147492-65-7

Basic information

• Product Name: C22 Dihydroceramide
• Synonyms: C22 Dihydroceramide;N-[(1S,2R)-2-Hydroxy-1-(hydroxymethyl)-heptadecyl]-docosanamide
• CAS NO: 147492-65-7
• Molecular Formula: C40H81NO3
• Molecular Weight: 624.08
• Product Categories: Protein Kinase Inhibitors and Activators;Fatty Acid Derivatives & Lipids;Inhibitors
• Mol File: 147492-65-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: 97-99°C
• Boiling Point: 732.2°C at 760 mmHg
• Flash Point: 396.6°C
• Appearance: /
• Density: 0.903g/cm³
• Vapor Pressure: 9.55E-25mmHg at 25°C
• Refractive Index: 1.473
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform (Slightly, Heated), Methanol (Slightly, Heated)
• CAS DataBase Reference: C22 Dihydroceramide(CAS DataBase Reference)
• NIST Chemistry Reference: C22 Dihydroceramide(147492-65-7)
• EPA Substance Registry System: C22 Dihydroceramide(147492-65-7)

Safety Data

• Hazardous Substances Data: 147492-65-7(Hazardous Substances Data)

Usage

Description

C22 Dihydroceramide, with the CAS number 147492-65-7, is a white solid compound that is useful in organic synthesis. It plays a significant role in various chemical reactions and processes due to its unique properties.

Uses

Used in Organic Synthesis:
C22 Dihydroceramide is used as a synthetic building block for the creation of more complex organic molecules. Its chemical properties make it a valuable component in the synthesis of various compounds, contributing to the development of new materials and substances with potential applications in different industries.
Used in Pharmaceutical Industry:
C22 Dihydroceramide is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties, potentially leading to the discovery of novel treatments for various medical conditions.
Used in Cosmetics Industry:
In the cosmetics industry, C22 Dihydroceramide is used as an ingredient in the formulation of skincare and beauty products. Its properties may contribute to the development of products with improved moisturizing, anti-aging, or protective effects, enhancing the overall performance and benefits of these products for consumers.
Used in Chemical Research:
C22 Dihydroceramide is also used as a research tool in the field of chemistry. Its unique properties and reactivity make it an interesting subject for studying various chemical reactions and mechanisms, potentially leading to new discoveries and advancements in the field.

InChI:InChI=1/C40H81NO3/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-24-26-28-30-32-34-36-40(44)41-38(37-42)39(43)35-33-31-29-27-25-23-16-14-12-10-8-6-4-2/h38-39,42-43H,3-37H2,1-2H3,(H,41,44)/t38-,39+/m0/s1

Upstream product

• 27888-44-4 (2S,3R)-N-(docosanoate)-1,3-dihydroxy-2-amino-octadeca-4-(E)-ene 

Relevant articles and documents

METHOD OF ISOLATING SPHINGOLIPIDS FROM CORDYCEPS AND THEIR USE

A method of isolating at least one sphingolipid portion selected from a sphingoid base portion, a ceramide portion, a glycosphingolipid portion or a phosphosphingolipid portion from Cordyceps, in particular from wild-type Cordyceps, allows for obtaining sphingolipid portions having an increased amount of one of sphingoid bases, ceramides, glycosphingolipids or phosphosphingolipids. The sphingolipid portions isolated contained significant amounts of sphingolipids not reported so far, and possess exceptional immunosuppressive activities. A method of treating a subject suffering from an inflammatory disease like an autoimmune disease or an allergic disease includes administering sphingolipids isolated from Cordyceps, in particular from wild-type Cordyceps. A method of treating a subject suffering from an inflammatory disease includes administering certain sphingolipids to the subject. Still further in accordance with the present invention is a composition, in particular a pharmaceutical composition comprising at least one sphingolipid portion.

COSMETIC COMPOSITION COMPRISING AT LEAST ONE CATIONIC COPOLYMER AND AT LEAST ONE ANIONIC ASSOCIATIVE POLYMER AND COSMETIC TREATMENT PROCESSES USING SAID COMPOSITION

The disclosure relates to novel cosmetic compositions comprising, in a cosmetically acceptable medium: (i) at least one cationic polymer which are produced by polymerization of a mixture of monomers comprising: a) at least one vinyl monomer substituted with at least one amino group, b) at least one hydrophobic nonionic vinyl monomer, c) at least one associative vinyl monomer, and e) at least one hydroxylated nonionic vinyl monomer, and (ii) at least one anionic associative polymers.

Dyeing processes comprising at least one multi-carbosite, multi-group coupling agent for wash-protecting the color of artificially dyed keratin fibers

Disclosed herein is a cosmetic process for wash-protecting the color of artificially dyed keratin fibers, comprising applying to the keratin fibers at least one composition comprising at least one multi-carbosite, multi-group coupling agent, the coupling agent being an electrophilic hydrocarbon-based compound comprising neither an aldehyde group, nor a carboxylic acid group, nor a formol-generating group, the coupling agent comprising at least two identical reactive groups, the reactive groups not being carried by the same atom, if said atom is a carbon atom, and the coupling agent having a molecular weight of less than 500 g/mol.