Sodium gentisate
- CAS NO.：4955-90-2
- Empirical Formula: C7H7NaO4
- Molecular Weight: 178.12
- MDL number: MFCD00016504
- EINECS: 225-598-2
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-04-24 14:58:44
What is Sodium gentisate?
Chemical properties
Off-White Solid
The Uses of Sodium gentisate
Sodium gentisate is an reactant involved in oxidative coupling reactions followed by the product use as an antioxidant and tyrosinase inhibitor1.
The Uses of Sodium gentisate
Analgesic; anti-inflammatory.
What are the applications of Application
Gentisic acid sodium salt is an analgesic antiinflammatory compound
Definition
ChEBI: Gentisic acid sodium is a hydroxybenzoic acid. It is functionally related to a salicylic acid.
Properties of Sodium gentisate
| Melting point: | >2200C (dec) |
| storage temp. | Inert atmosphere,Room Temperature |
| Water Solubility | Soluble in water |
| form | powder to crystal |
| color | White to Orange to Green |
| Merck | 14,4398 |
| CAS DataBase Reference | 4955-90-2(CAS DataBase Reference) |
| EPA Substance Registry System | Benzoic acid, 2,5-dihydroxy-, monosodium salt (4955-90-2) |
Safety information for Sodium gentisate
Computed Descriptors for Sodium gentisate
| InChIKey | MOIJZWWOFOQFMH-UHFFFAOYSA-M |
New Products
3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID Pentadecanoic acid Hendecanoic acid 2-AMINO-3-METHYLQUINOLINE HYDROCHLORIDE 3-Hydroxypropionitrile DL-3-Amino-3-(2-methoxyphenyl)propionic acid 5-Bromo-2-Fluoropyridine 2,3-Diamino-5-Chloropyridine 2-Amino-3-Hydroxypyridine 2,6-Diamino Pyridine 4-Amino-2-Chloropyridine 2-Hydroxy-4-Picoline 4-(4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 4-Bromo-3-(ethoxymethyl)benzoic acid 2,4-Dichloro-5-methoxyaniline 4,6-Dichloro-2-(propylthio)pyrimidin-5-amine N2-Isobutyryl-2'-O-methylguanosine 2-chloro-5-methylpyridin-4-amine 4-Bromobenzaldehyde 2-Chloro-6-nitro benzothiazole 2-Amino-4-phenyl-thiazole 4-Chloro-2-methyl quinoline 2-(Chloromethyl) quinazolin-4(3H)-one 5-Phenyl-[1,3,4]-thiadiazol-2-amineRelated products of tetrahydrofuran
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