ChemicalBook Product Catalog Organic Chemistry Ethers and derivatives Ethers, ether-alcohols, ether phenol derivatives 2-Methoxy-4-nitroaniline

2-Methoxy-4-nitroaniline

2-Methoxy-4-nitroaniline Basic information
Product Name:2-Methoxy-4-nitroaniline
Synonyms:redbasecibav;redbaseirgav;Brilliant Red Developing Base 4B;-Amino-5-nitrophenyl methyl ether;RED R BASE;4-Nitro-o-anisidine (NH2=1);Benzenamine, 2-methoxy-4-nitro-;4-NITRO-2-ANISIDINE ( 2-METHOXY-4-NITRO ANILINE )
CAS:97-52-9
MF:C7H8N2O3
MW:168.15
EINECS:202-588-6
Product Categories:Intermediates of Dyes and Pigments;Dyes and Pigments;Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Nitro Compounds
Mol File:97-52-9.mol
2-Methoxy-4-nitroaniline Structure
2-Methoxy-4-nitroaniline Chemical Properties
Melting point 140-142 °C(lit.)
Boiling point 337.07°C (rough estimate)
density 1,211 g/cm3
refractive index 1.6010 (estimate)
storage temp. Store below +30°C.
solubility 0.2g/l
pka1.02±0.10(Predicted)
form Crystalline Powder
color Yellow to orange
PH6.2 (0.2g/l, H2O, 20℃)
Water Solubility slightly soluble
BRN 879619
InChIKeyGVBHRNIWBGTNQA-UHFFFAOYSA-N
CAS DataBase Reference97-52-9(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenamine, 2-methoxy-4-nitro-(97-52-9)
EPA Substance Registry System2-Methoxy-4-nitroaniline (97-52-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-20/21/22
Safety Statements 26-37/39-36/37
RIDADR UN 3077 9 / PGIII
WGK Germany 2
RTECS BZ7170000
Hazard Note Irritant
TSCA Yes
HS Code 29222900
MSDS Information
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2-Methoxy-4-nitroaniline English
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ALFA English
2-Methoxy-4-nitroaniline Usage And Synthesis
Chemical Propertiesyellow to orange crystalline powder
Uses2-Methoxy-4-nitroaniline is used as a photometric reagent for the determination of ethinylestradiol (ETE), a semi-synthetic estrogen that is widely used in oral contraceptives.
General Description2-Methoxy-4-nitroaniline is an important inducer of CYP1A2 owing to its small molecular size.
Flammability and ExplosibilityNonflammable
Biochem/physiol ActionsThe metabolism of 2-methoxy-4-nitroaniline (MNA) occurs via the hydroxylation of the phenyl ring to form 6-hydroxy MNA in Harlan Sprague Dawley rats and B6C3F(1)/N mice.
Nitroaniline TIMTEC-BB SBB006349 2,5-Dimethoxy-4-nitroaniline 2-Chloro-N-(2-methoxy-4-nitro-phenyl)-acetamide N-(2-METHOXY-4-NITROPHENYL)ACETAMIDE 5-METHYL-4-NITRO-O-ANISIDINE 2-Methyl-4-methoxybenzenamine N-(2-METHOXY-4-NITRO-PHENYL)-METHANESULFONAMIDE N-(3-chloro-4-fluorophenyl)-4-methoxy-2-nitroaniline 4-METHOXY-2-NITROANILINE DIAZOTATE anisidine Methoxy 4-nitro-o-phenetidine 4-METHOXY-2-NITROANILINE,2-nitro-p-anisidine 4-methoxy-2-nitroaniline 4-(2,5-dibutoxy-4-nitrophenyl)morpholine 2-METHOXY-5-NITROANILINE,2-AMINO-4-NITROANISOLE(2-METHOXY-5-NITROANILINE),2-Methoxy-5-nitroaniline, 98+% 4-(2,5-Diethoxy-4-nitrophenyl)morpholine 2-METHOXY-4-NITROBENZENEDIAZONIUM TETRAFLUOROBORATE
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