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Encyclopedia results for Bis(trimethylsilyl)amine

Bis(trimethylsilyl)amine





Encyclopedia results for Bis(trimethylsilyl)amine

  1. Bis(trimethylsilyl)amine

    Chembox verifiedrevid 443984861 ImageFileL1 HMDS.png ImageNameL1 Structural formula of bis trimethylsilyl amine ImageFileR1 HMDS 3D.png ImageNameR1 Spacefill model of bis trimethylsilyl amine IUPACName Bis trimethylsilyl amine OtherNames Hexamethyldisilazane br 1,1,1,3,3,3 Hexamethyldisilazane Section1 Chembox Identifiers Abbreviations HMDS CASNo 999 97 3 CASNo Ref cascite correct CAS PubChem 13838 PubChem Ref Pubchemcite correct PubChem PubChem1 18913873 PubChem1 Comment amine PubChem1 Ref Pubchemcite correct PubChem PubChem2 45051731 PubChem2 Comment sodium PubChem2 Ref Pubchemcite correct PubChem PubChem3 45051783 PubChem3 Comment potassium PubChem3 Ref Pubchemcite correct PubChem ChemSpiderID 13238 ChemSpiderID Ref chemspidercite correct chemspider EINECS 213 668 5 UNNumber 2924, 3286 MeSHName Hexamethylsilazane RTECS JM9230000 SMILES C Si C C N Si C C C SMILES1 N Si C C C Si C C C StdInChI ... Bis trimethylsilyl amine is prepared by treatment of trimethylsilyl chloride with ammonia ... it hydrolysis hydrolyze s slowly in humid air. Alkali metal bis trimethylsilyl amides result from the deprotonation of bis trimethylsilyl amine. For example lithium bis trimethylsilyl amide LiHMDS is prepared ... Hexamethyldisilazan fr Bis trim thylsilyl amine ms Bis trimethylsilyl amine nl Hexamethyldisilazaan ... F 3 NFPA R 1 ExternalMSDS http hazard.com msds mf baker baker files h2066.htm External MSDS Bis trimethylsilyl amine also known as hexamethyldisilazane, or HMDS is an organosilicon compound with the molecular formula CH sub 3 sub sub 3 sub Si sub 2 sub NH. The molecule is a derivative of ammonia with trimethylsilyl ... sub 2 sub NLi C sub 4 sub H sub 10 sub Together with sodium bis trimethylsilyl amide NaHMDS and potassium bis trimethylsilyl amide KHMDS , LiHMDS is used as a non nucleophilic base . Reactions One of the uses ... 01 00936 0 pmid 11486868 ref See also Hexamethyldisiloxane Metal bis trimethylsilyl amides References ... s into trimethylsilyl ether s. HMDS can be used to silylate laboratory glassware and make it hydrophobic ...   more details



  1. Sodium bis(trimethylsilyl)amide

    and bis trimethylsilyl amine . Structure It is common that polar organometallic reagents are depicted ...Chembox Verifiedfields changed verifiedrevid 464400209 ImageFile1 Sodium bis trimethylsilyl amide.png ImageFile2 Sodium bis trimethylsilyl amide trimer from crystal.png PIN Sodium bis trimethylsilyl amide SystematicName Sodiobis trimethylsilyl amine OtherNames Sodium hexamethyldisilazane br Sodium hexamethyldisilazide Section1 Chembox Identifiers Abbreviations NaHMDS InChI 1 C6H18NSi2.Na c1 8 2,3 7 9 4,5 6 h1 6H3 q 1 1 rC6H18NNaSi2 c1 9 2,3 7 8 10 4,5 6 h1 6H3 InChIKey WRIKHQLVHPKCJU JSJAVMDOAQ InChI1 1S C6H18NSi2.Na c1 8 2,3 7 9 4,5 6 h1 6H3 q 1 1 InChIKey1 WRIKHQLVHPKCJU UHFFFAOYSA N CASNo Ref cascite changed ?? CASNo 1070 89 9 PubChem 2724254 PubChem Ref Pubchemcite ChemSpiderID 21169873 ChemSpiderID Ref chemspidercite correct chemspider EINECS 213 983 8 UNNumber UN 3263 SMILES C Si C C N Na Si C C C StdInChI Ref stdinchicite changed chemspider StdInChI 1S C6H18NSi2.Na c1 8 2,3 7 br 9 4,5 6 h1 6H3 q 1 1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey WRIKHQLVHPKCJU UHFFFAOYSA ... OtherAnions OtherCations Lithium bis trimethylsilyl amide Lithium br bis trimethylsilyl amide br LiHMDS br Potassium bis trimethylsilyl amide Potassium br bis trimethylsilyl amide OtherCpds Lithium diisopropylamide LDA br Potassium hydride KH Sodium bis trimethylsilyl amide is the chemical compound ... Trimethylsilyl TMS groups. ref Watson, B. T. Lebel, H. Sodium bis trimethylsilyl amide in Encyclopedia ... Bis trimethylsilyl amide year 1997 last1 Driess first1 Matthias last2 Pritzkow first2 Hans last3 .... To deprotonate precursors to give stable carbenes . See also Metal bis trimethylsilyl amides References Reflist Category Organosilicon compounds Category Bis trimethylsilyl amides Category Sodium compounds es Bis trimetilsilil amida de sodio fr Bis trim thylsilyl amidure de sodium id Natrium bis ... to give amine derivatives CH sub 3 sub sub 3 sub Si sub 2 sub NNa RBr &rarr CH sub 3 sub sub ...   more details



