5-Nitro-2-furfurolsemicarbazon

Nitrofurazone Struktur
59-87-0
CAS-Nr.
59-87-0
Bezeichnung:
5-Nitro-2-furfurolsemicarbazon
Englisch Name:
Nitrofurazone
Synonyma:
NFS;NF;semicarbazone;NITROFURAL;FURACILIN;5-NITRO-2-FURALDEHYDE SEMICARBAZONE;Actin-N;FURACIN;Furazone;Furfurin
CBNumber:
CB0492724
Summenformel:
C6H6N4O4
Molgewicht:
198.14
MOL-Datei:
59-87-0.mol

5-Nitro-2-furfurolsemicarbazon Eigenschaften

Schmelzpunkt:
242-244 °C (lit.)
Siedepunkt:
335.43°C (rough estimate)
Dichte
1.6031 (rough estimate)
Brechungsindex
1.6500 (estimate)
Flammpunkt:
2 °C
storage temp. 
2-8°C
Löslichkeit
Very slightly soluble in water, slightly soluble in ethanol (96 per cent).
pka
pKa 9.28± 0.03( EtOH,t =35±0.1,I=0.00) (Uncertain)
Farbe
Yellow to Dark Yellow
Wasserlöslichkeit
<0.1 g/100 mL at 19 ºC
Sensitive 
Light Sensitive
Merck 
14,6600
BRN 
86403
InChIKey
IAIWVQXQOWNYOU-FPYGCLRLSA-N
CAS Datenbank
59-87-0(CAS DataBase Reference)
IARC
3 (Vol. 50) 1990
NIST chemische Informationen
5-Nitro furfural semicarbazone(59-87-0)
EPA chemische Informationen
Nitrofurazone (59-87-0)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn,F
R-Sätze: 22-36-20/21/22-11
S-Sätze: 36-36/37-26-16
RIDADR  3249
WGK Germany  3
RTECS-Nr. LT7700000
8
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29321900
Giftige Stoffe Daten 59-87-0(Hazardous Substances Data)
Toxizität LD50 in rats (g/kg): 0.59 orally; 3.0 s.c. (Godwin)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H341 Kann vermutlich genetische Defekte verursachen. Keimzellmutagenität Kategorie 2 Warnung P201,P202, P281, P308+P313, P405,P501
H351 Kann vermutlich Krebs verursachen. Karzinogenität Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
H373 Kann die Organe schädigen bei längerer oder wiederholter Exposition. Spezifische Zielorgan-Toxizität (wiederholte Exposition) Kategorie 2 Warnung P260, P314, P501
H412 Schädlich für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 3 P273, P501
Sicherheit
P202 Vor Gebrauch alle Sicherheitshinweise lesen und verstehen.
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P308+P313 BEI Exposition oder falls betroffen: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.

5-Nitro-2-furfurolsemicarbazon Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R11:Leichtentzündlich.

S-Sätze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Beschreibung

Nitrofurazone is an antibacterial agent used in animal feed. Occupational dermatitis was reported in cattle breeders and farmers.

Chemische Eigenschaften

white to light yellow crystal powde

Verwenden

Nitrofurazone is a topical anti-infective and bactericide for most pathogens commonly causing surface infections; in the adjunctive therapy of patients with second and third degree bums when bacterial resistance to other agents is areal or potential problem; in skin grafting where bacterial contamination may cause graft rejection and/or donor-site infection; antibacterial agent for the treatment or prevention of infections in a variety of conditions involving skin, eyes, ears, nose and genito-urinary tract; used on pyodermas, ulcers, and wounds; affects some protozoa and is an effective prophylaxis against nosocomial infections; antiseptic lubricant for trans urethral resection; anti-microbial in veterinary medicine.

Indications

Nitrofurazone (Furacin), a synthetic nitrofuran derivative with a broad antibacterial spectrum. Although its exact mechanism of action is unknown, it is thought to inhibit bacterial enzymes involved in carbohydrate metabolism. It is not effective against fungal or viral organisms. It is used as adjunctive therapy in patients with second- and third-degree burns when bacterial resistance to other antiinfective agents is a potential problem. It is not effective in the treatment ofminor burns or superficial bacterial infections involving wounds, cutaneous ulcers, or various pyodermas. It is rarely used by dermatologists as it carries a high risk of acquired contact sensitivity.

Definition

ChEBI: A semicarbazone resulting from the formal condensation of semicarbazide with 5-nitrofuraldehyde. A broad spectrum antibacterial drug, although with little activity against Pseudomonas species, it is used as a local application for burns, ulcer , wounds and skin infections.

Weltgesundheitsorganisation (WHO)

Nitrofural, a nitrofuran derivative with broad-spectrum antibacterial activity, was introduced in the early 1940s for the topical treatment of various skin conditions. It has also been used systemically for the treatment of African trypasonomiasis. Following recent findings of in vitro mutagenicity and of carcinogenicity in experimental animals, use of topical preparations containing this substance was restricted in Germany. Nitrofural remains registered in several countries and the World Health Organization is not aware of restrictive action having been taken elsewhere.

