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Merck
CN

121258

3,5-Dinitrobenzoic acid

99%

Synonym(s):

DNBA

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About This Item

Linear Formula:
(O2N)2C6H3CO2H
CAS Number:
99-34-3
Molecular Weight:
212.12
NACRES:
NA.22
PubChem Substance ID:
24847456
eCl@ss:
39032062
UNSPSC Code:
12352100
EC Number:
202-751-1
MDL number:
MFCD00007253
Beilstein/REAXYS Number:
1914286

Key Documents

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Product Name

3,5-Dinitrobenzoic acid, 99%

InChI key

VYWYYJYRVSBHJQ-UHFFFAOYSA-N

InChI

1S/C7H4N2O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H,(H,10,11)

SMILES string

OC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O

assay

99%

form

solid

mp

204-206 °C (lit.)

solubility

ethanol: soluble 0.5 g/10 mL, clear, yellow to very deep greenish-yellow

functional group

carboxylic acid
nitro

Quality Level

200

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Application

3,5-Dinitrobenzoic acid was used in the derivatization of resins and determination of ampicillin.

General description

3,5-Dinitrobenzoic acid forms an adduct with 3,5-dimethylpyridine and the crystal structure of adduct has been studied at room temperature and 80K for both undeuterated and deuterated compounds. It forms 1:1 cocrystal with analgesic drug, ethenzamide and exists in two polymorphic forms.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7586V
WXBF7587V
WXBF4948V
WXBF4947V
WXBF4946V

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A J Bourque et al.
Analytical chemistry, 65(21), 2983-2989 (1993-11-01)
The effect of cross-linking, surface area, and porous nature of modified polystyrene-divinylbenzene (STY-DVB) reagents has been investigated. The supports were prepared via two techniques and modified to contain various chemical functionalities. These reagents were used in an on-line reactor for
The quasi-symmetric OHN and ODN bridges in the adducts of 3, 5-dimethylpyridine with 3, 5-dinitrobenzoic acid.
Jerzykiewicz LB, et al.
Journal of Molecular Structure, 440(1), 175-185 (1998)
Analytical Letters, 26, 2397-2397 (1993)
Polymorphs and solvates of a cocrystal involving an analgesic drug, ethenzamide, and 3, 5-dinitrobenzoic acid.
Aitipamula S, et al.
Crystal Growth & Design, 10(5), 2229-2238 (2010)
J Hall et al.
The Journal of biological chemistry, 262(23), 11046-11051 (1987-08-15)
In order to define the interaction domain on Rhodospirillum rubrum cytochrome c2 for the photosynthetic reaction center, positively charged lysine amino groups on cytochrome c2 were modified to form negatively charged carboxydinitrophenyl lysines. The reaction mixture was separated into six
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