What is the Diphenyl anilinophosphonate?

Diphenyl anilinophosphonate is , while it's Molecular Formula is C18H16 N O3 P. Used in Plastics and Polymer Industry: Diphenyl anilinophosphonate is used as a flame retardant and plasticizer for enhancing the fire safety and flexibility of plastics, polymers, and resins. Its incorporation into these materials helps to reduce their flammability, making it an essential additive in the production of electrical equipment, cables, and textiles. Used in Electrical Equipment Manufacturing: In the electrical equipment industry, Diphenyl anilinophosphonate is utilized as a flame retardant to ensure that the materials used in the construction of electrical components possess enhanced fire resistance. This contributes to the safety and durability of the equipment. Used in Cable Production: For cable production, Diphenyl anilinophosphonate serves as a critical component that improves the fire retardancy of the cables, thereby reducing the risk of fire hazards and ensuring the longevity of the cables in various applications. Used in Textile Industry: In the textile industry, Diphenyl anilinophosphonate is employed as a flame retardant to treat fabrics, providing them with fire-resistant properties. This is particularly important for applications where fire safety is a priority, such as in the production of upholstery, carpets, and protective clothing. Overall, Diphenyl anilinophosphonate's versatility, thermal stability, and resistance to leaching, coupled with its low toxicity and cost-effectiveness, make it a preferred choice for a wide range of applications across different industries.

What is the CAS number for Diphenyl anilinophosphonate?

The CAS number of Diphenyl anilinophosphonate is 3848-51-9.

What is Diphenyl anilinophosphonate (3848-51-9) used for?

Diphenyl anilinophosphonate, with the chemical formula C12H11NO2P, is a phosphonate ester characterized by a phosphorus atom bonded to two oxygen atoms and a carbon atom of an aniline group. It is recognized for its thermal stability, resistance to leaching, and low toxicity, which contribute to its value in various industrial applications.InChI:InChI=1/C18H16NO3P/c20-23(19-16-10-4-1-5-11-16,21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15H,(H,19,20)

What is the Diphenyl anilinophosphonate?

Diphenyl anilinophosphonate is , while it's Molecular Formula is C18H16 N O3 P. Used in Plastics and Polymer Industry: Diphenyl anilinophosphonate is used as a flame retardant and plasticizer for enhancing the fire safety and flexibility of plastics, polymers, and resins. Its incorporation into these materials helps to reduce their flammability, making it an essential additive in the production of electrical equipment, cables, and textiles. Used in Electrical Equipment Manufacturing: In the electrical equipment industry, Diphenyl anilinophosphonate is utilized as a flame retardant to ensure that the materials used in the construction of electrical components possess enhanced fire resistance. This contributes to the safety and durability of the equipment. Used in Cable Production: For cable production, Diphenyl anilinophosphonate serves as a critical component that improves the fire retardancy of the cables, thereby reducing the risk of fire hazards and ensuring the longevity of the cables in various applications. Used in Textile Industry: In the textile industry, Diphenyl anilinophosphonate is employed as a flame retardant to treat fabrics, providing them with fire-resistant properties. This is particularly important for applications where fire safety is a priority, such as in the production of upholstery, carpets, and protective clothing. Overall, Diphenyl anilinophosphonate's versatility, thermal stability, and resistance to leaching, coupled with its low toxicity and cost-effectiveness, make it a preferred choice for a wide range of applications across different industries.

What is the CAS number for Diphenyl anilinophosphonate?

The CAS number of Diphenyl anilinophosphonate is 3848-51-9.

What is Diphenyl anilinophosphonate (3848-51-9) used for?

Diphenyl anilinophosphonate, with the chemical formula C12H11NO2P, is a phosphonate ester characterized by a phosphorus atom bonded to two oxygen atoms and a carbon atom of an aniline group. It is recognized for its thermal stability, resistance to leaching, and low toxicity, which contribute to its value in various industrial applications.InChI:InChI=1/C18H16NO3P/c20-23(19-16-10-4-1-5-11-16,21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15H,(H,19,20)

3848-51-9

Product NameDiphenyl anilinophosphonate
Molecular FormulaC18H16 N O3 P
Molecular Weight325.304
Purity99%

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Product Details

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CasNo： 3848-51-9
Molecular Formula： C18H16 N O3 P
Purity： 99%

