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1,3-hydroxy-2-propyl dihydrogen phosphate is a versatile phosphoric acid ester that features a hydroxy group and a propyl group attached to the phosphate group. This chemical compound is known for its diverse applications across various industries due to its unique properties.

17181-54-3

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17181-54-3 Usage

Uses

Used in Flame Retardants:
1,3-hydroxy-2-propyl dihydrogen phosphate is used as a flame retardant for enhancing the fire resistance of materials, thereby improving safety standards in various applications.
Used in Plasticizers:
In the plastics industry, 1,3-hydroxy-2-propyl dihydrogen phosphate is used as a plasticizer to increase the flexibility and workability of polymers, making them more suitable for a range of uses.
Used as Stabilizers for Polymers:
1,3-hydroxy-2-propyl dihydrogen phosphate is used as a stabilizer for polyvinyl chloride (PVC) and other polymers to prevent degradation and extend the lifespan of these materials.
Used in Pharmaceutical Production:
1,3-hydroxy-2-propyl dihydrogen phosphate is utilized in the production of pharmaceuticals, contributing to the development of various medications and therapeutic agents.
Used as Corrosion Inhibitors:
In the metalworking industry, 1,3-hydroxy-2-propyl dihydrogen phosphate is used as a corrosion inhibitor to protect metal surfaces from rust and other forms of corrosion, ensuring the longevity and integrity of metal components.
Used as Surfactants in Personal Care and Cleaning Products:
1,3-hydroxy-2-propyl dihydrogen phosphate is used as a surfactant in the manufacture of personal care products and cleaning agents, enhancing their effectiveness in cleaning and emulsifying processes.
Overall, 1,3-hydroxy-2-propyl dihydrogen phosphate is a multifunctional chemical with a broad spectrum of applications in industries such as plastics, pharmaceuticals, metalworking, and personal care, making it an essential component in many products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17181-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,8 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17181-54:
(7*1)+(6*7)+(5*1)+(4*8)+(3*1)+(2*5)+(1*4)=103
103 % 10 = 3
So 17181-54-3 is a valid CAS Registry Number.

17181-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name glycerol 2-phosphate

1.2 Other means of identification

Product number -
Other names 1,3-dihydroxypropan-2-yl 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:17181-54-3 SDS

17181-54-3Relevant academic research and scientific papers

Direct Quantitative Analysis of Enzyme-Catalyzed Reactions by Two-Dimensional Nuclear Magnetic Resonance Spectroscopy: Adenylate Kinase and Phosphoglyceromutase

Mendz, George L.,Robinson, Gae,Kuchel, Philip W.

, p. 169 - 173 (1986)

The back-transformation method for the analysis of two-dimensional nuclear magnetic resonance cross-relaxation and exchange data has been employed to obtain the rate constants of the phosphoglyceromutase and adenylate kinase catalyzed reactions in vitro.The results are in excellent agreement with those obtained by other methods.It is shown that a single two-dimensional experiment for each catalyzed reaction is sufficient to calculate the rate constants.The study of the adenylate kinase reaction demonstrates the potential of the method for direct analysis of higher order reactions without having to simplify them in terms of pseudo-first-order steps.

Reactivities of some energy rich organic orthophosphates towards transition metal ion oxidants

Gupta, Kalyan Kali Sen,Mahapatra, Ambikesh,Sanyal, Ankan

, p. 332 - 334 (2007/10/02)

The orthophosphates, α- and β-glycerophosphates, react with HCrO-4 in HClO4 medium to give 1:1 intermediates which subsequently decomposes to give products of the reactions.The rate is directly proportional to +> in each reaction.Thermodynamic parameters associated with the equilibrium step and the activation parameters associated with the slowest step has been evaluated for each substrate.An attempt has been made to correlate the results obtained earlier with other transition metal ion oxidants.

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