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31141

Supelco

Prosulfocarb

PESTANAL®, analytical standard

Synonym(s):

S-Benzyl dipropylthiocarbamate

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About This Item

Empirical Formula (Hill Notation):
C14H21NOS
CAS Number:
52888-80-9
Molecular Weight:
251.39
Beilstein:
4804364
EC Number:
401-730-6
MDL number:
MFCD00145179
UNSPSC Code:
41116107
PubChem Substance ID:
329753665
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

SMILES string

CCCN(CCC)C(=O)SCc1ccccc1

InChI

1S/C14H21NOS/c1-3-10-15(11-4-2)14(16)17-12-13-8-6-5-7-9-13/h5-9H,3-4,10-12H2,1-2H3

InChI key

NQLVQOSNDJXLKG-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

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H317,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

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)

Lot/Batch Number
BCCF9466
BCCC8918
BCBZ3239
BCBV4720
BCBT9386

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Michèle Nègre et al.
Pest management science, 62(10), 957-964 (2006-08-04)
Adsorption isotherms of prosulfocarb were determined on soils with different physicochemical properties. The extent of adsorption increased with the organic carbon content, but the results also suggested the involvement of some inorganic soil surfaces. In order better to understand the
Roberto Busi et al.
Pest management science, 76(12), 3926-3934 (2020-07-09)
Resistance to the dinitroaniline herbicide trifluralin in Lolium rigidum (annual ryegrass) often is mediated by the enhanced capacity to metabolize the herbicide to less toxic polar conjugates and/or by functionally recessive target-site mutations in α-tubulin. In two L. rigidum populations
Mara Gennari et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 37(4), 297-305 (2002-06-26)
Active microbial degraders of the herbicide prosulfocarb (PSC) were isolated to evaluate their performance in soil with a view to their use for bioremediation. The isolated cultures (a microbial consortium and a Pseudomonas sp. strain) were active when tested in
Karsten E Braun et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 52(2), 122-130 (2016-11-08)
The fate of
Enhanced soil biodegradation of prosulfocarb herbicide in barley crop.
J Rouchaud et al.
Bulletin of environmental contamination and toxicology, 58(5), 752-757 (1997-05-01)
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