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Supelco

Phosalone

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H15ClNO4PS2
CAS Number:
Molecular Weight:
367.81
Beilstein:
694650
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

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

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

InChI key

IOUNQDKNJZEDEP-UHFFFAOYSA-N

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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.

Application

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

Legal Information

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

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Customers Also Viewed

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)
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)
Mohammad Reza Hadjmohammadi et al.
Journal of separation science, 33(8), 1044-1051 (2010-02-16)
A comparison between C(18) silica and multi-walled carbon nanotubes (MWCNTs) in the extraction of Chlorpyrifos and Phosalone in environmental water samples was carried out using HPLC. Parameters affecting the extraction were type and volume of elution solvent, pH and flow
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 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

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