Basic information Safety Supplier Related

Ethyl acetimidate hydrochloride

Basic information Safety Supplier Related

Ethyl acetimidate hydrochloride Basic information

Product Name:
Ethyl acetimidate hydrochloride
Synonyms:
  • EAH
  • ETHYL ACETAMIDATE HCL
  • ETHYL ACETIMIDATE HYDROCHLORIDE
  • 1-ethoxyethylideneammonium chloride
  • ACETIMIDIC ACID ETHYL ESTER
  • ETHYL ACETIMIDATE HCL
  • Ethyl acetimidate hydrochloride, 98.5%
  • EthyliminoacetateHCl
CAS:
2208-07-3
MF:
C4H10ClNO
MW:
123.58
EINECS:
218-631-7
Product Categories:
  • Amidates/Imidates
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
2208-07-3.mol
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Ethyl acetimidate hydrochloride Chemical Properties

Melting point:
112-114 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
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
Ethanimidic acid, ethyl ester, hydrochloride (2208-07-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
3-10-21
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29252900

MSDS

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Ethyl acetimidate hydrochloride Usage And Synthesis

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.

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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