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BENZOPHENONE-4,4'-DICARBOXYLIC ACID is an organic compound that belongs to the class of benzophenones. It is widely used as a chemical intermediate in the production of UV absorbers, pharmaceuticals, agrochemicals, and pigments. Known for its ability to absorb ultraviolet radiation, it is a valuable ingredient in sunscreen and other sun protection products. It also serves as an effective photoinitiator in the polymerization of various materials, including plastics and coatings. Furthermore, it is a key ingredient in the development of light-stable and weather-resistant materials used in the automotive and construction industries.

964-68-1

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964-68-1 Usage

Uses

Used in Sun Protection Products:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a UV absorber for its ability to absorb ultraviolet radiation, providing protection against harmful UV rays in sunscreen and other sun protection products.
Used in Polymerization:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a photoinitiator in the polymerization of various materials, including plastics and coatings, to enhance their properties and performance.
Used in Automotive and Construction Industries:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a key ingredient in the development of light-stable and weather-resistant materials, ensuring durability and longevity in automotive and construction applications.
Used in Pharmaceutical Synthesis:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a chemical intermediate in the synthesis of pharmaceuticals, contributing to the development of new and effective medications.
Used in Agrochemical Production:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a chemical intermediate in the production of agrochemicals, aiding in the development of agricultural products that enhance crop protection and yield.
Used in Pigment Industry:
BENZOPHENONE-4,4'-DICARBOXYLIC ACID is used as a chemical intermediate in the synthesis of pigments, contributing to the creation of vibrant and stable colorants for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 964-68-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 964-68:
(5*9)+(4*6)+(3*4)+(2*6)+(1*8)=101
101 % 10 = 1
So 964-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O5/c16-13(9-1-5-11(6-2-9)14(17)18)10-3-7-12(8-4-10)15(19)20/h1-8H,(H,17,18)(H,19,20)

964-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzophenone-4,4'-dicarboxylic Acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 4,4‘-carbonylbis-

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:964-68-1 SDS

964-68-1Relevant academic research and scientific papers

Effect of functional group polarity on the antimalarial activity of spiro and dispiro-1,2,4-trioxolanes

Dong, Yuxiang,Tang, Yuanqing,Chollet, Jacques,Matile, Hugues,Wittlin, Sergio,Charman, Susan A.,Charman, William N.,Tomas, Josefina Santo,Scheurer, Christian,Snyder, Christopher,Scorneaux, Bernard,Bajpai, Saroj,Alexander, Scott A.,Wang, Xiaofang,Padmanilayam, Maniyan,Cheruku, Srinivasa R.,Brun, Reto,Vennerstrom, Jonathan L.

, p. 6368 - 6382 (2007/10/03)

Based on the structures of several lipophilic trioxolane antimalarial prototypes, we set out to determine which functional groups were associated with good antimalarial profiles and identify more polar (lower Log P/Log D) lead compounds with good physicoc

Optimized liquid-phase oxidation

-

Page/Page column 39-41, (2008/06/13)

Disclosed is an optimized process and apparatus for more efficiently and economically carrying out the liquid-phase oxidation of an oxidizable compound. Such liquid-phase oxidation is carried out in a bubble column reactor that provides for a highly effic

Optimized liquid-phase oxidation

-

Page/Page column 39-41, (2008/06/13)

Disclosed is an optimized process and apparatus for more efficiently and economically carrying out the liquid-phase oxidation of an oxidizable compound. Such liquid-phase oxidation is carried out in a bubble column reactor that provides for a highly effic

PRODUCTION OF AROMATIC CARBOXYLIC ACIDS

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Page 28, (2008/06/13)

A process for the production of an aromatic carboxylic acid comprising contacting in the presence of a catalyst, within a continuous flow reactor, one or more precursors of the aromatic carboxylic acid with an oxidant, such contact being effected with sai

Synthesis and solubility properties of C60 fullerene derivatives bearing carboxy groups

Tomioka, Hideo,Yamamoto, Katsutoshi

, p. 63 - 66 (2007/10/03)

Bis(4-tert-butoxycarbonylphenyl)diazomethanes have been prepared and treated with fullerene (C60) to give the corresponding 1,2-methano derivatives which upon hydrolysis with CF3CO2H gave the title compounds. The solubility of the latter in aqueous THF has been measured.

Photochemistry of Meta-Substituted and Para-Substituted Aromatic Polycarbonyl Compounds

Ito, Yoshikatsu,Kawatsuki, Nobuhiro,Giri, Brij Pal,Yoshida, Masahiro,Matsuura, Teruo

, p. 2893 - 2904 (2007/10/02)

Spectroscopic (λmax and ET) and photochemical (quantum yield of benzocyclobutenol formation ΦCB and Stern-Volmer quenching constant with diene KSV) properties for meta-substituted polyketones 1b-f, 2, and 5b, pa

Purification of 4,4'-benzophenonedicarboxylic acid

-

, (2008/06/13)

A process is described for purifying 4,4'-benzophenonedicarboxylic acid, useful in preparing thermoplastic polyesters yielding molded articles having high impact strength, wherein the acid contains aromatic monocarboxylic acid genetic impurity, which comp

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