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Ethyl acetimidate hydrochloride

Names

[ CAS No. ]:
2208-07-3

[ Name ]:
Ethyl acetimidate hydrochloride

[Synonym ]:
Ethanimidic acid, ethyl ester, hydrochloride (1:1)
Ethyl ethanimidoate hydrochloride (1:1)
ACETIMIDIC ACID ETHYL ESTER
EthyliminoacetateHCl
Ethyl ethanimidoate
MFCD00012572
1-ethoxyethylideneammonium chloride
EAH
Ethyl ethanimidate hydrochloride (1:1)
ethyl ethaneimidate monohydrochloride
ethyl acetimidate monohydrochloride
EINECS 218-631-7
ethyl acetamidate hydrochloride
ETHYL ACETAMIDATE HCL
ethyl ethanimidate hydrochloride
ETHYL ACETIMIDATE HCL
ethanimidic acid ethyl ester hydrochloride
ethyl iminoacetate hydrochloride

Chemical & Physical Properties

[ Density]:
0.89g/cm3

[ Boiling Point ]:
57.3ºC at 760 mmHg

[ Melting Point ]:
112-114 °C(lit.)

[ Molecular Formula ]:
C4H10ClNO

[ Molecular Weight ]:
123.581

[ Flash Point ]:
22.3ºC

[ Exact Mass ]:
123.045090

[ PSA ]:
33.08000

[ LogP ]:
1.92180

[ Index of Refraction ]:
1.58 (20ºC)

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925290090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Involvement of lysine residues in the binding of ovine chorionic somatomammotropin to lactogenic and somatotropic receptors.

FEBS Lett. 166(2) , 352-6, (1984)

The biological activities of several ovine chorionic somatomammotropin (oCS) derivatives obtained by chemical modification of the lysine residues were studied by radioreceptor assays using rabbit mamm...

Rapid removal of acetimidoyl groups from proteins and peptides. Applications to primary structure determination.

Biochem. J. 199(2) , 335-40, (1981)

Methylamine buffers can be used for the rapid quantitative removal of acetimidoyl groups from proteins and peptides modified by treatment with ethyl or methyl acetimidate. The half-life for displaceme...

Studies on the structure of the ligand-binding site of the brain D1 dopamine receptor.

Biochem. Pharmacol. 44(2) , 325-34, (1992)

A series of group-specific modifying reagents were tested for their effects on [3H]SCH23390 binding to brain D1 dopamine receptors in order to identify amino acid residues at the ligand binding site o...


More Articles


Related Compounds