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140-98-7

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140-98-7 Usage

General Description

Butyl maleurate is a chemical compound that belongs to the ester group. It is formed by the reaction of maleic acid with butanol, resulting in a colorless liquid with a fruity odor. Butyl maleurate is commonly used as a fragrance ingredient in various consumer products such as perfumes, lotions, and personal care items. It is also used as a plasticizer in polymer and resin formulations. This chemical is considered to have low toxicity and is generally regarded as safe for use in cosmetics and other household products when used in accordance with regulations and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 140-98-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 140-98:
(5*1)+(4*4)+(3*0)+(2*9)+(1*8)=47
47 % 10 = 7
So 140-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O4/c1-2-3-6-15-8(13)5-4-7(12)11-9(10)14/h4-5H,2-3,6H2,1H3,(H3,10,11,12,14)/b5-4-

140-98-7SDS

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 N-Carbamoylmaleamic acid, butyl ester

1.2 Other means of identification

Product number -
Other names N-Carbamoyl-maleinamidsaeure-allylester

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:140-98-7 SDS

140-98-7Relevant articles and documents

NOVEL POLYMERIZABLE ACYL IMIDAZOLIDINONE MONOMERS

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Page/Page column 9, (2010/11/29)

Acyl imidazolidinones and compositions containing the same are disclosed, which are particularly suitable for use as self-crosslinkers and can also be used as wet adhesion properties, especially in latex-based polymer systems. Processes for preparing such compounds, compositions containing the same, as well as additional uses thereof are also disclosed.

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