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875-29-6

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875-29-6 Usage

Chemical Family

Furan-2,5-dione family

Physical State

Colorless to light yellow liquid

Odor

Strong

Common Uses

Solvent, manufacturing of pharmaceuticals, dyes, and pesticides, chemical intermediate for the production of other organic compounds

Potential Use

Bio-based building block for the production of renewable polymers and plastics

Safety Precautions

May be harmful if inhaled or ingested, can cause irritation to the skin and eyes. Handle with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 875-29-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 875-29:
(5*8)+(4*7)+(3*5)+(2*2)+(1*9)=96
96 % 10 = 6
So 875-29-6 is a valid CAS Registry Number.

875-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diethyl-succinic acid anhydride

1.2 Other means of identification

Product number -
Other names DL-2,3-Diethylbernsteinsaeureanhydrid

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:875-29-6 SDS

875-29-6Relevant articles and documents

Mechanism of trialkylborane promoted adhesion to low surface energy plastics

Sonnenschein, Mark F.,Webb, Steven P.,Kastl, Patrick E.,Arriola, Daniel J.,Wendt, Benjamin L.,Harrington, Daniel R.,Rondan, Nelson G.

, p. 7974 - 7978 (2004)

Excellent adhesion to low surface energy substrates such as polypropylene, polyethylene, poly(vinyl difluoride), and poly(tetrafluoroethylene) is obtained with acrylic polymerization initiated by trialkylboranes at room temperature and without need for surface pretreatment. The mechanism of adhesion is a consequence of a series of radical processes resulting from the initial oxidation of the trialkylborane followed by the production of alkoxy and alkyl radicals. This paper will elucidate the mechanism of adhesion using both experiment and theory.

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