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16791-94-9

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16791-94-9 Usage

General Description

Imidodicarbonicdiamide, N,N'-dimethyl-, also known as DMDM hydantoin, is a water-soluble preservative that is widely used in personal care and cosmetic products. It acts as a formaldehyde releaser and works by slowly releasing small amounts of formaldehyde to inhibit the growth of bacteria, fungi, and yeast in products such as shampoos, conditioners, and lotions. However, there are concerns about the potential health effects of formaldehyde exposure, including skin irritation and allergic reactions, which has led to the restriction or banning of DMDM hydantoin in certain products and regions. As a result, there is ongoing debate and research into the safety and effectiveness of this chemical in consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 16791-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,9 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16791-94:
(7*1)+(6*6)+(5*7)+(4*9)+(3*1)+(2*9)+(1*4)=139
139 % 10 = 9
So 16791-94-9 is a valid CAS Registry Number.

16791-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N''-dimethylbiuret

1.2 Other means of identification

Product number -
Other names Biuret, 1,5-dimethyl-

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:16791-94-9 SDS

16791-94-9Relevant articles and documents

Synthesis, characterization, and binding property of isoelectronic analogues of nucleobases, B(6)-substituted 5-aza-6-borauracils and-thymines

Ito, Hiroshi,Yumura, Kyohei,Saigo, Kazuhiko

supporting information; experimental part, p. 3386 - 3389 (2010/11/05)

(Equation Presented). As isoelectronic BN-containing analogues of 6-substituted uracil and thymine, a series of B(6)-substituted 5-aza-6-borauracils (UBNs) and-thymines (TBNs) were synthesized and fully characterized. The crystallographic and spectroscopic analyses of the analogues revealed that the framework and hydrogen-bonding pattern of TBNs were similar to those of the original nucleobase, thymine.

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