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Merck
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45365

Supelco

Captafol

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C10H9Cl4NO2S
Número CAS:
2425-06-1
Peso molecular:
349.06
Número CE:
219-363-3
Número MDL:
MFCD00041816
Código UNSPSC:
41116107
ID de substância PubChem:
329756675
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

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
cleaning products
cosmetics
environmental
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

ClC(Cl)C(Cl)(Cl)SN1C(=O)C2CC=CCC2C1=O

InChI

1S/C10H9Cl4NO2S/c11-9(12)10(13,14)18-15-7(16)5-3-1-2-4-6(5)8(15)17/h1-2,5-6,9H,3-4H2

chave InChI

JHRWWRDRBPCWTF-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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

Atenção

Restricted to professional users. Attention − Avoid exposure − obtain special instructions before use.

Informações legais

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

Palavra indicadora

Danger

Frases de perigo

H317,H350,H410

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1

Código de classe de armazenamento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análise (COA)

Lot/Batch Number
BCCG5803
BCCG2296
BCBT8609
BCBT5470
SZBC089XV

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H C Kim et al.
Cancer letters, 111(1-2), 15-20 (1997-01-01)
The modifying effects of captafol and protective effects of L-cysteine on the development of glutathione S-transferase placental form-positive (GST-P +) foci of the liver and expression of proliferating cell nuclear antigen (PCNA) in the kidney were investigated in a medium-term
M A Rodrigues et al.
Biomedical and environmental sciences : BES, 7(3), 278-283 (1994-09-01)
The cytotoxicity of captafol, a phthalimide-derived fungicide, was evaluated in IB-RS-2 cells. Captafol at 0.12-1.0 microgram/ml blocks the cell multiplication. This effect is concentration-dependent, only partially reversible and the degree of inhibition increases with time. The synthesis of DNA and
S Saxena et al.
Biochemistry and molecular biology international, 41(6), 1125-1136 (1997-05-01)
The mutagenic and genotoxic potential of four pesticides viz. captan, foltaf, phosphamidon and furadan was evaluated by the Ames mutagenicity assay and their DNA damaging ability on radiation repair defective E. coli K-12 strains respectively. The mutagenic spectrum revealed captan
H Tsuda et al.
Japanese journal of cancer research : Gann, 84(3), 230-236 (1993-03-01)
In a development trial for an initiation bioassay system, 7 known carcinogens and 1 suspected carcinogen were examined. In experiment 1, group 1 animals were initially subjected to partial hepatectomy (PH) 12 h before administration of diethylnitrosamine, 2-amino-3-methylimidazo[4,5-f]-quinoline (IQ), captafol
M Futakuchi et al.
Cancer letters, 104(1), 37-41 (1996-06-24)
Effects of quinoline and captafol, both of which are hemangiocarcinogenic agents, were investigated in spontaneously hypertensive rats (SHR). Male SHR and Wistar Kyoto rats (WKY), the parent strain of SHR, were administered quinoline (0.2%) or captafol (0.15%) supplemented in the
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