  1. Lithium bis(trimethylsilyl)amide

    also be prepared by deprotonation of bis trimethylsilyl amine with n butyllithium ref cite journal journal Inorg. Synth. doi 10.1002 9780470132395.ch6 title Lithium Bis Trimethylsilyl Amide and Tris Trimethylsilyl Amine series Inorganic Syntheses year 1966 last1 Amonoo Neizer first1 E. H. last2 ...chembox verifiedrevid 450703366 ImageFile LiHMDS.png ImageSize 200px IUPACName lithium bis trimethylsilyl azanide OtherNames Lithium bis trimethylsilyl amide and lithium hexamethyldisilazide Section1 Chembox Identifiers CASNo Ref cascite correct CAS CASNo 4039 32 1 PubChem SMILES C Si C C N Si C C C. Li Section2 Chembox Properties Formula C sub 6 sub H sub 18 sub LiNSi sub 2 sub MolarMass 167.326 g mol Appearance White solid Density MeltingPt 71 72 C BoilingPt 80 84 C 0.001 mm Hg Solubility decomposes in water SolubleOther THF, hexane Section3 Chembox Hazards MainHazards flammable FlashPt Autoignition Section8 Chembox Related OtherAnions OtherCations OtherFunctn Function OtherCpds Sodium bis trimethylsilyl amide , Potassium bis trimethylsilyl amide Lithium bis trimethylsilyl amide commonly abbreviated as LiHMDS , Li thium H exa M ethyl D i S ilazide is the organosilicon compound with the formula CH sub 3 sub sub 3 sub Si sub 2 sub NLi. This colourless solid is a strong non nucleophilic Base chemistry base used for deprotonation reactions and as a ligand . When solvent free, this compound ... journal Angew. Chem. title Assoziation im festen Zustand von Bis trimethylsilyl amidolithium und ..., Richard G. Copperthwaite Transition Metal Complexes of Bis Trimethyl silyl Amine 1,1,1,3,3,3 Hexamethyldisilazane ... with trimethylsilyl chloride gives tris trimethylsilyl amine, which features a planar, 3 coordinate ... 500px center See also Metal bis trimethylsilyl amides References references Category ... Bis trimethylsilyl amides Category Article Feedback 5 id Litium bis trimetilsilil amida nl Lithiumbis trimethylsilyl amide zh ...   more details



  1. Metal bis(trimethylsilyl)amides

    may be prepared from n butyllithium and bis trimethylsilyl amine ref cite journal journal Inorg. Synth. doi 10.1002 9780470132395.ch6 title Lithium Bis Trimethylsilyl Amide and Tris Trimethylsilyl ... chromium ref D. C. Bradley and Copperthwaite Transition Metal Complexes of Bis trimethylsilyl amine ... Complexes of Bis trimethylsilyl amine series Inorg. Synth. year 1978 volume 18 pages 112 120 doi ...File Hmds ligand.png thumb upright right The bis trimethylsilyl amide ligand Metal bis trimethylsilyl amides are coordination complex es of a metal cation with bis trimethylsilyl amide ligands. These ligands ... of metal amides . Metal bis trimethylsilyl amide complexes are lipophilic due to the ligand, thus ... Apart from group 1 and 2 complexes, a general method for preparing many metal bis trimethylsilyl ... year 1990 isbn 9780470132593 ref with one of the alkali metal bis trimethylsilyl amides ... may be removed by filtration. The resultant metal bis trimethylsilyl amide is often purified by distillation or sublimation. Group 1 complexes main lithium bis trimethylsilyl amide sodium bis trimethylsilyl amide potassium bis trimethylsilyl amide Lithium, sodium, and potassium bis trimethylsilyl amides ... journal Angew. Chem. title Assoziation im festen Zustand von Bis trimethylsilyl amidolithium ... Sodium Bis trimethylsilyl amide year 1997 last1 Driess first1 Matthias last2 Pritzkow first2 ... 10.1021 ic00333a029 journal Inorg. Chem. title Ion pairing in bis trimethylsilyl amido potassium The x ... Li hmds C sub 4 sub H sub 10 sub The direct reaction of these molten reactive metals with bis trimethylsilyl ... bases . In inorganic chemistry, these reagents are precursors for other bis trimethylsilyl amide complexes ... with the group 2 metals, but they may be prepared by reaction of tin II bis trimethylsilyl amide ... title Synthesis and spectroscopic properties of bis trimethylsilyl amides of the alkaline earth ... bis trimethylsilyl amide, but this method can result in potassium contamination. An improved ...   more details



  1. Bis(trimethylsilyl)acetamide

    Bis trimethylsilyl acetamide ? Talk Bis trimethylsilyl acetamide Requested move Discuss Current title is ambiguous. Orphan date February 2009 Chembox ImageFileL1 Bis trimethylsilyl acetamide.svg ImageSizeL1 121 ImageNameL1 Structural formula of E bis trimethylsilyl acetamide ImageFileR1 Bis trimethylsilyl acetamide 3D.png ImageSizeR1 121 ImageNameR1 Ball and stick model of E bis trimethylsilyl acetamide PIN N Trimethylsilyl 1 trimethylsilyloxyethanimine SystematicName Trimethylsilyl N trimethylsilyl ethanecarboximidate OtherNames N , O Bis trimethylsilyl acetamide Section1 Chembox Identifiers Abbreviations BSA CASNo 10416 59 8 CASNo Comment E CASNo Ref cascite correct ?? CASNo1 101660 04 2 CASNo Comment E , chlorotimethylsilane CASNo Ref cascite correct ?? PubChem 25248 PubChem Ref Pubchemcite correct PubChem PubChem1 6913588 PubChem1 Comment E PubChem1 Ref Pubchemcite correct PubChem PubChem2 5372922 PubChem2 Comment Z PubChem2 Ref Pubchemcite correct PubChem PubChem3 12412242 PubChem3 Comment E , tris sup 2 sup H sub 3 sub methyl , tris sup 2 sup H sub 3 sub methyl PubChem3 Ref Pubchemcite correct PubChem PubChem4 44149724 PubChem4 Comment E , chlorotimethylsilane PubChem4 Ref Pubchemcite correct PubChem ChemSpiderID 23581 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID1 4523073 ChemSpiderID1 Comment E ChemSpiderID1 Ref chemspidercite correct chemspider ChemSpiderID2 10516629 ChemSpiderID2 Comment Z ChemSpiderID2 Ref chemspidercite correct chemspider EINECS 233 892 7 UNNumber 2920 MeSHName N,O bis trimethylsilyl acetamide RTECS AK3000000 SMILES CC N Si C C ... S36 37 39 S45 Section8 Chembox Related Function Amide s OtherFunctn Dimethylacetamide Bis trimethylsilyl ... source of the trimethylsilyl group in Protecting group protecting functional groups in chemistry. See also Silyl ether Trimethylsilyl chloride References reflist Category Reagents for organic chemistry fr Bis trim thylsilyl ac tamide ...   more details



