Natriumazid Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
GERUCHLOSE FARBLOSE HEXAGONALE KRISTALLE.
CHEMISCHE GEFAHREN
Kann beim Erhitzen explodieren (oberhalb des Schmelzpunkts, besonders bei schnellem Erhitzen). Feuer- und Explosionsgefahr. Schwache Base in wässriger Lösung. Reagiert mit Kupfer, Blei, Silber, Quecksilber und Kohlenstoffdisulfid unter Bildung besonders schlagempfindlicher Verbindungen. Reagiert mit Säuren unter Bildung von giftigem und explosionsfähigen Wasserstoffazid.
ARBEITSPLATZGRENZWERTE
TLV: (als STEL, ceiling) als Stickstoffwasserstoffsäure-Dampf: 0,11 ppm; als Natriumazid: 0,29 mg/m? Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); (ACGIH 2005).
MAK: 0,2 mg/m?(Einatembarer Aerosolanteil); Spitzenbegrenzung: überschreitungsfaktor I(2); Schwangerschaft: Gruppe D (DFG 2006). EG Arbeitsplatz-Richtgrenzwerte: 0.1 mg/m?(als TWA), 0.3 mg/m?(als STEL); Hautresorption (EU 2000).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation, über die Haut und durch Verschlucken.
INHALATIONSGEFAHREN
Verdampfung bei 20°C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch schnell erreicht werden.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen, die Haut und die Atemwege. Exposition leicht oberhalb der Arbeitsplatzgrenzwerte kann zu Auswirkungen auf das Nervensystem führen.
LECKAGE
Gefahrenbereich verlassen! Fachmann zu Rate ziehen! Verschüttetes Material in Kunststoffbehältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. Persönliche Schutzausrüstung: Vollschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.
R-Sätze Betriebsanweisung:
R28:Sehr giftig beim Verschlucken.
R32:Entwickelt bei Berührung mit Säure sehr giftige Gase.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R52/53:Schädlich für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R22:Gesundheitsschädlich beim Verschlucken.
S-Sätze Betriebsanweisung:
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
Aussehen Eigenschaften
N3Na. Farblose Kristalle.
Gefahren für Mensch und Umwelt
Mit Säuren Bildung von explosiver und sehr giftiger Stickstoffwasserstoffsäure. Reagiert explosiv mit Brom, Chromylchlorid und Schwefelkohlenstoff. Kann explosiv reagieren mit Blei, Dimethylsulfat und Kupfer. Stark exotherme Reaktion mit Kaliumnitrat und Schwefelsäure.
Schleimhautreizungen nach Verschlucken im Mund, Rachen, Speiseröhre und Magen-Darmtrakt. Gefahr der Hautresorption. Systemische Wirkung: Herz-Kreislaufstörungen, ZNS-Störungen, Durchfall, Müdigkeit. Toxische Wirkung auf Nieren. Mengen von 5-10 mg können den Sehnerv lähmen, tiefe Ohnmacht usw. hervorrufen (Wirkung beruht auf der Blockade des Cytochromoxydase-Systems).
Wassergefährdend (WGK 2).
Schutzmaßnahmen und Verhaltensregeln
Im Abzug arbeiten.
Gummihandschuhe (nur als kurzfristiger Staubschutz).
Verhalten im Gefahrfall
Verschüttete Substanz vorsichtig trocken aufnehmen. Mit Wasser nachreinigen.
Löschpulver, Sand.
Keine wasserhaltigen Löschmittel verwenden.
Erste Hilfe
Nach Hautkontakt: Mit viel Wasser abwaschen, abtupfen mit Polyethylenglycol 400.
Nach Augenkontakt: Mit viel Wasser bei geöffnetem Lidspalt mindestens 15 Minuten spülen. Augenarzt!
Nach Verschlucken: Es besteht akute Lebengefahr. Viel Wasser mit Aktivkohle-Zusatz trinken, Erbrechen vervorrufen. Sofort Arzt hinzuziehen!
Nach Kleidungskontakt: Kontaminierte Kleidung sofort ausziehen.
Ersthelfer: siehe gesonderten Anschlag
Sachgerechte Entsorgung
Feststoffabfall als Sondermüll entsorgen. Nicht in Säure-/Lauge-Behälter geben.
Chemische Eigenschaften
Sodium azide is a colorless to white, odorless, crystalline solid. Combustible solid above 300°C.
Physikalische Eigenschaften
Colorless hexagonal crystals; density 1.846 g/cm
3 at 20°C; decomposes on heating to produce sodium and nitrogen; also decomposes in vacuum; soluble in water partially converting to hydrazoic acid, solubility in water, 41.7 g/100mL; slightly soluble in alcohol, 0.316g/100mL at 16°C; soluble in liquid ammonia.
