| Identification | More | [Name]
Dinitolmide | [CAS]
148-01-6 | [Synonyms]
2-METHYL-3,5-DINITROBENZAMIDE
3,5-DINITROBENZAMIDE
3,5-DINITRO-O-TOLUAMIDE
3,5-DINITRO TOLUAMIDE
AMIDE 3,5-DINITRO-O-TOLUIC ACID
bornylformiat
DINITOLMIDE
LABOTEST-BB LT00159528
NITROMID
NITROMIDE
ZOALENE
2-methyl-3,5-dinitro-benzamid
3,5-dinitro-o-toluamid
coccidinea
coccidot
d.o.t.
dinitolmid
zoamix
3,5-dinitro-toluamide(DOT) BPV93
Robenidine HCl, Vetranal | [EINECS(EC#)]
204-499-8 | [Molecular Formula]
C11H18O2 | [MDL Number]
MFCD00007985 | [Molecular Weight]
182.26 | [MOL File]
148-01-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Yellowish solid. Very slightly
soluble in water; soluble in acetone, acetonitrile,
dioxane, and dimethylformamide. | [Melting point ]
170-180 °C (lit.) | [Boiling point ]
366.66°C (rough estimate) | [density ]
1.5406 (rough estimate) | [refractive index ]
1.7400 (estimate) | [Fp ]
2 °C | [storage temp. ]
0-6°C | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
13.74±0.50(Predicted) | [color ]
Pale Beige to Light Beige | [Merck ]
13,3297 | [InChI]
InChI=1S/C8H7N3O5/c1-4-6(8(9)12)2-5(10(13)14)3-7(4)11(15)16/h2-3H,1H3,(H2,9,12) | [InChIKey]
ZEFNOZRLAWVAQF-UHFFFAOYSA-N | [SMILES]
C(N)(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1C | [CAS DataBase Reference]
148-01-6(CAS DataBase Reference) | [EPA Substance Registry System]
148-01-6(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,F | [Risk Statements ]
R22:Harmful if swallowed.
R36:Irritating to the eyes.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R11:Highly Flammable. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S16:Keep away from sources of ignition-No smoking . | [OEB]
B | [OEL]
TWA: 5 mg/m3 | [RIDADR ]
UN 1648 3/PG 2 | [WGK Germany ]
3
| [RTECS ]
XS4200000
| [HS Code ]
29242990 | [Safety Profile]
Poison by intravenous
route. Moderately toxic by ingestion.
Mutation data reported. A strong
exothermic reaction above 248OC has caused
industrial explosions. When heated to
decomposition it emits toxic fumes of NOx.
See also NITRO COMPOUNDS of
AROMATIC HYDROCARBONS.
| [Hazardous Substances Data]
148-01-6(Hazardous Substances Data) |
| Hazard Information | Back Directory | [General Description]
Yellowish, crystalline solid. Mp: 177°C. Very slightly soluble in water. Soluble in acetone, acetonitrile, and dimethylformamide. Used as an anti-parasite drug for poultry. Store in a cool, ventilated place, away from acute fire hazards and easily oxidized materials. | [Reactivity Profile]
DINITOLMIDE reacts as an oxidizing agent. Has been known on at least one occasion to explode destructively. Incompatible with easily oxidized materials. Emits toxic NOx fumes if heated to decomposition. | [Description]
Dinitolmide is a yellowish crystalline substance. Molecular weight= 225.18; Freezing/Meltingpoint = 177.2℃. Very slightly soluble in water. | [Chemical Properties]
Yellowish solid. Very slightly
soluble in water; soluble in acetone, acetonitrile,
dioxane, and dimethylformamide. | [Uses]
A fodder additive for poultry used to prevent coccidiosis infections. Antiprotozoan drug. | [Uses]
antiprotozoal | [Definition]
ChEBI: Dinitolmide is a dinitrotoluene. | [Hazard]
Liver damage | [Synthesis]
The ammoniation process of step C of the present invention is as follows: 400 L of concentrated ammonia (for ammoniation) and 15 kg of ammonium bicarbonate are added to the reactor, and the pre-prepared acyl chloride solution is slowly added to the reactor under stirring. During the reaction, the reaction temperature was controlled below 40℃ by cooling the brine. After the dropwise addition, the reaction was continued with stirring for 1 to 2 hours. Upon completion of the reaction, a filtration operation was carried out, and the filter cake was washed thoroughly with cold water and subsequently dried to obtain 102.6 kg of 3,5-dinitro-o-methylbenzamide, with a yield of 85.9% (in terms of nitro compounds) and a product purity of 98.5%. In step C of the present invention, an ammonia recovery process was designed to reuse ammonia. | [Potential Exposure]
AgriculturalChemical; Mutagen. Those involved in the manufacture,formulation, and application of this veterinary coccidiostat,an antiparasite medicine used in poultry. | [First aid]
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Note to physician: Treat for methemoglobinemia.Spectrophotometry may be required for precise determination of levels of methemoglobinemia in urine | [storage]
Store at -20°C | [Incompatibilities]
A weak oxidizing agent, but hightemperatures and pressures may cause violent reactions.Heat can cause a violent exothermic reaction above248℃. Contact with alkalies may form explosive metalsalts. | [References]
[1] Patent: CN105906523, 2016, A. Location in patent: Paragraph 0037; 0041
[2] Journal of the Society of Chemical Industry, London, 1940, vol. 59, p. 92,94
[3] Journal of the Society of Chemical Industry, London, 1940, vol. 59, p. 92,94 |
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