Sulfathiazolnatrium

Sodium sulfathiazole

HCID 12285822

Grundinformationen

CAS
144-74-1
Standard-SMILES
Nc1ccc(S(=O)(=O)[N-]c2nccs2)cc1.[Na+]
InChIKey
GWIJGCIVKLITQK-UHFFFAOYSA-N
Summenformel
C9H8N3NaO2S2
Durchschnittliche Molmasse
277,3 g/mol
Monoisotopische Masse
276,99556278

Überblick

Sulfathiazole sodium is a sulfonamide.

Namen und Bezeichner

Bevorzugter Name
Sodium sulfathiazole
IUPAC
sodium (4-aminophenyl)sulfonyl-(1,3-thiazol-2-yl)azanide
Lokaler Name
Sulfathiazolnatrium
Englischer Name
Sulfathiazole sodium
Summenformel
C9H10N3NaO2S2
Molmasse
279.31

Namen und Synonyme

Sulfathiazole sodium144-74-1Sodium sulfathiazoleDTXSID6051724PV16N742VMDTXCID2030279RefChem:186543205-638-5Sulfathiazole sodium saltMFCD00072133Sulfathiazole (sodium)sodium;(4-aminophenyl)sulfonyl-(1,3-thiazol-2-yl)azanide
Weitere Namen anzeigen
ST-NASulfathiazole(ST)Sulfathiazole Bp98sodiumnorsulfazoleSULFATHIAZOLESOUDIMsolublesulfathiazolesodiumsulphathiazole
Benzenesulfonamide, 4-amino-N-2-thiazolyl-, monosodium saltSodium ((4-aminophenyl)sulfonyl)(thiazol-2-yl)amideSodium norsulfazolesodium [(4-aminophenyl)sulfonyl](1,3-thiazol-2-yl)azanideSodium sulphathiazoleSoluble sulfathiazoleSodium 2-sulfanilamidothiazoleMonosodium 2-sulfanilamidothiazole

Datenbank-Bezeichner

CAS
144-74-1
PubChem CID
12285822
DTXSID
DTXSID6051724
ChEMBL
CHEMBL2107243
ChEBI
CHEBI:201399
UNII
PV16N742VM
EC Number
205-638-5
Nikkaji
J2.893.562E

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
111 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
3
Schwere Atome
17

Physikochemische Eigenschaften

storage temp.
-20 °C · Store at -20°C
Löslichkeit
2 O: · H2O: soluble50mg/mL
Aggregatzustand
powder
Farbe
white to off-white
Biologische Quelle
synthetic (Organic)
Wasserlöslichkeit
2 O: · H2O: soluble 50mg/mL

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 5 Einträge

This chemical does not meet GHS hazard criteria for 2.3% (1 of 43) of reports.

Warning

H315 (97.7%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 43 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Regulatory InformationStatus: Active Update: 11-12-2017 https://echa.europa.eu/registration-dossier/-/registered-dossier/21640
Other Safety InformationIMAP assessments - Benzenesulfonamide, 4-amino-N-2-thiazolyl-, monosodium salt: Human health tier I assessment
Hazard Classes and CategoriesSkin Irrit. 2 (97.7%)

Sicherheitsdaten

F
10
wgk
2
tsca
TSCA listed
RTECS-Nr.
WP2450000
risk_code
36/37/38
hazard_code
Xi

Chemie und Industrie

Pharmakologische Informationen

MeSH Pharmacological ClassificationSubstances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection.

Verwendung und Herstellung

General Manufacturing InformationBenzenesulfonamide, 4-amino-N-2-thiazolyl-, sodium salt (1:1): INACTIVE
Anwendungen · 2 Einträge

BeschreibungSulfathiazole sodium salt is a short-acting sulfa drug. It was a common oral and topical antibiotic until less toxic alternatives were discovered. It is no longer used in humans. Sulfathiazole is added to the diet of laboratory animals to inhibit folate formation by gut bacteria. This ensures that the animal′s only source of available folate is from their diet. Sulfathiazole is a sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfathiazole is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid. It is active against Gram positive bacteria, Gram negative bacteria and Chlamydia. Mode of resistance is via the alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.

VerwendenSulfathiazole sodium salt is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA). It can also be used in biological study of thermotherapy and sulfonamide antibiotics deciphered Cyanobacteria and Proteobacteria microbiome in huanglongbing-affected Citrus paradise and Citrus limon.

Anbieter100 Anbieter

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
武汉鹏垒生物科技有限公司15871464247 · [email protected]
武汉欣扬瑞和化学科技有限公司13720274133 · [email protected]
湖北金梭生物科技有限公司00123456789 · [email protected]

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