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2466-67-3

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2466-67-3 Usage

Description

Isopentyl dihydrogen phosphate, also known as IDP, is a phosphate ester chemical compound derived from isopentyl alcohol and phosphoric acid. It is recognized for its high thermal stability and is widely utilized as a flame retardant in various applications due to its effectiveness in reducing the flammability of materials. IDP operates by releasing water vapor and diluting flammable gases when exposed to heat, which helps to slow down the ignition and spread of fire.

Uses

Used in Plastics Industry:
Isopentyl dihydrogen phosphate is used as a flame retardant for enhancing the fire resistance of plastic materials. It is incorporated into the manufacturing process to reduce the risk of ignition and fire spread, thereby improving the safety of plastic products.
Used in Textile Industry:
In the textile industry, isopentyl dihydrogen phosphate is used as a flame retardant to treat fabrics and fibers. This application helps to lower the flammability of textiles, making them safer for use in various settings, including clothing, upholstery, and curtains.
Used in Industrial and Commercial Products:
Isopentyl dihydrogen phosphate is utilized as a flame retardant in a wide range of industrial and commercial products to improve their fire safety. This includes applications in electronic devices, construction materials, and automotive components, where reducing the risk of fire is crucial.
It is important to handle and use isopentyl dihydrogen phosphate with caution due to its potential toxicity and environmental impact. Proper safety measures should be taken during its application to minimize any adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 2466-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2466-67:
(6*2)+(5*4)+(4*6)+(3*6)+(2*6)+(1*7)=93
93 % 10 = 3
So 2466-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H13O4P/c1-5(2)3-4-9-10(6,7)8/h5H,3-4H2,1-2H3,(H2,6,7,8)

2466-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methylbutyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names 1-Butanol,3-methyl-,dihydrogen phosphate

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:2466-67-3 SDS

2466-67-3Downstream Products

2466-67-3Relevant articles and documents

Regioselective phosphorylation of carbohydrates and various alcohols by bacterial acid phosphatases; probing the substrate specificity of the enzyme from Shigella flexneri

Van Herk, Teunie,Hartog, Aloysius F.,Van Der Burg, Alida M.,Wever, Ron

, p. 1155 - 1162 (2007/10/03)

Bacterial non-specific acid phosphatases normally catalyze the dephosphorylation of a variety of substrates. As shown previously the enzymes from Shigella flexneri and Salmonella enterica are also able to catalyze the phosphorylation of inosine to inosine monophosphate and D-glucose to D-glucose 6-phosphate (D-G6P) using cheap pyrophosphate as the phosphate donor. After optimization high yields (95%) are achieved in the latter reaction and we show here that it is possible to use these enzymes in a preparative manner. This prompted us to investigate by using 31P NMR and HPLC also the phosphorylation of a broad range of carbohydrates and alcohols. Many cyclic carbohydrates are phosphorylated in a regioselective manner. Non-cyclic carbohydrates are phosphorylated as well. Phosphorylation of linear alcohols, cyclic and aromatic alcohols is also possible. In all cases the acid phosphatase from Shigella prefers a primary alcohol function above a secondary one. We conclude that these enzymes are an attractive alternative to existing chemical and enzymatic methods in the phosphorylation of a broad range of compounds.

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