Sulfanilamid

Sulfanilamide Struktur
63-74-1
CAS-Nr.
63-74-1
Bezeichnung:
Sulfanilamid
Englisch Name:
Sulfanilamide
Synonyma:
SN;Sulfonamide;4-AMINOBENZENESULFONAMIDE;PRONTOSIL;SULPHANILAMIDE;Sulphonamide;AVC;STREPTOCIDE;Sulfanilamid;Sulfonylamide
CBNumber:
CB6212562
Summenformel:
C6H8N2O2S
Molgewicht:
172.2
MOL-Datei:
63-74-1.mol

Sulfanilamid Eigenschaften

Schmelzpunkt:
164-166 °C(lit.)
Siedepunkt:
400.5±47.0 °C(Predicted)
Dichte
1.08
Dampfdruck
0.00001 hPa (70 °C)
Brechungsindex
1.6490 (estimate)
storage temp. 
2-8°C
Löslichkeit
5.37g/l
pka
pKa 10.65(H2O t = 25.0±0.5 I = 0.2) (Uncertain)
Aggregatzustand
powder
Farbe
white to faintly beige
PH
5.8-6.1 (5g/l, H2O, 20℃)
Geruch (Odor)
Odorless
Säure-Base-Indikators(pH-Indikatoren)
5.8 - 6.1 (0.5% aq.sol.)
Wasserlöslichkeit
7.5 g/L at 25 ºC
maximale Wellenlänge (λmax)
257nm(H2O)(lit.)
Merck 
14,8925
BRN 
511852
InChIKey
FDDDEECHVMSUSB-UHFFFAOYSA-N
LogP
-0.620
CAS Datenbank
63-74-1(CAS DataBase Reference)
NIST chemische Informationen
Benzenesulfonamide, 4-amino-(63-74-1)
EPA chemische Informationen
Sulfanilamide (63-74-1)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 40
S-Sätze: 24/25-36-22
WGK Germany  3
RTECS-Nr. WO8400000
10
TSCA  Yes
HazardClass  8
HS Code  29350090
Giftige Stoffe Daten 63-74-1(Hazardous Substances Data)
Toxizität LD50 orally in mice: 3.8 g/kg (Marshall)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H303 May be harmfulif swallowed Acute toxicity,oral Category 5 P312
H314 Verursacht schwere Verätzungen der Haut und schwere Augenschäden. Ätzwirkung auf die Haut Kategorie 1B Achtung GHS hazard pictogramssrc="/GHS05.jpg" width="20" height="20" /> P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P301+P330+P331 BEI VERSCHLUCKEN: Mund ausspülen. KEIN Erbrechen herbeiführen.
P303+P361+P353 BEI BERÜHRUNG MIT DER HAUT (oder dem Haar): Alle kontaminierten Kleidungsstücke sofort ausziehen. Haut mit Wasser abwaschen oder duschen.
P304+P340 BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P405 Unter Verschluss aufbewahren.

Sulfanilamid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R40:Verdacht auf krebserzeugende Wirkung.

S-Sätze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S22:Staub nicht einatmen.

Beschreibung

Sulfanilamide is an organic sulfur compound structurally similar to p-aminobenzoic acid (PABA) with antibacterial property. Sulfanilamide competes with PABA for the bacterial enzyme dihydropteroate synthase, thereby preventing the incorporation of PABA into dihydrofolic acid, the immediate precursor of folic acid. This leads to an inhibition of bacterial folic acid synthesis and de novo synthesis of purines and pyrimidines, ultimately resulting in cell growth arrest and cell death.

Chemische Eigenschaften

White granules or powder crystals, odorless. Taste slightly bitter. Slightly soluble in cold water, ethanol, methanol, ether and acetone, easily soluble in boiling water, glycerin, hydrochloric acid, potassium hydroxide and sodium hydroxide solution, insoluble in chloroform, ether, benzene and petroleum ether.

Verwenden

Sulfanilamide is an antibacterial agent and antimicrobial agent of sulfonamide type (topical and vaginal).

Definition

ChEBI: Sulfanilamide is a sulfonamide in which the sulfamoyl functional group is attached to aniline at the 4-position. It has a role as an EC 4.2.1.1 (carbonic anhydrase) inhibitor, an antibacterial agent and a drug allergen. It is a substituted aniline, a sulfonamide antibiotic and a sulfonamide.

synthetische

Sulfonamide is synthesized from acetanilide by chlorosulfonation, amination, hydrolysis, and neutralization:
Acetanilide is reacted with chlorosulfonic acid at 40~50℃, then cooled, slowly added to water for acid decomposition, precipitated at the same time, dried and filtered to obtain p-acetamidobenzenesulfonyl chloride, and then subjected to ammoniation, and the amination temperature is controlled at 40~ 45 ℃, and then hydrolyzed, acidified to obtain sulfonamide.

