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线性分子式:
O2NC6H4CO2H
化学文摘社编号:
分子量:
167.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39032047
UNSPSC Code:
12352100
EC Number:
204-508-5
MDL number:
Beilstein/REAXYS Number:
908644
产品名称
3-硝基苯甲酸, ReagentPlus®, 99%
InChI key
AFPHTEQTJZKQAQ-UHFFFAOYSA-N
InChI
1S/C7H5NO4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H,(H,9,10)
SMILES string
OC(=O)c1cccc(c1)[N+]([O-])=O
product line
ReagentPlus®
assay
99%
form
solid
mp
139-141 °C (lit.)
solubility
water: soluble 3 g/L at 25 °C
functional group
carboxylic acid
nitro
Quality Level
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Application
3-硝基苯甲酸被用于研究臭氧作为额外分解或整理剂在降解邻-、间-和对-硝基苯甲酸中的作用。
General description
3-硝基苯甲酸能够与具有重要商业价值的除草剂和杀虫剂( 氨基三唑)形成分子加合物。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
373.3 °F - Pensky-Martens closed cup
flash_point_c
189.6 °C - Pensky-Martens closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
W Jiang et al.
The Analyst, 122(3), 211-215 (1997-03-01)
In an attempt to produce complete oxidation of a biological matrix, bovine liver, ozone was investigated as an additional, potentially non-contaminating, oxidizing reagent after nitric acid digestion. Experiments were carried out to determine the decomposition efficiency of residual carbon species
Molecular co-crystals of carboxylic acids. 16. 1: 1 Adduct of 3-nitrobenzoic acid with 3-amino-1H-1, 2, 4-triazole.
Lynch DE, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 50(8), 1291-1294 (1994)
Zhiqiang Hu et al.
Water research, 39(4), 710-720 (2005-02-15)
The physical and biochemical characteristics of the biomass in three lab-scale sequencing batch reactors (SBR) treating a synthetic wastewater at a 20-day target solids retention time (SRT) were investigated. The synthetic wastewater feed contained biogenic compounds and 22 organic priming
Miguel A Providenti et al.
Applied and environmental microbiology, 72(4), 2651-2660 (2006-04-07)
In Comamonas sp. strain JS46, 3-nitrobenzoate (3Nba) is initially oxidized at the 3,4 position by a dioxygenase, which results in release of nitrite and production of protocatechuate. The locus coding for the 3Nba dioxygenase (designated mnb, for m-nitrobenzoate) was mobilized
Reproductive toxicology. m-Nitrobenzoic acid.
Environmental health perspectives, 105 Suppl 1, 325-326 (1997-02-01)
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