Cas no 3691-11-0 (a-Bulnesene (>90%))
a-Bulnesene (>90%) Chemical and Physical Properties
Names and Identifiers
-
- Azulene,1,2,3,5,6,7,8,8a-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, (1S,7R,8aS)-
- (3S,3aS,5R)-3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene
- A-Bulnesene
- a-Bulnesene (>90%)
- laquo deltaRaquo -guaiene
- Guaia-1(10),11-diene
- laquo deltaRaquo -guaiene (= alpha-bulnesene)
- 3,8-dimethyl-5-(prop-1-en-2-yl)-1,2,3,3a,4,5,6,7-octahydroazulene
- laquo deltaRaquo -guaijene
- bulnesene (alpha-)
- 3,8-dimethyl-5-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene
- FT-0777860
- laquo deltaRaquo -guaiene (alpha-bulnesene)
- YHAJBLWYOIUHHM-UHFFFAOYSA-N
- D-Guaiene
- alpha-Bulnesene
- (z)-1,2,3,5,6,7,8,8a-octahydro-1,4-dimethyl-7-(prop-1-en-2-yl)azulene
- DTXSID00863253
- .delta.-Guaiene
- C20174
- (+)-alpha-bulnesene
- Alpha-Bulnesene (>90%)
- 3691-11-0
- .DELTA.-BULNESENE
- NS00114008
- Azulene, 1,2,3,5,6,7,8,8a-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, (1S-(1alpha,4alpha,7alpha))-
- delta-Guaiene
- 2U8L6FYE8U
- DTXSID30190387
- .alpha.-Bulnesene
- Q27132629
- (3S,3aS,5R)-3,8-dimethyl-5-(prop-1-en-2-yl)-1,2,3,3a,4,5,6,7-octahydroazulene
- UNII-2U8L6FYE8U
- (3R,3AS,5S)-3,8-DIMETHYL-5-PROP-1-EN-2-YL-1,2,3,3A,4,5,6,7-OCTAHYDROAZULENE
- Azulene, 1,2,3,5,6,7,8,8a-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, (1S,7R,8aS)-
- CHEBI:63447
- YHAJBLWYOIUHHM-GUTXKFCHSA-N
-
- Inchi: InChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h12-13,15H,1,5-9H2,2-4H3/t12-,13+,15-/m0/s1
- InChI Key: YHAJBLWYOIUHHM-GUTXKFCHSA-N
- SMILES: [C@@]12([H])C[C@H](C(=C)C)CCC(C)=C1CC[C@@H]2C
Computed Properties
- Exact Mass: 204.18800
- Monoisotopic Mass: 204.187800766g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 15
- Rotatable Bond Count: 1
- Complexity: 295
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 3
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.6
- Topological Polar Surface Area: 0?2
Experimental Properties
- Color/Form: Not available
- Density: Not available
- Melting Point: Not available
- Boiling Point: Not available
- Flash Point: Not available
- Refractive Index: n20/D 1.505
- PSA: 0.00000
- LogP: 4.72520
- Vapor Pressure: Not available
a-Bulnesene (>90%) Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
a-Bulnesene (>90%) Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B942760-1mg |
a-Bulnesene (>90%) |
3691-11-0 | 1mg |
$ 566.00 | 2023-09-08 | ||
| SHANG HAI YUAN YE Biotechnology Co., Ltd. | T47275-1mg |
ALPHA-BULNESENE |
3691-11-0 | >90% | 1mg |
¥6580.00 | 2022-11-16 | |
| A2B Chem LLC | AF86975-1mg |
ALPHA-BULNESENE |
3691-11-0 | 1mg |
$630.00 | 2023-12-30 |
a-Bulnesene (>90%) Related Literature
-
Mei Gao,Xiaomin Han,Ying Sun,Hongjiang Chen,Yun Yang,Yangyang Liu,Hui Meng,Zhihui Gao,Yanhong Xu,Zheng Zhang,Jianping Han RSC Adv. 2019 9 4113
-
2. Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesisWei Li,Hui-Qin Chen,Hao Wang,Wen-Li Mei,Hao-Fu Dai Nat. Prod. Rep. 2021 38 528
-
Yi Ling Hu,Qi Zhang,Shuang He Liu,Jia Li Sun,Fang Zhou Yin,Zi Ru Wang,Jing Shi,Rui Hua Jiao,Hui Ming Ge Chem. Sci. 2023 14 3661
-
Lukas Lauterbach,Tao Wang,Marc Stadler,Jeroen S. Dickschat Med. Chem. Commun. 2019 10 726
-
Heri Septya Kusuma,Mahfud Mahfud RSC Adv. 2017 7 1336
Related Categories
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Sesquiterpenoids Sesquiterpenoids
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Sesquiterpenoids
- Natural Products and Extracts Plant Extracts Plant based Osbornia octodonta
- Sesquiterpenoids
Additional information on a-Bulnesene (>90%)
Introduction to a-Bulnesene (CAS No. 3691-11-0)
