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Octadecyl myristate, also known as Cetyl Myristate or Hexadecyl Octadecanoate, is a waxy, white, solid ester compound derived from the combination of myristic acid and octadecanol. It is widely used in the cosmetics and pharmaceutical industries as an emollient, providing a smooth, silky texture to creams, lotions, and ointments. Octadecyl myristate is known for its excellent skin feel, moisturizing properties, and ability to improve the stability of formulations. It is also used as a thickening agent and a solvent for various active ingredients. Due to its non-comedogenic nature, it is suitable for use in skincare products, particularly for sensitive or acne-prone skin types.

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  • 3234-81-9 Structure
  • Basic information

    1. Product Name: octadecyl myristate
    2. Synonyms: octadecyl myristate;Tetradecanoic acid, octadecyl ester;Octadecylmyristat;Myristic acid octadecyl ester;Einecs 221-785-8
    3. CAS NO:3234-81-9
    4. Molecular Formula: C32H64O2
    5. Molecular Weight: 480.84936
    6. EINECS: 221-785-8
    7. Product Categories: N/A
    8. Mol File: 3234-81-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 507°Cat760mmHg
    3. Flash Point: 269.8°C
    4. Appearance: /
    5. Density: 0.858g/cm3
    6. Vapor Pressure: 2.12E-10mmHg at 25°C
    7. Refractive Index: 1.455
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: octadecyl myristate(CAS DataBase Reference)
    11. NIST Chemistry Reference: octadecyl myristate(3234-81-9)
    12. EPA Substance Registry System: octadecyl myristate(3234-81-9)
  • 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: 3234-81-9(Hazardous Substances Data)

3234-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3234-81-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3234-81:
(6*3)+(5*2)+(4*3)+(3*4)+(2*8)+(1*1)=69
69 % 10 = 9
So 3234-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H64O2/c1-3-5-7-9-11-13-15-16-17-18-19-21-23-25-27-29-31-34-32(33)30-28-26-24-22-20-14-12-10-8-6-4-2/h3-31H2,1-2H3

3234-81-9SDS

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 octadecyl tetradecanoate

1.2 Other means of identification

Product number -
Other names octyldodecyl myristate

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:3234-81-9 SDS

3234-81-9Downstream Products

3234-81-9Relevant 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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