| Identification | More | [Name]
Ethyl acetimidate hydrochloride | [CAS]
2208-07-3 | [Synonyms]
EAH
ETHYL ACETAMIDATE HCL
ETHYL ACETIMIDATE HYDROCHLORIDE
1-ethoxyethylideneammonium chloride
ACETIMIDIC ACID ETHYL ESTER
ETHYL ACETIMIDATE HCL
Ethyl acetimidate hydrochloride, 98.5%
EthyliminoacetateHCl
ethylacetimidate,HCl98.5%
ethyl iminoacetate hydrochloride
Ethanimidic acid, ethyl ester, hydrochloride
(1-Ethoxyethane)imine hydrochloride
1-Ethoxy-1-iminoethane·hydrochloride | [EINECS(EC#)]
218-631-7 | [Molecular Formula]
C4H10ClNO | [MDL Number]
MFCD00012572 | [Molecular Weight]
123.58 | [MOL File]
2208-07-3.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
112-114 °C(lit.) | [storage temp. ]
2-8°C | [solubility ]
water: soluble50mg/mL, clear, colorless | [form ]
Crystalline Powder | [color ]
White | [Water Solubility ]
Soluble in water (50mg/L). | [Sensitive ]
Moisture Sensitive | [BRN ]
3552401 | [Stability:]
Hygroscopic, Moisture Sensitive | [InChIKey]
WGMHMVLZFAJNOT-UHFFFAOYSA-N | [CAS DataBase Reference]
2208-07-3(CAS DataBase Reference) | [EPA Substance Registry System]
2208-07-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [F ]
3-10-21 | [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29252900 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
Ethyl acetimidate hydrochloride was used in preparation of amidinated carbonic anhydrase via chemical modification of human erythrocyte carbonic anhydrase. It was also used in synthesis of methyl 2-methyl-2-thiazoline-4-carboxylate hydrochloride. | [Uses]
Ethyl acetimidate hydrochloride was used in preparation of amidinated carbonic anhydrase via chemical modification of human erythrocyte carbonic anhydrase. It was also used in synthesis of methyl 2-methyl-2-thiazoline-4-carboxylate hydrochloride. | [Purification Methods]
Recrystallise the hydrochloride by dissolving it in the minimum volume of super dry EtOH and adding dry Et2O or from dry Et2O. Dry it in a vacuum and store it in a vacuum desiccator with P2O5. Alternatively it could be crystallised from EtOH (containing a couple of drops of ethanolic HCl) and adding dry Et2O. Filter and dry it in a vacuum desiccator over H2SO4 and NaOH. [Pinner Chem Ber 16 1654 1883, Glickman & Cope J Am Chem Soc 67 1020 1945, Chaplin & Hunter J Chem Soc 1118 1937, McElvain & Schroeder J Am Chem Soc 71 40 1949, McElvain & Tate J Am Chem Soc 73 2233 1951, Methods Enzymol 25 585 1972, Beilstein 2 III 418.] |
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