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Merck
CN

45322

灭害威

PESTANAL®, analytical standard

别名:

(4-二甲基氨基-3-甲基苯基) N-甲基酸酯

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关于此项目

经验公式（希尔记法）:
C11H16N2O2
化学文摘社编号:
2032-59-9
分子量:
208.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756645
EC Number:
217-990-7
Beilstein/REAXYS Number:
2808681
MDL number:
MFCD00055440

主要文件

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InChI key

IMIDOCRTMDIQIJ-UHFFFAOYSA-N

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)

SMILES string

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

grade

analytical standard

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

Quality Level

100

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相关类别

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
GHS06,GHS09

signalword

Danger

Hazard Classifications

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

存储类别

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

wgk

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

法规信息

危险化学品
农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCH7437
BCBW1360

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Synthesis, relative insect toxicity, and anticholinesterase activity of aminocarb transformation products.
W D Marshall et al.
Archives of environmental contamination and toxicology, 15(4), 385-392 (1986-07-01)
R P Moody et al.
Journal of toxicology and environmental health, 20(1-2), 209-218 (1987-01-01)
The dermal penetration of 14C-ring-labeled fenitrothion and aminocarb was determined in rats and rhesus monkeys. In monkeys, 49 +/- 4% (t1/2 = 14 h) of the fenitrothion and 74 +/- 4% (t1/2 = 25 h) of aminocarb were absorbed from
S Y Szeto et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 20(5), 559-575 (1985-10-01)
In-vitro inhibitions of brain AChE in brook trout, Salvelinus fontinalis (Mitchill), by aminocarb (4-dimethylamino-m-tolyl N-methylcarbamate) and its toxic metabolites, MAA (4-methylamino-m-tolyl N-methylcarbamate), AA(4-amino-m-tolyl N-methylcarbamate), MFA (4-methylformamido-m-tolyl N-methylcarbamate) and FA (4-formamido-m-tolyl N-methylcarbamate) were investigated. The molar concentrations of inhibitors causing 50%
G M Richardson et al.
Ecotoxicology and environmental safety, 12(2), 180-186 (1986-10-01)
Young brown bullhead (Ictalurus nebulosus) were exposed to aminocarb (4-dimethylamino-3-methylphenyl N-methylcarbamate) at lethal and sublethal concentrations and the tissue distribution of total unspecified residues was examined. The concentration of residues in each tissue increased with the concentration of exposure. The
Acute toxicity of aminocarb in male rats and inhibition of tissue esterases.
I Vassilieff et al.
Bulletin of environmental contamination and toxicology, 31(3), 326-330 (1983-09-01)
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实验方案

US EPA Method 632: HPLC Analysis of Pesticides on Ascentis® C18

-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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