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DI-N-DECYL PHOSPHITE is an organic phosphite ester with the molecular formula C20H45O3P, belonging to the group of phosphites used as additives in various industrial processes.

7000-66-0

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7000-66-0 Usage

Uses

Used in Polymer Production:
DI-N-DECYL PHOSPHITE is used as a stabilizer and antioxidant for preventing degradation from heat and oxidation in the production of polymers such as polyethylene and polypropylene.
Used in PVC Resin Production:
DI-N-DECYL PHOSPHITE is used as a processing aid in the production of PVC resins.
Used in Synthetic Rubber Production:
DI-N-DECYL PHOSPHITE is used as a stabilizer in the production of synthetic rubbers.
Used in Lubricant and Metalworking Fluid Production:
DI-N-DECYL PHOSPHITE is used to improve thermal stability and resistance to oxidation in the production of lubricants and metalworking fluids.

Check Digit Verification of cas no

The CAS Registry Mumber 7000-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7000-66:
(6*7)+(5*0)+(4*0)+(3*0)+(2*6)+(1*6)=60
60 % 10 = 0
So 7000-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H42O3P/c1-3-5-7-9-11-13-15-17-19-22-24(21)23-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3/q+1

7000-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name didecoxy(oxo)phosphanium

1.2 Other means of identification

Product number -
Other names phosphonic acid bis-decyl ester

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:7000-66-0 SDS

7000-66-0Downstream Products

7000-66-0Relevant academic research and scientific papers

Phosphine catalyzed addition of long-chain dialkyl phosphites to electron-deficient alkenes

Il’in, Anton,Gubaev, Arthur,Antonova, Anna,Khannanov, Arthur,Galkin, Vladimir

, p. 3287 - 3297 (2020)

Conjugate addition of the long chain dialkyl phosphites to electron-deficient alkenes under PBu3 catalysis afforded the corresponding phosphonates in good yields in a short reaction time. Long chain alkyl groups in the phosphites were well tolerated in this transformation. The products of this reaction are of particular interest as components of lubrication oil composition.

Convenient preparation of long-chain dialkyl phosphates: Synthesis of dialkyl phosphates

Aitken, R. Alan,Collett, Chris J.,Mesher, Shaun T. E.

scheme or table, p. 2515 - 2518 (2012/09/05)

Reaction of phosphorus oxychloride with a primary alcohol (1.8 equiv) and triethylamine (1.8 equiv) in toluene, followed by filtration and treatment with steam, gives dialkyl phosphates in good yield and essentially free from trialkyl phosphate contamination. Georg Thieme Verlag Stuttgart · New York.

Synthesis of AZT 5′-O-hydrogen phospholipids and their derivatives

Xiao, Qiang,Sun, Jing,Sun, Qi,Ju, Yong,Zhao, Yu-fen,Cui, Yu-xin

, p. 107 - 111 (2007/10/03)

A series of AZT 5′-O-hydrogen phospholipids 5a-e were synthesized by a tandem transesterification of diphenyl phosphite (DPP) with AZT and a long-chain alcohol. This method has the merits of easy operation and high yields. The corresponding phosphonates, phosphorothionates and phosphoroselenoates of 5d and 5e and the phosphoramidates conjugated with L-amino acid methyl ester 9a and 9b were also synthesized.

Novel approach to the synthesis of AZT 5′-O-hydrogen phospholipids

Xiao, Qiang,Sun, Jing,Ju, Yong,Zhao, Yu-Fen,Cui, Yu-Xin

, p. 5281 - 5283 (2007/10/03)

A series of AZT 5′-O-hydrogen phospholipids were synthesized by a tandem transesterification of diphenyl phosphite with AZT and a long-chain alcohol. The method possesses the merits of ease of operation and high yields. It can also be extended to synthesize other biological phospholipids.

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