2-Amino-4,5-dihydroxybenzoic Acid

≥95%

Reagent Code: #139633
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CAS Number 114874-99-6

science Other reagents with same CAS 114874-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.13 g/mol
Formula C₇H₇NO₄
badge Registry Numbers
MDL Number MFCD14583132
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of antibiotics and anti-inflammatory agents. It also serves in the preparation of dyes and pigments due to its aromatic structure and functional groups that allow for various chemical modifications. Its hydroxyl and amino groups make it suitable for use in chelating agents and antioxidants, where it can stabilize metal ions and scavenge free radicals. Additionally, it finds application in research settings for the development of novel organic compounds and in the study of reaction mechanisms involving substituted benzoic acids.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,590.00
inventory 250mg
10-20 days ฿19,160.00
inventory 1g
10-20 days ฿34,500.00

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2-Amino-4,5-dihydroxybenzoic Acid
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of antibiotics and anti-inflammatory agents. It also serves in the preparation of dyes and pigments due to its aromatic structure and functional groups that allow for various chemical modifications. Its hydroxyl and amino groups make it suitable for use in chelating agents and antioxidants, where it can stabilize metal ions and scavenge free radicals. Additionally, it finds application in resea

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of antibiotics and anti-inflammatory agents. It also serves in the preparation of dyes and pigments due to its aromatic structure and functional groups that allow for various chemical modifications. Its hydroxyl and amino groups make it suitable for use in chelating agents and antioxidants, where it can stabilize metal ions and scavenge free radicals. Additionally, it finds application in research settings for the development of novel organic compounds and in the study of reaction mechanisms involving substituted benzoic acids.

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