Benzonitril Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
FARBLOSE FLüSSIGKEIT MIT CHARAKTERISTISCHEM GERUCH.
CHEMISCHE GEFAHREN
Zersetzung beim Erhitzen oder Verbrennen unter Bildung giftiger Rauche mit Cyanwasserstoff und Stickstoffoxiden. Reagiert sehr heftig mit starken Säuren unter Bildunghochgiftigen Cyanwasserstoffs. Greift einige Kunststoffe an.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation, über die Haut und durch Verschlucken.
INHALATIONSGEFAHREN
Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitsschädliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen, die Haut und die Atemwege. Möglich sind Auswirkungen auf die Zellatmung mit nachfolgender Zyanose. Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig.
LECKAGE
Ausgelaufene Flüssigkeit möglichst in abdichtbaren Behältern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Chemikalienschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.
R-Sätze Betriebsanweisung:
R21/22:Gesundheitsschädlich bei Berührung mit der Haut und beim Verschlucken.
S-Sätze Betriebsanweisung:
S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
Aussehen Eigenschaften
C7H5N; Benzoesäurenitril, Phenylcyanid; farblose, bittermandelartig riechende Flüssigkeit.
Gefahren für Mensch und Umwelt
Bei Verbrennung können cyanhaltige Gase entstehen.
Gesundheitsschädlich bei Berührung mit der Haut und beim Verschlucken.
Für Nitrile allgemein gilt: Höchste Vorsicht! Blausäurefreisetzung möglich - Blockade der Zellatmung, Herz-Kreislaufstörungen, Atemnot, Bewußtlosigkeit. Latenzzeit bis Wirkungseintritt.
Benzonitril ist wassergefährdend.
Schutzmaßnahmen und Verhaltensregeln
Im Abzug arbeiten.
Schutzhandschuhe (als kurzzeitiger Spritzschutz).
Verhalten im Gefahrfall
Mit flüssigkeitsbindendem Material (z.B. Rench-Rapid) aufnehmen. Ais Sondermüll entsorgen.
Kohlendioxid, Pulver
Im Brandfall können cyanhaltige Gase entstehen.
Erste Hilfe
Nach Hautkontakt: Betroffene Hautstellen gründlich mit Wasser und Seife abwaschen.
Nach Augenkontakt: Mindestens 15 Minuten unter fließendem Wasser bei geöffnetem Lidspalt spülen. Augenarzt konsultieren.
Nach Einatmen: Frischluft.
Nach Verschlucken: Viel Wasser trinken lassen; nur bei vollem Bewußtsein des Betroffenen Erbrechen auslösen. Bei Bewußtlosigkeit stabile Seitenlage. Arzt hinzuziehen.
Nach Kleidungskontakt: Kontaminierte Kleidung ausziehen.
Ersthelfer: siehe gesonderten Anschlag
Sachgerechte Entsorgung
Als Sondermüll entsorgen.
Chemische Eigenschaften
Bezonitrile is a colorless, oily liquid. It has a almond odor and a bitter taste. Slightly soluble in cold water, the solubility in water at 100°C is 1%; miscible with common organic solvents. When heated to decomposition, benzonitrile emits toxic hydrogen cyanide and oxides of nitrogen (HSDB 1988).
Occurrence
Benzonitrile is reported to be found in natural cocoa aroma), in milk products, roasted filberts and peanuts and cooked trassi . Benzonitrile also has been detected in the thermal decomposition
products of flexible polyurethane foam.
Verwenden
The most important commercial use for benzonitrile is the synthesis of benzoguanamine, which is a derivative of melamine and is used in protective coatings and molding resins. It is used intermediate for rubber chemicals; solvent for nitrile rubber, specialty lacquers, and many resins and polymers, and for many anhydrous metallic salts.
Application
Benzonitrile is a widely utilized as a solvent and an intermediate in industries making drugs, perfumes, dyes, rubber, textiles, resins and specialty lacquers. It finds application as a versatile precursor for many derivatives. It coordinates with transition metal to form complexes which act as synthetic intermediates.
synthetische
Benzonitrile can be prepared by following methods:
1) on a small scale by the dehydration in an inert solvent with phosphorus oxychloride or benzenesulfonyl chloride and an organic amine.
2) from benzoic acid by heating with lead thiocyanate.
3) by heating sodium benzenesulfonate with sodium cyanide.
4) by adding benzenediazonium chloride solution to a hot aq sodium cyanide solution containing cupric sulfate and distilling by ammoxidation of toluene.
Benzonitrile can also be produced in high yield by the vapor-phase catalytic ammoxidation of toluene.
Definition
ChEBI: Benzonitrile is a nitrile that is hydrogen cyanide in which the hydrogen has been replaced by a phenyl group. It is a member of benzenes and a nitrile.
Air & Water Reaktionen
Slightly soluble in water.
Reaktivität anzeigen
The cyano group can be readily hydrolyzed in the presence of mineral acids to produce stable, moderately toxic benzoic acid . When heated to decomposition, Benzonitrile emits highly toxic fumes of nitrogen oxides and hydrogen cyanide [Sax, 9th ed., 1996, p. 353].
Hazard
High toxicity; absorbed by skin.
