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68612

Supelco

Bakuchiol

analytical standard

Sinonimo/i:

(S)-Bakuchiol, 4-[(1E,3S)-3-Ethenyl-3,7-dimethyl-1,6-octadien-1-yl]phenol

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About This Item

Formula empirica (notazione di Hill):
C18H24O
Numero CAS:
10309-37-2
Peso molecolare:
256.38
Beilstein:
3611720
Numero MDL:
MFCD01707441
Codice UNSPSC:
85151701
ID PubChem:
329761022
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Attività ottica

[α]/D +24.0 to +30.0°, c = 0.1 in chloroform

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

−20°C

Stringa SMILE

C\C(C)=C/CC[C@@](C)(C=C)\C=C\c1ccc(O)cc1

InChI

1S/C18H24O/c1-5-18(4,13-6-7-15(2)3)14-12-16-8-10-17(19)11-9-16/h5,7-12,14,19H,1,6,13H2,2-4H3/b14-12+/t18-/m1/s1
LFYJSSARVMHQJB-QIXNEVBVSA-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.

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

363.2 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

184 °C - Pensky-Martens closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG7662
BCCG0499
BCCD6908
BCCB9679
BCBZ9454

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Sun-Hye Lim et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(5), 425-430 (2011-03-09)
Estrogenic activities of ethanol extract and its active components from Psoralea corylifolia L. were studied using various in vitro assays. The main components from ethanol extract were analyzed to be bakuchiol, psoralen, isobavachalcone, isobavachromene, and bavachinin. In a fractionation procedure
P-J Hsu et al.
Natural product research, 23(8), 781-788 (2009-05-07)
Bioactivity guided fractionation of an EtOAc extract from Psoralidium tenuiflorum (Pursh) Rydb. (family : Fabaceae) yielded the known compound bakuchiol as a racemic mixture. This compound was purified by liquid-liquid partitioning and chromatography followed by NMR and GCMS characterisation. This
Gang Zhao et al.
Biochemical pharmacology, 75(9), 1835-1847 (2008-03-11)
Monoamine transporters play key roles in controlling monoamine levels and modulating monoamine reuptake. The objective of the present study was to identify monoamine transporter inhibitors from herbal sources. We discovered that bakuchiol analogs isolated from Fructus Psoraleae inhibited monoamine transporter
Hong-li Chen et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 45(4), 467-470 (2011-03-02)
The in vitro antitumor activity of bakuchiol was exploited, compared with tamoxifen. The result of biological activities showed that bakuchiol could inhibit human breast cancer and the IC50 values were 2.89 x 10(-5) mol L(-1) and 8.29 x 10(-3) mol
Hongli Chen et al.
Bioorganic & medicinal chemistry, 16(5), 2403-2411 (2007-12-08)
A series of derivatives of bakuchiol were synthesized and tested in vitro for their cytotoxicity, and inhibition of T cell proliferation and B cell proliferation. The data obtained provided preliminary structure-activity relationships of the compounds as immunosuppressive activity.
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