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465-95-2

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465-95-2 Usage

Description

Primulagenin is a pentacyclic triterpenoid belonging to the oleanane family, characterized by the presence of a double bond between carbons 12 and 13, and featuring hydroxy groups at the 3β, 16α, and 28 positions. This unique molecular structure endows Primulagenin with a range of biological activities and potential applications across various fields.

Uses

Used in Pharmaceutical Industry:
Primulagenin is used as a bioactive compound for its potential therapeutic effects. Its chemical structure allows it to interact with various biological targets, making it a candidate for the development of new drugs. The presence of hydroxy groups at specific positions may contribute to its pharmacological properties, such as anti-inflammatory, anticancer, or antimicrobial activities.
Used in Cosmetic Industry:
In the cosmetic industry, Primulagenin is used as an active ingredient for its potential skin health benefits. The triterpenoid's ability to modulate biological processes may lead to applications in anti-aging, skin regeneration, or protection against environmental stressors. Its incorporation into cosmetic formulations could provide consumers with skincare products that promote healthier and more resilient skin.
Used in Nutraceutical Industry:
Primulagenin's potential health-promoting properties also make it a candidate for use in the nutraceutical industry. It could be incorporated into dietary supplements or functional foods to support overall health and well-being. The triterpenoid's bioactivity may contribute to immune system support, antioxidant activity, or other health benefits when consumed as part of a balanced diet.
Used in Agricultural Industry:
In agriculture, Primulagenin could be utilized as a natural compound to enhance crop protection or improve plant health. Its potential antimicrobial or antifungal properties might be harnessed to develop eco-friendly pesticides or to promote plant growth and resistance against diseases.
Overall, Primulagenin's unique structure and biological activities position it as a versatile compound with applications in various industries, ranging from pharmaceuticals and cosmetics to nutraceuticals and agriculture. Further research and development will be essential to fully explore and harness its potential for these diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 465-95-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 465-95:
(5*4)+(4*6)+(3*5)+(2*9)+(1*5)=82
82 % 10 = 2
So 465-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O3/c1-25(2)14-15-30(18-31)20(16-25)19-8-9-22-27(5)12-11-23(32)26(3,4)21(27)10-13-28(22,6)29(19,7)17-24(30)33/h8,20-24,31-33H,9-18H2,1-7H3/t20-,21?,22-,23+,24-,27+,28-,29-,30-/m1/s1

465-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,6aR,6bS,8R,8aS,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol

1.2 Other means of identification

Product number -
Other names Genin A

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:465-95-2 SDS

465-95-2Downstream Products

465-95-2Relevant articles and documents

Bischof,Jeger

, p. 1760,1761 Anm. 1 (1948)

Kitagawa et al.

, p. 5377 (1968)

SAPONINS IN CYCLAMEN SPECIES: CONFIGURATION OF CYCLAMIRETIN C AND STRUCTURE OF ISOCYCLAMIN

Reznicek, Gottfried,Jurenitsch, Johann,Robien, Wolfgang,Kubelka, Wolfgang

, p. 825 - 828 (2007/10/02)

Five sapogenins and three saponins were identified in bulbs of 14 cytologically defined Cyclamen species and their structures were determined by means of mass, 1H and 13C NMR spectroscopy.In addition to the known products of hydrolysis, primulagenin A was found, and cyclamiretin C was shown to be identical with cyclamigenin C.The new saponin isocyclamin was identified as 3β--O-β-D-glucopyranosyl-(1-4)--α-L-arabinopyranosyl>-16α-hydroxy-13β,28-epoxy-olean-30-al. - Key Word Index - Cyclamen; Primulaceae; saponin; sapogenin; chemotaxonomy.

Minor triterpenoid saponins from the leaves of Bupleurum rotundifolium L.

Akai,Takeda,Kobayashi,et al.

, p. 4685 - 4690 (2007/10/02)

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