Accéder au contenu
Merck
Toutes les photos(1)

Principaux documents

Voir toute la documentation

39303

Supelco

[6]-Shogaol

analytical standard

Synonyme(s) :

1-(4-Hydroxy-3-methoxyphenyl)-4-decen-3-one

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(1)

About This Item

Formule empirique (notation de Hill):
C17H24O3
Numéro CAS:
555-66-8
Poids moléculaire :
276.37
Beilstein:
2056098
Numéro MDL:
MFCD01736094
Code UNSPSC :
85151701
ID de substance PubChem :
329755838
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Essai

≥90.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

food and beverages

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CCCCC\C=C\C(=O)CCc1ccc(O)c(OC)c1

InChI

1S/C17H24O3/c1-3-4-5-6-7-8-15(18)11-9-14-10-12-16(19)17(13-14)20-2/h7-8,10,12-13,19H,3-6,9,11H2,1-2H3/b8-7+

Clé InChI

OQWKEEOHDMUXEO-BQYQJAHWSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Description générale

[6]-Shogaol is a pungent and one of the most abundant dehydrated form of gingerols present in the fresh ginger roots or dried and thermally treated roots. It may serve as a potential anti-inflammatory agent.

Application

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

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Autres remarques

This compound is commonly found in plants of the genus: zingiber

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
WXBF4194V
BCCJ9075
WXBF1851V
BCCG8779
BCCF8038

Vous ne trouvez pas la bonne version ?

Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Les clients ont également consulté

Slide 1 of 8

1 of 8

[6]-Gingerol, Zingiber officinale An antitumor, apoptosis-inducing compound of the ginger family that blocks EGF-induced cell transformation by inhibiting the activation of Activator Protein-1 (AP-1).

Sigma-Aldrich

345868

[6]-Gingerol, Zingiber officinale

[6]-Gingerol phyproof® Reference Substance

PHL89201

[6]-Gingerol

10-Shogaol phyproof® Reference Substance

PHL83911

10-Shogaol

10-Gingerol phyproof® Reference Substance

PHL89203

10-Gingerol

Zingerone analytical standard

Supelco

88787

Zingerone

Vanillylacetone ≥96%, FG

Sigma-Aldrich

W312401

Vanillylacetone

Sigma-Aldrich

Sigma-Aldrich

W252204

Ginger oil

Zerumbone ≥98% (HPLC)

Sigma-Aldrich

Z3902

Zerumbone

Po-Lin Kuo et al.
Journal of agricultural and food chemistry, 59(7), 3429-3438 (2011-03-05)
This study has two novel findings: it is not only the first to demonstrate inflammatory cytokines, which are produced by the bronchial epithelium after exposure to phthalate esters and contribute to airway remodeling by increasing human bronchial smooth muscle cells
Pharmacological studies on ginger. IV. Effect of (6)-shogaol on the arachidonic cascade
MS, et al.
Nihon Aruk?ru Yakubutsu Igakkai Zasshi = Japanese Journal of Alcohol Studies & Drug Dependence, 88, 263-269 (1986)
Ya-Ling Hsu et al.
Journal of agricultural and food chemistry, 60(3), 852-861 (2012-01-10)
4-Shogaol is one of the phytoconstituents isolated from dried red ginger, which is commercially available to consumers. Some active constituents from ginger have been found to have anti-inflammatory and antioxidant effects, but studies on 4-shogaol have been relatively rare. This
Chia-Jui Weng et al.
Molecular nutrition & food research, 56(8), 1304-1314 (2012-06-21)
We previously demonstrated that 6-shogaol and 6-gingerol, two active compounds in ginger (Zingiber officinale), possess antiinvasive activity against highly metastatic hepatoma cells. The aims of this study were to evaluate the inhibitory effect and molecular mechanism underlying the transcription and
Pharmacokinetics of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol and conjugate metabolites in healthy human subjects
Zick.MS, et al.
Cancer Epidemiology, Biomarkers & Prevention, 17, 1930-1936 (2008)
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique