Other grades of this product :
| 2,3-Dihydroxybenzoic acid Basic information |
| 2,3-Dihydroxybenzoic acid Chemical Properties |
| Melting point | 204-206 °C (lit.) | | Boiling point | 95-96/0.5mm | | density | 1,542 g/cm3 | | refractive index | 1.6400 (estimate) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | methanol: soluble50mg/mL, clear to faintly hazy, orange | | form | Crystalline Powder | | pka | pK1:2.98;pK2:10.14 (30°C) | | color | Beige to brown or pinkish-gray | | Water Solubility | Soluble in water, methanol and dimethyl sulfoxide. | | BRN | 2209117 | | InChIKey | GLDQAMYCGOIJDV-UHFFFAOYSA-N | | CAS DataBase Reference | 303-38-8(CAS DataBase Reference) | | NIST Chemistry Reference | Benzoic acid, 2,3-dihydroxy-(303-38-8) | | EPA Substance Registry System | 2,3-Dihydroxybenzoic acid (303-38-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 2 | | RTECS | DG8576490 | | Hazard Note | Irritant | | HS Code | 29182900 |
| 2,3-Dihydroxybenzoic acid Usage And Synthesis |
| Chemical Properties | Pale Brownish to Red Brownish Crystalline Powder | | Uses | 2,3-Dihydroxybenzoic Acid is a selected phenol as MMP (Matrix Metalloproteinase) inhibitor. | | Uses | 2,3-Dihydroxybenzoic acid was used to study the complexes of manganese with aliphatic and aromatic polyhydroxy ligands in basic media by electrochemical, spectrophotometric and magnetic methods. It was used in isolation of new siderophore named vulnibactin from low iron cultures of Vibrio vulnificus, a human pathogen. It was used as cocrystal former to study the influence of position isomerism on the co-crystals formation and physicochemical properties of piracetam. | | Definition | ChEBI: A dihydroxybenzoic acid that is benzoic acid substituted by hydroxy groups at positions 2 and 3. It occurs naturally in Phyllanthus acidus and in the aquatic fern Salvinia molesta. | | Biochem/physiol Actions | 2,3-Dihydroxybenzoic acid was found to be orally effective iron-chelating drug in hypertransfused rat model. It is monocatechol siderophore produced by Brucella abortus. |
| 2,3-Dihydroxybenzoic acid Preparation Products And Raw materials |
|
日本语
한국어
Français
Deutsch
España
Türkiye