3-(Carboxymethyl)benzoic acid

95%

Reagent Code: #161850
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CAS Number 2084-13-1

science Other reagents with same CAS 2084-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.16 g/mol
Formula C₉H₈O₄
badge Registry Numbers
MDL Number MFCD15523567
thermostat Physical Properties
Boiling Point 412.8°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.392g/cm3
Storage Room temperature, dry seal

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its dual carboxylic acid functionality allows for selective reactions, making it valuable in constructing complex molecules. Commonly employed in the development of metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Also utilized in the synthesis of polymers and resins where controlled cross-linking is required. Its aromatic structure with carboxyl groups supports applications in designing functional materials for catalysis and sensing.

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Test Parameter Specification
Appearance White to yellow to brown solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿313.50
inventory 1g
10-20 days ฿1,730.00
inventory 10g
10-20 days ฿12,590.00
inventory 25g
10-20 days ฿29,980.00

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3-(Carboxymethyl)benzoic acid
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Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its dual carboxylic acid functionality allows for selective reactions, making it valuable in constructing complex molecules. Commonly employed in the development of metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Also utilized in the synthesis of polymers and resins where controlled cross-linking is required. Its aromatic structure with carboxyl groups supports a

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its dual carboxylic acid functionality allows for selective reactions, making it valuable in constructing complex molecules. Commonly employed in the development of metal-organic frameworks (MOFs) due to its ability to chelate metal ions. Also utilized in the synthesis of polymers and resins where controlled cross-linking is required. Its aromatic structure with carboxyl groups supports applications in designing functional materials for catalysis and sensing.

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