Verwenden
Sodium azide is used in making othermetal azides, therapeutically to control bloodpressure, as a propellant for automotivesafety bags, as a preservative for laboratoryreagents, as an analytical reagent, andin organic synthesis. It is also used as anantifading reagent for immunofluorescence(Boeck et al. 1985).
Definition
sodium azide: A white or colourlesscrystalline solid, NaN
3, soluble inwater and slightly soluble in alcohol;hexagonal; r.d. 1.846; decomposes onheating. It is made by the action ofnitrogen(I) oxide on hot sodamide(NaNH
2) and is used as an organicreagent and in the manufacture ofdetonators.
synthetische
Sodium azide is prepared by reacting sodium amide with nitrous oxide. The amide is heated with nitrous oxide at 200°C or its solution in liquid ammonia is treated with nitrous oxide at ambient temperature: 2NaNH
2 + N
2O → NaN
3 + NaOH + NH
3.
Vorbereitung Methode
Sodium azide can be prepared from sodium metal and liquid
ammonia in the presence of ferric chloride. The amide
formed is treated with nitrous oxide to produce the azide.
Reaktivität anzeigen
Sodium azide is unstable. Decomposes rapidly or explosively at about 300°C [Hawley]. May explode if shocked. Forms violently explosive products if exposed to carbon disulfide. Can be sensitized toward decomposition by metal salts (especially heavy metal salts such as silver chloride) or by traces of strong acids [Sax, 9th ed., 1996, p. 298].
Hazard
Sodium azide is a toxic as well as an explosive substance (Patnaik, P. 1999. A Comprehensive Guide to the Hazardous Properties of Chemical Substances, 2
np ed. New York: John Wiley & Sons). Although inert to shock, violent decomposition can occur when heated at 275°C. Contact of solid or solution with lead and copper must be avoided. Reactions with halogens, carbon disulfide, or chromyl chloride can be explosive. Dissolution in water produces toxic vapors of hydrazoic acid. The salt is an acute poison causing headache, hypotension, hypothermia, and convulsion. LD
50 oral (rats): 27 mg/kg.
Health Hazard
The acute toxicity of sodium azide is high. Symptoms of exposure include lowered blood pressure, headache, hypothermia, and in the case of serious overexposure, convulsions and death. Ingestion of 100 to 200 mg in humans may result in headache, respiratory distress, and diarrhea. Target organs are primarily the central nervous system and brain. Sodium azide rapidly hydrolyzes in water to form hydrazoic acid, a highly toxic gas that can escape from solution, presenting a serious inhalation hazard. Symptoms of acute exposure to hydrazoic acid include eye irritation, headache, dramatic decrease in blood pressure, weakness, pulmonary edema, and collapse. Solutions of sodium azide can be absorbed through the skin. Sodium azide has not been found to be carcinogenic in humans. Chronic, low-level exposure may cause nose irritation, episodes of falling blood pressure, dizziness, and bronchitis.
Brandgefahr
When heated to decomposition, Sodium azide emits very toxic fumes of nitrogen oxides; explosive. Forms explosive-sensitive materials with some metals such as lead, silver, mercury or copper. May form toxic hydrazoic acid fumes in fire. Containers may explode in fire. Avoid acids, benzoyl chloride and potassium hydroxide; bromine; carbon disulfide; copper; lead; nitric acid; barium carbonate; sulfuric acid; chromium (II) hypochlorite, dimethyl sulfate, water, dibromomalononitrile, lead, silver, copper, mercury. Hazardous polymerization may not occur.
Flammability and Explosibility
Flammability hazard is low, but violent decomposition can occur when heated to
275 °C. Decomposition products include oxides of nitrogen and sodium oxide.
Sicherheitsprofil
Poison by ingestion, skin contact, intraperitoneal, intravenous, and subcutaneous routes. Human systemic effects by ingestion: general anesthesia, somnolence, and hdney changes. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. Violent reaction with benzoyl chloride combined with KOH, Br2, barium carbonate, CS2, Cr(OCl)2, Cu, Pb, HNO3, BaCO3, H2SO4, hot water, (CH3)2SO4, dibromomalononitrile, sulfuric acid. Incompatible with acids, ammonium chloride + trichloroacetonitrile, phosgene, cyanuric chloride ,2,5 -dinitro3 methylbenzoic acid + oleum, trifluroroacryloyl chloride. Reacts with heavy metals (e.g., brass, copper, lead) to form dangerously explosive heavy metal azides, a particular problem in laboratory equipment and drain traps. When heated to decomposition it emits very toxic fumes of NOx and Na2O. See also AZIDES.
mögliche Exposition
Sodium azide is used as preservative and diluent. It has been used for a wide variety of military, laboratory, medicine, and commercial purposes. It is used extensively as an intermediate in the production of lead azide, commonly used in detonators, and other explosives. Reported to be used in automobile air-bag inflation. One of the largest potential exposure is that to automotive workers, repairmen, and wreckers, if sodium azide is used as the inflation chemical. Commercial applications include use as a fungicide, nematocide, and soil sterilizing agent and as a preservative for seeds and wine. The lumber industry has used sodium azide to limit the growth of enzymes responsible for formation of brown stain on sugar pine, while the Japanese beer industry used it to prevent the growth of a fungus which darkens its product. The chemical industry has used sodium azide as a retarder in the manufacture of sponge rubber, to prevent coagulation of styrene and butadiene latexes stored in contact with metals; and to decompose nitrites in the presence of nitrates.
