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18-methyleicosanoic acid, also known as arachidic acid with a methyl group substitution at position 18, is a methyl-branched fatty acid that plays a crucial role in the outer layer of the epicuticle of human hair. 18-methyleicosanoic acid contributes to the hydrophobic properties of the hair surface, making it an essential component in the cosmetic industry.

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  • 36332-93-1 Structure
  • Basic information

    1. Product Name: 18-methyleicosanoic acid
    2. Synonyms: 18-methyleicosanoic acid;18-methylicosanoic acid;WSRCOZWDQPJAQT-UHFFFAOYSA-N
    3. CAS NO:36332-93-1
    4. Molecular Formula: C21H42O2
    5. Molecular Weight: 326.55698
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36332-93-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 18-methyleicosanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 18-methyleicosanoic acid(36332-93-1)
    11. EPA Substance Registry System: 18-methyleicosanoic acid(36332-93-1)
  • 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: 36332-93-1(Hazardous Substances Data)

36332-93-1 Usage

Uses

Used in Hair Cosmetics Industry:
18-methyleicosanoic acid is used as an additive in hair cosmetics for its hydrophobic properties, which help in conditioning the hair and providing a smooth, manageable, and healthy appearance. The application of this acid in hair care products enhances their effectiveness in maintaining the hair's natural moisture barrier and improving overall hair health.

Check Digit Verification of cas no

The CAS Registry Mumber 36332-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36332-93:
(7*3)+(6*6)+(5*3)+(4*3)+(3*2)+(2*9)+(1*3)=111
111 % 10 = 1
So 36332-93-1 is a valid CAS Registry Number.

36332-93-1SDS

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 18-methylicosanoic acid

1.2 Other means of identification

Product number -
Other names 18-MEA

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:36332-93-1 SDS

36332-93-1Downstream Products

36332-93-1Relevant articles and documents

METHOD FOR PRODUCING CROSS-COUPLING COMPOUND

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Page/Page column 20-22, (2010/01/29)

To provide a method for performing a cross-coupling reaction of a Grignard compound with an alkyl halide simply, efficiently and in high yield, a method for obtaining a ω-bromo long chain carboxylic acid simply and efficiently using an easily obtainable raw material and a method for producing a useful branched fatty acid simply and efficiently. [R1: an alkyl group having 1 to 15 carbon atoms, R2: an alkyl group having 1 to 30 carbon atoms with a carboxyl group and X and X': a halogen atom] [n : an integer of 9 to 17] [n : an integer of 9 to 17, R1a : a branched alkyl group having 3 to 8 carbon atoms and X: a halogen atom]

Chiral discrimination of branched-chain fatty acids by reversed-phase HPLC after labeling with a chiral fluorescent conversion reagent

Akasaka, Kazuaki,Ohrui, Hiroshi

, p. 153 - 158 (2007/10/03)

Anteiso fatty acids having 16 to 29 carbon atoms were labeled with the chiral fluorescent conversion reagents, (1R,2R)- and (1S,2S)-2-(2,3- anthracenedicarboximido)-cyclohexanol. The diastereomeric esters of anteiso acids having up to 20 carbon atoms were

Hair cosmetic composition

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, (2008/06/13)

A hair cosmetic composition comprising a branched fatty acids of the following formula (1), STR1 wherein R1 is a methyl or ethyl group, n is an integer of 4-16, and R2 is an amino, alkoxy, or glycerol group. The composition imparts excellent sensation to hair and prevents hairs from being damaged.

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