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(3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid is a saturated fatty acid with a carbon chain length of 16, featuring four methyl groups at the 3rd, 7th, 11th, and 15th positions. This white, waxy solid is insoluble in water but soluble in organic solvents, and is commonly sourced from natural products like plant waxes and oils.

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  • 18654-64-3 Structure
  • Basic information

    1. Product Name: (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid
    2. Synonyms: (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid;3D,7D,11D-Phytanic acid
    3. CAS NO:18654-64-3
    4. Molecular Formula: C20H40O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18654-64-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 422.3°Cat760mmHg
    3. Flash Point: 179.7°C
    4. Appearance: /
    5. Density: 0.88g/cm3
    6. Vapor Pressure: 2.58E-08mmHg at 25°C
    7. Refractive Index: 1.454
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid(18654-64-3)
    12. EPA Substance Registry System: (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid(18654-64-3)
  • 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: 18654-64-3(Hazardous Substances Data)

18654-64-3 Usage

Uses

Used in Cosmetics Industry:
(3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid is used as a raw material for producing synthetic esters, emollients, and other cosmetic ingredients due to its ability to improve the texture and feel of cosmetic products.
Used in Pharmaceutical Applications:
(3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid is used as an antimicrobial and anti-inflammatory agent for its potential in treating various skin conditions and infections, making it a promising candidate for pharmaceutical formulations.
Used in Skincare Applications:
(3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid is used as an active ingredient in skincare products for its beneficial properties in promoting skin health and combating inflammation and microbial growth.

Check Digit Verification of cas no

The CAS Registry Mumber 18654-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,5 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18654-64:
(7*1)+(6*8)+(5*6)+(4*5)+(3*4)+(2*6)+(1*4)=133
133 % 10 = 3
So 18654-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O2/c1-16(2)9-6-10-17(3)11-7-12-18(4)13-8-14-19(5)15-20(21)22/h16-19H,6-15H2,1-5H3,(H,21,22)

18654-64-3SDS

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 (3R,7R,11R)-3,7,11,15-Tetramethylhexadecanoic acid

1.2 Other means of identification

Product number -
Other names (3R,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid

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:18654-64-3 SDS

18654-64-3Downstream Products

18654-64-3Relevant articles and documents

Synthesis of stereoisomerically pure monoether lipids

Burns, Christopher J.,Field, Leslie D.,Hashimoto, Kikuko,Petteys, Brian J.,Ridley, Damon D.,Rose, Michael

, p. 387 - 394 (1999)

Four stereoisomerically pure lipids have been synthesized which contain chirally pure phytanol (obtained through resolution of a chiral amide) and chiral glycerol moieties. The lipids were obtained in 7-13% overall yield in eight steps from commercially available materials.

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