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5-Sulfoanthranilsure
2-AMINO-5-SULFOBENZOIC ACID · 5-Sulfoanthranilic a · 5-SULFOANTHRANILIC ACID · 5-sulphoanthranilic acid · 2-Carboxy-4-sulfoaniline · 4-sulfo-2-carboxyaniline · 5-Sulfoo-aminobenzoicacid · 2-amino-5-sulfo-benzoicaci

Identifikatoren & physikalische Daten
| CAS No. | 3577-63-7 |
|---|---|
| Summenformel | C7H7NO5S |
| Durchschnittliche Molmasse | 217,2 g/mol |
| Monoisotopische Masse | 217,0044935 g/mol |
| SMILES | Nc1ccc(S(=O)(=O)O)cc1C(=O)O |
| InChIKey | MJNYPLCGWXFYPD-UHFFFAOYSA-N |
| PubChem CID | 19151 |
| EC No. | 222-697-2 |
| DTXSID | DTXSID2026070 |
| Lokaler Name | 5-Sulfoanthranilsure |
Chemische & physikalische Eigenschaften
| XLogP | -0,3 |
|---|---|
| Polarare Oberfläche (TPSA) | 126 |
| H-Brücken-Donoren | 3 |
| H-Brücken-Akzeptoren | 6 |
| Frei drehbare Bindungen | 2 |
| Schwere Atome | 14 |
| Formalladung | 0 |
| Komplexität | 319 |
| Löslichkeit | 10 to 50 mg/mL at 68.9 °F (NTP, 1992) |
| Physical Description | 5-sulfoanthranilic acid is an off-pink powder. (NTP, 1992) |
| Schmelzpunkt | 317 °C |
| Dichte | 1.709±0.06 g/cm3(Predicted) |
| Lagerbedingungen | 2-8°C |
| Aggregatzustand | powder to crystal |
| pKa (Säurekonstante) | -1.59±0.50(Predicted) |
| Farbe | White to Light yellow to Light orange |
| InChI | InChI=1S/C7H7NO5S/c8-6-2-1-4(14(11,12)13)3-5(6)7(9)10/h1-3H,8H2,(H,9,10)(H,11,12,13) |
| InChIKey | MJNYPLCGWXFYPD-UHFFFAOYSA-N |
| SMILES | C(O)(=O)C1=CC(S(O)(=O)=O)=CC=C1N |
| CAS Datenbank | 3577-63-7(CAS DataBase Reference) |
| EPA chemische Informationen | 5-Sulfoanthranilic acid (3577-63-7) |
Sicherheit & Vorschriften
| GHS-Einstufung | This chemical does not meet GHS hazard criteria for 40% (2 of 5) of reports.WarningH302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P264, P264+P265, P270, P272, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 5 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
|---|---|
| Regulatorische Informationen | REACH registered substance: 5-sulphoanthranilic acid (EC: 222-697-2) |
| Brandgefahren | Flash point data for this material are not available, but it is probably combustible. (NTP, 1992) |
| Reaktive Gruppe | Acids, Carboxylic |
| Reactivity Profile | 5-SULFOANTHRANILIC ACID is an amino acid. |
| Air and Water Reactions | Soluble in hot water [Hawley]. Unstable to prolonged exposure to air (NTP, 1992). |
| Hazard Classes and Categories | Acute Tox. 4 (20%) |
| Brandbekämpfung | Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992) |
| Erste Hilfe | EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. |
| Freisetung ohne Brand | SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. |
Anwendungen & Verwendung
Beschreibung
5-Sulfoanthranilic acid is produced from anthranilic acid by sulfonation with chlorosulfuric acid in anhydrous sulfuric acid or nitrobenzene or by baking the sulfate of anthranilic acid at 200 ℃. This compound is used, like its N-alkyl derivatives, as a stabilizer for diazo compounds.