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2,2'-thiobis(4-nonylphenol) is a chemical compound belonging to the nonylphenol family, characterized by its endocrine-disrupting properties and potential environmental hazards. It is known for its persistence in the environment, being found in soil, water, and biota, and has been associated with negative impacts on aquatic life and potential toxic effects on human health.

1258-75-9

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1258-75-9 Usage

Uses

Used in Rubber Industry:
2,2'-thiobis(4-nonylphenol) is used as an antioxidant in rubber products to enhance their durability and resistance to degradation, thereby extending their service life and improving performance.
Used in Plastics Industry:
In the plastics industry, 2,2'-thiobis(4-nonylphenol) serves as a stabilizer, preventing the degradation of plastic materials and maintaining their structural integrity over time.
However, due to the growing concern about the environmental and health risks associated with 2,2'-thiobis(4-nonylphenol), regulatory restrictions have been imposed in some regions to limit its use and release into the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1258-75-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1258-75:
(6*1)+(5*2)+(4*5)+(3*8)+(2*7)+(1*5)=79
79 % 10 = 9
So 1258-75-9 is a valid CAS Registry Number.

1258-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxy-5-nonylphenyl)sulfanyl-4-nonylphenol

1.2 Other means of identification

Product number -
Other names EINECS 215-020-7

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:1258-75-9 SDS

1258-75-9Upstream product

1258-75-9Downstream Products

1258-75-9Relevant academic research and scientific papers

Synthesis and antioxidancy of some n-Alkyl, t-Alkyl, homologous and isomeric lipidic alkylthiobisphenols

Tyman, John H. P.,Johnson, Robert A.

, p. 573 - 578 (2008/09/21)

To study the relationship between structure and properties of members of the lipidic thiobis phenol series, as extreme pressure additives in lubricants, a series of homologous compounds has been synthesised by the reaction of alkylphenols with sulphur dichloride. The isomeric n-nonylphenols have been reacted to form the C9 isomeric 2,2′-and 4,4′-thiobisphenols. Longer alkyl side-chains resulted mainly in the formation of 4,4′-thiobisphenols and some of the 2,2′ isomer. With short alkyl, particularly t-alkyl side-chains, steric hindrance resulted in the 2,2′-compound. Additive studies have indicated that the longer chain 4,4′ compounds possessed antioxidant properties comparable and superior to former commercial branched chain 2,2′ compounds produced from petrochemical intermediates. AOCS 2007.

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