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Myristyl Behenate is a waxy compound derived from natural sources such as vegetable oils, commonly used in the cosmetic and personal care industry as an emollient and thickening agent. It is known for its moisturizing properties, making it a popular ingredient in skincare products.
Used in Cosmetic and Personal Care Industry:
Myristyl Behenate is used as an emollient and thickening agent for its moisturizing properties, improving the texture and spreadability of products, and providing a protective barrier on the skin to lock in moisture and prevent dryness. It is often used in conjunction with other emollients and conditioning agents to enhance the overall performance of skincare formulations.

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  • 42233-09-0 Structure
  • Basic information

    1. Product Name: MYRISTYL BEHENATE
    2. Synonyms: BEHENIC ACID MYRISTYL ESTER;MYRISTYL BEHENATE;behenic acid myristyl ester crystalline
    3. CAS NO:42233-09-0
    4. Molecular Formula: C36H72O2
    5. Molecular Weight: 536.96
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 42233-09-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 549.1°C at 760 mmHg
    3. Flash Point: 297°C
    4. Appearance: /
    5. Density: 0.857g/cm3
    6. Vapor Pressure: 4.14E-12mmHg at 25°C
    7. Refractive Index: 1.457
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: MYRISTYL BEHENATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: MYRISTYL BEHENATE(42233-09-0)
    12. EPA Substance Registry System: MYRISTYL BEHENATE(42233-09-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 42233-09-0(Hazardous Substances Data)

42233-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42233-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42233-09:
(7*4)+(6*2)+(5*2)+(4*3)+(3*3)+(2*0)+(1*9)=80
80 % 10 = 0
So 42233-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C36H72O2/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-26-28-30-32-34-36(37)38-35-33-31-29-27-25-16-14-12-10-8-6-4-2/h3-35H2,1-2H3

42233-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tetradecyl docosanoate

1.2 Other means of identification

Product number -
Other names Behenic acid myristyl ester

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:42233-09-0 SDS

42233-09-0Downstream Products

42233-09-0Relevant articles and documents

Efficient greener methodology for the preparation of bio-based phase change materials from lipids

Y?ld?r?m, Ayhan,K?raylar, Kaan

, p. 407 - 413 (2020/11/19)

In the present work, a new, highly efficient and simple strategy has been developed for the synthesis of long chain esters from fatty acids and fatty alcohols as phase change materials. Equivalent amounts of the selected starting compounds were taken to the esterification reaction at 110 °C in a solventless medium. In order to catalyze the esterification reaction, non-hygroscopic triphenylphosphine-sulfur trioxide adduct was used (0.83 mmol%) which is an easily accessible compound. The relevant reaction was completed in a very short time (2 h) and under optimized esterification conditions, excellent conversion were reached. The targeted mono ester compounds (15 examples) were obtained in good to excellent yields even after a simple crystallization step (72-99%). Additionally, a catalyst reuse investigation and study covering the scale-up production of stearyl stearate was also carried out. The triphenylphosphine-sulfur trioxide catalyzed solvent free process can compete with existing processes and proved to be a cheaper, practical and environmentally-friendly method for the esterification of fatty acids and alcohols.

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