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78-33-1

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78-33-1 Usage

Chemical Properties

Solid. Bp 320C (5 mm Hg), mp 102– 105C, flash p 545F (285C). Insoluble inwater.Combustible.

Uses

Tris(p-tert-butylphenyl) Phosphate is a compound with potential application to fire retardants, plasticizers and oils, due to its chemical composition.

Check Digit Verification of cas no

The CAS Registry Mumber 78-33-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78-33:
(4*7)+(3*8)+(2*3)+(1*3)=61
61 % 10 = 1
So 78-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C30H39O4P/c1-28(2,3)22-10-16-25(17-11-22)32-35(31,33-26-18-12-23(13-19-26)29(4,5)6)34-27-20-14-24(15-21-27)30(7,8)9/h10-21H,1-9H3

78-33-1SDS

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 Tris(4-Tert-Butylphenyl) Phosphate

1.2 Other means of identification

Product number -
Other names Phenol, 4-(1,1-dimethylethyl)-, phosphate (3:1)

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:78-33-1 SDS

78-33-1Relevant articles and documents

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

supporting information, 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.

Preparation of Flame-Resistant Liquids Based on Mixed Tri(phenyl, p-tert-butylphenyl) Phosphates by Transesterification of Triphenyl Phosphate with p-tert-Butylphenol

Karchevskaya, O. G.,Korneeva, G. A.,Kron, T. E.,Noskov, Yu. G.

, p. 1237 - 1243 (2020/10/02)

Abstract: The possibility of controlling the composition of a mixture of triphenyl phosphate, p-tert-butylphenyl diphenyl phosphate, di(p-tert-butylphenyl)phenyl phosphate, and tri(p-tert-butylphenyl) phosphate, formed by transesterification of triphenyl phosphate with p-tert-butylphenol, was demonstrated. The amount of p-tert-butylphenol necessary for transesterification of triphenyl phosphate to yield a mixture of phosphates of required composition was determined. If necessary, the composition of the phosphates can be adjusted by selective distillation of triphenyl phosphate in a vacuum.

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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