CAS 99-55-8
:2-Methyl-5-nitroaniline
Description:
2-Methyl-5-nitroaniline, with the CAS number 99-55-8, is an organic compound belonging to the class of anilines, which are aromatic amines. It features a methyl group and a nitro group attached to a benzene ring, specifically at the 2 and 5 positions, respectively. This compound typically appears as a yellow to orange crystalline solid and is known for its moderate solubility in water, with better solubility in organic solvents such as ethanol and acetone. 2-Methyl-5-nitroaniline is primarily used in the synthesis of dyes, pigments, and pharmaceuticals. It exhibits properties such as being a potential skin irritant and having toxic effects if ingested or inhaled, necessitating careful handling. The compound can undergo various chemical reactions, including nitration and reduction, making it versatile in organic synthesis. Additionally, it is important to consider its environmental impact and regulatory status, as nitroanilines can be hazardous to aquatic life and may require proper disposal methods.
Formula:C7H8N2O2
InChI:InChI=1S/C7H8N2O2/c1-5-2-3-6(9(10)11)4-7(5)8/h2-4H,8H2,1H3
InChI key:InChIKey=DSBIJCMXAIKKKI-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC(N)=C(C)C=C1
Synonyms:- (2-Methyl-5-nitrophenyl)amine
- 1-Amino-2-Methyl-5-Nitrobenzene
- 1-Methyl-2-amino-4-nitrobenzene
- 2-Amino-4-nitrotoluene
- 2-Amino-4-nitrotoluene~5-Nitro-o-toluidine
- 2-Methyl-5-Nitro Aniline
- 2-Methyl-5-Nitrobenzenamine
- 3-Nitro-6-methylaniline
- 4-Nitro-2-Aminotoluene
- 5-Nitro-2-methylaniline
- 5-Nitro-2-toluidine
- 5-Nitro-o-toluidine
- 5-Nitro-ortho-toluidine
- 6-Methyl-3-nitroaniline
- Amarthol Fast Scarlet G Base
- Amarthol Fast Scarlet G Salt
- Azoene Fast Scarlet G Salt
- Azoene Fast Scarlet Gc Base
- Azoene Fast Scarlet Gc Salt
- Azofix Scarlet G Salt
- Azogene Fast Scarlet G
- Benzenamine, 2-methyl-5-nitro-
- Conazoic Diazo AB
- Dainichi Fast Scarlet G Base
- Daito Scarlet Base G
- Devol Scarlet B
- Devol Scarlet G Salt
- Diabase Scarlet G
- Diazo Fast Scarlet G
- Dycosbase Scarlet G Base
- Fast Red G Base
- Fast Red Sg Base
- Fast Scarlet Base G
- Fast Scarlet Base J
- Fast Scarlet G
- Fast Scarlet G Base
- Fast Scarlet G Salt
- Fast Scarlet Gc Base
- Fast Scarlet J Salt
- Fast Scarlet M 4NT Base
- Fast Scarlet T Base
- Hiltonil Fast Scarlet G Base
- Hiltonil Fast Scarlet G Salt
- Hiltonil Fast Scarlet Gc Base
- Icho Salt Scarlet G
- Kayaku Scarlet G Base
- Lake Scarlet G Base
- Lithosol Orange R Base
- Mitsui Scarlet G Base
- NSC 8947
- Naphthanil Scarlet G Base
- Naphtoelan Fast Scarlet G Base
- Naphtoelan Fast Scarlet G Salt
- Pnot
- Scarlet Base Ciba Ii
- Scarlet Base G
- Scarlet Base Irga Ii
- Scarlet Base Nsp
- Scarlet G
- Scarlet G Base
- Sugai Fast Scarlet G Base
- Symulon Scarlet G Base
- fast scarlet mN4t base
- o-Toluidine, 5-nitro-
- C.I.Azoic Diazo Component 12
- C.I. 37105
- C.I. Azoic Diazo Component 12
- 5-NITRO-ortho-TOLUIDINE (2-METHYL-5-NITROANILINE)
- C.I. Azoic Diazo Component No. 12
- CI 37105
- 4-METHYL-M-NITROANILINE
- 2-amino-4-nitrotoluene[qr]
- 2-methyl-5-nitro-benzenamin
- 2-METHYL-5-NITROANILINE
- 2-Methyl-5-nitro-benzeneamine
- P-NITRO-P-TOLUIDINE
- TIMTEC-BB SBB007597
- 2-methyl-5-nitroaniline[qr]
- See more synonyms
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2-Methyl-5-nitroaniline, 98+%
CAS:It is applied in organic synthesis. 5-Nitro-o-toluidine finds application as an intermediate in the synthesis of Pigment Red 17 (C.I. 12 390) and Pigment Red 22 (C.I. 12 315). It is also employed in conjunction with certain C.I. coupling components. It also serves as a precursor for a wide assortmen
