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21954-96-1

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21954-96-1 Usage

General Description

2-[(carbamoylmethyl)amino]acetamide, also known as carbamoyl glycine, is a synthetic compound with the molecular formula C4H10N2O2. It is a derivative of glycine and is classified as an amide. This chemical is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in research and drug development studies due to its potential applications in the treatment of various diseases. 2-[(carbamoylmethyl)amino]acetamide is a white crystalline solid with a molecular weight of 118.13 g/mol and has a variety of potential applications in the field of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 21954-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,5 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21954-96:
(7*2)+(6*1)+(5*9)+(4*5)+(3*4)+(2*9)+(1*6)=121
121 % 10 = 1
So 21954-96-1 is a valid CAS Registry Number.

21954-96-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-amino-2-oxoethyl)amino]acetamide

1.2 Other means of identification

Product number -
Other names Bis-carbamoylmethyl-amin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21954-96-1 SDS

21954-96-1Relevant articles and documents

The Ion-exchange Chromatography of Imino Derivatives of Glycine

Kawashiro, Katsuhiro,Morimoto, Shiro,Yoshida, Hideyuki

, p. 792 - 795 (2007/10/02)

The resolution of the six imino derivatives of glycine (Gly) by ion-exchange chromatography is described.The imino compounds included iminodiacetonitrile (1), iminodiacetamide (2), iminodiacetic acid (3), α-(cyanomethylamino)acetamide (4), α-(cyanomethylamino)acetic acid (5), and α-(carbamoylmethylamino)acetic acid (6).A mixture of 1-6 was chromatographed along with Gly, glycinamide, aminoacetonitrile, and NH3 with an automatic amino acid analyzer using Aminex A-4 resin column (0.25φ x 50 cm) and sodium citrate buffers.When the initial buffer of pH 3.25 was changed to pH 6.50 15 min after beginning the analysis, these ten components were completely resolved.The analysis was completed in about 4.5 h.The stability of 1, 4, and 5 in aqueous media at room temperature was also studied.

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