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188840

Sigma-Aldrich

Ethyl acetimidate hydrochloride

97%

Synonym(s):

Ethyl acetoamidate hydrochloride, Ethyl acetocarboximidate hydrochloride, Ethyl acetoimidate hydrochloride, Ethyl ethanimidate hydrochloride, Ethyl ethanimidoate hydrochloride, Ethyl iminoacetate hydrochloride

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10 G
$46.90
50 G
$114.00
250 G
$417.00

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10 G
$46.90
50 G
$114.00
250 G
$417.00

About This Item

Linear Formula:
CH3C(=NH)OC2H5 · HCl
CAS Number:
2208-07-3
Molecular Weight:
123.58
Beilstein:
3552401
EC Number:
218-631-7
MDL number:
MFCD00012572
UNSPSC Code:
12352100
PubChem Substance ID:
24851324
NACRES:
NA.22

$46.90

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

97%

mp

112-114 °C (lit.)

solubility

water: soluble 50 mg/mL, clear, colorless

functional group

amine

SMILES string

Cl.CCOC(C)=N

InChI

1S/C4H9NO.ClH/c1-3-6-4(2)5;/h5H,3H2,1-2H3;1H

InChI key

WGMHMVLZFAJNOT-UHFFFAOYSA-N

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1 of 4

This Item
189944122769391549
Ethyl acetimidate hydrochloride 97%

188840

Ethyl acetimidate hydrochloride

Cyclopentylphenylacetic acid 97%

189944

Cyclopentylphenylacetic acid

Adipic acid monoethyl ester 97%

122769

Adipic acid monoethyl ester

Dimethyl aminomalonate hydrochloride 97%

391549

Dimethyl aminomalonate hydrochloride

solubility

water: soluble 50 mg/mL, clear, colorless

solubility

methanol: soluble 50 mg/mL, clear, colorless

solubility

H2O: soluble 50 mg/mL, clear, colorless

solubility

water: soluble 25 mg/mL, clear, colorless to faintly yellow

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

200

mp

112-114 °C (lit.)

mp

98-100 °C (lit.)

mp

28-29 °C (lit.)

mp

160 °C (dec.) (lit.)

functional group

amine

functional group

carboxylic acid, phenyl

functional group

-

functional group

amine, ester

Application

Ethyl acetimidate hydrochloride was used in preparation of amidinated carbonic anhydrase via chemical modification of human erythrocyte carbonic anhydrase[1]. It was also used in synthesis of methyl 2-methyl-2-thiazoline-4-carboxylate hydrochloride[2].

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
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    Lot/Batch Number
    BCBK9192V
    BCBB1741
    BCBB1739
    BCBB1739V
    BCBB1740

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    Inhibition and chemical modifications of human erythrocyte carbonic anhydrase B.
    P L Whitney et al.
    The Journal of biological chemistry, 242(18), 4212-4220 (1967-09-25)
    2-Methyl-2-thiazoline-4-carboxylic acid: formation from N-acetylcysteine and hydrolysis.
    SMITH HA and GORIN G.
    The Journal of Organic Chemistry, 26(3), 820-823 (1961)
    P de la Llosa et al.
    FEBS letters, 191(2), 211-215 (1985-10-28)
    The lactogenic activity (L.A.) of oPRL and hGH derivatives obtained by chemical modifications of lysine residues was studied by radioreceptor assay. Control treatment with borohydride had a slight effect on the L.A. of hGH but drastically reduced the oPRL activity;
    J A Kauffman et al.
    Toxicology and applied pharmacology, 79(2), 211-217 (1985-06-30)
    Blockade of neuromuscular transmission was produced in the lower hind limb of the rat by local injection of either type A or type F botulinum toxin (BoTx). At 1, 3, 7, and 10 days after injection, the extensor digitorum longus
    W M Keung et al.
    International journal of peptide and protein research, 42(6), 504-508 (1993-12-01)
    Lysine and arginine residues in trichosanthin were modified with ethyl acetimidate and phenylglyoxal, respectively. The effects of these chemical modifications on the cell-free protein-synthesis-inhibitory activity and the antigen-antibody (Ag-Ab) interaction between trichosanthin and its antibody were examined. Ethyl acetimidate modification
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