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S1647

Sigma-Aldrich

(−)-Sinigrin hydrate

≥98% (HPLC), from horseradish

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About This Item

Formula empirica (notazione di Hill):
C10H16KNO9S2 · xH2O
Numero CAS:
3952-98-5
Peso molecolare:
397.46 (anhydrous basis)
Numero MDL:
MFCD00149447
Codice UNSPSC:
12352201
ID PubChem:
24899488
NACRES:
NA.25
Prezzi e disponibilità al momento non sono disponibili

Origine biologica

horseradish

Livello qualitativo

200

Saggio

≥98% (HPLC)

Stato

powder

tecniche

HPLC: suitable

Colore

white

Punto di fusione

128 (dec.) (lit.)

Solubilità

water: 50 mg/mL, clear, colorless to faintly yellow

Cationi in tracce

K: 8.4-10.8% (anhydrous)

Temperatura di conservazione

room temp

Stringa SMILE

[K+].[H]O[H].OC[C@H]1O[C@@H](S\C(CC=C)=N\OS([O-])(=O)=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C10H17NO9S2.K.H2O/c1-2-3-6(11-20-22(16,17)18)21-10-9(15)8(14)7(13)5(4-12)19-10;;/h2,5,7-10,12-15H,1,3-4H2,(H,16,17,18);;1H2/q;+1;/p-1/b11-6+;;/t5-,7-,8+,9-,10+;;/m1../s1
IUBVMJHASFBYGW-WBMBWNLZSA-M

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Categorie correlate

Azioni biochim/fisiol

A β-D-thioglucopyranoside occurring in black mustard seeds and horseradish root. Substrate for thioglucosidase.

Altre note

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H317

Classi di pericolo

Skin Sens. 1

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

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
0000276192
0000276192
SLCG6448
SLBZ2023
SLBQ2588V

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Tahereh Aghajanzadeh et al.
Frontiers in plant science, 5, 704-704 (2015-01-08)
Brassica juncea seedlings contained a twofold higher glucosinolate content than B. rapa and these secondary sulfur compounds accounted for up to 30% of the organic sulfur fraction. The glucosinolate content was not affected by H2S and SO2 exposure, demonstrating that
Mohammad Salehin et al.
Nature communications, 10(1), 4021-4021 (2019-09-08)
A detailed understanding of abiotic stress tolerance in plants is essential to provide food security in the face of increasingly harsh climatic conditions. Glucosinolates (GLSs) are secondary metabolites found in the Brassicaceae that protect plants from herbivory and pathogen attack.
Katherine Cools et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 901, 115-118 (2012-06-30)
Glucosinolates are β-thioglycosides which are found naturally in Cruciferae including the genus Brassica. When enzymatically hydrolysed, glucosinolates yield isothiocyanates and give a pungent taste. Both glucosinolates and isothiocyanates have been linked with anticancer activity as well as antifungal and antibacterial
Sabine Montaut et al.
Journal of natural products, 72(5), 889-893 (2009-04-02)
Fruit extracts of Dithyrea wislizenii were analyzed for desulfoglucosinolates and intact glucosinolates using HPLC-APCI-MS and HPLC-ESI-MS, respectively. 2-Propenylglucosinolate (sinigrin) was shown to be present in the extracts. 6-Methylsulfanylhexyl- (glucolesquerellin 9), 6-methylsulfinylhexyl- (glucohesperin 10), 7-methylsulfanylheptyl- (11), and 5-methylsulfanylpentylglucosinolate (glucoberteroin 12) were
Verena Jeschke et al.
Frontiers in plant science, 10, 1560-1560 (2019-12-24)
Dynamically changing environmental conditions promote a complex regulation of plant metabolism and balanced resource investments to development and defense. Plants of the Brassicales order constitutively allocate carbon, nitrogen, and sulfur to synthesize glucosinolates as their primary defense metabolites. Previous findings
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