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Molecular Formula:C18H16 N O3 P
Molecular Weight:325.304
Vapor Pressure:6.66E-08mmHg at 25°C
Boiling Point:438.9°Cat760mmHg
Flash Point:219.2°C
PSA：57.37000
Density:1.284g/cm³
LogP:5.43760

Diphenyl anilinophosphonate(Cas 3848-51-9) Usage

General Description

Diphenyl anilinophosphonate is a chemical compound with the formula C12H11NO2P. It is a phosphonate ester, which means it contains a phosphorus atom that is bonded to two oxygen atoms and to a carbon atom of an aniline group. Diphenyl anilinophosphonate is commonly used as a flame retardant and plasticizer in various materials such as plastics, polymers, and resins. Its ability to reduce the flammability of these materials makes it a valuable additive in the manufacturing of items such as electrical equipment, cables, and textiles. Diphenyl anilinophosphonate is also known for its thermal stability and resistance to leaching, making it a reliable choice for long-term fire protection. Additionally, its low toxicity and relatively low cost make it a preferred option for many industrial applications.

InChI:InChI=1/C18H16NO3P/c20-23(19-16-10-4-1-5-11-16,21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15H,(H,19,20)

3848-51-9 Relevant articles

Kinetics and mechanism of the anilinolysis of aryl phenyl isothiocyanophosphates in acetonitrile

Barai, Hasi Rani,Lee, Hai Whang

, p. 615 - 620 (2013)

Kinetic studies on the reactions of Y-ar...

The Step-Wise Synthesis of Oligomeric Phosphoramidates

Data, Shailja,Leung Wai, Jeffery,Kumar, Saawan,Cameron, Alan J.,Trehet, Manon,Itumoh, Emeka J.,Feld, Joey,S?hnel, Tilo,Leitao, Erin M.

supporting information, p. 5468 - 5477 (2021/09/30)

In this study, the step-wise synthesis t...

Synthesis and extraction behavior of alkyl and cyclic aminophosphonates towards actinides

Das, Dhrubajyoti,Brahmmananda Rao,Sivaraman,Sivaramakrishna, Akella,Vijayakrishna, Kari

, p. 597 - 604 (2018/07/13)

Alkyl and cyclic substituted aminophosph...

Synthesis method of aromatic amide phosphate compound and flame retardant containing compound

-

Paragraph 0063; 0064; 0065; 0066, (2017/02/02)

The invention discloses a one-pot synthe...

METHOD FOR PRODUCING PHOSPHORIC ACID ESTER AMIDE

-

Paragraph 0105-0106, (2016/12/07)

PROBLEM TO BE SOLVED: To provide a metho...

3848-51-9 Process route

: 62-53-3
aniline

: 2524-64-3
chlorophosphoric acid diphenyl ester

: 3848-51-9
phenyl-amidophosphoric acid diphenyl ester

Conditions

Conditions	Yield
With water; In acetonitrile; at 25 ℃; Rate constant;	95%
With water; In acetonitrile; at 25 ℃;	95%
With α-picoline; In 1,3,5-trimethyl-benzene; at 165 - 175 ℃; for 0.5h; Reagent/catalyst; Solvent;	95.1%
With triethylamine; In tetrahydrofuran; Cooling with ice;	84.29%
In benzene; for 1h; Heating;	54%
With triethylamine; at 20 ℃; for 16h; Inert atmosphere;	52%
With tetrachloromethane;
With water;
With pyridine;
In benzene;

In acetonitrile; at 45 - 65 ℃; Rate constant; Mechanism; Kinetics;
In acetonitrile; at 55 ℃; Kinetics; Mechanism;
In acetonitrile; at 35 ℃; Kinetics;
In acetonitrile; at 55 ℃; Concentration; Kinetics;
In acetonitrile; at 55 ℃; Kinetics;
In acetonitrile; at 55 ℃; Kinetics;

: 62-53-3
aniline

: 108-95-2,27073-41-2
phenol

: 18995-02-3
phenyl (N,N'-phenyl)phosphorodiamidate

: 3848-51-9
phenyl-amidophosphoric acid diphenyl ester

Conditions

Conditions	Yield
phenol; With magnesium chloride; trichlorophosphate; In 1,2-dichloro-ethane; at 70 - 100 ℃; for 2h; aniline; With triethylamine; In dichloromethane; 1,2-dichloro-ethane; at 30 - 70 ℃; for 2h; Overall yield = 76.55 %; Overall yield = 48.54 g;