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Merck
CN

45372

Supelco

灭螨猛

PESTANAL®, analytical standard

别名:

灭螨猛

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About This Item

经验公式(希尔记法):
C10H6N2OS2
CAS号:
分子量:
234.30
Beilstein:
526833
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

SMILES字符串

Cc1ccc2nc3SC(=O)Sc3nc2c1

InChI

1S/C10H6N2OS2/c1-5-2-3-6-7(4-5)12-9-8(11-6)14-10(13)15-9/h2-4H,1H3

InChI key

FBQQHUGEACOBDN-UHFFFAOYSA-N

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应用

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

推荐产品

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.

法律信息

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

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警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 2 - Skin Sens. 1A - STOT RE 2 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

法规信息

农药列管产品
危险化学品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

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访问文档库

Jianying Qi et al.
Bioorganic & medicinal chemistry letters, 13(20), 3561-3563 (2003-09-25)
It is demonstrated for the first time in this report that chinomethionate is capable of causing efficient DNA cleavage under mild irradiation conditions, a fungicide molecule that processes the simple group of 1,3-dithio-2-one as its reactive functionality.
R T Krause et al.
Journal - Association of Official Analytical Chemists, 66(4), 1018-1022 (1983-07-01)
The AOAC multiresidue method for nonpolar pesticide residues in nonfatty foods has been coupled with a high performance liquid chromatographic (HPLC)-fluorometric system for determining quinomethionate residues on apples and oranges. Quinomethionate is extracted with acetonitrile, and coextractives are removed with
G Carrera et al.
Comptes rendus des seances de l'Academie des sciences. Serie III, Sciences de la vie, 296(21), 1001-1004 (1983-01-01)
The amount of nitrogen excreted in urines is higher in pair-fed Rats subjected to a diet containing 400 mg/kg of oxythioquinox. This is a consequence of specific effect of oxythioquinox on protein catabolism and not to a renal failure as
Maureen R Gwinn et al.
Journal of toxicology and environmental health. Part A, 71(5), 315-324 (2008-01-25)
Microarray technology has advanced toward analysis of toxic occupational exposures in biological systems. Microarray analysis is an ideal way to search for biomarkers of exposure, even if no specific gene or pathway has been identified. Analysis may now be performed
G Carrera et al.
Toxicology letters, 19(1-2), 159-164 (1983-10-01)
Oxythioquinox, administered in solution in the dietary lipids at 400 mg/kg fresh food for 21 days, caused liver hypertrophy with severe steatosis. The levels of liver triglycerides increased 40-fold, phospholipids 2-fold and cholesterol 7-fold respectively. The steatosis was thought to

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