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Di-n-butyl morpholinophosphonate (DBMP) is an organophosphorus compound with the chemical formula C10H23NO3P. It is a colorless liquid with a slight odor and is soluble in water. DBMP is primarily used as a flame retardant and plasticizer in various applications, including plastics, rubber, and textiles. It works by releasing phosphorus-based compounds when exposed to heat, which helps to suppress the combustion process. Due to its effectiveness and low toxicity, DBMP has become a popular choice in the flame retardant industry. However, concerns have been raised about its potential environmental impact, and further research is needed to fully understand its long-term effects on ecosystems and human health.

7264-96-2

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7264-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7264-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7264-96:
(6*7)+(5*2)+(4*6)+(3*4)+(2*9)+(1*6)=112
112 % 10 = 2
So 7264-96-2 is a valid CAS Registry Number.

7264-96-2SDS

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 di-n-butyl morpholinophosphonate

1.2 Other means of identification

Product number -
Other names Morpholino-phosphorsaeure-dibutylester

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:7264-96-2 SDS

7264-96-2Downstream Products

7264-96-2Relevant academic research and scientific papers

REACTION OF SULFENAMIDES WITH DI-ALKYL AND TRIALKYL PHOSPHITES. AN EFFICIENT SYNTHESIS OF PHOSPHORAMIDATES BY UNUSUAL SUBSTITUTION AT S-N BOND IN (2-BENZOTHIAZOLYL)SULFENAMIDES

Torii, Sigeru,Sayo, Noboru,Tanaka, Hideo

, p. 695 - 698 (2007/10/02)

Regioselective attack of the trivalent phosphorus atom of dialkyl and trialkyl phosphites on either nitrogen or sulfur atom of sulfenamides has been found.The reaction of phenylsulfenamides with dialkyl phosphites yielded phosphorothiolates, whereas the treatment of (2-benzothiazolyl)sulfenamides with dialkyl and trialkyl phosphites gave phosphoramidates in excellent yields.

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