185329
3-硝基苯甲酸
ReagentPlus®, 99%
别名:
间硝基苯甲酸
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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
Assay:
99%
Form:
solid
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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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。
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。
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
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)
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
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
Zhiqiang Hu et al.
Water research, 39(15), 3501-3510 (2005-07-30)
Biodegradation rates of benzoate and related aromatic compounds, 3-nitrobenzoate, 4-chlorobenzoate, 4-chlorophenol, and 2,4-dichlorophenol by unexposed (unacclimated) and long-term exposed (acclimated) biomass were quantified using a modified fed-batch technique. The acclimated biomass was taken after approximately 1-year of operation from three
C R Bloom et al.
Biochemistry, 37(31), 10937-10944 (1998-08-07)
The positive and negative cooperativity and apparent half-site reactivity of the Co(II)-substituted insulin hexamer are well-described by a three-state allosteric model involving ligand-mediated interconversions between the three states: T3T3' right harpoon over left harpoon T3o R3o right harpoon over left
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