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C14 Ceramide, also known as N-acetylsphing-8-enine, is a lipid molecule belonging to the ceramide family. It is a naturally occurring sphingolipid that plays a crucial role in cellular processes such as cell signaling, growth, and differentiation. C14 Ceramide is an off-white solid and is useful in organic synthesis.

34227-72-0

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34227-72-0 Usage

Uses

Used in Pharmaceutical Industry:
C14 Ceramide is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties make it a valuable building block for the development of new drugs targeting various diseases.
Used in Cosmetic Industry:
C14 Ceramide is used as an active ingredient in the formulation of cosmetics and skincare products. It is known for its ability to maintain the skin's natural barrier, improve skin hydration, and reduce the appearance of fine lines and wrinkles.
Used in Research and Development:
C14 Ceramide is used as a research tool in the study of cellular processes and the development of new therapeutic strategies. Its role in cell signaling and growth makes it an important compound for understanding the underlying mechanisms of various diseases and conditions.
Used in Organic Synthesis:
C14 Ceramide is used as a starting material or intermediate in the synthesis of complex organic molecules. Its unique structure and properties make it a versatile building block for the creation of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 34227-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34227-72:
(7*3)+(6*4)+(5*2)+(4*2)+(3*7)+(2*7)+(1*2)=100
100 % 10 = 0
So 34227-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C32H63NO3/c1-3-5-7-9-11-13-15-16-18-19-21-23-25-27-31(35)30(29-34)33-32(36)28-26-24-22-20-17-14-12-10-8-6-4-2/h25,27,30-31,34-35H,3-24,26,28-29H2,1-2H3,(H,33,36)/b27-25+/t30-,31+/m0/s1

34227-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name C14 CERAMIDE

1.2 Other means of identification

Product number -
Other names Raiser

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:34227-72-0 SDS

34227-72-0Relevant academic research and scientific papers

Chiral combinatorial preparation and biological evaluation of unique ceramides for inhibition of sphingomyelin synthase

Koolath, Sajeer,Monde, Kenji,Murai, Yuta,Suga, Yoshiko

supporting information, (2020/02/04)

Enantiomers or diastereomers of chiral bioactive compounds often exhibit different biological and toxicological properties. Here, we report the efficient synthesis of four stereoisomers of sphingosine and derivatization of unique chiral ceramides through a combinatorial chemistry by solid-phase activated resin ester. In addition, to test the effectivity of stereochemistry of ceramide, we demonstrated a cell-based assay of sphingomyelin synthase inhibition in the presence ofchiral unique ceramides, which suggested that libraries of this sort will be a rich source of biologically active synthetic molecules.

Ceramide compound and application

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Paragraph 0036; 0045-0047; 0050, (2017/07/06)

The invention relates to a ceramide compound; in the structural general formula, m=2-12; n=0-20. The ceramide compound has significant pseudo neural growth factor activity, and is the small molecule compound capable of passing through blood-brain barrier. The structural general formula is shown as Figure.

Inhibitory activity of a ceramide library on interleukin-4 production from activated T cells

Park, Jin,Li, Qian,Chang, Young-Tae,Kim, Tae Sung

, p. 2589 - 2595 (2007/10/03)

Allergic diseases are hypersensitivity disorders associated with the production of specific immunoglobulin E (IgE) to environmental allergens. Interleukin (IL)-4, produced primarily by CD4+ T cells, is an important stimulus for the switch of th

The synthesis and biological characterization of a ceramide library

Chang, Young-Tae,Choi, Jaehwa,Ding, Sheng,Prieschl, Eva E.,Baumruker, Thomas,Lee, Jae-Mok,Chung, Sung-Kee,Schultz, Peter G.

, p. 1856 - 1857 (2007/10/03)

A facile synthesis of a combinatorial ceramide library and their activities in the NF-κB pathway and in apoptosis induction/prevention were demonstrated. A novel NF-κB activating molecule was discovered among ceramide containing β-galactose, and the structural requirements of ceramides for apoptosis induction was elucidated. Copyright

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