AMINOCARB

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C11H16N2O2
Molecular Weight	208.2569
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of AMINOCARB

Structure Search

SMILES

CNC(=O)OC1=CC=C(N(C)C)C(C)=C1

InChI

InChIKey=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)

HIDE SMILES / InChI

Molecular Formula	C11H16N2O2
Molecular Weight	208.2569
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

PubMed

Title	Date	PubMed
Application of chemometrics methods for the simultaneous kinetic spectrophotometric determination of aminocarb and carbaryl in vegetable and water samples.	2009-09-15	19349118
Immunomodulatory effect of various anti-parasitics: a review.	2006-03	16332285
[Lipoxygenase-mediated N-demethylation of pesticides in vitro].	2002-12	14694585
Photolysis of pesticides: influence of epicuticular waxes from Persica laevis DC on the photodegradation in the solid phase of aminocarb, methiocarb and fenthion.	2001-06	11407028
Comparison of the activity of topically applied pesticides and the herbicide 2,4-D in two short-term in vivo assays of genotoxicity in the mouse.	1990-11	2086312

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:56:16 GMT 2025` Edited by `admin` on `Mon Mar 31 18:56:16 GMT 2025`
Record UNII	767M03K32Y
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

AMINOCARB [HSDB]

Preferred Name

English

AMINOCARB

Common Name

English

4-(DIMETHYLAMINO)-3-METHYLPHENYL N-METHYLCARBAMATE

Systematic Name

English

AMINOCARB [ISO]

Common Name

English

AMINOCARB [MI]

Common Name

English

4-DIMETHYLAMINO-M-TOLYL METHYLCARBAMATE

Systematic Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

44401

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

Code System Code Type Description

WIKIPEDIA

AMINOCARB

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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MESH

C006511

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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CAS

2032-59-9

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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ALANWOOD

aminocarb

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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CHEBI

2653

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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EPA CompTox

DTXSID7022172

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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MERCK INDEX

m1698

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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Merck Index

FDA UNII

767M03K32Y

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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HSDB

561

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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ECHA (EC/EINECS)

217-990-7

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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NCI_THESAURUS

C163585

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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PUBCHEM

16247

Created by admin on Mon Mar 31 18:56:16 GMT 2025 , Edited by admin on Mon Mar 31 18:56:16 GMT 2025

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