  1. Potassium bis(trimethylsilyl)amide

    ic00333a029 journal Inorg. Chem. title Ion pairing in bis trimethylsilyl amido potassium The x ray ... Timothy P. last3 Huffman first3 John C. volume 29 issue 8 pages 1584 1586 ref See also Metal bis trimethylsilyl ... compounds Category Bis trimethylsilyl amides organic compound stub de Kaliumhexamethyldisilizan ...   more details



  1. Bis(trimethylsilyl)mercury

    Chembox verifiedrevid 433184657 ImageFile Bis trimethylsilyl mercury.png ImageSize ImageFile1 Bis trimethylsilyl mercury 3D vdW.png IUPACName OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 21106419 InChI 1 2C3H9Si.Hg c2 1 4 2 3 h2 1 3H3 rC6H18HgSi2 c1 8 2,3 7 9 4,5 6 h1 6H3 InChIKey RKCQQCXHUWKHGR GMLBIIQIAA StdInChI Ref stdinchicite correct chemspider StdInChI 1S 2C3H9Si.Hg c2 1 4 2 3 h2 1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey RKCQQCXHUWKHGR UHFFFAOYSA N CASNo Ref cascite correct ?? CASNo PubChem SMILES C Si C C Hg Si C C C Section2 Chembox Properties Hg 1 Si 2 C 6 H 18 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Bis trimethylsilyl mercury a chemical reagent with formula CH sub 3 sub sub 3 sub Si Hg Si CH sub 3 sub sub 3 sub . Synthesis This compound was first synthesized by Wiberg et al. in 1963, by the reaction of trimethylsilyl bromide with sodium amalgam ref name wiberg cite journal doi 10.1002 anie.196305071 title Recent Developments in the Chemistry of Metal Silyls of the Type M SiR3 n year 1963 author Wiberg, E. journal Angew. Chem. Int. Ed. Engl. volume 2 pages 507 last2 Stecher first2 O. last3 Andrascheck first3 H. J. last4 Kreuzbichler first4 L. last5 Staude first5 E. issue 9 ref 2 Na Hg TMSBr &rarr TMS sub 2 sub Hg 2 NaBr Reactions On prolonged heating at 100 160 C, or when stood under light as an ethereal solution, it decomposes to hexamethyldisilane ref name wiberg TMS sub 2 sub Hg &rarr CH sub 3 sub sub 3 sub Si Si CH sub 3 sub sub 3 sub Hg Reaction with hydrogen chloride gives trimethylsilane and trimethylsilyl chloride ref name wiberg TMS sub 2 sub Hg HCl &rarr TMSH TMSCl Hg References references Further reading cite journal doi 10.1107 S0108270199016339 year 2000 month Apr author Pickett, Nl Just, O Vanderveer, Dg Rees, Ws, Jr title Reinvestigation of bis trimethylsilyl mercury volume 56 issue 4 pages 412 ...   more details



  1. Bis(trimethylsilyl)sulfide

    Chembox verifiedrevid 401708703 ImageFile Bis trimethylsilyl sulfide.png ImageSize 200 ImageName Stereo structural formula of bis trimethylsilyl sulfide PIN Bis trimethylsilyl sulfide SystematicName Trimethyl trimethylsilyl sulfanyl silane OtherNames Hexamethyldisilathiane Section1 Chembox Identifiers CASNo 3385 94 2 CASNo Ref cascite correct ?? PubChem 76920 PubChem Ref Pubchemcite correct PubChem ChemSpiderID 69371 ChemSpiderID Ref chemspidercite correct chemspider EINECS 222 201 4 UNNumber 1993 SMILES C Si C C S Si C C C SMILES1 S Si C C C Si C C C StdInChI Ref stdinchicite correct chemspider StdInChI 1S C6H18SSi2 c1 8 2,3 7 9 4,5 6 h1 6H3 InChI 1 C6H18SSi2 c1 8 2,3 7 9 4,5 6 h1 6H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey RLECCBFNWDXKPK UHFFFAOYSA N InChIKey RLECCBFNWDXKPK UHFFFAOYAN Beilstein 1698358 Section2 Chembox Properties C 6 H 18 Si 2 S 1 ExactMass 178.066774332 g mol sup 1 sup Appearance colourless liquid, stench Density 0.846 g cm sup 3 sup Solubility hydrolysis Solvent other solvents SolubleOther ethers br arenes BoilingPtC 163 RefractIndex 1.4586 Section3 Chembox Structure Dipole 1.85 Debye D Section7 Chembox Hazards ExternalMSDS MainHazards toxic RPhrases 10 23 24 25 SPhrases 36 37 39 45 Section8 Chembox Related OtherCpds B sub 2 sub S sub 3 sub , SiS sub 2 sub Bis trimethylsilyl sulfide is the chemical compound with the formula CH sub 3 sub sub 3 sub Si sub 2 sub S. Often abbreviated trimethylsilyl tms sub 2 sub S, this colourless, vile smelling liquid is a useful aprotic source of S sup 2 sup in chemical synthesis. ref cite journal author Matulenko, M. A. title Bis trimethylsilyl Sulfide journal Encyclopedia of Reagents for Organic Synthesis Ed L. Paquette , J. Wiley & Sons, New York year 2004. doi 10.1002 047084289. volume 1 pages 5 ref Synthesis The reagent is prepared by treating trimethylsilyl chloride with anhydrous sodium sulfide ... thione s. ref cite journal title Synthetic Applications of Bis trimethylsilyl sulfide Part II. Synthesis ...   more details



