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Supelco

Carbofuran-3-hydroxy

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H15NO4
CAS Number:
Molecular Weight:
237.25
Beilstein:
1383873
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

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

impurities

≤2% water (Karl Fischer)

mp

140-148 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

storage temp.

−20°C

SMILES string

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)

InChI key

RHSUJRQZTQNSLL-UHFFFAOYSA-N

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General description

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

Application

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.

Legal Information

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

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Customers Also Viewed

Carbofuran metabolism and toxicity in the rat.
Ferguson PW, et al.
Toxicological Sciences, 4(1), 14-21 (1984)
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, 212(1-3), e10-e14 (2011-06-07)
We present two non fatal cases of intoxication with carbofuran (CBF) documented by hair analysis. Carbofuran and 3-hydroxycarbofuran (OHCBF, its main metabolite) hair concentrations were determined using a liquid chromatography-tandem mass spectrometry method. The obtained results were surprising if we
D L Suett
Food additives and contaminants, 3(4), 371-376 (1986-10-01)
Commercially-grown quick-maturing carrots which had been treated with insecticides to protect them from damage by carrot fly were analysed for residues of carbofuran (4 samples), disulfoton (17 samples) or phorate (20 samples). Intervals between treatment and harvest ranged from 10

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