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Merck
CN

45814

Iprobenfos

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H21O3PS
CAS Number:
26087-47-8
Molecular Weight:
288.34
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756969
EC Number:
247-449-0
Beilstein/REAXYS Number:
1974687
MDL number:
MFCD00191226

Key Documents

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Product Name

Iprobenfos, PESTANAL®, analytical standard

InChI key

FCOAHACKGGIURQ-UHFFFAOYSA-N

InChI

1S/C13H21O3PS/c1-11(2)15-17(14,16-12(3)4)18-10-13-8-6-5-7-9-13/h5-9,11-12H,10H2,1-4H3

SMILES string

CC(C)OP(=O)(OC(C)C)SCc1ccccc1

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

Quality Level

100

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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

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCM8693
BCCD6682
BCCB2786

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Donghao Li et al.
Marine pollution bulletin, 51(8-12), 966-974 (2005-11-18)
In order to investigate spatial and temporal distribution of organic pollutants in the Saemangeum Bay, organophosphorus pesticides (10), alkylphenols (8), chlorophenols (2), bisphenol A were analyzed from the surface seawater taken in 2002-2003. Most of the analytes were not detected
J Hemingway
Bulletin of the World Health Organization, 62(3), 445-449 (1984-01-01)
Malathion resistance in an Anopheles stephensi strain from Pakistan is dependent on a single gene, which results in increased degradation of malathion to the monocarboxylic acid. Mixtures of malathion and the fungicide IBP (O, O-bis(1-methylethyl) S-phenylmethyl phosphorothioate) were tested against
M Ueji et al.
Bulletin of environmental contamination and toxicology, 24(2), 204-210 (1980-02-01)
When BPMC was applied as single or mixed preparation with IBP to rice plants, BPMC absorbed through roots and translocated to upper portions. The uptake and dissipation of BPMC in rice plants were not different between both preparations. The disappearance
S Chen et al.
Cell death & disease, 4, e842-e842 (2013-10-12)
Interferon regulatory factor-4 binding protein (IBP) is a novel upstream activator of Rho GTPases. Our previous studies have shown that ectopic expression of IBP was correlated with malignant behaviors of human breast cancer cells, and invasive human breast cancer had
Li-Ming Tao et al.
Pest management science, 62(1), 86-90 (2005-10-20)
A malathion-resistant (RM) strain of Culex pipiens pallens Coq was obtained by successively selecting a field population with malathion in the laboratory. The synergistic effect of iprobenfos on malathion toxicity and alpha-naphthyl acetate (alpha-NA) esterase assay revealed that malathion resistance
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