Basic information Safety Supplier Related

Methyl 4-amino-3-hydroxybenzoate

Basic information Safety Supplier Related

Methyl 4-amino-3-hydroxybenzoate Basic information

Product Name:
Methyl 4-amino-3-hydroxybenzoate
Synonyms:
  • 3-HYDROXY-4-AMINOBENZOIC ACID ETHYL ESTER
  • 4-AMINO-3-HYDROXYBENZOIC ACID ETHYL ESTER
  • METHYL-3-HYDROXY-4-AMINOBENZOATE
  • METHYL 4-AMINO-3-HYDROXYBENZENECARBOXYLATE
  • METHYL 4-AMINO-3-HYDROXYBENZOATE
  • 4-Amino-3-hydroxybenzoic acid methyl ester
  • 2-Amino-5-(methoxycarbonyl)phenol, 2-Hydroxy-4-(methoxycarbonyl)aniline
  • Methyl 4-aMino-3-hydroxybenzenecarboxylate, 95+%
CAS:
63435-16-5
MF:
C8H9NO3
MW:
167.16
Product Categories:
  • Aromatic Esters
  • Benzoic acid
Mol File:
63435-16-5.mol
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Methyl 4-amino-3-hydroxybenzoate Chemical Properties

Melting point:
120-122°C
Boiling point:
364.5±27.0 °C(Predicted)
Density 
1.305±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
solid
pka
8.94±0.10(Predicted)
color 
Brown
BRN 
608716
InChI
InChI=1S/C8H9NO3/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4,10H,9H2,1H3
InChIKey
OCZXDVNSNDITBS-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(N)C(O)=C1
CAS DataBase Reference
63435-16-5(CAS DataBase Reference)
NIST Chemistry Reference
Methyl 4-amino-3-hydroxybenzoate(63435-16-5)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2922500090

MSDS

  • Language:English Provider:ALFA
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Methyl 4-amino-3-hydroxybenzoate Usage And Synthesis

Uses

Methyl 4-amino-3-hydroxybenzoate is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.

Synthesis

67-56-1

2374-03-0

63435-16-5

1. 4-Amino-3-hydroxybenzoic acid (5.0 g, 32.6 mmol) was slowly added dropwise to a mixture of 1.25 M HCl solution (100 mL) and methanol (100 mL) at 0 °C. 2. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature with continuous stirring overnight. 3. The reaction process was monitored by HPLC and it was found that there was still raw material left, so the mixture was continued to be stirred at room temperature for 48 hours. 4. After completion of the reaction, the solvent was removed by distillation under reduced pressure. 5. 5. The residue was treated with saturated aqueous sodium bicarbonate solution, followed by extraction of the aqueous phase with ethyl acetate (2×). 6. The organic extracts were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to dryness to afford the title compound methyl 4-amino-3-hydroxybenzoate (5.37 g, 97% yield) as a crystalline solid. 7. The molecular weight of the product was confirmed to be 168 (M+1)+ by low resolution mass spectrometry (LRMS) analysis.

References

[1] Patent: WO2013/68552, 2013, A1. Location in patent: Page/Page column 70
[2] Patent: WO2013/68554, 2013, A1. Location in patent: Page/Page column 80
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 10, p. 1257 - 1260
[4] Patent: EP1382607, 2004, A2. Location in patent: Page 43
[5] Organic and Biomolecular Chemistry, 2016, vol. 14, # 15, p. 3782 - 3786

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