95426
(−)-α-甜没药醇
analytical standard
别名:
(-)-6-甲基-2-(4-甲基-3-环己烯-1-基)-5-庚烯-2-醇, 左美诺醇
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关于此项目
经验公式（希尔记法）:
C15H26O
化学文摘社编号:
分子量:
222.37
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
85151701
EC Number:
208-205-9
MDL number:
InChI key
RGZSQWQPBWRIAQ-CABCVRRESA-N
InChI
1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m1/s1
SMILES string
C\C(C)=C\CC[C@](C)(O)[C@H]1CCC(C)=CC1
grade
analytical standard
assay
≥93% (GC)
optical activity
[α]/D -60±2°, neat
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
storage temp.
2-8°C
Quality Level
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General description
(−)-α-Bisabolol is a monocyclic sesquiterpene alcohol naturally found in the essential oil of different plants like Vanillosmopsis erythropappa and Matricaria chamomilla. It finds applications in clinical and cosmetic industries due to its pharmacological properties like anti-inflammatory, anti-irritant, antimicrobial and skin healing property. It also shows effective action against malignant tumor cells.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
This compound is commonly found in plants of the genus: angelica
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
289.4 °F - closed cup
flash_point_c
143 °C - closed cup
Insight into the apoptosis-inducing action of α-bisabolol towards malignant tumor cells: Involvement of lipid rafts and Bid
Darra E, et al.
Archives of Biochemistry and Biophysics, 476(2), 113-123 (2008)
Dennis Dienst et al.
Scientific reports, 10(1), 5932-5932 (2020-04-05)
Cyanobacteria and microalgae are attractive photoautotrophic host systems for climate-friendly production of fuels and other value-added biochemicals. However, for economic applications further development and implementation of efficient and sustainable cultivation strategies are essential. Here, we present a comparative study on
Orazio Taglialatela-Scafati et al.
Journal of natural products, 75(3), 453-458 (2012-02-09)
Apart from a large amount (ca. 2.0%) of α-bisabolol β-D-fucopyranoside (2a), the aerial parts of the Mediterranean weed Carthamus glaucus afforded an unusual triglyceride (E-2-crotonyl-1,3-distearolylglycerol, 7), two lipophilic flavonoids (6a,b), and a series of bisabolane fucopyranosides variously acylated on the
Jaekwan Kim et al.
Pharmaceutical research, 29(7), 2017-2029 (2012-03-09)
To evaluate the ability of a novel radiofrequency (RF) microporation technology based on ablation of the skin barrier to enhance topical delivery of active ingredients The influence of RF fluence and the molecular size of the absorbent on the permeation
Chiaki Nakano et al.
Chembiochem : a European journal of chemical biology, 12(15), 2271-2275 (2012-10-30)
Now found in bacteria: An increasing number of genome sequences indicate that bacteria possess a variety of terpenoid cyclase genes. The characterization of two sesquiterpene cyclase (SC) genes found in the draft genome sequence of Streptomyces citricolor is described here.
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