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Behenic anhydride is a long-chain fatty acid derivative that is produced through the oxidation of behenic acid, a saturated fatty acid found in natural sources such as peanut oil and rapeseed oil. It has a high melting point, is insoluble in water, and is known for its high stability and resistance to oxidation, making it suitable for use in various industrial applications.

55726-23-3

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55726-23-3 Usage

Uses

Used in Surfactant Production:
Behenic anhydride is used as a raw material in the production of surfactants, which are compounds that lower the surface tension of a liquid, allowing it to mix with another substance. Its high stability and resistance to oxidation make it suitable for use in various surfactant formulations.
Used in Lubricant Production:
Behenic anhydride is used as a component in the manufacturing of lubricants, which are substances that reduce friction between surfaces in relative motion. Its high melting point and insolubility in water make it suitable for use in high-temperature applications, ensuring the lubricants' performance and longevity.
Used in Industrial Chemicals:
Behenic anhydride is used as a raw material in the synthesis of various industrial chemicals, such as behenyl alcohol and behenamide. These compounds are widely used in personal care and cosmetic products, providing emollient, moisturizing, and conditioning properties to the formulations.
Used in Personal Care and Cosmetic Products:
Behenic anhydride is used as a starting material for the synthesis of behenyl alcohol and behenamide, which are incorporated into personal care and cosmetic products for their emollient, moisturizing, and conditioning properties. These compounds help improve the texture, feel, and performance of the products, providing benefits to the users.

Check Digit Verification of cas no

The CAS Registry Mumber 55726-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,2 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55726-23:
(7*5)+(6*5)+(5*7)+(4*2)+(3*6)+(2*2)+(1*3)=133
133 % 10 = 3
So 55726-23-3 is a valid CAS Registry Number.
InChI:InChI=1/C44H86O3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39-41-43(45)47-44(46)42-40-38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-42H2,1-2H3

55726-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Behenic Anhydride

1.2 Other means of identification

Product number -
Other names docosanoyl docosanoate

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:55726-23-3 SDS

55726-23-3Relevant academic research and scientific papers

Mild and efficient synthesis of carboxylic acid anhydrides from carboxylic acids and triazine coupling reagents

Kaminski, Zbigniew J.,Kolesinska, Beata,Malgorzata, Marcinkowska

, p. 3349 - 3358 (2007/10/03)

Anhydrides of carboxylic acids were obtained in 53%-95% yield by treatment of appropriate carboxylic acids with 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) or 2,4-dichloro-6-methoxy-1,3,5-triazine (DCMT) in the presence of N-methylmorpholine. It has been proved that synthesis proceeds via triazine active esters 3a,b, which are able to acylate carboxylate anion but not less nucleophilic carboxylic acid.

N-docosahexaenoyl, 3 hydroxytyramine: A dopaminergic compound that penetrates the blood-brain barrier and suppresses appetite

Shashoua, Victor E.,Hesse, Gary W.

, p. 1347 - 1357 (2007/10/03)

Fatty acids with varying chain lengths (2-22 carbon atoms long) and degrees of unsaturation (0-6 double bonds) were used to synthesize dopaminergic compounds for a study of the carrier mediated transport of dopamine (DA) to the brain. The most active carrier was the all cis C22:6 fatty acid [docosahexaenoic acid,( DHA)]which increased DA uptake through the blood-brain barrier by greater than 7.5 fold. The DHA-DA compound, NMI 8739, depressed the general locomotor activity of mice in a dose dependent manner. It also suppressed the appetite of Balb c mice and Charles River rats by 50% and 95% respectively at a dose of 10 mg/kg. Daily administration of NMI-8739 for a three week period did not induce tolerance. These results demonstrate DHA's potential for the carrier mediated transport of small molecules to the brain.

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