  1. Bis(trimethylsilyl)acetylene

    Chembox verifiedrevid 427189984 ImageFile Bis trimethylsilyl acetylene.png ImageSize ImageAlt IUPACName Bis trimethylsilyl acetylene OtherNames BTMSA Section1 Chembox Identifiers CASNo 14630 40 1 SMILES Section2 Chembox Properties Formula C sub 8 sub H sub 18 sub Si sub 2 sub MolarMass 170.40192 Appearance Colorless to white Liquid Density 0.791 g cm sup 3 sup MeltingPt 26 C BoilingPt 134.6 8.0 C Solubility 0.031 g L Section3 Chembox Hazards MainHazards Flammable, Irritant Bis trimethylsilyl acetylene BTMSA is an organosilicon compound with the formula C sub 2 sub Si CH sub 3 sub sub 3 sub sub 2 sub . It is a colorless liquid that is soluble in organic solvents. This compound is used as a surrogate for acetylene . BTMSA is prepared by treating acetylene with butyl lithium followed by addition of chlorotrimethylsilane ref Holmes, A. Sporikou, C. Org. Synth. 1993, Coll. Vol. 8, 606. ref ref Walton, D. R. M. Waugh, F., J. Organomet. Chem. 1972, 37, 45. DOI 10.1016 S0022 328X 00 89260 8 ref Li sub 2 sub C sub 2 sub 2 CH sub 3 sub sub 3 sub SiCl CH sub 3 sub sub 3 sub Si sub 2 sub C sub 2 sub 2 LiCl Applications BTMSA is used as a nucleophile in Friedel Crafts reaction Friedel Crafts type acylation s and alkylation s and a precursor to lithium trimethylsilylacetylide. The TMS groups can be removed with tetra n butylammonium fluoride TBAF and replaced with protons. BTMSA is also a useful reagent in cycloaddition reactions. Illustrating its versatility, BTMSA was used in a concise total synthesis of estrone . ref Curtain, M. L. Wang, C. Bis trimethylsilyl acetylene. e EROS. ref A key step in this synthesis was the formation of the steroidal skeleton, catalyzed by Cyclopentadienylcobalt dicarbonyl CpCo CO sub 2 sub BTMSA also serves as a ligand in organometallic chemistry . For example, it forms stable adduct s with metallocene s. ref Rosenthal, U. Burlakov, V. V. Arndt, P. Baumann, W. Spannenberg, A. Organometallics 2003, 22, 884. DOI 10.1021 om0208570 ref Cp sub 2 sub TiCl ...   more details



  1. Trimethylsilyl

    sub 3 sub are formed on the molecule. A couple of examples of trimethylsilylating agents include trimethylsilyl chloride and bis trimethylsilyl acetamide . Trimethylsilyl groups on a molecule have a tendency ...Chembox Name Trimethylsilyl radical ImageFile Trimethylsilyl group.PNG ImageSize 121 ImageName Skeletal formula of tetramethylsilane with some implicit hydrogens shown IUPACName Trimethylsilyl OtherNames Trimethyl sup 3 sup silyl Section1 Chembox Identifiers CASNo 16571 41 8 PubChem 123362 PubChem Ref Pubchemcite correct pubchem ChemSpiderID 109962 ChemSpiderID Ref chemspidercite correct chemspider SMILES C Si C C StdInChI 1S C3H9Si c1 4 2 3 h1 3H3 StdInChI Ref stdinchicite correct chemspider StdInChIKey ... . A trimethylsilyl group abbreviated TMS is a functional group in organic chemistry . This group ... inertness and a large molecular volume which makes them useful in a number of applications. A trimethylsilyl ... as well. Compounds with trimethylsilyl groups are not normally found in nature. Chemists sometimes use ... s, phenols , or carboxylic acid s by substituting a trimethylsilyl group for a hydrogen in the hydroxyl ... to certain functional groups in a reactant molecule, trimethylsilyl groups may also be used as temporary ... phase with trimethylsilyl groups is referred to as endcapping . In an NMR spectroscopy NMR spectrum , signals from atoms in trimethylsilyl groups in compounds will commonly have chemical shifts close ... can be isolated when enveloped by bulky trimethylsilyl groups. This effect can be observed in tetrahedrane s. Super silyl groups Image Tri trimethylsilyl silyl.png 150px right the Tri trimethylsilyl ... two varieties A silicon group connected to three trimethylsilyl groups makes a tri trimethylsilyl ... ja0693542 ref ref Tris trimethylsilyl silyl Governed Aldehyde Cross Aldol Cascade Reaction Boxer ... ether by reaction with tris trimethylsilyl silane and triflic acid with evolution of hydrogen. The aldol reaction is catalyzed by Bistriflimide bis trifluoromethane sulfonimide ref Image Supersilylapplication.png ...   more details



  1. Amine

    other uses class wikitable style margin auto 1em auto 1em align right Primary amine Secondary amine Tertiary amine center Image Primary amine 2D general.png 100px primary amine center center Image Secondary amine 2D general.png 100px secondary amine center center Image Amine 2D general.png 100px tertiary amine center Amines are organic compound s and functional group s that contain a base chemistry .... ref McMurray3rd ref Important amines include amino acid s, biogenic amine s, trimethylamine , and aniline ... . N methylpiperidine is a cyclic tertiary amine. It is also possible to have four alkyl substituents ... amine Aromatic amines have the nitrogen atom connected to an aromatic ring as in aniline s. The aromatic ring decreases the base chemistry alkalinity of the amine, depending on its substituents. The presence of an amine group strongly increases the reactivity of the aromatic ring, due to an electron ... the prefix amino or the suffix amine. The prefix N shows substitution on the nitrogen atom. An organic ... amines are named with the suffix amine . br Image Methylamine.png 100px br methylamine Higher amines ... br or sometimes pent 2 yl amine or pentane 2 amine Physical properties Hydrogen bonding significantly ... 200px right amine inversion Chirality Amines of the type NHRR and NRR R are chirality chemistry .... The degree of solvation of the protonated amine. The nitrogen atom features a lone electron .... Thus the basicity of an amine may be expected to increase with the number of alkyl groups on the amine ... to trimethyl amine due to the predominance of steric hindrance offered by the three methyl ... on the aromatic ring, and their positions relative to the amine group may also considerably ... form is not well solvated. For this reason the parent amine is less basic than expected. In the case ... or iron with an acid . valign top Amine alkylation valign top haloalkane valign top Delepine reaction ... specific for aryl amines valign top Menshutkin reaction valign top tertiary amine reaction product ...   more details



