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Ethyl hydrazinoacetate hydrochloride

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Ethyl hydrazinoacetate hydrochloride Basic information

Product Name:
Ethyl hydrazinoacetate hydrochloride
Synonyms:
  • ETHYL HYDRAZINOACETATE HCL
  • ETHYL HYDRAZINOACETATE HYDROCHLORIDE
  • ETHYL HYDRAZINEACETATE HCL
  • HYDRAZINO-ACETIC ACID ETHYL ESTER HYDROCHLORIDE
  • ETHYL HYDRAZINOACETATE HYDROCHLORIDE, 97 %
  • HYDRAZINO-ACETIC ACID ETHYL ESTER HCL
  • EthylHydrzinocetateHydrochloride
  • Acetic acid, hydrazino-, ethyl ester, monohydrochloride
CAS:
6945-92-2
MF:
C4H11ClN2O2
MW:
154.6
EINECS:
230-104-3
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • COOR
  • Hydrazines
  • Nitrogen Compounds
  • Organic Building Blocks
  • Miscellaneous
Mol File:
6945-92-2.mol
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Ethyl hydrazinoacetate hydrochloride Chemical Properties

Melting point:
152-154 °C(lit.)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
DMSO (Sparingly), Methanol (Slightly)
form 
Liquid
color 
Clear colorless to pale yellow
BRN 
3912112
Stability:
Hygroscopic
InChI
InChI=1S/C4H10N2O2.ClH/c1-2-8-4(7)3-6-5;/h6H,2-3,5H2,1H3;1H
InChIKey
HZZRIIPYFPIKHR-UHFFFAOYSA-N
SMILES
C(OCC)(=O)CNN.[H]Cl
CAS DataBase Reference
6945-92-2(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29280000
Storage Class
11 - Combustible Solids

MSDS

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Ethyl hydrazinoacetate hydrochloride Usage And Synthesis

Chemical Properties

White to off-white powder

Uses

Ethyl hydrazinoacetate hydrochloride has been used in the preparation of three novel copper(II) complexes as condensation derivatives of 2-pyridinecarboxaldehyde, 2-acetylpyridine and 2-quinolinecarboxaldehyde.

Synthesis

Ethyl hydrazinoacetate hydrochloride is prepared by using chloroacetic acid as a raw material and reacted with sodium hydroxide in the presence of a catalyst to obtain sodium chloroacetate, which is then reacted with hydrazine hydrate in the presence of sodium hydroxide, and the intermediate obtained is acidified and esterified to obtain ethyl hydrazinoacetate hydrochloride, the target product of the present invention.

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