Basic information Application Safety Supplier Related

1-Methyl-1H-imidazole-4-carboxylic acid

Basic information Application Safety Supplier Related

1-Methyl-1H-imidazole-4-carboxylic acid Basic information

Product Name:
1-Methyl-1H-imidazole-4-carboxylic acid
Synonyms:
  • BUTTPARK 90\06-31
  • 1-Methyl-1H-4carboxylicacid
  • 1-Methyl-1H-imidazole-4-carboxylic acid, 90+%
  • 1-METHYLIMIDAZOLE-4-CARBOXYLIC ACID
  • 1-METHYL-1H-IMIDAZOLE-4-CARBOXYLIC ACID
  • 1-Methyl-1H-imidazole-4-carboxylic acid ,95%
  • 1-methyl-1H-imidzole-4-carboxylic acid
  • 1-methyl-4-imidazole-carboxylic acid
CAS:
41716-18-1
MF:
C5H6N2O2
MW:
126.11
EINECS:
636-992-2
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • blocks
  • Carboxes
  • Imidazoles
  • Carboxylic Acids
  • Imidazoles & Benzimidazoles
  • Carboxylic Acids
  • Imidazoles & Benzimidazoles
Mol File:
41716-18-1.mol
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1-Methyl-1H-imidazole-4-carboxylic acid Chemical Properties

Melting point:
245 °C
Boiling point:
399.1±15.0 °C(Predicted)
Density 
1.34±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
DMSO, Methanol
pka
1.61±0.10(Predicted)
form 
Solid
color 
Off-White to Light Brown
Sensitive 
Hygroscopic
InChI
InChI=1S/C5H6N2O2/c1-7-2-4(5(8)9)6-3-7/h2-3H,1H3,(H,8,9)
InChIKey
WZTRQGJMMHMFGH-UHFFFAOYSA-N
SMILES
C1N(C)C=C(C(O)=O)N=1
CAS DataBase Reference
41716-18-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900
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1-Methyl-1H-imidazole-4-carboxylic acid Usage And Synthesis

Application

1-Methyl-4-imidazolium carboxylic acid belongs to the imidazolium derivative class. It has certain acidity and is mainly used as an intermediate in organic synthesis and pharmaceutical chemistry. It can be used in the synthesis of bioactive molecules and biological hormones.

Chemical Properties

White to light brown solid

Definition

ChEBI: 1-methyl-imidazole-4-carboxylic acid is an imidazolyl carboxylic acid. It has a role as a metabolite.

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