  1. BIS

    wiktionary bis Bis is a prefix or suffix designating the second instance of a thing, thus preceding ter . Bis can also refer to Bis band , a Scottish pop band Bis magazine Bis magazine , a high teens magazine published by Kobunsha of Japan The 14 bis , an early fixed wing aircraft derived by Alberto Santos Dumont from his Number 14 airship aircraft hybrid Bis is used in chemical nomenclature sometimes instead of the prefix di Bis Bisulfite or Bisulfite sequencing in Genomics, to differentiate between methylated and non methylated cytosine in the Genome Epigenetic . BIS may refer to Bank for International Settlements , an international organization for cooperation among Central Banks Bureau of Industry and Security , a component of the United States Department of Commerce The Department for Business, Innovation and Skills of the United Kingdom government Bureau of Indian Standards Benevolent Irish Society British Interlingua Society , a society that promotes Interlingua in the UK British Interplanetary Society , the oldest space advocacy society Best in Show, the highest placing in a conformation dog show , cat show, or other show or exposition Bezpe nostn informa n slu ba, the Czech Security Information Service BIS band , or Believe in Style, a Japanese pop punk band BIS Records , a Scandinavian record label focusing on classical works Bislama language ISO 639 alpha 3 code bis Bismarck Municipal Airport IATA code BIS Block Island Sound Bloque Institucional Social D mocrata Bohemia Interactive Studio Science & Technology Barratt Impulsivity Scale , a self administered test to measure impulsivity Behavioural Inhibition System BIS monitor or bispectral index, to assess the depth of anaesthesia Business Information Server , a new name for the Unisys MAPPER product Boot Integrity ... , a middle school in Burlingame, California disambiguation cs BIS de BIS fr BIS ko BIS it BIS nl BIS ja BIS no BIS ru fi Bis sv Bis ...   more details



  1. Trimethylsilyl chloride

    chembox verifiedrevid 412832233 Name Trimethylsilyl chloride ImageFile tmscl stick2.png ImageSize 150px ImageName TMSCl ImageFileL1 Trimethylsilyl chloride from xtal 2006 3D balls.png ImageSizeL1 150px ImageNameL1 Ball and stick model of the trimethylsilyl chloride molecule ImageFileR1 Trimethylsilyl chloride from xtal 2006 3D vdW.png ImageSizeR1 150px ImageNameR1 Space filling model of the trimethylsilyl chloride molecule IUPACName Trimethylsilyl chloride OtherNames Chlorotrimethylsilane br TMSCl ... 400 C Section8 Chembox Related Function halosilane s OtherFunctn Trimethylsilyl fluoride br Trimethylsilyl bromide br Trimethylsilyl iodide br Trimethylsilyl chloride , also known as chlorotrimethylsilane ... the compound is readily available commercially. Uses Trimethylsilyl chloride has variety of uses in chemistry, both as a source of the trimethylsilyl group, and as an anhydrous source of chlorides. Functional groups such as alcohols and amine s readily undergo reaction with trimethylsilyl chloride, giving trimethylsilyl ether s and trimethylsilyl amine s. These new groups can be used as protecting group s for the original functional group, however the lability of the trimethylsilyl group restricts their utility. Trimethylsilyl ation can also be used to increase the volatility of a compound, enabling gas chromatography of normally non volatile substances such as glucose . Trimethylsilyl chloride also reacts with metal acetylides to give trimethylsilyl alkynes , which are useful protected forms of alkynes. The reaction of trimethylsilyl chloride with alcohols gives rise to an equivalent ... isable aldehyde s, ketone s and ester s are converted to trimethylsilyl enol ether s. Despite their hydrolytic ... with an alcohol group at the alpha carbon. The trimethylsilyl enol ether s can also be used as masked enolate equivalents in the Mukaiyama aldol addition . Trimethylsilyl chloride can also be used as a starting material to prepare other trimethylsilyl halides and pseudohalide s, such as Trimethylsilyl ...   more details



  1. Trimethylsilyl azide

    chembox verifiedrevid 418908466 ImageFile Trimethylsilyl azide.png ImageSize 120px IUPACName Azido trimethyl silane OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 70747 InChI 1 C3H9N3Si c1 7 2,3 6 5 4 h1 3H3 InChIKey SEDZOYHHAIAQIW UHFFFAOYAJ StdInChI Ref stdinchicite correct chemspider StdInChI 1S C3H9N3Si c1 7 2,3 6 5 4 h1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey SEDZOYHHAIAQIW UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 4648 54 8 PubChem 78378 Beilstein 1903730 EINECS 225 078 5 SMILES N N N Si C C C Section2 Chembox Properties C 3 H 9 N 3 Si 1 Appearance clear liquid, color less Density 0.8763 g cm3 20 C MeltingPt 95 C BoilingPt 52 53 C at 175mmHg 92 95 C at 760mmHg Solubility Section7 Chembox Hazards ExternalMSDS EUClass EUIndex MainHazards NFPA H 4 NFPA F 3 NFPA R 0 NFPA O RPhrases R11 , R23 , R24 , R25 , R29 , R50 , R51 , R52 , R53 SPhrases S16 , S29 , S36 , S37 , S45 , S57 , S8 , RSPhrases FlashPt 6 C Autoignition 300 C ExploLimits LD50 PEL Trimethylsilyl azide CH sub 3 sub sub 3 sub SiN sub 3 sub is a chemical compound used as a reagent in organic chemistry . Preparation Trimethylsilyl azide is commercially available. It may be prepared by the reaction of trimethylsilyl chloride and sodium azide ref OrgSynth author L. Birkofer and P. Wegner title Trimethylsilyl azide collvol 6 collvolpages 1030 year 1988 prep cv6p1030 ref TMSCl NaN sub 3 sub &rarr TMSN sub 3 sub NaCl TMS CH sub 3 sub sub 3 sub Si Applications It is considered a safer replacement for hydrazoic acid in many reactions. It will however over time hydrolysis hydrolyze to hydrogen azide and therefore it must be stored free of moisture ref cite journal doi 10.1055 s 2007 984895 title Trimethylsilyl Azide TMSN sub 3 sub A Versatile Reagent in Organic Synthesis year 2007 author Jafarzadeh, Mohammad journal Synlett volume 2007 issue 13 pages 2144 ref It has been used in the Oseltamivir total synthesis . Safety Trimethylsilyl ...   more details



