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Supelco

Dialifos

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H17ClNO4PS2
CAS Number:
10311-84-9
Molecular Weight:
393.85
Beilstein/REAXYS Number:
1550800
EC Number:
233-689-3
MDL number:
MFCD00055503
UNSPSC Code:
41116107
PubChem Substance ID:
329755356

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

storage temp.

2-8°C

SMILES string

CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O

InChI

1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3

InChI key

MUMQYXACQUZOFP-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

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
SZBD304XV
SZBA277XV
7169X
3203X

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M Kalafatić et al.
The International journal of developmental biology, 35(3), 335-340 (1991-09-01)
Investigations showed that the three insecticides used had the most damaging effect upon hydra immediately after treatment. The tentacles and the hypostome are the parts most often damaged. Inse the affected cells, lesions appear in the intracellular membranes, the nucleus
R Besser et al.
Neurology, 40(8), 1275-1277 (1990-08-01)
Two patients with acute severe organophosphate intoxication showed (1) single evoked compound muscle action potentials (CMAP) with repetitive discharges and (2) prominent decremental responses of CMAP with 20 and 50 Hz supramaximal nerve stimulation. Following the intravenous injection of single
Prashant Shankarrao Adole et al.
Analytical biochemistry, 621, 114158-114158 (2021-03-12)
Intentional or unintentional intake of anticholinesterase pesticides became common due to their extensive use in agricultural and domestic purposes, resulting in numerous poisoning cases. A simple, accurate, and sensitive gas chromatography-ion trap mass spectrometry-based method for the quantification of 12
Environmental fate of dialifor and formation of its oxygen analogue following application on grape vines in the San Joaquin Valley, California.
W Winterlin et al.
Journal of agricultural and food chemistry, 28(6), 1078-1083 (1980-11-01)
H N Nigg et al.
Archives of environmental contamination and toxicology, 10(4), 497-504 (1981-07-01)
Surface residue disappearance rates of dioxathion, malathion, oxydemetonmethyl, and dialifor were the same for fruit and leaves, and they increase with temperature. Disappearance rates were in the order of malathion greater than or equal to oxydemetonmethyl greater than dialifor greater
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