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Merck

45687

Supelco

Thiobencarb

PESTANAL®, analytical standard

Synonym(e):

Benthiocarb

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About This Item

Empirische Formel (Hill-System):
C12H16ClNOS
CAS-Nummer:
Molekulargewicht:
257.78
Beilstein:
1968440
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

CCN(CC)C(=O)SCc1ccc(Cl)cc1

InChI

1S/C12H16ClNOS/c1-3-14(4-2)12(15)16-9-10-5-7-11(13)8-6-10/h5-8H,3-4,9H2,1-2H3

InChIKey

QHTQREMOGMZHJV-UHFFFAOYSA-N

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Allgemeine Beschreibung

Thiobencarb is a thiocarbamate herbicide, widely used for the control of pests in rice fields.

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Thiobencarb may be used as a reference standard for the determination of thiobencarb residues in fruits and vegetables by matrix solid-phase dispersion and liquid chromatography coupled with mass spectrometry.

Rechtliche Hinweise

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

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

Determination of carbamate residues in fruits and vegetables by matrix solid-phase dispersion and liquid chromatography--mass spectrometry.
Fernandez M, et al.
Journal of Chromatography A, 871(1-2), 43-56 (2000)
E Sancho et al.
Ecotoxicology and environmental safety, 56(3), 434-441 (2003-10-25)
European eels (Anguilla anguilla) were exposed to a sublethal thiobencarb concentration of 0.22 mg/L in a flow-through system for 96 h. Mg(2+) and Na(+)-K(+) adenosine triphosphatase (ATPase) activities were evaluated in gill and muscle tissues at 2, 12, 24, 48
Kara R Schmelzer et al.
Pest management science, 61(1), 68-74 (2004-12-14)
The herbicide thiobencarb is suspected of causing delayed phytotoxicity syndrome (DPS) in rice plants. While the ultimate agent appears to be its dechlorinated product (deschlorothiobencarb), the influence of organic carbon on the formation of deschlorothiobencarb in California rice field soils
Comparative cytotoxicity of the aqueous chlorination products of thiobencarb, a thiocarbamate herbicide, in cultured rat hepatocytes
Jinno H, et al.
Toxicology in vitro, 11(6) (1997)
Jianrong Xia
Chemosphere, 59(4), 561-566 (2005-03-25)
Effects of thiobencarb on growth, photosynthesis and photoinhibition of Nostoc sphaeroides colonies were examined. Thiobencarb concentrations higher than 2 mg/l led to a significant decrease in phycoerythrin, phycocyanin and allophycocyanin content, but no significant effect on chlorophyll a (chl a)

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