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Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester is a chemical compound that serves as a stabilizer, UV absorber, antioxidant, and plant growth regulator. It is widely used in various industries to protect materials from degradation and enhance their performance.

980-17-6

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980-17-6 Usage

Uses

Used in Plastics Industry:
Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester is used as a stabilizer for plastics to protect them from degradation caused by exposure to UV radiation. It acts as an antioxidant to prevent the oxidation of plastics, thereby enhancing their durability and performance.
Used in Polymers Industry:
In the polymers industry, Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester is used as a UV absorber to protect polymers from the harmful effects of UV radiation. This helps maintain the integrity and appearance of the polymers over time.
Used in Coatings, Adhesives, and Sealants Production:
Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester is used in the production of coatings, adhesives, and sealants to enhance their resistance to UV radiation and oxidation. This improves the overall performance and longevity of these products.
Used in Agricultural Industry:
In the agricultural industry, Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester is used as a plant growth regulator. It helps in promoting healthy plant growth and development, contributing to increased crop yields.
However, it is important to handle Phosphonic acid, [[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]-, bis(1-methylethyl) ester with caution due to its potential health hazards and environmental impact. Proper safety measures should be taken to minimize any risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 980-17-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 980-17:
(5*9)+(4*8)+(3*0)+(2*1)+(1*7)=86
86 % 10 = 6
So 980-17-6 is a valid CAS Registry Number.

980-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diisopropyl (3,5-di-tert-butyl-4-hydroxybenzyl)phosphonate

1.2 Other means of identification

Product number -
Other names (3,5-Di-tert-butyl-4-hydroxy-benzyl)-phosphonic acid diisopropyl 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:980-17-6 SDS

980-17-6Relevant academic research and scientific papers

Silver(I) Promoted the C4-H Bond Phosphonation of 1-Naphthylamine Derivatives with H-Phosphonates

Zhao, Lixiao,Sun, Mengmeng,Yang, Fan,Wu, Yangjie

, p. 11519 - 11530 (2021/09/02)

A simple and efficient protocol for silver-promoted direct C-H phosphonation of 1-naphthylamine derivatives with H-phosphonates was described. This reaction proceeded smoothly for 1-naphthylamine derivatives at the C4 site, providing a facile and efficient route to 4-phosphonated 1-naphthylamine derivatives. This phosphonation could tolerate a diverse type of functional groups at the pyridinyl and naphthyl moieties. Further functionalization of the phosphonated product was also explored at the C2 and C8 sites, such as fluoridation, methylation, methoxylation, and amination. In addition, DFT studies of the reaction intermediate showed that the most electrophilic reactive site is at the C4 site in the naphthyl ring.

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