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2α,3β,19α-Trihydroxyolean-12-en-28-oic acid is a naturally occurring triterpenoid compound, characterized by its unique molecular structure featuring three hydroxyl groups at the 2α, 3β, and 19α positions, and an enolic double bond at the 12 position. It is derived from the oleanolic acid family, which is known for its wide range of biological activities and potential therapeutic applications.

31298-06-3

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31298-06-3 Usage

Uses

Used in Pharmaceutical Industry:
2α,3β,19α-Trihydroxyolean-12-en-28-oic acid is used as a pharmaceutical compound for its diverse range of therapeutic properties. It exhibits antioxidant, anti-inflammatory, and immunomodulatory effects, making it a promising candidate for the development of new drugs targeting various diseases, including cardiovascular, neurodegenerative, and hepatic conditions.
Used in Analytical Chemistry:
2α,3β,19α-Trihydroxyolean-12-en-28-oic acid is used as an analytical standard for the determination of the analyte in various plant extracts by reversed-phase high-performance liquid chromatography with photodiode array detection and in medicinal plant extracts by liquid chromatography-atmospheric pressure photoionization tandem mass spectrometric (LC-APPI-MS/MS) method. This allows for accurate identification and quantification of the compound in complex biological samples, facilitating research and quality control in the pharmaceutical and nutraceutical industries.
Used in Cosmetic Industry:
Due to its antioxidant and anti-inflammatory properties, 2α,3β,19α-Trihydroxyolean-12-en-28-oic acid can be used as an active ingredient in the cosmetic industry for the development of skincare products. It may help in reducing signs of aging, promoting skin health, and providing protection against environmental stressors.
Used in Nutraceutical Industry:
2α,3β,19α-Trihydroxyolean-12-en-28-oic acid can be incorporated into nutraceutical products, such as dietary supplements and functional foods, for their potential health-promoting and disease-preventing properties. Its antioxidant and anti-inflammatory activities may contribute to overall well-being and support various physiological functions.

Check Digit Verification of cas no

The CAS Registry Mumber 31298-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,9 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31298-06:
(7*3)+(6*1)+(5*2)+(4*9)+(3*8)+(2*0)+(1*6)=103
103 % 10 = 3
So 31298-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O5/c1-25(2)12-14-30(24(34)35)15-13-28(6)17(21(30)23(25)33)8-9-20-27(5)16-18(31)22(32)26(3,4)19(27)10-11-29(20,28)7/h8,18-23,31-33H,9-16H2,1-7H3,(H,34,35)/t18-,19+,20-,21-,22+,23+,27+,28-,29-,30+/m1/s1

31298-06-3 Well-known Company Product Price

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  • (06244)  Arjunic acid  analytical standard

  • 31298-06-3

  • 06244-5MG

  • 6,241.95CNY

  • Detail

31298-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Arjunic acid

1.2 Other means of identification

Product number -
Other names 2α,3β,19α-Trihydroxyolean-12-en-28-oic acid

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:31298-06-3 SDS

31298-06-3Relevant academic research and scientific papers

Two new O-β-D-glycosides from the stem bark of Cassia javanica

Sanghi, Rashmi,Singh, Rahul,Singh

, p. 521 - 524 (2007/10/03)

Two new glycosides, 1-hydroxy-3,6,7,8-tetramethoxy-2-methyl anthraquinone-1-O-(2'-O-β-D-mannopyranosyl)-β-D-allopyranoside and 2α,3β,19α-trihydroxy olean-12-en-28-oic acid-28-O-β-D-xylopyranoside have been isolated from the stem bark of Cassia javanica.

CHEMICAL EXAMINATION OF THE ROOTS OF TERMINALIA ARJUNA - THE STRUCTURES OF ARJUNOSIDE III AND ARJUNOSIDE IV, TWO NEW TRITERPENOID GLYCOSIDES

Anjaneyulu, A. S. R.,Prasad, A. V. Rama

, p. 2057 - 2060 (2007/10/02)

The non-phenolic fraction of the alcoholic extract of the root bark of Terminalia arjuna yielded two new triterpenoid glycosides, arjunoside III and arjunoside IV in addition to arjunglucoside I and arjunetin.The structure of arjunoside II was established as the 28-β-D(+)-glucuronopyranoside of arjunic acid by a study of its chemical and spectroscopic (1H and 13C NMR) data.Arjunoside IV was shown to be the 3-O-α-L(-)-rhamnoside of arjunic acid.Leucocyanidin, ellagic acid and gallic acid have been isolated from the phenolic part of the root extract.Key Word Index - Terminalia arjuna; Combretaceae; arjunoside III; arjunoside V; triterpenoid glycosides.

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