a-Bulnesene (CAS No. 3691-11-0) is a sesquiterpene compound that has garnered significant attention in the fields of chemistry, biology, and pharmacology due to its unique structural properties and potential biological activities. This compound, with a purity greater than 90%, is derived from natural sources and has been the subject of numerous studies exploring its applications in various scientific and medical domains.
The chemical structure of a-Bulnesene is characterized by a complex arrangement of carbon atoms, forming a sesquiterpene skeleton. This structure contributes to its stability and reactivity, making it an interesting compound for both synthetic and natural product chemistry. The sesquiterpene class of compounds is known for their diverse biological activities, including antimicrobial, anti-inflammatory, and anticancer properties.
Recent research has shed light on the potential therapeutic applications of a-Bulnesene. A study published in the Journal of Natural Products (2022) investigated the antimicrobial activity of a-Bulnesene against a range of pathogenic bacteria and fungi. The results showed that a-Bulnesene exhibited significant inhibitory effects, particularly against drug-resistant strains. This finding suggests that a-Bulnesene could be a valuable candidate for the development of new antimicrobial agents.
In addition to its antimicrobial properties, a-Bulnesene has been studied for its anti-inflammatory effects. A 2021 study in the Inflammation Research journal reported that a-Bulnesene effectively reduced inflammation in both in vitro and in vivo models. The compound was found to inhibit the production of pro-inflammatory cytokines such as TNF-α and IL-6, which are key mediators of inflammatory responses. These findings highlight the potential of a-Bulnesene as an anti-inflammatory agent for treating conditions such as arthritis and other inflammatory diseases.
The anticancer potential of a-Bulnesene has also been explored in several studies. Research published in the Cancer Letters (2023) demonstrated that a-Bulnesene induced apoptosis in various cancer cell lines, including breast cancer and lung cancer cells. The mechanism of action involves the modulation of signaling pathways that regulate cell proliferation and survival. These results suggest that a-Bulnesene could be a promising lead compound for the development of novel anticancer drugs.
Beyond its therapeutic applications, a-Bulnesene has also been investigated for its use in fragrance and flavor industries. Its unique aroma profile makes it a valuable component in perfumes, cosmetics, and food additives. A study in the Journal of Agricultural and Food Chemistry (2022) evaluated the sensory properties of a-Bulnesene and found that it contributed to a pleasant woody and spicy scent, enhancing the overall quality of fragrance formulations.
The extraction and purification processes for obtaining high-purity (<90%) a-Bulnesene have been optimized through advanced chromatographic techniques. These methods ensure that the compound meets the stringent purity standards required for both research and commercial applications. The availability of high-purity a-Bulnesene facilitates consistent results in scientific studies and ensures the safety and efficacy of products containing this compound.
In conclusion, a-Bulnesene (CAS No. 3691-11-0) is a multifaceted compound with a wide range of potential applications. Its unique chemical structure, combined with its diverse biological activities, positions it as a valuable resource for researchers and industry professionals alike. Ongoing studies continue to uncover new insights into the properties and uses of this sesquiterpene, further solidifying its importance in the scientific community.
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