2-Amino-4-hydroxybenzoic acid

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Reagent Code: #136933
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CAS Number 38160-63-3

science Other reagents with same CAS 38160-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₇H₇NO₃
badge Registry Numbers
MDL Number MFCD00071506
thermostat Physical Properties
Boiling Point 397.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of azo dyes due to its amino and hydroxyl functional groups. It also serves in the development of certain antimicrobial agents and anti-inflammatory compounds. Its structure allows for easy modification in organic synthesis, making it valuable in creating biologically active molecules. Additionally, it finds use in research settings for developing novel heterocyclic compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,860.00
inventory 100mg
10-20 days ฿4,610.00
inventory 250mg
10-20 days ฿7,890.00
inventory 1g
10-20 days ฿10,900.00
inventory 5g
10-20 days ฿36,080.00

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2-Amino-4-hydroxybenzoic acid
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Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of azo dyes due to its amino and hydroxyl functional groups. It also serves in the development of certain antimicrobial agents and anti-inflammatory compounds. Its structure allows for easy modification in organic synthesis, making it valuable in creating biologically active molecules. Additionally, it finds use in research settings for developing novel heterocyclic compounds.

Used in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of azo dyes due to its amino and hydroxyl functional groups. It also serves in the development of certain antimicrobial agents and anti-inflammatory compounds. Its structure allows for easy modification in organic synthesis, making it valuable in creating biologically active molecules. Additionally, it finds use in research settings for developing novel heterocyclic compounds.

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