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631-45-8

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631-45-8 Usage

Description

Tri-o-tolylthiophosphate is a phosphorothioate ester of o-tolyl, known for its high thermal stability and extreme pressure properties. It is commonly used as an antiwear and antioxidant additive in lubricants and hydraulic fluids.
Used in Lubricant Industry:
Tri-o-tolylthiophosphate is used as an antiwear and antioxidant additive for improving the performance and longevity of moving mechanical parts by reducing friction and minimizing wear and tear.
Used in Hydraulic Fluid Industry:
Tri-o-tolylthiophosphate is used as an additive in hydraulic fluids to enhance their thermal stability and extreme pressure properties, ensuring smooth operation and maintenance of machinery and equipment.
Used in Grease Formulation:
Tri-o-tolylthiophosphate is used as a key component in the formulation of greases to provide protection against wear and tear, as well as to improve the thermal stability of the grease.
Used in Gear Oil Industry:
Tri-o-tolylthiophosphate is used as an additive in gear oils to enhance their antiwear and antioxidant properties, ensuring efficient operation and reducing wear in gears.
Used in Metalworking Fluid Industry:
Tri-o-tolylthiophosphate is used in the formulation of metalworking fluids to improve their performance, reduce friction, and minimize wear during metalworking processes.
Note: The use of Tri-o-tolylthiophosphate should be handled with caution and in compliance with safety regulations due to its potential environmental and health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 631-45-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 631-45:
(5*6)+(4*3)+(3*1)+(2*4)+(1*5)=58
58 % 10 = 8
So 631-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H21O3PS/c1-16-10-4-7-13-19(16)22-25(26,23-20-14-8-5-11-17(20)2)24-21-15-9-6-12-18(21)3/h4-15H,1-3H3

631-45-8SDS

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 tris(2-methylphenoxy)-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names O,O,O-Tris(2-methylphenyl) thiophosphate

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:631-45-8 SDS

631-45-8Downstream Products

631-45-8Relevant articles and documents

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Gottlieb

, ()

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Method for preparing phosphate ester derivatives from white phosphorus

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Paragraph 0065-0067, (2021/06/23)

A method for preparing phosphate ester derivatives from white phosphorus relates to the field of chemical engineering, and comprises the following steps: adding alkali, a catalyst, a white phosphorus solution, ROH or RSH (R represents alkyl or aromatic group) into a reaction container in an inert atmosphere, and heating and stirring the mixture in a mixed solvent of toluene and DMSO (dimethyl sulfoxide) to react for a certain time, so as to obtain three-coordinated phosphate ester derivatives; and 2) continuing to add H2O2, air or sulfur powder until the oxidation is completed, thereby obtaining the tetra-coordinated phosphate ester derivative. According to the method, chlorine, phosphorus trichloride and halogen are not needed, phosphite ester is directly prepared from elementary white phosphorus in an efficient, green and environment-friendly manner, and phosphate and thiophosphate can be directly prepared after oxidation. High pollution and high corrosivity of a traditional method are avoided in the whole process; meanwhile, white phosphorus is completely converted in the whole process, white phosphorus residues are avoided, and the post-reaction treatment process is safe.

NEW METHOD FOR THE SYNTHESIS OF O,O-DIARYL HYDROGEN PHOSPHORODITHIOATES, O,O,O-TRIARYL PHOSPHOROTHIOATES, AND TETRAKIS(ARYLOXY)DIPHOSPHINE

Mazitova, F. N.,Khairullin, V. K.

, p. 652 - 658 (2007/10/02)

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