3,5-Dinitrobenzoic acid structure
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Common Name | 3,5-Dinitrobenzoic acid | ||
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CAS Number | 99-34-3 | Molecular Weight | 212.117 | |
Density | 1.7±0.1 g/cm3 | Boiling Point | 395.5±32.0 °C at 760 mmHg | |
Molecular Formula | C7H4N2O6 | Melting Point | 204-206 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 179.2±13.6 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 3,5-Dinitrobenzoic acid |
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Synonym | More Synonyms |
Density | 1.7±0.1 g/cm3 |
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Boiling Point | 395.5±32.0 °C at 760 mmHg |
Melting Point | 204-206 °C(lit.) |
Molecular Formula | C7H4N2O6 |
Molecular Weight | 212.117 |
Flash Point | 179.2±13.6 °C |
Exact Mass | 212.006943 |
PSA | 128.94000 |
LogP | 1.69 |
Vapour Pressure | 0.0±1.0 mmHg at 25°C |
Index of Refraction | 1.658 |
Stability | Stable. Contact with strong bases may lead to fire. Incompatible with strong bases, strong oxidizing agents. |
Water Solubility | 1350 mg/L (25 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335-H413 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | F:Flammable;Xn:Harmful; |
Risk Phrases | R11;R22;R36/37/38;R68 |
Safety Phrases | S26-S36/37/39-S16 |
RIDADR | UN1325 |
WGK Germany | 3 |
RTECS | DG9140700 |
Packaging Group | III |
Hazard Class | 4.1 |
HS Code | 2916399090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2916399090 |
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Summary | 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
A method for rapid screening of ketone biotransformations: detection of whole cell Baeyer-Villiger monooxygenase activity.
Enzyme Microb. Technol. 50(2) , 101-6, (2012) A method for screening of ketone biotransformations was developed and applied to the identification of Baeyer-Villiger monooxygenase (BVMO) activity. The method was based on the formation of a purple ... |
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Electronic, infrared, and 1HNMR spectral studies of the novel charge-transfer complexes of o-tolidine and p-toluidine with alternation pi-acceptors (3,5-dinitro benzoic acid and 2,6-dichloroquinone-4-chloroimide) in CHCl3 solvent.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 64(3) , 778-88, (2006) The rapid interaction between o-tolidine and p-toluidine (pi-donors) with the pi-acceptors, e.g., 3,5-dinitrobenzoic acid (DNB) and 2,6-dichloroquinone-4-chloroimide (DCQ) results in the formation of ... |
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Method development in quantitative NMR towards metrologically traceable organic certified reference materials used as (31)P qNMR standards.
Anal. Bioanal. Chem 407 , 3115-3123, (2015) Quantitative nuclear magnetic resonance (qNMR) spectroscopy is employed by an increasing number of analytical and industrial laboratories for the assignment of content and quantitative determination o... |
Benzoic acid, 3,5-dinitro- |
3,5-Dinitro Benzoic Acid |
Dinitrobenzoic acid |
WNR CVQ ENW |
Benzoic acid,3,5-dinitro |
3,5-di-NO2PhCOOH |
DNBA |
3-Carboxy-1,5-dinitrobenzene |
EINECS 202-751-1 |
3,5-Dinitro-benzoic acid |
MFCD00007253 |