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Octyl caprate, also known as caprylic acid octyl ester, is a synthetic chemical compound that serves as an emollient and skin conditioning agent in the cosmetic and personal care industry. Derived from caprylic acid, it is known for its low viscosity and easy absorption by the skin, which contributes to its popularity in various skincare, hair care, and makeup products. It provides a smooth, creamy texture and helps moisturize and soften the skin, making it a valuable ingredient in lotions, creams, and other topical treatments. Furthermore, octyl caprate is also used as a fragrance ingredient and a solvent in various formulations, and is considered safe and effective for cosmetic use.

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  • 2306-92-5 Structure
  • Basic information

    1. Product Name: OCTYL CAPRATE
    2. Synonyms: OCTYL CAPRATE;Octyl decanoate;Decanoic acid, octyl ester;Capric acid octyl ester
    3. CAS NO:2306-92-5
    4. Molecular Formula: C18H36O2
    5. Molecular Weight: 284.48
    6. EINECS: 218-983-1
    7. Product Categories: N/A
    8. Mol File: 2306-92-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 334.7 °C at 760 mmHg
    3. Flash Point: 158.5 °C
    4. Appearance: /
    5. Density: 0.864 g/cm3
    6. Vapor Pressure: 0.000126mmHg at 25°C
    7. Refractive Index: 1.442
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: OCTYL CAPRATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: OCTYL CAPRATE(2306-92-5)
    12. EPA Substance Registry System: OCTYL CAPRATE(2306-92-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2306-92-5(Hazardous Substances Data)

2306-92-5 Usage

Uses

Used in Cosmetic and Personal Care Industry:
Octyl caprate is used as an emollient and skin conditioning agent for its ability to provide a smooth, creamy texture and help moisturize and soften the skin. Its low viscosity and easy absorption make it a popular ingredient in lotions, creams, and other topical treatments.
Used in Fragrance Industry:
Octyl caprate is used as a fragrance ingredient due to its ability to enhance the scent of various products while also providing additional skin conditioning benefits.
Used in Solvent Applications:
In various formulations, octyl caprate is used as a solvent to dissolve and stabilize other ingredients, contributing to the overall performance and effectiveness of the product.

Check Digit Verification of cas no

The CAS Registry Mumber 2306-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2306-92:
(6*2)+(5*3)+(4*0)+(3*6)+(2*9)+(1*2)=65
65 % 10 = 5
So 2306-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H36O2/c1-3-5-7-9-11-12-14-16-18(19)20-17-15-13-10-8-6-4-2/h3-17H2,1-2H3

2306-92-5SDS

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 octyl decanoate

1.2 Other means of identification

Product number -
Other names Octyl caprate

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:2306-92-5 SDS

2306-92-5Downstream Products

2306-92-5Relevant articles and documents

Esterification of free fatty acids (Biodiesel) using nano sulfated-titania as catalyst in solvent-free conditions

Hosseini-Sarvari, Mona,Sodagar, Esmat

, p. 229 - 238 (2013/05/09)

Nano sulfated titania was tested as catalyst for esterification of free fatty acids, specially methanolic and ethanolic esterification of stearic acid (biodiesels). Factorial design evidenced a positive effect of reaction temperature, amount of catalyst, and solvents on ester conversion. This nano-sized sulfated titania has been prepared by a sol-gel hydrothermal process. This prepared sulfated titania showed high catalytic activity in direct esterification of fatty acids as well as benzoic acids with various alcohols and phenols under solvent-free conditions. This method is of great value because of its environmentally benign character, easy handling, high yields, convenient operation, and green. FT-IR studies are shown that the catalyst can be reused for acylation without loss of catalytic activity.

Covalently bound benzyl ligand promotes selective palladium-catalyzed oxidative esterification of aldehydes with alcohols

Liu, Chao,Tang, Shan,Zheng, Liwei,Liu, Dong,Zhang, Heng,Lei, Aiwen

supporting information; experimental part, p. 5662 - 5666 (2012/07/01)

It's a benzyl kind of magic: In the title reaction proceeding with benzyl chloride as the oxidant, the benzyl group serves as a carbon ligand, thus having an 3-coordination effect on palladium (see scheme). A variety of aldehydes and alcohols were selectively converted into the corresponding esters in good to excellent yields. Copyright

Use of water-in-oil microemulsions and gelatin-containing microemulsion-based gels for lipase-catalysed ester synthesis in organic solvents

Rees, G D,Jenta, T R J,Nascimento, M G,Catauro, M,Robinson, B H,et al.

, p. 30 - 34 (2007/10/02)

Chromobacterium viscosum (CV) lipase and lipoprotein lipase ex Pseudomonas have been solubilised in AOT water-in-oil microemulsions at two different R-values, and used to catalyse the lactonisation of 16-hydroxyhexadecanoic acid at 40 deg C.CV lipase has also been immobilised in gelatin-containing microemulsion-based gels (MBGs) with retention of catalytic activity.These lipase-containing MBGs prove to be novel solid-phase catalysts for use in apolar organic solvents.MBGs do not dissolve in their parent nor, oil, when pelletted, do they self-associate in the organicsolvent in which they are placed in contact.CV lipase-containing MBGs have been used to synthesise on a preparative scale, a variety of different esters under mild conditions and both regio- and stereoselective syntheses have been demonstrated.Lipase-containing MBGs have also been shown to effectively catalyse esterifications at temperatures as low as -20 deg C.

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