Lager
In particular,
work with sodium azide should be conducted in a fume hood to prevent exposure by
inhalation, and appropriate impermeable gloves and splash goggles should be worn
at all times to prevent skin and eye contact. Containers of sodium azide should be
stored in secondary containers in a cool, dry place separated from acids.
Versand/Shipping
UN1687 Sodium azide, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
läuterung methode
Crystallise sodium azide from hot water or from water by adding absolute EtOH or acetone. Also purify it by repeated crystallisation from an aqueous solution saturated at 90o by cooling it to 10o, and adding an equal volume of EtOH. The crystals are washed with acetone, and the azide is dried at room temperature under vacuum for several hours in an Abderhalden pistol. Its solubility in H2O is 42% at 18o, and in EtOH it is 0.22% at 0o. [Das et al. J Chem Soc, Faraday Trans 1 78 3485 1982, Schenk in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol I pp 474-475 1963, Browne Inorg Synth 1 79 1939, Frierson Inorg Synth II 139 1946.] HIGHLY POISONOUS and potentially explosive.
Inkompatibilitäten
Reacts explosively and/or forms explosive and/or shock sensitive compounds with acids and many metals. Contact with water forms hydrazoic acid. Combustible solid (if heated above 275C). May explode when heated above its melting point, especially if heating is rapid. Reacts with acids; producing toxic, shock-sensitive, and explosive hydrogen azide. It forms explosive compounds with phosgene, brass, zinc, trifluoroacrylol fluoride, and nitrogendiluted bromine vapor. Reacts with benzoyl chloride and potassium hydroxide, bromine, carbon disulfide; copper, lead, nitric acid; barium carbonate; sulfuric acid; chromium (II) hypochlorite; dimethyl sulfate; dibromomalononitrile, silver, mercury. Over a period of time, sodium azide may react with copper, lead, brass, or solder in plumbing systems to form an accumulation of the highly explosive and shock-sensitive compounds of lead azide and copper azide
Waste disposal
Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Disposal may be accomplished by reaction with sulfuric acid solution and sodium nitrate in a hard rubber vessel.Nitrogen dioxide is generated by this reaction and the gas is run through a scrubber before it is released to the atmosphere. Controlled incineration is also acceptable (after mixing with other combustible wastes) with adequate scrubbing and ash disposal facilities.
Natriumazid Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Candesartan
1-Phenyltetrazol-5-thiol
2,4,6-Triisopropylbenzene-sulfonyl azide
Zidovudine
Pentylamin
TETRAHYDROTHIOPHENE SULFOXIMINE
5-AMINOMETHYL-PYRROLIDIN-2-ONE
PYRIDINE-2,4-DIAMINE
2,6-DICHLORO-4-ISOCYANATOPYRIDINE
ZENIPLATIN
2-ISOCYANATO-1-METHYL-1H-PYRROLE
Gabapentin
Azidotrimethylsilan
3-ISOCYANATO-1,5-DIMETHYL-1H-PYRAZOLE
Methyl-1H-indol-2-carboxylat
1-[2-(Dimethylamino)ethyl]-1,2-dihydro-5H-tetrazol-5-thion
Irbesartan
METHYL 6-(TRIFLUOROMETHYL)-1H-INDOLE-2-CARBOXYLATE
2,5-Dihydro-5-thioxo-1H-tetrazol-1-methansulfonsure
1,5-DIMETHYL-1 H-PYRAZOL-3-YLAMINE
Azosemid
PEMIROLAST
1-METHYL-1H-IMIDAZOL-5-YL ISOCYANATE
1,5-Diazobicyclo[4.3.0]non-5-en
2-THIOPHENAMINE
Rotenon
S-(1-BUTYL)-S-(5-BUTYLNONAN-5-YL) SULFOXIMINE
Methoxymethylisocyanat
4-FLUORO-2,1,3-BENZOXADIAZOLE
α,α,α-Trifluor-p-tolylisocyanat
Losartan
1,2-Dihydro-1-methyl-5H-tetrazol-5-thion
2-ISOCYANATO-4,6-DIMETHOXYPYRIMIDINE
1,4-OXATHIANE SULFOXIMINE
Benzenesulfonylazide
diazepam-polyhydroxybutyrate microspheres
cis-1,2-Diaminocyclohexane
5-METHOXYQUINOLIN-6-AMINE
S-METHYL-S-(2-METHYLPYRAZINYL) SULFOXIMINE
Azimsulfuron
