CAS 10483-91-7

Germanicol acetate

Description:

Germanicol acetate, with the CAS number 10483-91-7, is an organic compound derived from germanicol, a triterpenoid alcohol. This substance is characterized by its acetate functional group, which is formed through the esterification of germanicol with acetic acid. Germanicol acetate typically appears as a colorless to pale yellow liquid and is known for its pleasant, floral aroma, making it of interest in the fragrance and flavor industries. It is relatively soluble in organic solvents but has limited solubility in water. The compound exhibits properties typical of esters, including volatility and the potential for reactivity under certain conditions. Additionally, germanicol acetate may possess biological activities, which could include antimicrobial or anti-inflammatory effects, although specific studies on its pharmacological properties may be limited. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards in laboratory or industrial settings.

Formula: C₃₂H₅₂O₂

InChI: InChI=1S/C32H52O2/c1-21(33)34-26-13-14-30(7)24(28(26,4)5)12-15-32(9)25(30)11-10-22-23-20-27(2,3)16-17-29(23,6)18-19-31(22,32)8/h20,22,24-26H,10-19H2,1-9H3/t22-,24+,25-,26+,29-,30+,31-,32-/m1/s1

InChI key: InChIKey=FKMDSFSBFAGDCK-SPFANWNTSA-N

SMILES: C[C@]12[C@@]([C@]3(C)[C@@](CC1)(C(C)(C)[C@@H](OC(C)=O)CC3)[H])(CC[C@]4([C@@]2(C)CC[C@]5(C)C4=CC(C)(C)CC5)[H])[H]

Synonyms:

• Germanicyl acetate
• Germanicol acetate
• Olean-18-en-3β-ol, acetate
• Olean-18-en-3-ol, acetate, (3β)-
• Olean-18-en-3-ol, 3-acetate, (3β)-
• Olean-18-en-3-ol, acetate, (3b)- (9CI)
• Olean-18-en-3b-ol, acetate (7CI,8CI)
• Germanicolacetate (6CI)
• Germanicylacetate

Germanicol acetate

CAS: 10483-91-7

Germanicol acetate shows some slight cytotoxic activity against Jurkat cells .

Formula: C₃₂H₅₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 468.75

Ref: TM-TN4131

Germanicol acetate

Controlled Product

CAS: 10483-91-7

Germanicol acetate is a triterpenoid compound, which is derived from natural sources such as plants. This compound is predominantly isolated from the bark and leaves of various plant species where it exists as a secondary metabolite. With its complex structure, germanicol acetate possesses notable therapeutic potential attributed to its anti-inflammatory, anti-tumor, and anti-microbial properties. The mode of action primarily involves the inhibition of specific signaling pathways and the modulation of molecular targets associated with inflammation and cellular proliferation.

Formula: C₃₂H₅₂O₂

Purity: Min. 95%

Molecular weight: 468.8 g/mol

Ref: 3D-KAA48391

Olean-18-en-3-ol, 3-acetate, (3β)-

CAS: 10483-91-7

Formula: C₃₂H₅₂O₂

Molecular weight: 468.7541

Ref: IN-DA01SJNA