  1. Trimethylsilyl cyanide

    chembox Watchedfields changed verifiedrevid 412009295 ImageFileL1 Trimethylsilyl cyanide skeletal.png ImageSizeL1 120px ImageFileR1 Trimethylsilyl cyanide 3D vdW.png ImageSizeR1 120px IUPACName trimethylsilylformonitrile OtherNames Cyanotrimethylsilane TMS cyanide Trimethylsilylnitrile Trimethylsilanecarbonitrile Trimethylsilylcarbonitrile Section1 Chembox Identifiers Abbreviations TMSCN ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 74110 InChI 1 C4H9NSi c1 6 2,3 4 5 h1 3H3 InChIKey LEIMLDGFXIOXMT UHFFFAOYAM StdInChI Ref stdinchicite correct chemspider StdInChI 1S C4H9NSi c1 6 2,3 4 5 h1 3H3 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey LEIMLDGFXIOXMT UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 7677 24 9 EINECS PubChem 82115 SMILES C Si C C C N InChI RTECS MeSHName ChEBI Ref ebicite correct EBI ChEBI KEGG Ref keggcite correct kegg KEGG ATCCode Section2 Chembox Properties C 4 H 9 Si 1 N 1 Appearance Density 0.793 g mL at 20 C MeltingPtCL 8 MeltingPtCH 11 Melting notes BoilingPtCL 114 BoilingPtCH 117 Boiling notes Solubility organic solvents SolubleOther reacts with water Solvent pKa pKb IsoelectricPt SpecRotation RefractIndex 1.392 Viscosity Dipole Section3 Chembox Structure CrystalStruct Coordination MolShape Dipole Section7 Chembox Hazards ExternalMSDS EUClass EUIndex MainHazards NFPA H NFPA F NFPA R NFPA O RPhrases R11 R26 27 28 R29 SPhrases S16 S36 37 39 S45 RSPhrases FlashPt convert 1 C F Autoignition ExploLimits PEL Section8 Chembox Related OtherAnions OtherCations OtherFunctn Function OtherCpds Trimethylsilyl cyanide is the chemical compound with the chemical formula formula CH sub 3 sub sub 3 sub SiCN. This volatile liquid consists of a cyanide group, that is CN, attached to a trimethylsilyl group. The molecule is used in organic ... and trimethylsilyl chloride ref OrgSynth author Livinghouse, T. title Trimethylsilyl Cyanide Cyanosilation ... Trimethylsilyl cyanide is treated with care since it hydrolyzes to give hydrogen cyanide 2 CH sub ...   more details



  1. Amine Chermiti

    Use dmy dates date March 2011 Infobox football biography fullname Mohamed Amine Chermiti image File Amine Chermiti Hertha BSC Berlin 2 .jpg 175px dateofbirth birth date and age 1987 12 26 df yes cityofbirth Sfax countryofbirth Tunisia height height m 1.76 precision 0 ref cite web url http www.transfermarkt.de de spieler 61682 chermiti mohamed amine profil.html title 9 Mohamed Amine Chermiti language German publisher transfermarkt.de accessdate 5 March 2011 ref currentclub FC Z rich clubnumber 9 position Forward association football Striker youthyears1 2002 2005 youthclubs1 Jeunesse Sportive Kairouanaise JS Kairouan years1 2005 2006 clubs1 Jeunesse Sportive Kairouanaise Kairouan caps1 10 goals1 ... 20 30, 21 November 2011 UTC ntupdate 23 59, 22 January 2010 UTC Mohamed Amine Chermiti born 26 December ... sport hertha bsc amine chermiti der kleine kommt zurueck 1370116.html title Amine Chermiti ... Jeddah Al Ittihad for one year ref cite web url http www.berlin aktuell.de hertha bsc amine chermiti auf leihbasis nach saudi arabien id1347.html title Hertha BSC Amine Chermiti auf Leihbasis nach Saudi ... ref and returned on 30 June 2010. ref cite web url http bazonline.ch sport fussball FCZ pokert um Amine Chermiti story 28122137 title FCZ pokert um Amine Chermiti language German publisher Basler Zeitung ... with FC Z rich ref cite web url http www.fcz.ch profis news detail.htm?id 885 title Amine Chermiti unterschreibt bis Sommer 2014 language German publisher FC Z rich date 5 July 2010 accessdate 5 March ... team . ref nfteams 24077 ref References Reflist External links Fussballdaten chermitiamine Amine ... squad Persondata Metadata see Wikipedia Persondata . NAME Chermiti, Mohamed Amine ALTERNATIVE NAMES ... PLACE OF DEATH DEFAULTSORT Chermiti, Mohamed Amine Category 1987 births Category Living people ... de Amine Chermiti es Amine Chermiti fr Mohamed Amine Chermiti it Amine Chermiti lt Amine Chermiti ja pl Mohamed Amine Chermiti ru , fi Amine Chermiti ...   more details



  1. Amine (disambiguation)

    distinguish Anime wiktionary amine amino Amine or Amino may refer to In chemistry Amine , an organic compound and a type of functional group that contains nitrogen as the key atom An Amino acid , a molecule that contains both amine and carboxyl functional groups An Amino alcohol , a molecule that contains both an amine and an alcohol functional group An Amino sugar , a sugar that contains an amine group in place of a hydroxyl group In other uses Amine , an alternate spelling of the Arabic male name Amin name , female form Amina Amine Women s magazine , the largest online magazine for Danish women Amine singer , Moroccan born French R&B singer, full name Amine Mounder Yoshihiko Amino 1929 2004 , a Japanese historian See also Ammine , the ammonia ligand, not to be confused with the amine functional group NH2, chemical formula for amine functional group with subscripted 2 , refers to National Highway 2, as indicated in List of highways numbered 2 disambiguation Amin disambiguation disambig fa fr Amine ...   more details



