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Benfuracarb

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C20H30N2O5S
CAS-Nummer:
82560-54-1
Molekulargewicht:
410.53
MDL-Nummer:
MFCD00210247
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329753802
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

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

InChIKey

FYZBOYWSHKHDMT-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

>212.0 °F

Flammpunkt (°C)

> 100 °C

Persönliche Schutzausrüstung

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

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Analysenzertifikate (COA)

Lot/Batch Number
BCCJ0073
BCCB7712
BCBW8924
BCBS3726V
SZBD077XV

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Mutagenic and cytotoxic activities of benfuracarb insecticide.
Eren Y, et al.
Cytotechnology, 68(4), 637-643 (2016)
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
K Ameno et al.
Forensic science international, 116(1), 59-61 (2000-12-19)
We describe four fatal cases due to ingestion of carbofuran, a carbamate insecticide. Carbofuran was detected in the gastric contents using thin layer chromatography (TLC) and gas chromatography/mass spectrophotometry (GC/MS), and quantified in the blood using a gas chromatograph equipped
S Kilani-Morakchi et al.
Communications in agricultural and applied biological sciences, 71(2 Pt B), 555-562 (2007-03-28)
In order to complete previous studies conducted on Blattella germanica, three insecticides from different groups were evaluated: boric acid, an inorganic compound, benfuracarb, a carbamate, and halofenozide, a non-steroidal ecdysone agonist. Boric acid (8.20%, LD50) and benfuracarb (2%, LD50) were
Maria Rosaria Iesce et al.
Environmental science and pollution research international, 13(2), 105-109 (2006-04-15)
N-methylcarbamate insecticides are widely used chemicals for crop protection. This study examines the hydrolytic and photolytic cleavage of benfuracarb, carbosulfan and carbofuran under natural conditions. Their toxicity and that of the corresponding main degradation products toward aquatic organisms were evaluated.
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