Allgemeine Beschreibung

Odorless pale yellow needles or yellow powder. pH (saturated aqueous solution) 6.0 - 6.5. Alkaline solutions are dark orange.

Air & Water Reaktionen

Insoluble in water.

Reaktivität anzeigen

Furacilin darkens on prolonged exposure to light. Furacilin can react violently with reducing materials. .

Brandgefahr

Flash point data for Furacilin are not available; however, Furacilin is probably combustible.

Pharmazeutische Anwendungen

A synthetic compound used in the topical treatment of wounds and burns and as an instillation for bladder washout. A nitrofurazone-impregnated urinary catheter is said to reduce infection in catheterized patients. Activity against the common bacterial pathogens is sufficient to cover most pathogens that cause infections of burns and wounds, with the important exception of Ps. aeruginosa. Attention has been drawn to its activity against methicillin-resistant Staphylococcus aureus, and its use in clearing carriage has been suggested. Slight absorption occurs from intact skin (c. 1%) and burned skin (5%). It is neither a primary irritant nor a sensitizer, but some preparations contain polyethylene glycol as a vehicle, and absorption can cause problems in patients with reduced renal function. Of limited availability.

Kontakt-Allergie

Nitrofurazone is an antibacterial agent used in animal feeds. Occupational dermatitis was reported in cattle breeders or farmers.

Clinical Use

5-Nitro-2-furaldehyde semicarbazone (Furacin) occurs asa lemon-yellow crystalline solid that is sparingly solublein water and practically insoluble in organic solvents.Nitrofurazone is chemically stable, but moderately lightsensitive.It is used topically in the treatment of burns, especiallywhen bacterial resistance to other agents may be a concern.It may also be used to prevent bacterial infection associatedwith skin grafts. Nitrofurazone has a broad spectrumof activity against Gram-positive and Gram-negative bacteria,but it is not active against fungi. It is bactericidalagainst most bacteria commonly causing surface infections,including S. aureus, Streptococcus spp., E. coli,Clostridium perfringens, Enterobacter (Aerobacter) aerogenes,and Proteus spp.; however, P. aeruginosa strainsare resistant.Nitrofurazone is marketed in solutions, ointments, andsuppositories in a usual concentration of 0.2%.

Sicherheitsprofil

Poison by ingestion and intraperitoneal routes. Moderately toxic by subcutaneous route. Questionable carcinogen with experimental carcinogenic, neoplas tigenic, tumorigenic, and teratogenic data, Experimental reproductive effects. A human sensitizer. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

5-Nitro-2-furfurolsemicarbazon Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


5-Nitro-2-furfurolsemicarbazon Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 401)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Mojin Biotechnology Co., Ltd
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sales@hbmojin.com China 12456 58
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+8617531190177
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15069388126 15069388126
sales@sjzlpharm.com China 61 58
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sales8@anhuiyiao.com China 253 58
Sigma Audley
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Shanghai Aosiris new Material Technology Co., LTD
86-15139564871 +8615139564871
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Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
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+86-21-33585366 - 03@
sales03@shyrchem.com CHINA 738 60
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+86-0551-65418679 +86-18949832763
info@tnjchem.com China 2989 55

59-87-0(5-Nitro-2-furfurolsemicarbazon)Verwandte Suche:


  • 2-Furaldehyde, 5-nitro-, semicarbazone
  • 2-Furancarboxaldehyde, 5-nitro-, semicarbazone
  • 5-Nitro-2-furaldehyde semicarbazole
  • 5-nitro-2-furaldehydsemicarbazone
  • 5-Nitro-2-furancarboxaldehyde semicarbazone
  • 5-nitro-2-furancarboxaldehydesemicarbazone
  • 5-Nitro-2-furfuraldehyde semicarbazone
  • 5-nitro-2-furfuraldehydesemicarbazone
  • 5-Nitrofuraldehyde semicarbazide
  • 5-nitrofuraldehydesemicarbazide
  • 5-Nitrofuran-2-aldehyde semicarbazone
  • Fedacin
  • Flavazone
  • Fracine
  • Furacine
  • furacin-e
  • Furacinetten
  • Furacin-Hc
  • Furacoccid
  • Furacort
  • Furacycline
  • Furaderm
  • Furagent
  • Furalcyn
  • Furaldon
  • Furalone
  • Furametral
  • Furan-Ofteno
  • Furaplast
  • Furaseptyl
  • Furaskin
  • Furatsilin
  • Furaziline
  • Furazin
  • Furazina
  • Furazol W
  • furazolw
  • Furazyme
  • Furesol
  • Furosem
  • Fuvacillin
  • Hemofuran
  • Hydrazinecarboxamide, 2-[(5-nitro-2-furanyl)methylene]-
  • Ibiofural
  • Mammex
  • Mastofuran
  • Monafuracin
  • Monafuracis
  • Monofuracin
  • NCI-C56064
  • Nefco
  • NF-7
  • Nfz mix
  • Nifucin
  • Nifurid
  • Nifuzon
  • Nitrofuraldehyde semicarbazone
  • nitrofuraldehydesemicarbazone
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