  1. Amine Lecomte

    Infobox football biography playername Amine Lecomte image fullname Amine Lecomte Addani birth date birth date and age 1990 4 26 cityofbirth Reims countryofbirth France height convert 1.94 m abbr on currentclub Lekhwiya clubnumber 40 position Goalkeeper association football Goalkeeper youthyears1 youthclubs1 FC Sochaux Montb liard years1 2006 2010 clubs1 FC Sochaux Montb liard caps1 ? goals1 ? years2 2010 clubs2 Lekhwiya caps2 3 goals2 0 nationalyears1 nationalteam1 nationalcaps1 nationalgoals1 pcupdate ntupdate Amine Lecomte born 26 April 1990 is a Morocco Moroccan Association football footballer who plays as a Goalkeeper association football goalkeeper for Lekhwiya in Qatar . Career Amine won the Qatar League with his club Lekhwiya in the 2010 2011 season. The team, coached by Djamel Belmadi , included Bakari Kone , Aruna Dindane , Abdeslam Ouaddou , Jasur Hasanov and Karim Boudiaf , among others. International career In August 2011, Amine was called up by Eric Gerets in the Morocco national football team for the friendly game against Senegal . However, Amine had to call off few days before the game because of an injury. ref http www.theatlaslions.com news center 4552104279 Senegal vs Morocco Iassam Badda replaces Amine Lecomte 32474 Senegal vs Morocco Iassam Badda replaces Amine Lecomte ref References reflist External links http www.qsl.com.qa users Teams popup.aspx?pregno 17981 QSL.com.qa Player Profile http aminel a.skyrock.com Official Blog Persondata Metadata see Wikipedia Persondata . NAME Lecomte, Amine ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH 26 April 1990 PLACE OF BIRTH Reims , France DATE OF DEATH PLACE OF DEATH DEFAULTSORT Lecomte, Amine Category 1990 births Category Living people Category People from Reims Category French people of Moroccan descent Category French footballers Category Qatar Stars League players fr Amine Lecomte Addani ...   more details



  1. Amine sulfotransferase

    enzyme Name amine sulfotransferase EC number 2.8.2.3 CAS number 9026 08 8 IUBMB EC number 2 8 2 3 GO code 0047685 image width caption In enzymology , an amine sulfotransferase EC number 2.8.2.3 is an enzyme that catalysis catalyzes the chemical reaction 3 phosphoadenylyl sulfate an amine math rightleftharpoons math adenosine 3 ,5 bisphosphate a sulfamate Thus, the two substrate biochemistry substrates of this enzyme are 3 phosphoadenylyl sulfate and amine , whereas its two product chemistry products are adenosine 3 ,5 bisphosphate and sulfamate . This enzyme belongs to the family of transferase s, specifically the sulfotransferases, which transfer sulfur containing groups. The systematic name of this enzyme class is 3 phosphoadenylyl sulfate amine N sulfotransferase . Other names in common use include arylamine sulfotransferase , and amine N sulfotransferase . This enzyme participates in sulfur metabolism . References reflist 1 cite journal author Ramaswamy SG, Jakoby WB date 1987 title Amine N sulfotransferase journal J. Biol. Chem. volume 262 pages 10039&ndash 43 pmid 3475273 issue 21 cite journal author Roy, AB date 1960 title The enzymic synthesis of aryl sulphamates journal Biochem. J. volume 74 pages 49&ndash 56 transferase stub Category EC 2.8.2 Category Enzymes of unknown structure ...   more details



  1. Amine oxide

    Image Amine Oxides General Formulae.png thumb right 170px General structure of an amine oxide An amine oxide , also known as amine N oxide and N oxide , is a chemical compound that contains the functional ... sub 3 sub N O. In the strict sense the term amine oxide applies only to oxides of tertiary amine s. Sometimes it is also used for the analogous derivatives of primary and secondary amines. Examples of amine ... C, and N Methylmorpholine N oxide N methylmorpholine N oxide , which is an oxidant. Properties Amine ... chain alkyl amine oxides are used as nonionic surfactant s and foam stabilizers. Amine oxides are highly ... s. Small amine oxides are very hydrophilic and have an excellent water molecule water solubility and a very poor solubility in most organic solvent s. Amine oxides are weak base chemistry bases with a Acid ... ic hydroxylamine s, upon protonation at a pH below their p K sub a sub . Synthesis Amine oxides are prepared ...?VIEW MANUSCRIPT&MSID 180 Link ref . Reactions Pyrolytic elimination. Amine oxides, when heated ... elimination . Reduction to amines. Amine oxides are readily converted to the parent amine by common ... Czako ISBN 0 12 429785 4 ref Image PolonovskiReaction.svg Polonovski reaction Metabolites Amine oxides ... , Zolmitriptan , and morphine . Amine oxides of chemotherapy anti cancer drugs have been developed ... drug. See also Functional group Amine , NR sub 3 sub Hydroxylamine , NR sub 2 sub OH Phosphine ... TEMPO 2,2,6,6 Tetramethylpiperidine 1 oxyl , a stable amine oxide radical References reflist External links http www.cem.msu.edu reusch VirtualText amine2.htm Chemistry of amine oxides http nanoparticles.org ... aminehomepage.html The amine oxides homepage http www.chem.qmul.ac.uk iupac class oneN.html Nomenclature of nitrogen compounds http www.iupac.org goldbook A00273.pdf IUPAC definition pdf DEFAULTSORT Amine Oxide Category Amine oxides Category Functional groups de Aminoxide es Nitr xido fr Amine oxyde nl Amine oxide ja pl Tlenki amin pt xido de amina zh ...   more details



  1. Amine Amamou

    Orphan date November 2010 Infobox football biography image name Amine Amamou fullname Amine Amamou birth date birth date and age 1987 4 20 birth place Marrakech , Morocco height height m 1.83 currentclub Kawkab Marrakech clubnumber position Forward youthyears1 ? 2007 youthclubs1 Kawkab Marrakech years1 2007 clubs1 Kawkab Marrakech caps1 14 goals1 1 nationalyears1 nationalteam1 nationalcaps1 nationalgoals1 pcupdate april 16, 2009 ntupdate October 17, 2008 Amine Amamou is a Morocco Moroccan football soccer footballer . He usually plays as forward association football forward . Amamou is currently attached to Kawkab Marrakech . ref cite web publisher Kawkabi.com title Info Joueur Amine Amamou url http www.kawkabi.com index.php component option,com joomleague Itemid,54 func,showPlayer p,5 pid,45 accessdate 2009 08 01 Dead link date October 2010 bot H3llBot ref References reflist Persondata Metadata see Wikipedia Persondata . NAME Amamou, Amine ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH April 20, 1987 PLACE OF BIRTH Marrakech , Morocco DATE OF DEATH PLACE OF DEATH DEFAULTSORT Amamou, Amine Category Moroccan footballers Category 1987 births Category Living people Category People from Marrakech Morocco footy bio stub ...   more details



