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Phosphinic acid, (aminomethyl)-, also known as (aminomethyl)phosphinic acid or Aminomethylphosphonic acid, is an organic compound with the chemical formula C2H8NO2P. It is a colorless, crystalline solid that is soluble in water and has a molecular weight of 109.07 g/mol. Phosphinic acid, (aminomethyl)- is a derivative of phosphinic acid, which is a type of phosphorus-containing organic acid. It is characterized by the presence of an aminomethyl group (-CH2NH2) attached to the phosphorus atom. (Aminomethyl)phosphinic acid is used in various applications, including as a chelating agent, a flame retardant, and a precursor in the synthesis of other phosphorus-containing compounds. It is also known for its potential use in the treatment of metal poisoning and as a corrosion inhibitor.

996-28-1

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996-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 996-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 996-28:
(5*9)+(4*9)+(3*6)+(2*2)+(1*8)=111
111 % 10 = 1
So 996-28-1 is a valid CAS Registry Number.

996-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name aminomethyl-H-phosphinic acid

1.2 Other means of identification

Product number -
Other names 1-aminomethylphosphinic acid

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:996-28-1 SDS

996-28-1Relevant academic research and scientific papers

A CONVENIENT SYNTHESIS OF AMINOMETHYLPHOSPHONOUS ACID

Grobelny, Damian

, p. 1177 - 1180 (2007/10/02)

Aminomethylphosphonous acid has been prepared in excellent yield by alkylation of bis(trimethylsilyl)ethoxycarbonylphosphonite 2 with N-(bromomethyl)phthalimide 1, followed by acidic removal of protecting groups.

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