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Merck
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Documentos

45371

Supelco

Carboxine

PESTANAL®, analytical standard

Sinônimo(s):

5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide, Carbathiine

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About This Item

Fórmula empírica (Notação de Hill):
C12H13NO2S
Número CAS:
Peso molecular:
235.30
Beilstein:
983249
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

CC1=C(SCCO1)C(=O)Nc2ccccc2

InChI

1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

chave InChI

GYSSRZJIHXQEHQ-UHFFFAOYSA-N

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Aplicação

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

Produtos recomendados

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.

Informações legais

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2

Órgãos-alvo

Kidney

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

212.0 °F - closed cup

Ponto de fulgor (°C)

100 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Certificados de análise (COA)

Lot/Batch Number

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Supelco

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Sigma-Aldrich

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Sigma-Aldrich

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Toshikazu Irie et al.
Bioscience, biotechnology, and biochemistry, 67(9), 2006-2009 (2003-10-02)
We cloned a gene for the iron sulfur protein (Ip) subunit from an edible mushroom, Lentinula edodes, and introduced a point mutation that confers carboxin resistance into it. The mutant gene successfully transformed L. edodes with high efficiency (9 transformants/2.5
Yoko Shima et al.
Bioscience, biotechnology, and biochemistry, 75(1), 181-184 (2011-01-14)
Five carboxin-resistant mutants from Aspergillus oryzae were characterized by the sensitivities of their mycelial growth and succinate dehydrogenase (SDH) activity to carboxin and three related fungicides. Despite a significant resistance to carboxin, exhibited by all the mutants, their patterns of
David Obermayer et al.
The Journal of organic chemistry, 76(16), 6657-6669 (2011-07-05)
A series of 4-(pyrazol-1-yl)carboxanilides active as inhibitors of canonical transient receptor potential channels were synthesized in an efficient three-step protocol using controlled microwave heating. The general synthetic strategy involves condensation of 4-nitrophenylhydrazine with appropriate 1,3-dicarbonyl building blocks, followed by reduction
Willem G van Herk et al.
Environmental entomology, 36(6), 1441-1449 (2008-02-21)
A bioassay for observing wireworm behavior in soil is described. The bioassay permits analysis of orientation, feeding, repellency, and postcontact toxicity behaviors of wireworms in response to insecticide-treated wheat seeds. Wireworm positions were recorded every 5 min for 3 h
Gabriel Scalliet et al.
PloS one, 7(4), e35429-e35429 (2012-04-27)
A range of novel carboxamide fungicides, inhibitors of the succinate dehydrogenase enzyme (SDH, EC 1.3.5.1) is currently being introduced to the crop protection market. The aim of this study was to explore the impact of structurally distinct carboxamides on target

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