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C34H33O6P, also known as bis(2-ethylhexyl) 4-methyl-2,6-dinitrophenyl phosphate or BPMN, is an organophosphate flame retardant. It is commonly used in various plastics, rubber, and other materials to enhance their fire resistance properties. BPMN acts as a flame retardant by releasing a non-flammable gas when exposed to heat, which helps suppress the spread of flames. This chemical is often used in combination with other flame retardants to provide comprehensive fire protection.

2635339-85-2

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2635339-85-2 Usage

Uses

Used in Plastics Industry:
C34H33O6P is used as a flame retardant in plastics for enhancing their fire resistance properties. It helps in reducing the risk of fire and improving the safety of plastic products.
Used in Rubber Industry:
C34H33O6P is used as a flame retardant in rubber products to improve their fire resistance. This is particularly important in applications where rubber products are exposed to high temperatures or potential fire hazards.
Used in Other Materials:
C34H33O6P is also used in other materials to enhance their fire resistance properties. It can be incorporated into textiles, coatings, and adhesives to provide additional protection against fire.
However, due to environmental and health concerns associated with BPMN, there have been efforts to develop alternative, more environmentally friendly flame retardants to replace it in various applications. These concerns stem from its persistence in the environment and potential toxicity, which may pose risks to both human health and the ecosystem.

Check Digit Verification of cas no

The CAS Registry Mumber 2635339-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,6,3,5,3,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2635339-85:
(9*2)+(8*6)+(7*3)+(6*5)+(5*3)+(4*3)+(3*9)+(2*8)+(1*5)=192
192 % 10 = 2
So 2635339-85-2 is a valid CAS Registry Number.

2635339-85-2Upstream product

2635339-85-2Downstream Products

2635339-85-2Relevant academic research and scientific papers

A convenient protocol for the synthesis of axially chiral Br?nsted acids

Bartoszek, Michael,Beller, Matthias,Deutsch, Jens,Klawonn, Markus,K?ckritz, Angela,Nemati, Navid,Pews-Davtyan, Anahit

, p. 1316 - 1322 (2008)

Partially hydrogenated binaphthol monophosphoric acids were prepared via an improved four-step sequence. It is demonstrated that typical protection and deprotection of the phenolic groups are dispensable. The vinyl-substituted derivative has been polymerized to give a novel polymerized organocatalyst.

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