Formula:C7H8N2O2Purity:98+%Color and Shape:Yellow to pale brown, PowderMolecular weight:152.15Ref: IN-DA003HNL
25g20.00€5kg162.00€100g30.00€250g47.00€500g50.00€50kgTo inquire100kgTo inquire250kgTo inquireGB/T 17592-2011 Azo Dyes Mixture 128 1000 µg/mL in Acetonitrile
CAS:Controlled Product- 101-14-4
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- 139-65-1
- 60-09-3
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- 87-62-7
- 90-04-0
- 91-59-8
- 91-94-1
- 92-67-1
- 92-87-5
- 95-53-4
- 95-68-1
- 95-69-2
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Color and Shape:ColourlessEPA Method 8270 App. IX Calibration Mixture 602 1000 µg/mL in Dichloromethane
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- 924-16-3
- 930-55-2
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- 95-53-4
- 95-94-3
- 98-86-2
- 99-35-4
- 99-55-8
- 99-65-0
Color and Shape:Mixture2-Amino-4-nitrotoluene 10 µg/mL in Acetonitrile
CAS:Formula:C7H8N2O2Color and Shape:Single SolutionMolecular weight:152.152-Methyl-5-nitroaniline
CAS:Formula:C7H8N2O2Purity:>98.0%(GC)(T)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:152.152-Amino-4-nitrotoluene
CAS:Controlled ProductFormula:C7H8N2O2Color and Shape:NeatMolecular weight:152.15GB 31604.52-2021 Primary Aromatic Amine Mixtures 36 1000 µg/mL in Acetonitrile
CAS:Controlled Product- 101-14-4
- 101-77-9
- 101-80-4
- 106-47-8
- 106-50-3
- 108-45-2
- 119-90-4
- 119-93-7
- 120-71-8
- 1208-52-2
- 137-17-7
- 139-65-1
- 60-09-3
- 615-05-4
- 62-53-3
- 6582-52-1
- 838-88-0
- 87-62-7
- 90-04-0
- 91-59-8
- 91-94-1
- 92-67-1
- 92-87-5
- 95-53-4
- 95-68-1
- 95-69-2
- 95-80-7
- 97-56-3
- 99-55-8
Color and Shape:Mixture2-Methyl-5-nitroaniline
CAS:Controlled ProductApplications 2-Methyl-5-nitroaniline is used as a reagent in the synthesis of imatinib base derivatives which show antibacterial and antifungal activity. Also used as a reagent in the synthesis of pyrimidinylaminobenzene derivatives which exhibit antiproliferative activity against melanoma. Dyes and metabolites, Environmental Testing. It is a COVID19-related research product.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Patoliya, M.J., et al.: J. Chem., no vol., no pp. (2013); Kim, H.J., et al.: B. Korean Chem. Soc., 34, 2311 (2013)Formula:C7H8N2O2Color and Shape:YellowMolecular weight:152.152-Methyl-5-nitroaniline
CAS:2-Methyl-5-nitroaniline (2MNA) is a chemical that has been found to be toxic to humans. It is used in wastewater treatment and as a reagent for the production of dyes, rubber products, pesticides, and plastics. 2MNA is oxidized by cytochrome P450 enzymes to create reactive intermediates that react with DNA bases or nucleic acids. 2MNA has also been shown to cause cancer in animals and humans at high doses. It is unclear whether this effect is due to the 2MNA itself or the reactive intermediate formed during metabolism. 2MNA binds to proteins on the surface of cells which may interfere with their function, including enzyme activities and signal transduction pathways. The carcinogenic potential of 2MNA may be due to its ability to form covalent bonds with cellular components such as fatty acids and proteins.Formula:C7H8N2O2Purity:Min. 98%Color and Shape:Slightly Yellow Orange PowderMolecular weight:152.15 g/mol2-Methyl-5-nitroaniline
CAS:Formula:C7H8N2O2Purity:95.0%Color and Shape:Solid, No data available.Molecular weight:152.153
