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Supelco

Aminocarb

PESTANAL®, analytical standard

Synonym(s):

(4-Dimethylamino-3-methylphenyl) N-methylcarbamate

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About This Item

Empirical Formula (Hill Notation):
C11H16N2O2
CAS Number:
Molecular Weight:
208.26
Beilstein/REAXYS Number:
2808681
EC Number:
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
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CNC(=O)Oc1ccc(N(C)C)c(C)c1

InChI

1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)

InChI key

IMIDOCRTMDIQIJ-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

Skull and crossbonesEnvironment

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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M Fournier et al.
Journal of toxicology and environmental health, 25(1), 103-118 (1988-01-01)
Interaction of two potential immunosuppressive factors, sublethal pesticide exposure and viral inhibition of lymphocyte mitogenesis, was examined in mixed lymphocyte reaction (MLR). Inbred (C57Bl/6 x A/J)F mice, semisusceptible to mouse hepatitis virus 3 (MHV3) infection were exposed to selected pesticides
P Weinberger et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 20(2), 263-273 (1985-04-01)
Ceratophyllum demersum exposed to a constant 1 microgram/ml aminocarb exhibited a large capacity for the sorption of the pesticide, up to 400 micrograms/g fresh weight in the dark and 1000 micrograms/g fresh weight in the light. Smaller, actively growing sprigs
G H Hottendorf et al.
Journal of toxicology and environmental health, 22(1), 101-111 (1987-01-01)
The toxicity of three cephalosporin antibiotics to rabbit kidney cells in culture was compared to their known nephrotoxic potential in vivo (cephaloridine greater than cefazolin greater than cephalothin). While cephalothin is considered to be a relatively nonnephrotoxic cephalosporin when administered
G M Richardson et al.
Ecotoxicology and environmental safety, 7(6), 552-557 (1983-12-01)
Acute toxicity of aminocarb to the aquatic isopod Caecidolea racovitzai racovitzai was found to be proportional to exposure temperature with the potency of the insecticide increasing 1.3 to 5.2 times when the temperature was increased from 12 to 20 degrees
Yongnian Ni et al.
Journal of hazardous materials, 168(2-3), 1239-1245 (2009-04-08)
A procedure for the simultaneous kinetic spectrophotometric determination of aminocarb and carbaryl in vegetable and water samples was described. The method was based on the differential oxidation rate of aminocarb and carbaryl when they were reacted with the oxidant, potassium

Protocols

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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