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Supelco

Carbofuran-3-hydroxy

PESTANAL®, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C12H15NO4
Numero CAS:
Peso molecolare:
237.25
Beilstein:
1383873
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
NMR: suitable
gas chromatography (GC): suitable

Impurezze

≤2% water (Karl Fischer)

Punto di fusione

140-148 °C

Compatibilità

passes test for identity (NMR)

applicazioni

agriculture
environmental

Formato

neat

Temperatura di conservazione

−20°C

Stringa SMILE

CNC(=O)Oc1cccc2C(O)C(C)(C)Oc12

InChI

1S/C12H15NO4/c1-12(2)10(14)7-5-4-6-8(9(7)17-12)16-11(15)13-3/h4-6,10,14H,1-3H3,(H,13,15)
RHSUJRQZTQNSLL-UHFFFAOYSA-N

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Descrizione generale

Carbofuran-3-hydroxy is one of the metabolites of the insecticide, carbofuran.

Applicazioni

Carbofuran-3-hydroxy may be used as a reference standard for the determination of carbofuran-3-hydroxyn in rape plants by reverse phase high pressure liquid chromatography.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

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

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 2 Oral

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificati d'analisi (COA)

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Direct analysis of carbofuran and 3-hydroxycarbofuran in rape plants by reverse-phase high-pressure liquid chromatography.
Y W Lee et al.
Journal of agricultural and food chemistry, 28(4), 719-722 (1980-07-01)
P W Ferguson et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 4(1), 14-21 (1984-02-01)
The influence of carbofuran metabolism on acetylcholinesterase inhibition has been defined after low dose (50 micrograms/kg, iv and oral) [carbonyl-14C]carbofuran exposures to male Sprague-Dawley rats. Red blood cell acetylcholinesterase (RBC AchE) inhibition (83% at 2 min, 37% at 15 min
S Dulaurent et al.
Forensic science international, 176(1), 72-75 (2007-11-07)
We reported two non-fatal cases of intoxication with pesticides namely alachlor and carbofuran. Hair stand samples were collected from two men approximately 1 year after alachlor intoxication for case 1, and 14 days after the last exposure for case 2.
Carbofuran metabolism and toxicity in the rat.
Ferguson PW, et al.
Toxicological Sciences, 4(1), 14-21 (1984)
Adsorption and degradation of benfuracarb in three soils in Hunan, People's Republic of China.
N Xue et al.
Bulletin of environmental contamination and toxicology, 76(4), 720-727 (2006-05-12)

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