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Merck
모든 사진(1)

주요 문서

N27314

Sigma-Aldrich

3-Nitrotoluene

99%

동의어(들):

1-Methyl-3-nitrobenzene

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About This Item

Linear Formula:
CH3C6H4NO2
CAS Number:
Molecular Weight:
137.14
Beilstein:
1906910
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.73 (vs air)

Quality Level

vapor pressure

1 mmHg ( 50.2 °C)

분석

99%

형태

liquid

refractive index

n20/D 1.541 (lit.)

bp

230-231 °C (lit.)

mp

14-16 °C (lit.)

density

1.157 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(c1)[N+]([O-])=O

InChI

1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3

InChI key

QZYHIOPPLUPUJF-UHFFFAOYSA-N

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픽토그램

Health hazardExclamation markEnvironment

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class Code

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

WGK

WGK 3

Flash Point (°F)

208.4 °F

Flash Point (°C)

98 °C

개인 보호 장비

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


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문서 라이브러리 방문

이미 열람한 고객

J P Chism et al.
Drug metabolism and disposition: the biological fate of chemicals, 13(6), 651-657 (1985-11-01)
2-Nitrotoluene (2NT) induces DNA repair in the in vivo-in vitro hepatocyte unscheduled DNA synthesis assay in male, but not female, Fischer-344 rats. 3-Nitrotoluene (3NT) and 4-nitrotoluene (4NT) are inactive in both sexes. The structurally related rat hepatocarcinogen, 2,6-dinitrotoluene, which also
G Allenby et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 16(4), 710-724 (1991-05-01)
A method for culturing isolated seminiferous tubules (ST) from adult rats for 1-3 days has been developed and optimized rigorously on the basis of the secretion of immunoactive inhibin under basal conditions and after maximal stimulation with rat FSH or
Daniel Meyer et al.
Applied and environmental microbiology, 71(11), 6624-6632 (2005-11-05)
Escherichia coli JM101(pSPZ3), containing xylene monooxygenase (XMO) from Pseudomonas putida mt-2, catalyzes specific oxidations and reductions of m-nitrotoluene and derivatives thereof. In addition to reactions catalyzed by XMO, we focused on biotransformations by native enzymes of the E. coli host
J P Chism et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(5), 596-602 (1984-09-01)
The metabolism and excretion of 2-, 3-, and 4-nitrotoluene (2NT, 3NT, and 4NT, respectively) were studied in male Fischer 344 rats. Excreta were collected for 72 hr after an oral dose (200 mg/kg) of radiolabeled 2NT, 3NT, or 4NT. Radiolabel
J D deBethizy et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(1), 45-50 (1984-01-01)
2-Nitrotoluene (2NT), but not 3-nitrotoluene (3NT) or 4-nitrotoluene (4NT), is genotoxic in the in vivo-in vitro hepatic DNA repair assay. These differences in genotoxicity may be due to hepatic metabolism. For this reason, the metabolism of the nitrotoluenes was compared

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