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o-Decylphenol, also known as 2-phenyl-1-decanol, is an organic compound with the chemical formula C16H26O. It is a colorless to pale yellow liquid with a mild, aromatic odor. This phenolic compound is derived from the reaction of o-cresol and decanol and is commonly used as a nonionic surfactant, emulsifier, and stabilizer in various industrial applications, including the manufacturing of lubricants, fuels, and detergents. Due to its potential environmental and health concerns, the use of o-deylphenol is subject to regulations in many countries.

2985-64-0

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2985-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2985-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2985-64:
(6*2)+(5*9)+(4*8)+(3*5)+(2*6)+(1*4)=120
120 % 10 = 0
So 2985-64-0 is a valid CAS Registry Number.

2985-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name o-dodecylphenol

1.2 Other means of identification

Product number -
Other names decyl phenol

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:2985-64-0 SDS

2985-64-0Relevant academic research and scientific papers

Alkylation of Phenol by 1-Dodecene and 1-Decanol. A Literature Correction

Campbell, Curt B.,Onopchenko, Anatoli,Santilli, Donald S.

, p. 3665 - 3669 (2007/10/02)

A recent literature report that 1-dodecene reacts with phenol in the presence of sulfated zirconium oxide (superacid), or 1-dodecanol with phenol in the presence of H-Mordenite (zeolite), to afford mostly para-substituted alkylphenols has been shown to be incorrect.The product with zirconium is a mixture of ortho/para isomers (ca. 50-65/50-35), and not the exclusive para isomer as reported.The major product in the case of zeolite catalysis is the o-alkylphenol, with a high degree of end attachment, and not the predominantly claimed para isomers.The selectivity obtained with H-Mordenite during alkylation of phenol differs from the a lkylation of alkylbenzenes and anisole, and is best explained on the basis of a surface catalysis phenomenon.

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