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N-Capric acid N-heptyl ester, also known as heptyl caprate, is a chemical compound with the molecular formula C15H30O2. It is an ester formed by the condensation of capric acid and heptyl alcohol, characterized by its emollient and emulsifying properties.

60160-17-0

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60160-17-0 Usage

Uses

Used in Cosmetics and Personal Care Industry:
N-Capric acid N-heptyl ester is used as an emollient and emulsifier for its ability to soften and hydrate the skin, improving the texture and consistency of cosmetic and personal care products.
Used in Industrial Applications:
In the industrial sector, N-capric acid N-heptyl ester is utilized as a lubricant and plasticizer due to its lubricating and smoothing properties, contributing to the production of various industrial goods that require these characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 60160-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60160-17:
(7*6)+(6*0)+(5*1)+(4*6)+(3*0)+(2*1)+(1*7)=80
80 % 10 = 0
So 60160-17-0 is a valid CAS Registry Number.

60160-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Heptyl Decanoate

1.2 Other means of identification

Product number -
Other names 2-heptyl decanoate

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:60160-17-0 SDS

60160-17-0Downstream Products

60160-17-0Relevant academic research and scientific papers

Specific enzyme-catalyzed hydrolysis and synthesis in aqueous and organic medium using biocatalysts with lipase activity from Aspergillus niger MYA 135

Romero, Cintia M.,Pera, Licia M.,Loto, Flavia,Baigori, Mario D.

, p. 1361 - 1368 (2013/01/15)

In the present study, the specific hydrolytic activity of three biocatalysts such as the constitutive mycelium-bound lipase, the induced mycelium-bound lipase and the lyophilized induced supernatant from A. niger MYA 135 was evaluated in both aqueous and organic media.A direct correlation between activity in water and n-hexane was not observed for the same hydrolytic reaction. The n-hexane/water activity ratio (RO/A) was applied to characterize the activity in organic medium. The three biocatalysts showed RO/A values higher than 1 for hydrolysis of long-chain fatty acid esters, demonstrating a higher specific hydrolytic activity in organic solvent than in water. A different behavior was observed during hydrolysis of middle-chain fatty acid esters, which was higher in aqueous medium (R O/Adw) observed in a reaction mixture containing propanol and p-nitrophenyl laurate. Finally, both p-nitrophenyl caprate (C10) and p-nitrophenyl laurate (C12) were preferentially methanolized by the lyophilized induced supernatant, being this lipase activity the most specific biocatalyst preparation under transesterification conditions. A selectivity-based analysis of each lipase preparation toward transesterification or hydrolysis in organic medium was evaluated as well. Springer Science+Business Media, LLC 2012.

ESSENTIAL OIL PRODUCED BY CHRYSOSPORIUM XEROPHILUM IN COCONUT

Kinderlerer, Judith L.,Hatton, Paul V.,Chapman, Amanda J.,Rose, Malcolm E.

, p. 2761 - 2764 (2007/10/02)

An essential oil (0.3percent v/w) was produced after fermentation of coconut for nine months by Chrysosporium xerophilum.Sixty per cent of the volatiles were aliphatic methyl ketones (C5-C13), esters and secondary alcohols whilst 38percent were present as free medium chain length fatty acids (C6-C12).A new class of ester, 2-heptyl esters of C8, C10 and C12 fatty acids, was identified by GC-MS and confirmed by synthesis.It is suggested that ester formation, ketone formation and alkane synthesis are mechanisms for removing medium chain fatty acids (C6-C12) which, if allowed to accumulate in the substrate, would be toxic to the fungus.Key Word Index - Cocos nucifera; Palmae; Chrysosporium xerophilum; fungus; substrate conversion coconut; methyl ketones; 2-heptyl esters; detoxification.

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