  1. Hussein Amine

    BLP sources date February 2008 Infobox football biography name Hussein Amine image fullname Hussein Hassan Amine height 1.80 m birth date Birth date and age 1985 4 15 cityofbirth countryofbirth Lebanon currentclub Al Ansar FC Al Ansar clubnumber 13 position Defender football Defender years1 2002 clubs1 Al Ansar FC Al Ansar caps1 64 goals1 2 nationalyears1 ?? nationalteam1 flagicon LIB Lebanon national football team Lebanon nationalcaps1 ?? nationalgoals1 0 Hussein Hassan Amine born 15 March 1985 is a Lebanon Lebanese Football soccer footballer , who plays for the Lebanese side Al Ansar FC in the Defence. He Began with Al Ansar when he signed in 2002. His First official appearance was against Al Nejmeh in a 0 1 loss on September 9, 2003. His first official goal was in a 2 0 victory over Al Hikma on March 5, 2005. International career Hussein plays for Lebanon. External links nfteams 24576 Al Ansar Squad Persondata Metadata see Wikipedia Persondata . NAME Amine, Hussein ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH 1985 04 15 PLACE OF BIRTH Lebanon DATE OF DEATH PLACE OF DEATH DEFAULTSORT Amine, Hussein Category 1985 births Category Living people Category Lebanese footballers Hussein Amine Category Lebanon international footballers Lebanon footy bio stub pt Hussein Amine ...   more details



  1. Amine Rzig

    MedalTableTop MedalSport Men s Basketball MedalCountry TUN MedalCompetition FIBA Africa Championship African Championships MedalBronze 2009 FIBA Africa Championship 2009 Libya Tunisia MedalGold 2011 FIBA Africa Championship 2011 Madagascar Tunisia MedalBottom Amine Rzig born August 25, 1980 is a Tunisia n basketball player currently playing for Geish Army in the Egyptian Basketball League. ref http www.fiba.com pages eng fc news lateNews arti.asp?newsid 31619 Amine Rzig shouldering Tunisia challenge at FIBA.com ref Rzig is a member of the Tunisia national basketball team that finished third at the 2009 FIBA Africa Championship to qualify for the country s first FIBA World Championship . Rzig averaged 16.4 PPG and 5.4 RPG for the Tunisians en route to being named to the All Tournament team. ref http www.fiba.com pages eng fc news lateNews fibaEven fibaAfriCham p newsid 31702 arti.html LBA Gomes Leads All Star Team ref ref http libya2009.fiba.com pages eng fe 09 fafcm player p eid 4047 pid 60270 sid 6599 tid 375 profile.html Amine Rzig Profile at FIBA.com ref Highlights for Rzig included scoring a team leading 20 points in the bronze medal game against Cameroon to lead the Tunisians to the 2010 FIBA World Championship . ref http www.eurobasket.com boxScores African 20Championships 2009 0815 TUN CMR.asp Tunisia vs. Cameroon report at Eurobasket.com ref References reflist Tunisia squad FIBA Africa Championship 2009 Tunisia Squad 2010 FIBA World Championship Tunisia squad 2011 FIBA Africa Championship Persondata Metadata see Wikipedia Persondata . NAME Rzig, Amine ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH August 25, 1980 PLACE OF BIRTH DATE OF DEATH PLACE OF DEATH DEFAULTSORT Rzig, Amine Category Tunisian basketball players Category 1980 births Category Living people Tunisia basketball bio stub fr Amine Rzig fi Amine Rzig ...   more details



  1. Amine (singer)

    Infobox musical artist image See Wikipedia WikiProject Musicians name Amine image size background solo singer alias origin Casablanca, Morocco genre R&B years active label Capitol Records Capitol , EMI associated acts website http www.aminemusic.com Amine current members past members notable instruments Amine Mounder Arabic language Ar is a French Moroccan R&B singer born in Casablanca, Morocco . He is known for his singular music style, Ra n B , which is a mix of R&B and Ra . His biggest hits are Sobri notre Destin , a duet with French singer Leslie singer Leslie , and J voulais . Both reached the 1 spot on the French singles chart. Discography Albums Au del des r ves 31 December 2005 16 FR Autour d eux April 2009 89 FR Singles 2004 Sobri feat.leslie Bourgoin 2005 Ma Vie 15 FR 2006 Finiki writted by Mouad Hamich Prod.by Dj kore & Bellek 3 MA 2006 J voulais 1 FR 2006 My Girl Amine song My Girl 29 FR 2006 Sobri 2 feat.leslie Bourgoin 2009 Juste un oui 2009 Juste un oui arabe version writted by Mouad Hamich Prod.by Dj kore & Bellek 13 2009 Tu ne m as pas laiss le choix 2009 Maat Lohiche feat. Cheb Bilal External links fr icon http www.aminemusic.com Official website fr icon http www.emi.fr EMI Music France fr icon http www.wikimusique.net index.php Amine Amine Author Mario Scolas on WikiMusique GNU fr icon http beurgeoisie.fr La Beurgeoisie The French website for successful Beurs . Use dmy dates date September 2010 Persondata Metadata see Wikipedia Persondata . NAME Amine ALTERNATIVE NAMES SHORT DESCRIPTION DATE OF BIRTH PLACE OF BIRTH DATE OF DEATH PLACE OF DEATH DEFAULTSORT Amine Category French male singers Category French language singers Category Living people Category People from Casablanca Category French people of Moroccan descent Category French people of Arab descent France singer stub fr Amine chanteur ...   more details



  1. Polyethylene amine

    Polyethylene amine is a polymer of aziridine with the molecular formula CH sub 2 sub CH sub 2 sub NH sub n sub . It is a structural analogue of polyethylene glycol with NH in place of oxygen atoms. It is produced by the polymerization of aziridine. Oligomeric polyethylene amines with a small number of units are used as Curing chemistry curing agents for epoxy resin s. They are water soluble. The gelling properties of higher polyethylene amines are useful for resin formulas that require high viscosity during application and curing. Polyethylene amine can form gel s. Due to the rich content of easily protonated amine groups, in acidic solutions it behaves as a polyelectrolyte polycation . Polyethylene amine may have applications as a component of ion exchange resin s. High selectivity semipermeable membranes, permeable for carbon dioxide and retaining oxygen , can be made from this material as well. These are important for life support systems. http www.dsls.usra.edu meetings bio2001 pdf EVAcomplete.pdf See also Ethylene diamine Diethylene triamine Triethylene tetramine Polyethylenimine Category Organic polymers Category Polyelectrolytes Category Polyamines ...   more details




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