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4-Amino-2-methylbenzoic acid

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4-Amino-2-methylbenzoic acid Basic information
Product Name:4-Amino-2-methylbenzoic acid
Synonyms:4-amino-2-methylbenozoic acid;4-azanyl-2-methyl-benzoic acid;4-AMino-2-Methylbenzoic acid, 95+%;2-METHYL-4-AMINO-BENZOIC ACID;4-AMINO-2-METHYLBENZOIC ACID;Benzoic acid, 4-amino-2-methyl- (9CI);4-Amino-o-toluic;4-Amino-2-methybenzoic acid
CAS:2486-75-1
MF:C8H9NO2
MW:151.16
EINECS:200-297-9
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Aromatic Amino AcidsCarbonyl Compounds;C8;Carboxylic Acids;Peptide Synthesis;Unnatural Amino Acid Derivatives;CARBOXYLICACID;Amino Acids and Derivatives
Mol File:2486-75-1.mol
4-Amino-2-methylbenzoic acid Structure
4-Amino-2-methylbenzoic acid Chemical Properties
Melting point 160-165 °C
Boiling point 339.5±30.0 °C(Predicted)
density 1.254±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
pka4.86±0.25(Predicted)
form Solid
color Light orange to Yellow to Green
Major Applicationpeptide synthesis
InChIInChI=1S/C8H9NO2/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4H,9H2,1H3,(H,10,11)
InChIKeyXRSQZFJLEPBPOZ-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC=C(N)C=C1C
CAS DataBase Reference2486-75-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 26
WGK Germany 3
HS Code 29224999
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
4-Amino-2-methylbenzoic acid Usage And Synthesis
Chemical PropertiesWhite powder
Usespeptide synthesis
reaction suitabilityreaction type: solution phase peptide synthesis
Synthesis
2-Methyl-4-nitrobenzoic acid

1975-51-5

4-Amino-2-methylbenzoic acid

2486-75-1

GENERAL STEPS: Prior to each experiment, the tubular reaction apparatus was equilibrated by pumping solvent for 30 min at 16 bar hydrogen pressure (see Fig. 4). An Omnifit reaction cartridge (20.0 mm outer diameter, 15.0 mm inner diameter) containing 1 g Pd/C catalyst was used. To prevent overpressurization of the system in case of blockage, the upper pressure of the Knauer pump was set to 25 bar. with the injection ring disconnected from the flow line, the injection ring was opened and manually injected with 3.6 mL of a 0.076 M ethanol solution of 2-methyl-4-nitrobenzoic acid (excess feedstock solution in the ring was recovered for reuse). The injection ring was then closed and plugged into the flow stream. Collect the product at the outlet of the system downstream of the backpressure regulator for 120 min. The solvent is removed by reduced pressure distillation (first using a rotary evaporator and then a secondary rotary vane pump) to give 4-amino-2-methylbenzoic acid.

References[1] Tetrahedron, 2018, vol. 74, # 47, p. 6795 - 6803
[2] Chemische Berichte, 1884, vol. 17, p. 161
[3] Patent: US2012/46467, 2012, A1. Location in patent: Page/Page column 26
4-Amino-2-methylbenzoic acid Preparation Products And Raw materials
Raw materials2-Methyl-4-nitrobenzoic acid-->Hydrogen-->Ethanol-->Activated carbon-->Palladium
Preparation Products2-Methyl-4-(2-methylbenzamido)benzoic acid
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