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Key Documents

31611

Supelco

Phenthoate

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H17O4PS2
CAS Number:
Molecular Weight:
320.36
Beilstein:
2474108
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

format

neat

storage temp.

2-8°C

SMILES string

CCOC(=O)C(SP(=S)(OC)OC)c1ccccc1

InChI

1S/C12H17O4PS2/c1-4-16-12(13)11(10-8-6-5-7-9-10)19-17(18,14-2)15-3/h5-9,11H,4H2,1-3H3

InChI key

XAMUDJHXFNRLCY-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.

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Legal Information

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

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

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Certificates of Analysis (COA)

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Customers Also Viewed

Fish mortality following application of phenthoate to Florida citrus.
H N Nigg et al.
Bulletin of environmental contamination and toxicology, 32(5), 587-596 (1984-05-01)
P K Gupta
Toxicology letters, 22(1), 69-73 (1984-07-01)
This study was designed to provide information on the cumulative effects of phenthoate, an organophosphorus insecticide. Male rats were given the test compound orally 6 days/week for a minimum of 10 weeks and until the cumulative LD50 (CLD50) remained constant
S Kawabata et al.
Journal of toxicology. Clinical toxicology, 32(1), 49-60 (1994-01-01)
Five metabolites were detected in the plasma and urine of a patient following ingestion of the organophosphate insecticide, phenthoate. Intact phenthoate was detected only in gastric lavage fluid. After methylation of acidic extracts of plasma and urine, phenthoate acid, demethyl
Min Liao et al.
Journal of environmental sciences (China), 16(5), 738-741 (2004-11-24)
Adsorption of phenthoate and acetochlor onto kaolin, montmorillonite, bentonite clays and respective organoclays prepared by the exchange of quaternary ammonium as tetradecyltrimethyl ammonium bromide(TTAB), dodecyltrimethylammonium bromide (DTAB), and cetylpyridinium chloride (CPC) were studied. The adsorption equilibrium data points were fitted
T Imamura et al.
Toxicology and applied pharmacology, 70(1), 140-147 (1983-08-01)
Malathion and phenthoate carboxylesterase activities were investigated in pulmonary alveolar macrophages (PAM) in Sprague-Dawley rats. PAM was found to be capable of hydrolyzing phenthoate at a faster rate than malathion. Oral administration to rats with O,O,S-trimethyl phosphorothioate (OOS-Me), a pneumotoxic

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