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Benfuracarb

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C20H30N2O5S
CAS Number:
82560-54-1
Molecular Weight:
410.53
MDL number:
MFCD00210247
UNSPSC Code:
41116107
PubChem Substance ID:
329753802
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

format

neat

SMILES string

CCOC(=O)CCN(SN(C)C(=O)Oc1cccc2CC(C)(C)Oc12)C(C)C

InChI

1S/C20H30N2O5S/c1-7-25-17(23)11-12-22(14(2)3)28-21(6)19(24)26-16-10-8-9-15-13-20(4,5)27-18(15)16/h8-10,14H,7,11-13H2,1-6H3

InChI key

FYZBOYWSHKHDMT-UHFFFAOYSA-N

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General description

Benfuracarb belongs to the benzofuranyl methylcarbamate insecticide group of pesticides used to control insect pests in citrus, maize, sugar beet and vegetables.

Application

Benfuracarb may be used as a reference standard for the determination of the analyte:
  • In bananas by application of a modified QuEChERS procedure followed by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS).
  • In honeybees, honey and bee pollen by liquid chromatography coupled to tandem mass spectrometry.

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

Signal Word

Danger

Hazard Statements

H301 + H331,H361f,H410

Hazard Classifications

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

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

>212.0 °F

Flash Point(C)

> 100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL1809
BCCJ0073
BCCB7712
BCBW8924
BCBS3726V

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Khaled Abass et al.
Toxicology letters, 224(2), 290-299 (2013-08-21)
In vitro metabolism of benfuracarb in liver microsomes from seven species was studied in order to quantitate species-specific metabolic profiles and enhance benfuracarb risk assessment by interspecies comparisons. Using LC-MS/MS, a total of seven phase-I-metabolites were detected from the extracted
Raju Chandra et al.
Bulletin of environmental contamination and toxicology, 83(3), 348-351 (2009-04-01)
The fate of benfuracarb was studied under field conditions in brinjal fruits and soil following foliar spray application at 0.25 and 0.50 microg g(-1) by HPLC. At 0.25 microg g(-1), benfuracarb persisted up to 7 days both in soil and
S Ichikawa et al.
The Journal of toxicological sciences, 20(2), 143-148 (1995-05-01)
The antidotal action of atropine sulfate and 2-pyridine aldoxime methiodide (2-PAM) against poisoning attributable to the new procarbamate insecticide benfuracarb [(ethyl N-[2,3-dihydro-2,2-dimethylbenzofuran-7-yloxycarbonyl (methyl) aminothio]-N-isopropyl-beta-alaninate] was compared utilizing rats as our experimental model. Both the intraperitoneal and oral administrations of these
P Stehrer-Schmid et al.
Mutation research, 345(3-4), 111-125 (1995-12-01)
The carbamate insecticides benfuracarb, carbosulfan and furathiocarb were investigated in the mouse bone marrow micronucleus assay to establish whether they show cytogenetic activity in vivo. Two doses of each substance were administered intraperitoneally to NMRI mice. All of the three
A Maiza et al.
Communications in agricultural and applied biological sciences, 69(3), 257-266 (2005-03-12)
Blatta germanica is the more prevalent cockroach species in Algeria. In the present study, we tested the effect on reproduction in B. germanica of two insect growth regulators, RH-0345, a benzoylhydrazine analogue that mimics the action of 20-hydroxyecdysone, and methoprene
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