506-23-0

Basic information

• Product Name: ALPHA-ELEOSTEARIC ACID
• Synonyms: ALPHA-ELEOSTEARIC ACID;9(Z),11(E),13(E)-OCTADECATRIENOIC ACID;(9E,11Z,13E)-9,11,13-octadecatrienoic acid;a-EleostearicAcid;(9E,11Z,13E)-9,11,13-Octadecatriensure;(9Z,11E,13E)-9,11,13-Octadecatrienoic acid;C08315;(9Z,11E,13E)-octadeca-9,11,13-trienoic acid
• CAS NO: 506-23-0
• Molecular Formula: C₁₈H₃₀O₂
• Molecular Weight: 278.43
• EINECS: 208-029-2
• Mol File: 506-23-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 49°C
• Boiling Point: 361.24°C (rough estimate)
• Flash Point: 287.4°C
• Appearance: /
• Density: 0.9028
• Vapor Pressure: 3.45E-07mmHg at 25°C
• Refractive Index: 1.5112
• Storage Temp.: Amber Vial, -20°C Freezer, Under inert atmosphere
• Solubility: Aqueous Base (Slightly), Chloroform (Slightly), Methanol (Very Slightly)
• PKA: 4.78±0.10(Predicted)
• Stability: Light Sensitive
• CAS DataBase Reference: ALPHA-ELEOSTEARIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: ALPHA-ELEOSTEARIC ACID(506-23-0)
• EPA Substance Registry System: ALPHA-ELEOSTEARIC ACID(506-23-0)

Safety Data

• Hazardous Substances Data: 506-23-0(Hazardous Substances Data)

Usage

Description

ALPHA-ELEOSTEARIC ACID, also known as α-Eleostearic Acid, is a conjugated polyunsaturated fatty acid predominantly found in plant seed oil. It has demonstrated potential as a tumor growth suppressor, making it a promising candidate for various pharmaceutical and health-related applications.

Uses

Used in Pharmaceutical Applications:
ALPHA-ELEOSTEARIC ACID is used as a tumor growth suppressor for its ability to induce apoptosis in colon cancer Caco-2 cells through the up-regulation of GADD45, p53, and PPARγ. This suggests its potential use in the development of novel cancer treatments and therapies.
Used in Health and Nutrition Industry:
ALPHA-ELEOSTEARIC ACID is used as a beneficial component in the health and nutrition industry due to its potential tumor growth suppression properties. It can be incorporated into dietary supplements or functional foods to provide consumers with added health benefits, particularly in the context of cancer prevention and management.

InChI:InChI=1/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h5-10H,2-4,11-17H2,1H3,(H,19,20)/b6-5+,8-7+,10-9-

Upstream product

• 95168-90-4 octadeca-11t,13t-dien-9-ynoic acid 
• 4175-47-7 methyl α-eleostearate 
• 111699-15-1 (+/-)-t-butyl coriolate 
• 112-77-6 (Z)-9-octadecenoyl chloride 
• 110-53-2 1-Bromopentane 
• 16792-04-4 tert-butyl (9Z)-9-octadecenoate 
• 106369-41-9 1-methyl 13-t-butyl (2E,4Z)-2,4-tridecadiene-1,13-dioate 
• 111699-10-6 t-butyl 9-oxononanoate 
• 111699-11-7 t-butyl 9-hydroxy-10-undecynoate 
• 111699-14-0 t-butyl (9Z,11E)-13-oxo-9,11-tridecadienoate 
• 111699-13-9 t-butyl (9Z,11E)-13-hydroxy-9,11-tridecadienoate 
• 111699-12-8 13-t-butyl 1-methyl 3,4-tridecadiene-1,13-dioate 
• 26076-75-5 (E)-hex-1-enyldiisobutylaluminum 
• 96251-48-8 (E,E)-1-chloro-1,3-octadiene 

Downstream Products

• 544-73-0 (9E,11E,13E)-9,11,13-octadecatrienoic acid 
• 71599-29-6 octadeca-9,11,13-trienoic acid ethyl ester 
• 822-10-6 (9Z,11E)-methyl octadeca-9,11-dienoate 
• 57-11-4 stearic acid 
• 123-99-9 azelaic acid 
• 131543-46-9 Glyoxal 
• 109-52-4 valeric acid 
• 505-48-6 octane-1,8-dioic acid 
• 107-92-6 butyric acid 

Relevant articles and documents

Stereoselective Synthesis of Octadeacpolyenoic Esters as an Insecticide

Octadecapolyenoic acid derivatives such as (+/-)-t-butyl coriolate, α-eleostearic acid, t-butyl punicate, and t-butyl (9Z,11E)-13-hydroxy-9,11-octadien-15-ynoate were synthesized starting from oleic acid with high stereoselectivity and their insecticidal