Weltgesundheitsorganisation (WHO)

Sulfanilamide, a sulfonamide anti-infective agent, was introduced in 1936 for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing resistance and their replacement by antibiotics which are generally more active and less toxic. The sulfonamides are known to cause serious adverse effects such as renal toxicity, sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Sulfanilamide is still used in some countries as a pessaries or as vaginal cream.

Allgemeine Beschreibung

White powder. pH of 0.5% aqueous solution: 5.8-6.1.

Air & Water Reaktionen

May be unstable if exposed for long periods air and light . Slightly water soluble.

Reaktivität anzeigen

Sulfanilamide is an amino acid. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May react with azo and diazo compounds to generate toxic gases.

Brandgefahr

Flash point data for Sulfanilamide are not available but Sulfanilamide is probably combustible.

Sicherheitsprofil

Poison by intraperitoneal route. Moderately toxic by ingestion, subcutaneous, and intravenous routes. Human teratogenic effects by unspecified route: developmental abnormalities of the blood and lymphatic systems (including the spleen and bone marrow). Experimental reproductive effects. Questionable carcinogen with experimental carcinogenic data. Mutation data reported. Implicated in aplastic anemia. When heated to decomposition it emits very toxic fumes of NOx and SOx.

Sulfanilamid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Sulfanilamid Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 632)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739
info@dycnchem.com CHINA 52867 58
LEAP CHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 24738 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
sales@tnjchem.com China 34572 58
Anhui Zhongda Biotechnology Co., Ltd
+8615689548120
linda@zhongda-biotech.com China 204 58
Shandong Huisheng Import & Export Co., Ltd.
+86-13176845580 +86-13176845580
da@zhongda-biotech.com China 248 58
Anhui Zhongda Biotechnology Co., Ltd
+8619956560829
justine@zhongda-biotech.com China 300 58
Anhui Ruihan Technology Co., Ltd
+8617756083858
daisy@anhuiruihan.com China 994 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+86-13474506593 +86-13474506593
sarah@tnjone.com China 794 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21695 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714
fandachem@gmail.com China 9352 55

63-74-1(Sulfanilamid)Verwandte Suche:


  • p-amino-benzenesulfonamid
  • p-Aminobenzensulfonamide
  • p-Aminophenylsulfonamide
  • Prontalbin
  • Prontosil i
  • Prontosil white
  • prontosilalbum
  • prontosili
  • prontosilwhite
  • Prontylin
  • Pronzin album
  • pronzinalbum
  • Proseptal
  • Proseptine
  • Proseptol
  • p-Sulfamidoaniline
  • p-Sulfamoylaniline
  • Pysococcine
  • Rubiazol A
  • SULFANILAMIDE (BEST QUALITY)
  • sulfanilic amide
  • Sulfanilamide crystalline
  • 4-Aminobenzene sulphonamide
  • SULFANILAMIDE STANDARD SOLUTION
  • SULFANILAMIDE VETRANAL, 250 MG
  • SULFANILAMIDE, 99+%
  • SulfanilamideBp(Vet)
  • SulphanilamideGr
  • Sulfanilamide,Pharma
  • SulphanilamideExtraPure
  • Benzenesulfonamide, 4-amino- (9CI)
  • Sulfanilamide,98%
  • Sulfanilamide,97+%
  • Sulfanilamide (technical)
  • anilin-4-sufonic acid amide
  • sulfanilamide solution
  • 4-AMINOBENZENESULFONAMIDE(SULFANILAMIDE)
  • PARA-AMINOBENZENESULPHONAMIDE
  • SULPHONILAMIDE
  • Sulfanilamide [for Diazotization Titration]
  • SULFANILAMINE PURE
  • Sulphanyl acid amide
  • Sulfanilamide melting point standard
  • CHGC
  • EM66
  • SgII
  • ANTI-CHROMOGRANIN-C (CENTER) antibody produced in rabbit
  • SCG2
  • Secretogranin II
  • Secretogranin-2
  • IndustrialSulfanilamide
  • Sulfanilamide Melting Point Standard (1 g) (Approximately 165 degrees)
  • Sulfanilamide solution,100ppm
  • Sulfanilamide puriss. p.a., >=99% (calc. to the dried substance)
  • Sulfanilamide Vetec(TM) reagent grade, 98%
  • SULFANILAMIDE, VETEC
  • 1162 F
  • 1162f
Copyright 2019 © ChemicalBook. All rights reserved