Basic Information |
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Product Name: | GLYCINE ETHYL ESTER HYDROCHLORIDE |
CAS: | 623-33-6 |
English Synonyms: | ETHYL GLYCINATE HYDROCHLORIDE ; ETHYL 2-AMINOACETATE HYDROCHLORIDE ; GLYCINE ETHYL ESTER HYDROCHLORIDE ; GLY-OET-HCL ; H-GLY-OET HCL ; GEE HYDROCHLORIDE ; H-GLY-OET·HCL ; H-GLY-OET HYDROCHLORIDE ; GLYCINE ETHYL ESTER HYDROCHLORIDE SALT ; GLY-OET HCL ; GLYCINE ETHYL ESTER HCL ; GLYCINE,ETHYL ESTER,HYDROCHLORIDE ; ETHYL AMINOACETATE HYDROCHLORIDE ; AMINO-ACETIC ACID ETHYL ESTER HCL ; GLYCINE ETHYL ESTER HYDROCHLORIDE 99% ; AMINO-ACETIC ACID ETHYL ESTER HYDROCHLORIDE |
MDL Number.: | MFCD00012871 |
H bond acceptor: | 3 |
H bond donor: | 1 |
Smile: | CCOC(=O)CN.Cl |
InChi: | InChI=1S/C4H9NO2.ClH/c1-2-7-4(6)3-5;/h2-3,5H2,1H3;1H |
InChiKey: | InChIKey=TXTWXQXDMWILOF-UHFFFAOYSA-N |
Property |
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Melting Point: | 145-146 DEG C(LIT)/143~146℃ |
Comments: | APPLICATION: GLYCINE ETHYL ESTER (GEE) IS USED IN CONJUNCTION WITH N-(3-DIMETHYLAMINOPROPYL)-N'-ETHYLCARBODIIMIDE (EDC) FOR CARBOXYL-FOOTPRINTING STUDIES OF PROTEINS. THE GEE/EDC PROTOCOL EFFECTS SPECIFIC DERIVATIZATION OF GLUTAMATE AND ASPARTATE CARBOXYL SIDE CHAINS ON INTACT PROTEINS. THIS REACTION IS READILY DONE UNDER AQUEOUS CONDITIONS AT PHYSIOLOGICAL PH RTECS: MC0525000 UNSPSC: 12352100 WGK: 3 |
Safety information |
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Symbol: | GHS05 |
Signal word: | Danger |
Hazard statements: | H318 |
Precautionary statements: | P280-P305 + P351 + P338 |
hazard symbol: | Xi |
Risk Code: | R:41 |
Safe Code: | S:26-39 |
WGK Germany: | 3 |
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