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Phosphoric acid, 2-naphthalenyl diphenyl ester, also known as diphenyl 2-naphthyl phosphate, is an organophosphorus compound that is synthesized through an esterification reaction between phosphoric acid and 2-naphthol. It is an ester, a class of organic compounds formed by the condensation of acids and alcohols, and is known for its strong effectiveness in enhancing flame retardancy.

18872-49-6

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18872-49-6 Usage

Uses

Used in Material Science:
Phosphoric acid, 2-naphthalenyl diphenyl ester is used as a flame retardant for materials that require high fire resistance. Its strong effectiveness in enhancing flame retardancy makes it a valuable component in the production of materials that need to meet stringent safety standards.
Used in Flame Retardancy Applications:
In the flame retardancy industry, phosphoric acid, 2-naphthalenyl diphenyl ester is used as a key ingredient in the formulation of flame retardant products. Its ability to improve the fire resistance of materials is crucial for applications in various industries where safety is a priority.
Safety Considerations:
Due to its potential health risks upon exposure, careful handling of phosphoric acid, 2-naphthalenyl diphenyl ester is recommended to ensure the safety of workers and the environment. Proper safety measures and guidelines should be followed during its synthesis, use, and disposal to minimize any adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 18872-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18872-49:
(7*1)+(6*8)+(5*8)+(4*7)+(3*2)+(2*4)+(1*9)=146
146 % 10 = 6
So 18872-49-6 is a valid CAS Registry Number.

18872-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Naphthalen-2-yl diphenyl phosphate

1.2 Other means of identification

Product number -
Other names Phosphorsaeure-[2]naphthylester-diphenylester

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:18872-49-6 SDS

18872-49-6Downstream Products

18872-49-6Relevant academic research and scientific papers

Phosphorylation Organocatalysts Highly Active by Design

Dobrovetsky, Roman,Fallek, Amit,Kramer, Maria,Portnoy, Moshe,Weiss-Shtofman, Mor

supporting information, (2020/05/01)

The activity of nucleophilic organocatalysts for alcohol/phenol phosphorylation was enhanced through attaching oligoether appendages to a benzyl substituent on imidazole- or aminopyridine-based active units, presumably because of stabilizing n-cation interactions of the ethereal oxygens with the positively charged aza-heterocycle in the catalytic intermediates, and was substantially higher than that of known benchmark catalysts for a range of substrates. Density functional theory calculations and the study of analogues having a lower potential for such stabilizing interactions support our hypothesis.

DBN hexafluorophosphate salts as convenient sulfonylating and phosphonylating agents

Jones, Caroline S.,Bull, Steven D.,Williams, Jonathan M. J.

, p. 8452 - 8456 (2016/09/28)

Air-stable N-sulfonyl and N-phosphonyl DBN hexafluorophosphate salts have been synthesised under mild conditions as sulfonylating and phosphonylating agents. These salts are highly efficient in the sulfonylation and phosphonylation of a range of N- and O-nucleophiles to generate sulfonamides, sulfonate esters, phosphoramidates and phosphonate esters in good yields.

Organocatalytic phosphorylation of alcohols using pyridine- N -oxide

Murray, James I.,Woscholski, Rudiger,Spivey, Alan C.

supporting information, p. 985 - 990 (2015/04/27)

Phosphorylation of alcohols by phosphoryl chlorides catalysed by pyridine-N-oxide is reported. The utility of this method is demonstrated through phosphorylation of primary, secondary and a tertiary alcohol as well as phenols under mild reaction conditions and with low catalyst loading (5 mol%).

PROCESS FOR PREPARATION OF PHOSPHORIC ESTERS

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Page 7-8, (2010/11/30)

A process for preparing a phosphoric ester, comprising: Step (1) of reacting naphthol with phosphorus oxychloride in a molar ratio of 1:1.3 or more in the presence of a metallic halide and removing unreacted phosphorus oxychloride and Step (2) of reacting the reaction product of Step (1) with phenol in a molar ratio (molar ratio of chlorine contained in the reaction product to phenol) of 1:1-1.5 and removing hydrogen chloride produced as a by-product to thereby obtain a phosphoric ester represented by the general formula (I): wherein n is 1 or 2.

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