Basic information Safety Supplier Related

Hydroxyacetic Acid Hydrazide

Basic information Safety Supplier Related

Hydroxyacetic Acid Hydrazide Basic information

Product Name:
Hydroxyacetic Acid Hydrazide
Synonyms:
  • 2-Hydroxy-acetic Acid Hydrazide
  • Glicolic Acid Hydrazide
  • Hydroxyacetic Acid Hydrazide
  • 2-hydroxyethanehydrazide
  • Hydroxyacethydrazide
  • Acetic acid, 2-hydroxy-, hydrazide
  • Hydroxyacetylhydrazine
CAS:
3530-14-1
MF:
C2H6N2O2
MW:
90.08
Product Categories:
  • All Aliphatics
  • Aliphatics
  • Amines
Mol File:
3530-14-1.mol
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Hydroxyacetic Acid Hydrazide Chemical Properties

Melting point:
90-930C
Boiling point:
395.0±25.0 °C(Predicted)
Density 
1.311±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Acetone, Chloroform, Dichloromethane, Ethyl Acetate, Methanol
form 
Solid
pka
12.46±0.18(Predicted)
color 
White to Off-White
InChI
InChI=1S/C2H6N2O2/c3-4-2(6)1-5/h5H,1,3H2,(H,4,6)
InChIKey
LIUCWHQVLKSECA-UHFFFAOYSA-N
SMILES
C(NN)(=O)CO
CAS DataBase Reference
3530-14-1
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Hydroxyacetic Acid Hydrazide Usage And Synthesis

Chemical Properties

White Crystalline Solid

Uses

Hydroxyacetic Acid Hydrazide (cas# 3530-14-1) is a compound useful in organic synthesis.

Synthesis

623-50-7

3530-14-1

A. Synthesis of 2-hydroxyacetylhydrazine. Ethyl 2-hydroxyacetate (1.00 g, 9.60 mmol), hydrazine (0.324 mg, 10.1 mmol) and ethanol (20 mL) were mixed in a reaction vial, heated to 85 °C and kept for 3 hours. After completion of the reaction, the reaction mixture was concentrated to afford the target compound 2-hydroxyacetylhydrazine (0.702 g, 81% yield). The product was analyzed by mass spectrometry (ESI) and showed m/z 91.1 [M + 1]+.

References

[1] Molecules, 2016, vol. 21, # 11,
[2] Patent: WO2008/51493, 2008, A2. Location in patent: Page/Page column 196
[3] Chemical Biology and Drug Design, 2016, vol. 88, # 6, p. 873 - 883
[4] Patent: WO2011/77098, 2011, A1. Location in patent: Page/Page column 150
[5] Combinatorial Chemistry and High Throughput Screening, 2011, vol. 14, # 2, p. 132 - 137

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