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72915

Sigma-Aldrich

Sodium 3-nitrobenzoate

≥95.0% (HPLC)

Synonym(s):

3-Nitrobenzoic acid sodium salt

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About This Item

Linear Formula:
3-O2NC6H4CO2Na
CAS Number:
827-95-2
Molecular Weight:
189.10
Beilstein/REAXYS Number:
4166479
EC Number:
212-578-3
MDL number:
MFCD00051097
UNSPSC Code:
12352100
PubChem Substance ID:
57652348
NACRES:
NA.22

assay

≥95.0% (HPLC)

form

solid

SMILES string

[Na+].[O-]C(=O)c1cccc(c1)[N+]([O-])=O

InChI

1S/C7H5NO4.Na/c9-7(10)5-2-1-3-6(4-5)8(11)12;/h1-4H,(H,9,10);/q;+1/p-1

InChI key

MUADFEZFSKAZLT-UHFFFAOYSA-M

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Application

Sodium 3-nitrobenzoate may be used in the synthesis of [Ni(cyclam)(3-nitrobenzoate)2] complex. [Cyclam = 1,4,8,11-tetraazacyclotetradecane][1]

pictograms

FlameExclamation mark
GHS02,GHS07

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Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
STBH6055
STBH6056
STBH6057
STBH6058
STBH6059

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Novel nickel cyclam complexes with potent antimicrobial and cytotoxic properties.
Al-Bari MAA
Journal of Applied Sciences Research, 3(11), 1251-1261 (2007)
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
L J Nadeau et al.
Applied and environmental microbiology, 61(2), 840-843 (1995-02-01)
Pseudomonas sp. strain JS51 grows on m-nitrobenzoate (m-NBA) with stoichiometric release of nitrite. m-NBA-grown cells oxidized m-NBA and protocatechuate but not 3-hydroxybenzoate, 4-hydroxy-3-nitrobenzoate, 4-nitrocatechol, and 1,2,4-benzenetriol. Protocatechuate accumulated transiently when succinate-grown cells were transferred to media containing m-NBA. Respirometric experiments
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
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
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