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ChemicalBook > Product Catalogue >Organic Chemistry >Amides >Glycinamide

Glycinamide

Glycinamide Structure
  • ₹13905 - ₹76509
  • Product name: Glycinamide
  • CAS: 598-41-4
  • MF: C2H6N2O
  • MW: 74.08
  • EINECS:209-932-4
  • MDL Number:MFCD01859715
  • Synonyms:2-Aminoacetamide;Acetamide, 2-amino-;Glycinamide;AMINOACETAMIDE;2-amino-acetamid;2-Amino-1-iminoethanol;Aminoacetimidic acid;2-azanylethanamide
2 prices
Selected condition:

Brand

  • ottokemi

Package

  • 1gm
  • 5gm
  • Manufacturerottokemi
  • Product number A 2543
  • Product description2-Aminoacetamide, 95%
  • Packaging1gm
  • Price₹13905
  • Updated2022-05-26
  • Buy
  • Manufacturerottokemi
  • Product number A 2543
  • Product description2-Aminoacetamide, 95%
  • Packaging5gm
  • Price₹76509
  • Updated2022-05-26
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
ottokemi A 2543 2-Aminoacetamide, 95% 1gm ₹13905 2022-05-26 Buy
ottokemi A 2543 2-Aminoacetamide, 95% 5gm ₹76509 2022-05-26 Buy

Properties

Melting point :65-67 °C
Boiling point :281.3±23.0 °C(Predicted)
Density :1.122±0.06 g/cm3(Predicted)
storage temp. :Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka :pK1: 7.95(+1) (25°C)
NIST Chemistry Reference :H2NCH2CONH2 (glycinamide)(598-41-4)
EPA Substance Registry System :Acetamide, 2-amino- (598-41-4)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352 IF ON SKIN: wash with plenty of soap and water.
P332+P313 IF SKIN irritation occurs: Get medical advice/attention.

Description

2-Aminoacetamide is a derivative of the amino acid glycine . It has been shown to inhibit the conversion of proparathyroid hormone to parathyroid hormone. It can be useful in the identification of yeasts. It can also be useful in the synthesis of Oxiracetam , which is a derivative of Piracetam and a nootropic drug useful for improving cognition and memory impairments.

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