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DI-N-PROPYLPHOSPHATE (1:1 mixture of mono and di) is a chemical compound consisting of a 50/50 blend of mono and di-n-propylphosphate esters. It is an organophosphorus compound with the molecular formula C6H15O4P. This mixture is primarily used as a flame retardant and plasticizer in various industrial applications, such as plastics, rubber, and adhesives. Due to its phosphorus content, it exhibits excellent flame-retardant properties, making it a valuable additive in the production of materials that require resistance to fire. However, it is essential to handle this chemical with care, as it may have potential health and environmental risks, and proper safety measures should be taken during its use and disposal.

1804-93-9

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1804-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1804-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1804-93:
(6*1)+(5*8)+(4*0)+(3*4)+(2*9)+(1*3)=79
79 % 10 = 9
So 1804-93-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H15O4P/c1-3-5-9-11(7,8)10-6-4-2/h3-6H2,1-2H3,(H,7,8)

1804-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dipropyl hydrogen phosphate

1.2 Other means of identification

Product number -
Other names di-n-propylphosphate

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:1804-93-9 SDS

1804-93-9Downstream Products

1804-93-9Relevant academic research and scientific papers

METHOD FOR PRODUCING PHOSPHOESTER COMPOUND

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Paragraph 0023; 0026-0028, (2021/09/27)

PROBLEM TO BE SOLVED: To provide a method whereby, a phosphate compound selected from the group consisting of orthophosphoric acid, phosphonic acid, phosphinic acid, and anhydrides of them is used as raw material and, by one stage reaction, a corresponding phosphoester compound is produced. SOLUTION: To an aqueous solution of a phosphate compound, added is an organic silane or siloxane compound having an alkoxy group or an aryloxy group, and the mixture is subjected to a heating reaction, thereby producing a corresponding phosphoester compound without requiring a catalyst. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Reactivity of an electrophilic hypervalent iodine trifluoromethylation reagent with hydrogen phosphates - A mechanistic study

Santschi, Nico,Geissbühler, Patrik,Togni, Antonio

, p. 83 - 86 (2012/03/27)

The electrophilic trifluoromethylation of hydrogen phosphates with the reagent trifluoromethyl-1,3-dihydro-3,3-dimethyl-1,2-benziodoxole (1) was studied by means of initial rates determined for pseudo first order setups and subsequent Taft analysis of the calculated relative rates. A positive polar sensitivity factor, indicative of a negative charge forming during the rate-determining step, was found for the whole data set.

Oxidative alkoxylation of zinc phosphide in alcoholic solutions of copper(II) chloride

Dorfman,Ibraimova,Polimbetova

, p. 50 - 55 (2007/10/03)

Oxidative alkoxylation of Zn3P2 with the formation of valuable phosphoric and phosphorous acid esters occurred at a high rate and with a high selectivity in alcoholic solutions of CuCl2 under the action of oxygen at 30-60°C. Depending on the nature of the alcohol, two products were formed, namely, trialkyl phosphates (RO)3PO and dialkyl phosphites (RO)2HPO. Water favored the formation of dialkyl phosphates (RO)2(HO)PO. The kinetics and mechanism of the new catalytic reaction were studied, and the optimal conditions for conducting this reaction were found. The reaction proceeded in a topochemical mode by a separate redox mechanism.

Synthesis of Trialkyl Phosphates from White Phosphorus

Romakhin,Nikitin

, p. 1023 - 1026 (2007/10/03)

A new method was proposed for preparing trialkyl phosphates directly from white phosphorus by its electrolysis in a mixture of acetonitrile, alcohol, and water with tetraethylammonium iodide as supporting electrolyte. To increase the amount of the product synthesized in the unit volume of the electrolyte solution and the productivity of the process, phosphorus and water are added to the electrolyte in portions, which allows synthesis of up to 1 mol of trialkyl phosphate in 1 1 of the electrolyte solution.

Synthesis of dialkyl phosphites and trialkyl phosphates by oxidation of sodium hypophosphite by copper(II) chloride

Dorfman, Ya. A.,Aleshkova. M. M.

, p. 515 - 520 (2007/10/03)

Sodium hypophosphite oxidazies in alcoholic solution of CuCl2 at 50-80 deg C to give dialkyl phosphite and trialkyl phosphate.The yield of trialkyl phosphate increases with decreasing molecular weight of the alcohol and reaches ca. 100percent for MeOH and EtOH.The optimal conditions were found, and the mechanism of oxidation of NaPH2O2 to (RO)2PHO and (RO)3PO by copper(II) chloride was studied.The reaction proceeds via the formation of alkyl hypophosphite and copper(II) complexes with alkyl hypophosphite and dialkyl phosphite, which undergo inner-sphere two-electron redox decomposition with the liberation of dialkyl phosphite and trialkyl phosphate, respectively.

CONVENIENT SYNTHETIC ROUTE TO MONO- OR DIAKLYL PHOSPHATE FROM INORGANIC PHOSPHORUS ACIDS

Okamoto, Yoshiki,Kusano, Tetuya,Takamuku, Setsuo

, p. 195 - 200 (2007/10/02)

Mono- or dialkyl phosphate was synthesized in a favorable yield by oxidation of phosphonic or phosphinic acid in alcohol with oxygen at the presence of a catalytic amount of copper(II)chloride.The reaction may proceed via the formation of corresponding phosphorochloridate or phosphorochloridite.

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