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22255-10-3

Alpha-Amyrin palmitate is a natural product derived from plants, specifically from the resin of certain tree species. It is a compound composed of a terpene called alpha-Amyrin and palmitic acid, a fatty acid. This chemical exhibits various biological activities, including anti-inflammatory, antitumor, and antiparasitic properties. It has been studied for its potential use in pharmaceuticals and as a natural remedy for various health conditions. Furthermore, alpha-Amyrin palmitate has demonstrated antioxidant and hepatoprotective effects, positioning it as a promising candidate for further research and development.

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  • [(3S,6aR,6bS,8aR,11R,12S,12aS,14aS,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] hexadecanoate

    Cas No: 22255-10-3

  • USD $ 100.0-100.0 / Gram

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  • 22255-10-3 Structure

  • Basic information

    1. Product Name: alpha-Amyrin palmitate
    2. Synonyms: (3beta)-urs-12-en-3-yl hexadecanoate; alpha-amyrin palmitate; hexadecanoic acid, (3beta)-urs-12-en-3-yl ester
    3. CAS NO:22255-10-3
    4. Molecular Formula: C46H80O2
    5. Molecular Weight: 665.1262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22255-10-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 663.8°Cat760mmHg
    3. Flash Point: 355.6°C
    4. Appearance: /
    5. Density: 0.97g/cm3
    6. Vapor Pressure: 1.73E-17mmHg at 25°C
    7. Refractive Index: 1.515
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: alpha-Amyrin palmitate(CAS DataBase Reference)
    11. NIST Chemistry Reference: alpha-Amyrin palmitate(22255-10-3)
    12. EPA Substance Registry System: alpha-Amyrin palmitate(22255-10-3)

  • 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: 22255-10-3(Hazardous Substances Data)

22255-10-3 Usage

Uses

Used in Pharmaceutical Industry:
Alpha-Amyrin palmitate is used as a pharmaceutical compound for its anti-inflammatory, antitumor, and antiparasitic properties. Its diverse biological activities make it a valuable candidate for the development of new drugs to treat various health conditions.
Used in Natural Remedies:
Alpha-Amyrin palmitate is used as a natural remedy for its potential therapeutic effects on various health conditions. Its natural origin and biological activities contribute to its appeal as a safe and effective alternative to synthetic drugs.
Used in Antioxidant Applications:
Alpha-Amyrin palmitate is used as an antioxidant agent for its ability to neutralize free radicals and protect cells from oxidative damage. Its antioxidant properties make it a promising candidate for use in skincare products and supplements to promote overall health and well-being.
Used in Hepatoprotective Applications:
Alpha-Amyrin palmitate is used as a hepatoprotective agent for its ability to protect the liver from damage and support liver health. Its hepatoprotective effects make it a valuable component in formulations aimed at maintaining liver function and reducing the risk of liver-related diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 22255-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22255-10:
(7*2)+(6*2)+(5*2)+(4*5)+(3*5)+(2*1)+(1*0)=73
73 % 10 = 3
So 22255-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C46H80O2/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(47)48-39-28-30-44(7)37(42(39,4)5)27-31-46(9)38(44)25-24-36-41-35(3)34(2)26-29-43(41,6)32-33-45(36,46)8/h24,34-35,37-39,41H,10-23,25-33H2,1-9H3/t34-,35+,37?,38-,39+,41-,43-,44+,45-,46-/m1/s1

22255-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl palmitate

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:22255-10-3 SDS

22255-10-3Relevant articles and documents

Identification and quantification of important steryl esters in aspen wood

Serreqi, Alessio N.,Leone, Robert,Del Rio, Luis F.,Mei, Shirley,Fernandez, Marc,Breuil, Colette

, p. 413 - 418 (2000)

Steryl esters make up a major portion of the total lipids in aspen wood, and contribute significantly to pitch deposit problems during pulping. Fungal treatment of aspen is an attractive method for removing these compounds because it is inexpensive and environmentally acceptable; however, the mechanism of steryl ester removal remains unclear. Identification of the steryl esters will lead to a better understanding of how they are removed by fungi. The steryl ester fraction from aspen wood was obtained by acetone extraction then further purified by silica gel column chromatography and argentation-silica gel column chromatography. This led to the isolation of three major fractions: fraction I, fraction II, and fraction III. The major steryl esters of fractions I and II were identified by gas chromatography, gas chromatography-mass spectroscopy, and proton nuclear magnetic resonance analysis of the intact fraction as well as sterol and fatty acid moieties obtained after base hydrolysis. Identification of the steryl esters was carried out by mass spectra comparisons with steryl ester standards synthesized in the laboratory and comparison with mass spectra libraries (Wiley and NIST) by mass fragmentography. Fraction I contained primarily the palmitate, stearate, and eicosanoate esters of α- and β-amyrin. Fraction II consisted mainly of the palmitate, stearate, and eicosanoate esters of tirucalla-7,24-dien-3β-ol and lupeol.

Growth inhibition of streptococcus from the oral cavity by α-Amyrin esters

Diaz-Ruiz, Gloria,Hernandez-Vazquez, Liliana,Luna, Hector,Del Carmen Wacher-Rodarte, Maria,Navarro-Ocana, Arturo

, p. 12603 - 12611 (2013/02/23)

Five terpenoids were tested by the macrodilution broth method to determine their inhibition activity on cariogenic bacterial growth. In general, α-, β-amyrin and α-amyrin phenylacetate proved to be active, reducing the bacterial viability to less than 20%.

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