alpha-Amyrin

Modify Date: 2024-01-02 12:26:40

alpha-Amyrin Structure
alpha-Amyrin structure
Common Name alpha-Amyrin
CAS Number 638-95-9 Molecular Weight 426.717
Density 1.0±0.1 g/cm3 Boiling Point 493.8±45.0 °C at 760 mmHg
Molecular Formula C30H50O Melting Point 178-183°C
MSDS Chinese USA Flash Point 218.6±21.0 °C

 Use of alpha-Amyrin


α-Amyrin is a pentacyclic triterpenoid. α-Amyrin has long-lasting antinociceptive and anti-inflammatory properties. α-Amyrin can be used for the research of inflammatory[1].

 Names

Name α-amyrin
Synonym More Synonyms

 alpha-Amyrin Biological Activity

Description α-Amyrin is a pentacyclic triterpenoid. α-Amyrin has long-lasting antinociceptive and anti-inflammatory properties. α-Amyrin can be used for the research of inflammatory[1].
Related Catalog
References

[1]. J. L. Powers; W. E. Powers (1940). The isolation and identification of alpha- and beta-amyrin from the bark of Viburnum opulus. , 29(4), 175–178.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 493.8±45.0 °C at 760 mmHg
Melting Point 178-183°C
Molecular Formula C30H50O
Molecular Weight 426.717
Flash Point 218.6±21.0 °C
Exact Mass 426.386169
PSA 20.23000
LogP 11.01
Vapour Pressure 0.0±2.8 mmHg at 25°C
Index of Refraction 1.538
Storage condition 2-8℃

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport

 Synthetic Route

 Articles39

More Articles
β-Amyrin biosynthesis: the critical role of steric volume at C-19 of 2,3-oxidosqualene for its correct folding to generate the pentacyclic scaffold.

Org. Lett. 16(13) , 3548-51, (2014)

The effect of the steric volume at C-19 of (3S)-2,3-oxidosqualene 1 on the polycyclization reaction by β-amyrin synthase was examined. The substrate analogs, in which the methyl group at C-19 of 1 was...

Comparative analysis of CYP93E proteins for improved microbial synthesis of plant triterpenoids.

Phytochemistry 108 , 47-56, (2014)

Cytochrome P450-dependent monooxygenases (P450s) belonging to the CYP93E subfamily catalyze the C-24 oxidation of the triterpene backbone during the biosynthesis of triterpenoid saponins, which are bi...

Antitrypanosomal triterpenoid with an ε-lactone E-ring from Salvia urmiensis.

J. Nat. Prod. 76(9) , 1806-9, (2013)

A new triterpenoid, urmiensolide (1), was isolated from Salvia urmiensis. The structure was elucidated by a combination of 1D and 2D NMR, HRESIMS, and X-ray crystallographic analyses. The absolute con...

 Synonyms

α-Amyrenol
4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a
12a,14,14a,14b-icosahydropicen-3-ol
a-Amyrenol
Urs-12-en-3b-ol
VIMINALOL
(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octaméthyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydro-3-picénol
AMYRIN,A
MFCD00016754
(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-eicosahydro-picen-3-ol
α-Amyrin
EINECS 211-352-1
(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-icosahydro-3-picenol
Urs-12-en-3β-ol
alpha-amyrin
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-ol
Urs-12-en-3-ol, (3β)-
Urs-12-en-3-ol
(3β)-Urs-12-en-3-ol
a-amyrin
Top Suppliers:I want be here




Get all suppliers and price by the below link:

alpha-Amyrin suppliers

alpha-Amyrin price