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Merck
CN

124478

N-Isopropylaniline

97%

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About This Item

Linear Formula:
C6H5NHCH(CH3)2
CAS Number:
Molecular Weight:
135.21
EC Number:
212-196-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2205871
MDL number:
Assay:
97%
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refractive index

n20/D 1.539 (lit.)

bp

55 °C/0.3 mmHg (lit.)

density

0.934 g/mL at 25 °C (lit.)

InChI key

FRCFWPVMFJMNDP-UHFFFAOYSA-N

InChI

1S/C9H13N/c1-8(2)10-9-6-4-3-5-7-9/h3-8,10H,1-2H3

SMILES string

CC(C)Nc1ccccc1

assay

97%

General description

N-Isopropylaniline is an intermediate in propachlor degradation.

Application

N-Isopropylaniline has been used to study the mechanism of metabolism of propachlor by Pseudomonas sp.strain PEM1.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

wgk

WGK 3

flash_point_f

189.9 °F - Cleveland open cup

flash_point_c

87.7 °C - Cleveland open cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Propachlor and N-isopropylaniline residues in onions (Allium cepa) and muck soils.
B S Clegg et al.
Bulletin of environmental contamination and toxicology, 47(1), 104-111 (1991-07-01)
Sebastian R Sørensen et al.
Pest management science, 59(10), 1118-1124 (2003-10-17)
Mineralisation of the phenylurea herbicide isoproturon (3-(4-isopropylphenyl)-1,1-dimethylurea) and two of its known metabolites, 3-(4-isopropylphenyl)-1-methylurea (monodesmethyl-isoproturon) and 4-isopropylaniline, was studied in Danish agricultural soils with or without previous exposure to isoproturon. A potential for rapid mineralisation of isoproturon and the two
M Martin et al.
Applied and environmental microbiology, 65(2), 802-806 (1999-01-30)
Propachlor (2-chloro-N-isopropylacetanilide) is an acetamide herbicide used in preemergence. In this study, we isolated and characterized a soil bacterium, Acinetobacter strain BEM2, that was able to utilize this herbicide as the sole and limiting carbon source. Identification of the intermediates

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