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CAS

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20248-08-2

α-Amyrenone is a triterpenoid compound found in various plant species, such as the bark of the White birch tree (Betula pubescens) and the resin of the gumbo-limbo tree (Bursera simaruba). It is recognized for its bioactive properties, including anti-inflammatory, antioxidant, and anticancer activities, making it a promising candidate for the development of new drugs and natural products for various diseases. Additionally, its antioxidant properties have attracted interest in the cosmetic and skincare industry.

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  • 20248-08-2 Structure

  • Basic information

    1. Product Name: α-Amyrenone
    2. Synonyms: α-Amyrenone;δ-Amyrenane;5α-Olean-13(18)-en-3-one;Olean-13(18)-en-3-one;13(18)-Oleanen-3-one
    3. CAS NO:20248-08-2
    4. Molecular Formula: C30H48O
    5. Molecular Weight: 424.70152
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20248-08-2.mol
    9. Article Data: 2

  • Chemical Properties

    1. Melting Point: 198-201 °C
    2. Boiling Point: 488.8±44.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.01±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: α-Amyrenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-Amyrenone(20248-08-2)
    11. EPA Substance Registry System: α-Amyrenone(20248-08-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 20248-08-2(Hazardous Substances Data)

20248-08-2 Usage

Uses

Used in Pharmaceutical Industry:
α-Amyrenone is used as a potential therapeutic agent for various diseases due to its anti-inflammatory, antioxidant, and anticancer properties. It is being studied for its potential in the development of new drugs and natural products that can target a range of health conditions.
Used in Cosmetic and Skincare Industry:
α-Amyrenone is used as an ingredient in cosmetic and skincare products for its antioxidant properties. Its ability to protect the skin from oxidative stress and promote overall skin health makes it a valuable component in formulations aimed at maintaining youthful and radiant skin.

Check Digit Verification of cas no

The CAS Registry Mumber 20248-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,4 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20248-08:
(7*2)+(6*0)+(5*2)+(4*4)+(3*8)+(2*0)+(1*8)=72
72 % 10 = 2
So 20248-08-2 is a valid CAS Registry Number.

20248-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aR,6bS,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,13,14,14a-dodecahydro-1H-picen-3-one

1.2 Other means of identification

Product number -
Other names -

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:20248-08-2 SDS

20248-08-2Downstream Products

20248-08-2Relevant articles and documents

Hepatoprotective triterpenes from Sedum sarmentosum

He, Aimin,Wang, Mingshi,Hao, Hongyan,Zhang, Decheng,Lee, Kuo-Hsiung

, p. 2607 - 2610 (1998)

The known δ-amyrone, 3-epi-δ-amyrin, δ-amyrin as well as a new hydroperoxy triterpene, 18β-hydroperoxy-olean-12-en-3-one (named sarmentolin) were isolated as hepatoprotective agents from Sedum sarmentosum. Their structures were elucidated by spectral analysis and chemical reactions.

New oleanene triterpenes from root bark of Calotropis procera (Ait.) R.Br.

Ansari,Ali

, p. 287 - 290 (2007/10/03)

The structures of three oleanene type triterpenes, calotropoleanyl ester, proceroleanenol-A and proceroleanenol B, isolated from the root bark of Calotropis procera, have been elucidated as olean-13(18)-en-3β-yl acetate, olean-13(18)-en-9α-ol and olean-5, 13(18)-dien-3α-ol, respectively, on the basis of spectral data, elemental analyses and chemical reactions.

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