Ordering
Available Variants5 g
CHA.45198-5g
Price
€58.40
Available – Dispatch in 14 days
25 g
CHA.45198-25g
Price
€122.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.45198-5g | €58.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.45198-25g | €122.40 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | H2NC6H3(OH)CO2H |
|---|---|
| CAS Number | 2374-03-0 |
| Molecular Weight | 153.14 |
| NACRES | NA.22 |
| PubChem Substance ID | 24860651 |
| eCl@ss | 32160406 |
| UNSPSC Code | 12352106 |
| MDL number | MFCD00017094 |
| Beilstein/REAXYS Number | 509859 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
4-Amino-3-hydroxybenzoic acid, with the CAS registry number 2374-03-0, is a chemical compound that belongs to the class of aromatic carboxylic acids. It is characterized by the presence of an amino group and a hydroxyl group attached to a benzene ring, which also bears a carboxyl group. This compound exhibits unique chemical and physical properties due to the combination of these functional groups. The amino group contributes to its basicity, while the hydroxyl group imparts acidity, and the carboxyl group is responsible for its carboxylic acid properties. As a result, 4-amino-3-hydroxybenzoic acid can participate in various chemical reactions, including condensation and substitution reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, dyes, and other specialty chemicals. Its chemical structure and properties make it an important compound in various industrial and research applications.
