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Documenti

75934

Supelco

3β-Taraxerol

analytical standard

Sinonimo/i:

(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

Formula empirica (notazione di Hill):
C30H50O
Numero CAS:
127-22-0
Peso molecolare:
426.72
Numero MDL:
MFCD13186859
Codice UNSPSC:
85151701
ID PubChem:
329766775
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Stringa SMILE

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
GGGUGZHBAOMSFJ-GADYQYKKSA-N

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Applicazioni

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL4486
BCCH8354
BCCC9135
BCBZ9455
BCBT5837

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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
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
Ru-Mei Lu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(7), 1056-1059 (2009-10-31)
To study the chemical constituents of Uvaria microcarpa. The constituents were repeatedly separated and purified with silica gel column and Sephadex LH-20 column, and identified by physico-chemical properties and spectral methods. Nine compounds were separated and identified as beta-sitosterol palmitate
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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