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Merck
CN

36194

伏杀磷

PESTANAL®, analytical standard

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关于此项目

经验公式（希尔记法）:
C12H15ClNO4PS2
化学文摘社编号:
2310-17-0
分子量:
367.81
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755336
EC Number:
218-996-2
Beilstein/REAXYS Number:
694650
MDL number:
MFCD00055499

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产品名称

伏杀磷, PESTANAL®, analytical standard

InChI key

IOUNQDKNJZEDEP-UHFFFAOYSA-N

InChI

1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3

SMILES string

CCOP(=S)(OCC)SCN1C(=O)Oc2cc(Cl)ccc12

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

100

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相关类别

Application

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

General description

Phosalone is a commonly used, organophosphate insecticide, which can find applications in agricultural production. It can act effectively on lipid peroxidation and other antioxidant enzymes like superoxide dismutase, catalase and also glutathione peroxidase.

Legal Information

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

存储类别

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

wgk

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCJ6272
BCBX3928

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Role of reactive oxygen species in organophosphate insecticide phosalone toxicity in erythrocytes in vitro
Altuntas.I, et al.
Toxicology in vitro, 17, 153-157 (2003)
Synergism of resistance to phosalone and comparison of kinetic properties of acetylcholinesterase from four field populations and a susceptible strain of Colorado potato beetle
Mohamadi M.M, et al.
Pesticide Biochemistry and Physiology, 98, 254-262 (2010)
K Balasandaram et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 118(2), 229-231 (1998-01-24)
An acute dose of phosalone, intraperitoneally injected to Rana tigrina alters the bioelectrical activity of the brain. The frequency levels of delta, theta, alpha, and beta waves remained similar in both control and experimental groups, while the amplitude of the
V Issert et al.
Amino acids, 17(4), 377-389 (2000-03-09)
Hapten synthesis for the production of specific insecticide phosalone polyclonal antibodies was carried out starting from an intermediate of the phosalone synthesis, 6-chloro-2-benzoxazolone 1. Two haptens containing different spacers have been prepared: N-5-carboxypentyl-6-chloro-2-benzoxazolone 7 and N-(2-oxo-3-aza-5-carboxypentyl)-6-chloro-2-benzoxazolone 12. Each of these
K Lai et al.
Archives of biochemistry and biophysics, 318(1), 59-64 (1995-04-01)
The extensive use of organophosphorothioate insecticides in agriculture has resulted in the risk of environmental contamination with a variety of broadly based neurotoxins that inhibit the acetylcholinesterases of many different animal species. Organophosphorus hydrolase (OPH, EC 3.1.8.1) is a broad-spectrum
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