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Phenol, 4-methyl-2-octyl-, also known as 4-Methyl-2-octylphenol or 2-(4-Methylphenyl)octanol, is an organic compound with the chemical formula C15H24O. It is a derivative of phenol, featuring a phenolic hydroxyl group attached to a branched octyl chain with a methyl group at the 4-position. Phenol, 4-methyl-2-octyl- is characterized by its aromatic ring and a long aliphatic chain, which gives it unique properties such as low water solubility and high boiling point. It is primarily used as an intermediate in the synthesis of various chemicals, including antioxidants, UV stabilizers, and other specialty chemicals. Due to its chemical structure, it may exhibit certain toxicological properties, and therefore, it is essential to handle it with care and follow proper safety guidelines.

886-00-0

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886-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 886-00-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 886-00:
(5*8)+(4*8)+(3*6)+(2*0)+(1*0)=90
90 % 10 = 0
So 886-00-0 is a valid CAS Registry Number.

886-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-octylphenol

1.2 Other means of identification

Product number -
Other names 2-n-octyl-p-cresol

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:886-00-0 SDS

886-00-0Downstream Products

886-00-0Relevant academic research and scientific papers

Phenol transalkylation process

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, (2008/06/13)

Phenols having an unsubstituted ortho position are transalkylated in the ortho position by mixing them with an ortho-alpha-branched alkylphenol (e.g., 2,6-di-sec-butylphenol) and an aluminum phenoxide catalyst and heating the mixture to 100°-350°C., preferably in a closed system and in the presence of olefin corresponding in structure to the ortho-alpha-branched alkyl group.

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