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Merck
CN

45322

Supelco

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
CAS Number:
2032-59-9
分子量:
208.26
Beilstein:
2808681
EC 号:
217-990-7
MDL编号:
MFCD00055440
UNSPSC代码:
41116107
PubChem化学物质编号:
329756645
NACRES:
NA.24

主要文件

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等级

analytical standard

质量水平

100

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

包装形式

neat

SMILES字符串

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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相关类别

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

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

象形图

Skull and crossbonesEnvironment
GHS06,GHS09

警示用语：

Danger

危险声明

H300 - H311 - H410

危险分类

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

储存分类代码

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCH7437
BCBW1360

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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%
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
R N Schop et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 15(4), 666-675 (1990-11-01)
Genotoxicity of eight topically applied compounds was determined using the bone marrow micronucleus (MN) test and hair follicle nuclear aberration (NA) assay in CD1 mice. Twenty-four hours after a single treatment, cyclophosphamide (CY), applied at doses corresponding to 1/4, 1/8
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
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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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