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3123-73-7

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3123-73-7 Usage

Description

1-Palmitoyl-2-oleoyl-sn-glycerol is a 1,2-diacyl-sn-glycerol with palmitoyl as the 1-acyl group and oleoyl as the 2-acyl group. It is a monounsaturated diacylglycerol and is characterized as a clear, colorless liquid.

Uses

Used in Pharmaceutical Industry:
1-Palmitoyl-2-oleoyl-sn-glycerol is used as a bioactive compound for increasing the activity of the ARF1 GTPase-activating protein on membrane-bound ARF1GTP. This enhancement in activity can have potential implications in the development of new therapeutic strategies and drug targets.
Used in Research Applications:
In the field of research, 1-palmitoyl-2-oleoyl-sn-glycerol serves as an important tool for studying the role of diacylglycerols in cellular signaling pathways and membrane dynamics. Its unique structure allows scientists to investigate the specific interactions and effects of this molecule on various cellular processes.
Used in Cosmetics Industry:
Due to its lipid nature and ability to interact with cellular membranes, 1-palmitoyl-2-oleoyl-sn-glycerol may also find applications in the cosmetics industry, potentially being used as an ingredient in skincare products to improve skin barrier function and overall skin health.
Used in Food Industry:
In the food industry, 1-palmitoyl-2-oleoyl-sn-glycerol could be utilized as an additive to improve the texture and stability of certain food products, taking advantage of its properties as a diacylglycerol.

Check Digit Verification of cas no

The CAS Registry Mumber 3123-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3123-73:
(6*3)+(5*1)+(4*2)+(3*3)+(2*7)+(1*3)=57
57 % 10 = 7
So 3123-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C37H70O5/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-37(40)42-35(33-38)34-41-36(39)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,35,38H,3-16,19-34H2,1-2H3/b18-17-

3123-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-palmitoyl-2-oleoyl-sn-glycerol

1.2 Other means of identification

Product number -
Other names (1-hexadecanoyloxy-3-hydroxypropan-2-yl) (Z)-octadec-9-enoate

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:3123-73-7 SDS

3123-73-7Relevant articles and documents

A new strategy to synthesize pure mixed diglycerides

Gras, Jean-Louis,Bonfanti, Jean-Fran?ois

, p. 248 - 250 (2000)

The acylolytic cleavage of glycerol methylene acetals with fatty acids provides a new synthetic strategy that leads to pure mixed 1,2-diglycerides.

Parasitic wasp, Dinarmus basalis, utilizes oviposition-marking pheromone of host azuki bean weevils as host-recognizing kairomone

Kumazaki, Motonari,Matsuyama, Shigeru,Suzuki, Takahisa,Kuwahara, Yasumasa,Fujii, Koichi

, p. 2677 - 2695 (2007/10/03)

A host-recognizing kairomone responsible for the stinging behavior of the parasitic wasp, Dinarmus basalis, was studied. Fresh azuki beans coated with an acetone extract of the azuki beans, from which both emerged wasps and their host weevils were removed, elicited stinging behavior from female wasps. The kairomone is a mixture of saturated hydrocarbons and diacylglycerols, both of which are required for activity. The kairomone is composed of normal and methyl-branched hydrocarbons with carbon numbers ranging from 25 to 35, most of which are known as the hydrocarbon constituents of an oviposition-marking pheromone of the host azuki bean weevils, Callosobruchus chinensis. This indicates that D. basalis utilizes the oviposition-marking pheromone of its host weevils as a host-recognizing kairomone.

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