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Phosphonic acid, propyl-, bis(1-methylethyl) ester, also known as isopropyl bis(2-propylphosphonate), is a chemical compound characterized by its clear, colorless liquid form with a fruity odor. It is soluble in organic solvents and is recognized for its high thermal stability and low volatility, which makes it suitable for use in high-temperature environments. Phosphonic acid, propyl-, bis(1-methylethyl) ester is widely utilized across various industries due to its flame retardant and anti-corrosive properties.

18812-55-0

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18812-55-0 Usage

Uses

Used in Plastics Industry:
Phosphonic acid, propyl-, bis(1-methylethyl) ester is used as a flame retardant and anti-corrosive agent in the manufacturing of plastics, enhancing the safety and durability of the final products.
Used in Coatings Industry:
In the coatings industry, Phosphonic acid, propyl-, bis(1-methylethyl) ester serves as a crucial ingredient that imparts flame retardancy and corrosion resistance to coatings, thereby improving the protective qualities of the applied surfaces.
Used in Adhesives Industry:
Phosphonic acid, propyl-, bis(1-methylethyl) ester is used as an additive in adhesive formulations to provide flame retardancy and corrosion resistance, ensuring the adhesives' performance and longevity.
Used in Agricultural Chemicals Production:
Phosphonic acid, propyl-, bis(1-methylethyl) ester is utilized in the production of agricultural chemicals, where its flame retardant and anti-corrosive properties contribute to the safety and effectiveness of these products.
Used in Pharmaceuticals Production:
Phosphonic acid, propyl-, bis(1-methylethyl) ester is used in the pharmaceutical industry, potentially for its flame retardant and anti-corrosive properties, which can be beneficial in the manufacturing process or in the stability of the final product.
Used in Semiconductor Material Production:
As a processing aid in the production of semiconductor materials, Phosphonic acid, propyl-, bis(1-methylethyl) ester contributes to the manufacturing process by enhancing the quality and performance of the semiconductors.
Used in Polyurethane Foam Production:
Phosphonic acid, propyl-, bis(1-methylethyl) ester is used as a stabilizer in the production of polyurethane foams, ensuring the stability and uniformity of the foam structure.

Check Digit Verification of cas no

The CAS Registry Mumber 18812-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18812-55:
(7*1)+(6*8)+(5*8)+(4*1)+(3*2)+(2*5)+(1*5)=120
120 % 10 = 0
So 18812-55-0 is a valid CAS Registry Number.

18812-55-0SDS

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 1-di(propan-2-yloxy)phosphorylpropane

1.2 Other means of identification

Product number -
Other names propyl-phosphonic acid diisopropyl ester

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:18812-55-0 SDS

18812-55-0Relevant academic research and scientific papers

PHOSPHORYLNITRILE OXIDES. 5. REACTIONS OF 3-(DIALKOXYPHOSPHORYL)ISOXAZOLES AND -ISOXAZOLINES WITH NUCLEOPHILIC REAGENTS

Pavlov, V. A.,Kurdyukov, A. I.,Gorin, B. I.,Sagitova, F. R.,Aristova, N. V.,et al.

, p. 718 - 723 (2007/10/02)

3-Phosphorylated isoxazoles and isoxazolines react with nucleophiles either with cleavage of the P-C bond and subsequent ring opening or with retention of the heterocyclic ring depending on the structure of the ring substituents, nature of the nucleophile, and reaction conditions.This permits the selective chemical modification of the starting compounds.

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