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4-(1-Butylpentyl)-phenol, also known as 4-(1-butylpentan-1-yl)phenol, is an organic compound with the molecular formula C15H24O. It is a colorless to pale yellow liquid with a molecular weight of 220.35 g/mol. This chemical is characterized by a phenol group attached to a long alkyl chain, which consists of a butyl group and a pentyl group. 4-(1-Butylpentyl)-phenol is primarily used as an intermediate in the synthesis of various chemicals, including antioxidants, plasticizers, and other specialty chemicals. It is also known for its potential applications in the pharmaceutical and fragrance industries. Due to its chemical structure, it exhibits properties such as low solubility in water and high solubility in organic solvents.

6465-76-5

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6465-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6465-76-5 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 6465-76:
(6*6)+(5*4)+(4*6)+(3*5)+(2*7)+(1*6)=115
115 % 10 = 5
So 6465-76-5 is a valid CAS Registry Number.

6465-76-5SDS

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-(1-Butylpentyl)-phenol

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

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More Details:6465-76-5 SDS

6465-76-5Relevant academic research and scientific papers

The monolayer structure of the branched nonyl phenol oxyethylene glycols at the air-water interface

Green,Su,Lu,Penfold

, p. 1507 - 1515 (2007/10/03)

The behavior of the para-substituted nonyl phenol ethoxylates with branched nonyl chains at the air-water interface was studied to examine the effect of branching in the alkyl chain and the insertion of a benzyl ring in the alkyl chain on the monolayer structure of the nonionic surfactant. A series of para-(C4H9)2CHC6H4(OC2H4)nOH (BNPE), where n=4,8, and 12 were used in the surface tension measurements. The CMC was 1.1 ± 0.3 x 10-5 M for BNPE4, 4.0 ± 0.3 x 10-5 M for BNPE8, and 8.0 ± 0.3 x 10-5 M for BNPE12; the limiting area per molecule (Acmc) at the cmc was 46 ± 3, 61 ± 4, and 75 ± 5 sq A, respectively. For the same size of headgroups, the Acmc values were almost the same as those obtained from dodecyl ethoxylates. This indicated that Acmc for these nonionic surfactants are dependent on the size of headgroups and independent of the chemical structure of the hydrophobic chains. Nonyl phenol layers projected onto the surface normal direction were 18 ± 3 A (BNPE4), 19 ± 3 A (BNPE8), and 22 ± 3 A (BNPE12). These layers, in all cases, were nearly twice as thick as the fully extended chain, suggesting that the hydrophobic chain are widely distributed across the layer an extensive resulting in a strong mixing of the chain with the ethoxylate groups.

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