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经验公式(希尔记法):
C12H16ClNOS
化学文摘社编号:
分子量:
257.78
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
248-924-5
Beilstein/REAXYS Number:
1968440
MDL number:
产品名称
禾草丹, PESTANAL®, analytical standard
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
InChI key
QHTQREMOGMZHJV-UHFFFAOYSA-N
SMILES string
CCN(CC)C(=O)SCc1ccc(Cl)cc1
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
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Application
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.
General description
Thiobencarb is a thiocarbamate herbicide, widely used for the control of pests in rice fields.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
农药列管产品
此项目有
Bülent Kaya et al.
Mutation research, 557(1), 53-62 (2004-01-07)
In the present study, the herbicides bentazone, molinate, thiobencarb and trifluralin were evaluated for mutagenic and recombinagenic effects using the wing spot test of Drosophila melanogaster (somatic mutation and recombination test, SMART). Both standard (ST) and high-bioactivation (HB) fly crosses
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
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)
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
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)
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