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45333

Supelco

Azinphos-methyl

PESTANAL®, analytical standard

Synonym(s):

Guthion®, Methyltriazotin

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About This Item

Empirical Formula (Hill Notation):
C10H12N3O3PS2
CAS Number:
86-50-0
Molecular Weight:
317.32
Beilstein:
280476
EC Number:
201-676-1
MDL number:
MFCD00041814
UNSPSC Code:
41116107
PubChem Substance ID:
329756655
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

storage temp.

2-8°C

SMILES string

COP(=S)(OC)SCN1N=Nc2ccccc2C1=O

InChI

1S/C10H12N3O3PS2/c1-15-17(18,16-2)19-7-13-10(14)8-5-3-4-6-9(8)11-12-13/h3-6H,7H2,1-2H3

InChI key

CJJOSEISRRTUQB-UHFFFAOYSA-N

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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.

Legal Information

Guthion is a registered trademark of Makhteshim Chemical Works Ltd.
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Storage Class Code

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL9129
BCCG5166
BCCC6365
BCBV5129
BCBS2969V

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Ana Ferrari et al.
Aquatic toxicology (Amsterdam, Netherlands), 93(1), 37-44 (2009-04-14)
Amphibian embryos are naturally exposed to prooxidant conditions throughout their development. Environmental exposure to contaminants may affect their capacity to respond to challenging conditions, to progress in a normal ontogenesis, and finally to survive and succeed in completing metamorphosis. We
Gisela Kristoff et al.
Aquatic toxicology (Amsterdam, Netherlands), 112-113, 19-26 (2012-03-01)
Cholinesterases and carboxylesterases belong to the group of B-esterases, the serine superfamily of esterases that are inhibited by organophosphorus compounds. It is now generally accepted that before using the B-esterases as biomarkers of exposure to organophosphorus and carbamates in a
Martine S Jordaan et al.
Ecotoxicology (London, England), 21(3), 649-661 (2011-11-17)
The use of organophosphate pesticides is an integral part of commercial farming activities and these substances have been implicated as a major source of environmental contamination and may impact on a range of non-target fauna. The extent to which soil
Luis Claudio Cacciatore et al.
Chemosphere, 88(4), 450-458 (2012-03-23)
In this study, the cholinesterase (ChE) and carboxylesterase (CES) activities present in whole organism homogenates from Planorbarius corneus and their in vitro sensitivity to organophosphorous (OP) pesticides were studied. Firstly, a characterization of ChE and CES activities using different substrates
Jianshe Tang et al.
Journal of immunoassay & immunochemistry, 29(4), 356-369 (2008-09-30)
Organophosphorus Pesticides (OPPs) are a group of artificially synthesized substances used in farms to control pests and to enhance agricultural production. Although these compounds show preferential toxicity to insects, they are also toxic to humans and mammals by the same
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