Health Hazard
Benzonitrile may enter the human body by ingestion, absorption through the skin, or inhalation. The earliest symptoms of cyano compound intoxication may be weakness, headaches, confusion, and occasionally nausea and vomiting. The respiratory rate and depth will usually be increased at the beginning and at later stages become slow and gasping. Blood pressure is usually normal, especially in the mild or moderately severe cases, although the pulse rate is usually more rapid than normal.
Brandgefahr
Special Hazards of Combustion Products: Toxic hydrogen cyanide and oxides of nitrogen may form in fire.
Industrielle Verwendung
Benzonitrile is used as an intermediate for rubber chemicals and as a solvent for
nitrile rubber, specialty lacquers, many resins, polymers and for many anhydrous
metallic salts (HSDB 1988; Hawley 1981). It is principally used as an intermediate
for benzoguanamine (HSDB 1988). It is also used as an additive in nickel-plating
baths, separating naphthalene and alkylnaphthalenes from non-aromatics by
azetropic distillation; as jet-fuel additive; in cotton bleaching baths; as a drying
additive for acrylic fibers; and in the removal of titanium tetrachloride and
vanadium oxychloride from silicon tetrachloride (HSDB 1988; Smiley 1981).
Benzonitrile is also used in perfumes at a maximum level of 0.2% in the final
product (Opdyke 1979).
Sicherheitsprofil
Poison by intraperitoneal andsubcutaneous routes. Moderately toxic by ingestion,inhalation, and skin contact. A skinirritant. Combustible liquid. When heated todecomposition it emits toxic fumes of CN
- and NOx.
Stoffwechsel
Benzonitrile is mainly hydroxylated in vivo to cyanophenols, a small amount being
hydrolysed to benzoic acid (Williams 1959). Benzonitrile also forms 6>-hydroxybenzonitrile,
m-hydroxybenzonitrile, and /p-hydroxybenzonitrile in rabbits (HSDB
1988). In rabbit, 50% of a dose of 150 mg/kg was converted to conjugated
cyanophenols and 10% of the benzonitrile fed was excreted as benzoic acid.
Hydrogen cyanide is not a metabolite of benzonitrile (Williams 1959) and cyanide
was not found to be formed by benzonitrile either in vivo or in vitro (Tanii and
Hashimoto 1984). The in vivo microsomal hydroxylation of specifically deuterated
benzonitrile in the rat yielded mainly 4-hydroxybenzonitrile with 41%
retention of deuterium (Daly et al 1968).
Versand/Shipping
UN2224 Benzonitrile, Hazard Class: 6.1; Labels:
6.1—Poisonous materials.
läuterung methode
Dry benzonitrile with CaSO4, CaCl2, MgSO4 or K2CO3, and distil it from P2O5 in an all-glass apparatus, under reduced pressure (b 69o/10mm), collecting the middle fraction. Distillation from CaH2 causes some decomposition of benzonitrile. Isonitriles can be removed by preliminary treatment with conc HCl until the odour of isonitrile (carbylamine) has gone, followed by preliminary drying with K2CO3. (This treatment also removes amines.) Steam distil (to remove small quantities of carbylamine). The distillate is extracted into ether, washed with dilute Na2CO3, dried overnight with CaCl2, and the ether is removed by evaporation. The residue is distilled at 40mm (b 96o) [Kice et al. J Am Chem Soc 82 834 1960]. Conductivity grade benzonitrile (specific conductance 2 x 10-8 mho) is obtained by treatment with anhydrous AlCl3, followed by rapid distillation at 40-50o under vacuum. After washing with alkali and drying with CaCl2, the distillate is redistilled in a vacuum several times at 35o before fractionally crystallising several times by partial freezing. It is dried over finely divided activated alumina from which it is withdrawn when required [Van Dyke & Harrison J Am Chem Soc 73 402 1951]. [Beilstein 9 IV 892.]
Inkompatibilitäten
Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. They are incompatible Benzonitrile with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions.
Waste disposal
(1) Mix with calcium hypochlorite
and flush to sewer with water or (2) incinerate.
Benzonitril Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Ethyl N-(diphenylmethylene)glycinate
6-Phenyl-1,3,5-triazin-2,4-diamin
CYCLOPROTHRIN
7α-Chlor-11β,17,21-trihydroxy-16α-methylpregna-1,4-dien-3,20-dion-17,21-di(propionat)
3-Nitrobenzonitril
3-BENZOYL PROPIOPHENONE
4-CHLORO-2,5-DIPHENYLTHIENO[2,3-D]PYRIMIDINE
4,4'-(p-Phenylendiethen-2,1-diyl)bisbenzonitril
Bromoxynil (ISO)
Lanolin
3,4,5-Trimethoxybenzaldehyd
Chlorothalonil
4-tert-Butylbenzylamin
Bis(benzonitril)palladiumchlorid
3,8-Diamino-5-methyl-6-phenylphenanthridiniumbromid
Azosemid
2,6-Dimethoxybenzonitril
Phenol, 4-[(4-Amino-3-methylphenyl)amino]-, Reaktionsprodukte mit Natriumsulfid (Na2(Sx))
1,3,5-Triazine, 2-phenyl- (9CI)
METHYL(5-MERCAPTO-1H-BENZIMIDAZOL-2-YL)CARBAMATE
Prazosin
Benzamidoxim
Bunazosin hydrochloride
N-Methylbis(2,4-xylyliminomethyl)-amin
5-Phenyl-1H-tetrazol
Benzophenone imine
