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Tetrabutyl diphosphate (TBuDP) is a phosphorus-based chemical compound consisting of four butyl groups and a diphosphate functional group. It is used as a catalyst, solvent, and reagent in various chemical processes.

1474-75-5

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1474-75-5 Usage

Uses

Used in Plastics and Rubber Industry:
Tetrabutyl diphosphate is used as a flame retardant for plastics and rubber products, as it inhibits the combustion process.
Used in Organic Compound Synthesis:
Tetrabutyl diphosphate is used as a reagent in the synthesis of organic compounds.
Used in Polymer Production:
Tetrabutyl diphosphate is used as a stabilizer in the production of polymers.
Used in Pharmaceutical Industry:
Tetrabutyl diphosphate is used as a reagent in organic chemistry reactions within the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1474-75-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1474-75:
(6*1)+(5*4)+(4*7)+(3*4)+(2*7)+(1*5)=85
85 % 10 = 5
So 1474-75-5 is a valid CAS Registry Number.

1474-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl dibutoxyphosphoryl phosphate

1.2 Other means of identification

Product number -
Other names Tetrabutyl diphosphate

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:1474-75-5 SDS

1474-75-5Downstream Products

1474-75-5Relevant academic research and scientific papers

Electrochemical Oxidation of Metal Dialkyl Phosphites and Their Reaction with Halogens

Romakhin,Zagumennov,Nikitin

, p. 1022 - 1026 (2007/10/03)

Electrochemical oxidation of sodium dialkyl phosphites with alkyl radicals of normal structure leads to formation of tetraalkyl pyrophosphites as the main products, while electrochemical oxidation of litium dialkyl phosphites and sodium salts with branched alkyl radicals yields tetraalkyl hypophosphates. The reaction of metal dialkyl phosphites with halogens leads to analogous results.

ELECTROCHEMICALLY INDUCED PROCESSES OF FORMATION OF PHOSPHORIC ACID DERIVATIVES. 3. ELECTROSYNTHESIS FROM WHITE PHOSPHORUS IN ALCOHOL-WATER SOLUTIONS

Budnikova, Yu. G.,Kargin, Yu. M.,Zaripov, I. M.,Romakhin, A. S.,Ignat'ev, Yu. A.,et al.

, p. 1580 - 1584 (2007/10/02)

It has been established that the process of splitting of the P-P bonds of the white phosphorus molecules is initiated by cathode-generated nucleophiles (HO-, RO-), while functionalization of the P-H bond formed in phosphoric oligomers occurs under the action only of alcohol.The primary product after splitting of all the P-P bonds in phosphoric oligomers is dialkylphosphite (in alcohol-water media), or trialkylphosphite (in absolute alcohol), in the course of electrolysis being transformed into trialkylphosphate.Formation of esters of pyrophosphoric acid with reduced protogenic character of the medium was examined.It is proposed that under these conditions nucleophilic reagents of the type (>P)c-O- form and participate in splitting of the P-P bonds. Keywords: phosphoric acid derivatives, white phosphorus, electrosynthesis, alcohol-water solution.

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