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HEPTYL CAPRYLATE, also known as Heptyl octanoate, is an ester compound prepared by direct esterification of n-heptanol with n-octanoic acid. It has an oily, green odor and flavor, with taste characteristics described as waxy, fatty, and tropical fruity at 50 ppm.

4265-97-8

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4265-97-8 Usage

Uses

Used in Flavor and Fragrance Industry:
HEPTYL CAPRYLATE is used as a flavoring agent for its waxy, fatty, and tropical fruity taste, adding unique and pleasant aromas to various products.
Used in Cosmetics and Personal Care Industry:
HEPTYL CAPRYLATE is used as a fragrance ingredient, providing a green and oily scent to enhance the sensory experience of cosmetics and personal care products.
Used in the Food Industry:
HEPTYL CAPRYLATE is used as an additive to impart specific flavors and aromas to the food products, enhancing their overall taste and appeal.

Preparation

By direct esterifcation of n-heptanol with n-octanoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 4265-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4265-97:
(6*4)+(5*2)+(4*6)+(3*5)+(2*9)+(1*7)=98
98 % 10 = 8
So 4265-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-3-5-7-9-11-13-15(16)17-14-12-10-8-6-4-2/h3-14H2,1-2H3

4265-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name heptyl octanoate

1.2 Other means of identification

Product number -
Other names Octanoic acid, heptyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:4265-97-8 SDS

4265-97-8Downstream Products

4265-97-8Relevant articles and documents

ESSENTIAL OIL PRODUCED BY CHRYSOSPORIUM XEROPHILUM IN COCONUT

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

, p. 2761 - 2764 (1988)

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.

Kolbe Electrolysis of Biomass-Derived Fatty Acids Over Pt Nanocrystals in an Electrochemical Cell

Yuan, Gang,Wu, Chan,Zeng, Guorong,Niu, Xiaopo,Shen, Guoqiang,Wang, Li,Zhang, Xiangwen,Luque, Rafael,Wang, Qingfa

, p. 642 - 648 (2019/12/24)

Electrochemical valorization of non-food biomass-derived carboxylates into fuels is promising for the conversion, storage, and distribution of renewable electricity. Herein, we demonstrate that biofuels, hydrogen, and bicarbonate can be simultaneously produced in an electrochemical cell by one-step electrolysis of free fatty acids under ambient conditions on 3D self-supported ultralow Pt loading (2 wt %) electrode. The three valuable products can naturally separate from each other during the electrolysis in the alkaline aqueous solution. The experimental suggests that Pt(100) and Pt(110) are favorable for the production of non-Kolbe and Kolbe hydrocarbons, respectively. DFT calculation further clarifies the adsorption and stabilization of the reaction intermediates on Pt(100) and Pt(110).

Boosting the Catalytic Performance of Metal–Organic Frameworks for Steroid Transformations by Confinement within a Mesoporous Scaffold

Cirujano, Francisco G.,Luz, Ignacio,Soukri, Mustapha,Van Goethem, Cedric,Vankelecom, Ivo F. J.,Lail, Marty,De Vos, Dirk E.

supporting information, p. 13302 - 13306 (2017/10/17)

Solid-state crystallization achieves selective confinement of metal–organic framework (MOF) nanocrystals within mesoporous materials, thereby rendering active sites more accessible compared to the bulk-MOF and enhancing the chemical and mechanical stability of MOF nanocrystals. (Zr)UiO-66(NH2)/SiO2 hybrid materials were tested as efficient and reusable heterogeneous catalysts for the synthesis of steroid derivatives, outperforming the bulk (Zr)UiO-66(NH2) MOF. A clear correlation between the catalytic activity of the dispersed Zr sites present in the confined MOF, and the loading of the mesoporous SiO2, is demonstrated for steroid transformations.

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