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Merck
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Documentos

75934

Supelco

3β-Taraxerol

analytical standard

Sinónimos:

(3β)-D-Friedoolean-14-en-3-ol, (3β13α)-13-Methyl-27-norolean-14-en-3-ol, Alnulin, Skimmiol, Taraxerol, Tiliadin

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About This Item

Fórmula empírica (notación de Hill):
C30H50O
Número de CAS:
127-22-0
Peso molecular:
426.72
MDL number:
MFCD13186859
UNSPSC Code:
85151701
PubChem Substance ID:
329766775
NACRES:
NA.24

grade

analytical standard

Quality Level

100

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

SMILES string

CC1(C)CC[C@]2(C)CC=C3[C@]4(C)CC[C@@]5([H])C(C)(C)[C@@H](O)CC[C@]5(C)[C@@]4([H])CC[C@@]3(C)[C@]2([H])C1

InChI

1S/C30H50O/c1-25(2)17-18-27(5)13-9-21-29(7)14-10-20-26(3,4)24(31)12-16-28(20,6)22(29)11-15-30(21,8)23(27)19-25/h9,20,22-24,31H,10-19H2,1-8H3/t20-,22+,23+,24-,27-,28-,29-,30+/m0/s1

InChI key

GGGUGZHBAOMSFJ-GADYQYKKSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
BCCL4486
BCCH8354
BCCC9135
BCBZ9455
BCBT5837

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Xiangyang Yao et al.
International immunopharmacology, 15(2), 316-324 (2013-01-22)
Taraxerol, a triterpenoid compound, has potent anti-inflammatory effects. However, the molecular mechanisms are not clear. In the study, taraxerol concentration dependently inhibited nitric-oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the protein and mRNA levels and these inhibitions decreased the production
Venkatesan Kumar et al.
Phytochemical analysis : PCA, 19(3), 244-250 (2007-11-13)
A new, simple, sensitive, selective and precise HPTLC method has been developed for the determination of taraxerol in Clitoria ternatea L. Determination of taraxerol was performed on TLC aluminium plates. Linear ascending development was carried out in twin trough glass
Min-Qing Tian et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 33(4), 405-408 (2008-06-07)
To study the chemical constituents of Excoecaria agallocha L. The constituents were isolated and purified by repeated column chromatography and their structures were elucidated by spectroscopic analysis. Six triterpenoids including taraxerone (1), beta-amyrin acetate (2), 3beta-[(2E,4E)-6-oxo-decadienoyloxy]-olean-12-ene (3), taraxerol (4), acetylaleuritolic
Bernd R T Simoneit et al.
Chemosphere, 74(4), 543-550 (2008-11-22)
The reactivity of higher plant derived 3-oxy-triterpenoids to sunlight was investigated using a series of pure reference standards both under simulated and real solar exposure. The majority of the exposed compounds showed reactivity to light, particularly to simulated sunlight and
Yan Shi et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 33(16), 1994-1996 (2008-12-18)
To study the chemical constituents from the roots of Pterospermum heterophyllum. The chemical constituents of P. heterophyllum were isolated and purified by silica gel and sephadex LH-20 column chromatography. Their structures were identified on the basis of spectroscopic data and
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