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[1,1'-Biphenyl]-4-ol, phosphate (3:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3871-23-6

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3871-23-6 Usage

Uses

Used in Flame Retardant Industry:
[1,1'-Biphenyl]-4-ol, phosphate (3:1) is used as a flame retardant for enhancing the fire resistance of various materials. The phosphate group in the compound allows it to be easily incorporated into polymers and other materials, making it useful for creating flame-resistant products.
Used in Industrial Stabilizers:
[1,1'-Biphenyl]-4-ol, phosphate (3:1) is used as a stabilizer in industrial processes to maintain the stability and quality of products during manufacturing.
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-4-ol, phosphate (3:1) has potential applications in the pharmaceutical field, possibly due to its antioxidant properties and ability to be incorporated into various formulations.
Used in Agrochemical Industry:
[1,1'-Biphenyl]-4-ol, phosphate (3:1) also has potential uses in the agrochemical industry, where its properties might be beneficial for the development of new products or the enhancement of existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 3871-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3871-23:
(6*3)+(5*8)+(4*7)+(3*1)+(2*2)+(1*3)=96
96 % 10 = 6
So 3871-23-6 is a valid CAS Registry Number.

3871-23-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylphenol,phosphoric acid

1.2 Other means of identification

Product number -
Other names Tris-(biphenylyl-(4))-phosphat

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:3871-23-6 SDS

3871-23-6Downstream Products

3871-23-6Relevant academic research and scientific papers

Diphenyl Diselenide-Catalyzed Synthesis of Triaryl Phosphites and Triaryl Phosphates from White Phosphorus

Zhang, Yue,Cai, Ziman,Chi, Yangyang,Zeng, Xiangzhe,Chen, Shuanghui,Liu, Yan,Tang, Guo,Zhao, Yufen

, p. 5158 - 5163 (2021/07/20)

Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a diphenyl diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds. Subsequent oxidation of triaryl phosphites produces triaryl phosphates and triaryl thiophosphates. Phosphorotrithioates are also prepared efficiently from aromatic thiols and aliphatic thiols.

METHOD OF PREPARING BIPHENYL-4-YL DIPHENYL PHOSPHATE COMPOSITION

-

Paragraph 0027, (2013/07/19)

Provided is a method of preparing a biphenyl-4-yl diphenyl phosphate composition for use as a flame retardant or a plasticizer for resin, including mixing phosphoryl chloride (POCl3), 4-phenylphenol, and a catalyst, so that first dehydrochlorination occurs; and further adding phenol, so that second dehydrochlorination occurs.

Process for producing triaryl phosphate

-

, (2008/06/13)

A process for producing triaryl phosphate, comprising reacting at least one specific aromatic hydroxy compound with phosphorus pentachloride to form a chlorophosphorane compound and reacting water, an alcohol, an alcohol aqueous solution or an alkaline aqueous solution with the chlorophosphorane compound. The process permits the production of triaryl phosphate at high yields at a low temperature for a relatively short period of time, making the removal and treatment of a catalyst simply and obviating the use of the catalyst in some cases.

SYNTHESIS OF TRIARYL PHOSPHATES CATALYZED BY POLYETHYLENE GLYCOLS IN A TWO-PHASE SYSTEM: PHASE TRANSFER CATALYSIS

Krishnakumar, V. K.

, p. 189 - 196 (2007/10/02)

The synthesis of triaryl phosphates has been accomplished, at room temperature, in nearly quantitative yields in a two-phase system with poly(ethylene glycol) as a phase transfer catalyst.

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