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Phenol, 4-(1-butylhexyl)-, also known as 4-(1-butylhexyl)phenol or 4-n-butylphenol, is an organic compound with the chemical formula C14H22O. It is a derivative of phenol, where a butylhexyl chain is attached to the para position (4th position) of the phenol ring. Phenol, 4-(1-butylhexyl)- is a colorless to pale yellow liquid with a mild, characteristic odor. It is used as an intermediate in the synthesis of various chemicals, including antioxidants, plasticizers, and resins. Due to its chemical structure, it exhibits properties such as low solubility in water and high solubility in organic solvents. Phenol, 4-(1-butylhexyl)-, is also known for its potential environmental and health concerns, as it can be toxic and may cause skin irritation or other adverse effects.

6465-79-8

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6465-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6465-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6465-79:
(6*6)+(5*4)+(4*6)+(3*5)+(2*7)+(1*9)=118
118 % 10 = 8
So 6465-79-8 is a valid CAS Registry Number.

6465-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-decan-5-ylphenol

1.2 Other means of identification

Product number -
Other names -

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:6465-79-8 SDS

6465-79-8Relevant academic research and scientific papers

Equilibria for the isomerization of (secondary-alkyl)phenols and cyclohexylphenols

Nesterova, T. N.,Pimerzin, A. A.,Rozhnov, A. M.,Karlina, T. N.

, p. 385 - 396 (2007/10/02)

Equilibria of a series of isomerizations and trans-alkylations of alkylphenols have been investigated in the liquid phase over a wide range of temperatures.Equilibria of isomerizations connected with the displacement of a substituent on a benzene nucleus were studied for secondary-butyl, -amyl, -hexyl, and cyclohexyl-phenols, and di-(secondary-butyl)phenols.Equilibria of positional isomerization connected with the displacement of an oxyphenyl radical in an alkyl chain were investigated for oxyphenyl-pentanes, -hexanes, -octanes, and -decanes.Trans-alkylation was investigated for di- and tri-(secondary-butyl)phenols.Values of ΔrH0m and ΔrS0m were found for all investigated reactions.An analysis was made of the thermodynamic quantities for the reactions.Enthalpies of formation of isopropylphenols (IPP) in the gaseous state were calculated.The values of ΔfH0m/(kJ * mol-1) were found at 298.15 K: o-IPP, -(175.3 +/- 2.4); p-IPP, -(175.3 +/- 2.4); m-IPP, -(175.3 +/-2.4); 2,4-di-IPP, -(254.1 +/- 2.8); 2,5-di-IPP, -(254.1 +/- 2.8); 2,6-di-IPP, -(254.1 +/- 2.8); 3,5-di-IPP, -(254.1 +/- 2.8); 2,4,6-tri-IPP, -(333.0 +/- 3.1).

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