Pular para o conteúdo
Merck
Todas as fotos(2)

Documentos Principais

Visualizar Toda a Documentação

00290

Supelco

(−)-Sinigrin hydrate

analytical standard

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(2)

About This Item

Fórmula empírica (Notação de Hill):
C10H16KNO9S2 · xH2O
Número CAS:
3952-98-5
Peso molecular:
397.46 (anhydrous basis)
Número MDL:
MFCD00149447
Código UNSPSC:
85151701
ID de substância PubChem:
329747031
NACRES:
NA.24

Nível de qualidade

100

grau

analytical standard

Ensaio

≥99.0% (TLC)

atividade óptica

[α]/D -17.0±1°, c = 1 in H2O

prazo de validade

limited shelf life, expiry date on the label

Impurezas

≤6.0% water

pf

128 (dec.) (lit.)

aplicação(ões)

food and beverages

Formato

neat

cadeia de caracteres SMILES

[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

chave InChI

IUBVMJHASFBYGW-WBMBWNLZSA-M

Procurando produtos similares? Visita Guia de comparação de produtos

Ações bioquímicas/fisiológicas

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

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H317

Classificações de perigo

Skin Sens. 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCD2474
BCBW5081

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 10

1 of 10

Glucoraphani potassium salt phyproof® Reference Substance

PHL89215

Glucoraphani potassium salt

Glucobarbarin potassium salt phyproof® Reference Substance

PHL89684

Glucobarbarin potassium salt

Glucoiberin potassium salt phyproof® Reference Substance

PHL89687

Glucoiberin potassium salt

vibrant-m

ERMBC366

Rapeseed (S, total glucosinolate)

vibrant-m

ERMBC190

Rapeseed (S, total glucosinolate)

Gluconapin potassium salt phyproof® Reference Substance

PHL89688

Gluconapin potassium salt

3-Methylbenzylamine 98%

Sigma-Aldrich

126829

3-Methylbenzylamine

Sulfatase from Helix pomatia Type H-1, sulfatase ≥10,000 units/g solid

Sigma-Aldrich

S9626

Sulfatase from Helix pomatia

Allyl isothiocyanate PESTANAL®, analytical standard

Supelco

36682

Allyl isothiocyanate

Allyl isothiocyanate ≥95%, FCC

Sigma-Aldrich

W203408

Allyl isothiocyanate

Richard A Lankau et al.
The American naturalist, 171(2), 150-161 (2008-01-17)
Plants interact with many different species throughout their life cycle. Recent work has shown that the ecological effects of multispecies interactions are often not predictable from studies of the component pairwise interactions. Little is known about how multispecies interactions affect
Tianxin Wang et al.
Phytochemical analysis : PCA, 22(3), 205-213 (2010-11-04)
Sinigrin, a major glucosinolate present in Indian mustard (Brassica juncea L.) seeds as the precursor of the anticancer compound allyl isothiocyanate, shows a wide range of biological activities. It's necessary to optimize the extraction methods and conditions, in order to
Kody A Belliveau et al.
Natural product research, 24(1), 24-33 (2009-12-17)
A simple procedure for extracting and purifying sinigrin from Oriental mustard (Brassica juncea) meal using cold water was developed. Subsequently, the chemical degradation of sinigrin due to enzymatic activity was monitored using (1)H NMR spectroscopy over the course of 30
Gaetan Glauser et al.
Phytochemical analysis : PCA, 23(5), 520-528 (2012-02-11)
The analysis of glucosinolates (GS) is traditionally performed by reverse-phase liquid chromatography coupled to ultraviolet detection after a time-consuming desulphation step, which is required for increased retention. Simpler and more efficient alternative methods that can shorten both sample preparation and
Richard A Lankau
Proceedings of the National Academy of Sciences of the United States of America, 109(28), 11240-11245 (2012-06-27)
Although reciprocal evolutionary responses between interacting species are a driving force behind the diversity of life, pairwise coevolution between plant competitors has received less attention than other species interactions and has been considered relatively less important in explaining ecological patterns.
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica