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2,6-di-tert-butyl-4-[(phenylsulfanyl)methyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17258-84-3

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17258-84-3 Usage

Commonly Known As

DSTP

Physical Form

White to off-white crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Functionality

Hindered phenolic antioxidant and ultraviolet light stabilizer

Antioxidant Mechanism

Inhibits oxidation of polymers by scavenging free radicals

UV Stabilization

Absorbs and stabilizes UV radiation, protecting polymers from sunlight damage

Thermal Stability

Exhibits high thermal stability

Volatility

Low volatility

Industrial Applications

Used in plastics, rubber, and adhesives production

Safety

Non-toxic and non-carcinogenic

Consumer Applications

Suitable for food packaging and other consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 17258-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,5 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17258-84:
(7*1)+(6*7)+(5*2)+(4*5)+(3*8)+(2*8)+(1*4)=123
123 % 10 = 3
So 17258-84-3 is a valid CAS Registry Number.

17258-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(phenylsulfanylmethyl)phenol

1.2 Other means of identification

Product number -
Other names 3,5-Di-t-butyl-4-hydroxybenzylsulfid

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:17258-84-3 SDS

17258-84-3Downstream Products

17258-84-3Relevant academic research and scientific papers

SYNTHESIS OF SOME THIOMETHYL DERIVATIVES OF 2,6-DI-tert-BUTYLPHENOL AND THEIR ANTIOXIDANT CHARACTERISTICS

Bilalov, S. B.,Alieva, F. D.,Gasanov, B. R.

, p. 1355 - 1357 (2007/10/02)

The reactions of 3,5-di-tert-butyl-4-hydroxybenzyl-N-N-dimethylamine with various thiols leads to the formation of 3,5-di-tert-butyl-4-hydoxybenzyl alkyl (aryl) sulfides.By means of their electrochemical oxidation at a stationary graphite microelectrode in aqueous media over a wide range of pH it was established that the new sulfides have the same level of antiradical activity as ionole. 3,5-Ditert-butyl-4-hydroxybenzyl sulfide is the most easily oxidized.

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