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Pentyl dihydrogen phosphate, with the chemical formula C5H10PO4, is a versatile chemical compound composed of a pentyl group—a five-carbon alkyl chain—and a dihydrogen phosphate group, which includes two hydrogen atoms and a phosphate group. It is recognized for its high solubility in organic solvents, surfactant properties, and its potential in biomedical applications such as drug delivery systems and tissue engineering. Its flame-retardant properties and utility as a plasticizer make it valuable across various industries.

2382-76-5

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2382-76-5 Usage

Uses

Used in Flame Retardants:
Pentyl dihydrogen phosphate is utilized as a flame retardant in various materials to enhance their fire resistance. Its chemical structure allows it to interrupt the combustion process, making it an effective component in flame-retardant formulations.
Used as a Plasticizer:
In the plastics industry, pentyl dihydrogen phosphate serves as a plasticizer, improving the flexibility and workability of plastic materials. Its ability to increase the plasticity of polymers without compromising their structural integrity is highly beneficial.
Used in Surfactants:
Due to its surfactant properties, pentyl dihydrogen phosphate is employed in the formulation of detergents, cleaners, and other products that require the reduction of surface tension between different substances.
Used in Biomedical Applications:
Pentyl dihydrogen phosphate is studied for its potential use in drug delivery systems, where it can enhance the solubility and bioavailability of drugs. Additionally, it is being explored for its application in tissue engineering, where it may contribute to the development of scaffolds for tissue regeneration.
Used in Organic Solvent Industry:
Its high solubility in organic solvents makes pentyl dihydrogen phosphate a component in various solvent formulations, facilitating its use in a range of industrial processes that require the dissolution of specific compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2382-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2382-76:
(6*2)+(5*3)+(4*8)+(3*2)+(2*7)+(1*6)=85
85 % 10 = 5
So 2382-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H13O4P/c1-2-3-4-5-9-10(6,7)8/h2-5H2,1H3,(H2,6,7,8)

2382-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Pentyl phosphate, (C5H11O)(OH)2PO

1.2 Other means of identification

Product number -
Other names Phosphoric acid dihydrogen pentyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Agricultural chemicals (non-pesticidal),CBI
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:2382-76-5 SDS

2382-76-5Upstream product

2382-76-5Downstream Products

2382-76-5Relevant academic research and scientific papers

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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