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Iminodimethanol, also known as 2-(hydroxymethyl)-2-methyl-1,3-propanediamine or 2-amino-2-(hydroxymethyl)-1-methylethanol, is an organic compound with the chemical formula C4H11NO2. It is a colorless liquid with a molecular weight of 105.14 g/mol. Iminodimethanol is a derivative of 1,3-propanediamine, featuring a hydroxymethyl group and a methyl group attached to the nitrogen atom. iminodimethanol is used as a crosslinking agent in the production of polyurethane foams and elastomers, as well as a curing agent for epoxy resins. It is also employed in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, iminodimethanol is an important intermediate in the chemical industry.

7487-32-3

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7487-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7487-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7487-32:
(6*7)+(5*4)+(4*8)+(3*7)+(2*3)+(1*2)=123
123 % 10 = 3
So 7487-32-3 is a valid CAS Registry Number.

7487-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (hydroxymethylamino)methanol

1.2 Other means of identification

Product number -
Other names Methanol,iminobis

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:7487-32-3 SDS

7487-32-3Upstream product

7487-32-3Relevant academic research and scientific papers

Carbon-13 NMR Study of Reaction of Aqueous Formaldehyde with Amine Salts: Evidences for Reductive Methylation by Intramolecular Hydride Transfer

Narasimhan, S.,Balakrishnan, M.,Kumar, A. S.,Venkatasubramanian, N.

, p. 568 - 570 (2007/10/02)

Reductive methylation of amine salts by aqueous formaldehyde under acidic conditions proceeds through the initial formation of hydroxymethylamine intermediates, followed by intramolecular hydride transfer. 13C NMR studies on this reaction and the mechanism are discussed.

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