N27314
3-Nitrotoluene
99%
Sinónimos:
1-Methyl-3-nitrobenzene
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Fórmula lineal:
CH3C6H4NO2
Número CAS:
Peso molecular:
137.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-728-6
Beilstein/REAXYS Number:
1906910
MDL number:
Assay:
99%
Form:
liquid
Servicio técnico
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Permítanos ayudarlevapor density
4.73 (vs air)
Quality Level
vapor pressure
1 mmHg ( 50.2 °C)
assay
99%
form
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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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT RE 2
Clase de almacenamiento
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
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
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 K Dunnick et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 22(3), 411-421 (1994-04-01)
Nitrotoluenes are high-production-volume chemicals used in the synthesis of agricultural chemicals and in various dyes. Because of differences in the metabolism of the three isomers and their capabilities to bind to DNA, comparative toxicity studies of o-, m-, and p-nitrotoluene