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DIETHYL 1-DECYLPHOSPHONATE is an organophosphorus compound characterized by its colorless to pale yellow liquid appearance and a faint odor. It is a plasticizer and serves as an intermediate in the synthesis of other chemicals. DIETHYL 1-DECYLPHOSPHONATE exhibits low volatility, is insoluble in water, and is soluble in organic solvents. It is relatively stable under normal conditions but can react violently with strong oxidizing agents. Due to potential health hazards, it requires careful handling in industrial applications.

16165-68-7

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16165-68-7 Usage

Uses

Used in Chemical Industry:
DIETHYL 1-DECYLPHOSPHONATE is used as a plasticizer to increase the flexibility and workability of various plastics, making them more suitable for specific applications.
Used in Pharmaceutical Industry:
DIETHYL 1-DECYLPHONATE is used as an intermediate in the production of pharmaceuticals, contributing to the synthesis of active ingredients or other essential components of medications.
Used in Agrochemical Industry:
DIETHYL 1-DECYLPHONATE is employed as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides, to enhance their effectiveness in agricultural applications.
Used in Industrial Chemical Production:
DIETHYL 1-DECYLPHONATE is utilized as an intermediate in the manufacturing process of various industrial chemicals, playing a crucial role in the development of new compounds with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 16165-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16165-68:
(7*1)+(6*6)+(5*1)+(4*6)+(3*5)+(2*6)+(1*8)=107
107 % 10 = 7
So 16165-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H31O3P/c1-4-7-8-9-10-11-12-13-14-18(15,16-5-2)17-6-3/h4-14H2,1-3H3

16165-68-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L13038)  Diethyl 1-decylphosphonate, 97%   

  • 16165-68-7

  • 5g

  • 339.0CNY

  • Detail
  • Alfa Aesar

  • (L13038)  Diethyl 1-decylphosphonate, 97%   

  • 16165-68-7

  • 25g

  • 1250.0CNY

  • Detail

16165-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-diethoxyphosphoryldecane

1.2 Other means of identification

Product number -
Other names diethyl n-decylphosphonate

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:16165-68-7 SDS

16165-68-7Downstream Products

16165-68-7Relevant academic research and scientific papers

Structural and vibrational characteristics of amphiphilic phosphonate salts

Boczula, Dorota,Ca?y, Alicja,Dobrzyńska, Danuta,Janczak, Jan,Zoń, Jerzy

, p. 220 - 226 (2012)

1-Decylphosphonic acid (1), ammonium 1-decylphosphonate (NH 4C10H21PO3H) (2), ethylenediaminium 1-decylphosphonate 1,5 hydrate (enH2C10H 21PO3·1.5H2O) (3) and calcium 1-decylphosphonate (Ca(C10H21PO3H)2) (4) were prepared and characterized by IR and Raman spectroscopy. The structures of 2 and 3 were determined by single crystal X-ray diffraction analysis. Compound 2 crystallizes in the P1? space group of triclinic system with two molecules in the asymmetric unit cell whereas compound 3 crystallizes in C2/c space group of monoclinic system with four molecules in the unit cell and both exhibit layered supramolecular structures generated by ionic interaction, H-bonding and alkyl chain interdigitation in the case of 3. The FT-IR and Raman spectra have been assigned in the range 4000-500 cm-1 for all compounds, and reveal the trans conformation of alkane chain in all compounds.

Copper-catalyzed allylic C-H phosphonation

Yang, Bin,Zhang, Hong-Yu,Yang, Shang-Dong

supporting information, p. 3561 - 3565 (2015/03/30)

An efficient copper-catalyzed allylic C-H phosphonation reaction has been developed under mild reaction conditions. This method exhibits high regioselectivity and stereoselectivity. Various alkenes with useful functional groups are compatible in this tran

Phosphorus containing compounds as antihypercholesterolemic and antiatherosclerotic agents

-

, (2008/06/13)

Novel phosphorus containing compounds are described, as well as methods for the preparation and pharmaceutical composition of same, which are useful in preventing the intestinal absorption of cholesterol and thus are useful in the treatment of hypercholesterolemia and atherosclerosis.

Phosphonate Complexes. Part 6. Influence of Steric Effects, Solvation, and Chelation on Stability

Wozniak, Michel,Nowogrocki, Guy

, p. 2423 - 2428 (2007/10/02)

The interaction of some phosphonic acids RPO(OH)2, chosen to introduce different controlling factors (R=But, cyclo-C6H11, pH, n-C10H21, Me2NCMe2, CH2SEt, CH2CH2CO2(-)), with Ca(II) and Cu(II) has been investigated by potentiometry at 25 deg C, I=0.1 mol dm-3 (K).The selection of the species and the refinement of the stability constants illustrates the applicability of a new version of the program MUCOMP.Examination of linear free-energy plots indicates that factors other than polar effects are of significance, i.e. chelate formation with the potentially bidentate ligands and particularly solvation effects which preferentially stabilize the complexes of α- branched-chain phosphonates.Other features (steric hindrance, predominance of some microscopic forms) are discussed.

Organophosphonic acids or esters containing an epoxy group

-

, (2008/06/13)

A method for protecting the surface of a metal surface which comprises applying to said surface an organophosphorus compound of the formula STR1 wherein A IS 0 OR 1 R is a branched or unbranched chained bivalent alkylene radical of 1 to 12 carbon atoms which is substituted or unsubstituted and can contain in the chain structure --O--, --S--, STR2 R' is a branched or unbranched alkyl radical of 1 to 12 carbon atoms which can be halogen substituted and can contain in the chain structure STR3 X is an epoxy ring, halogen, alkylene, carboxylic acid ester residue, amino, isocyanato, isothiocyanato, urea, thiourea, urethano, alkyl substituted thio radical or the radical or a heterocyclic ring containing O, S or N in the ring structure; a new organophosphorus compounds having the formula set forth above and more particularly defined by specific chemical structures.

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