Propan-2-ol Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
FARBLOSE FLüSSIGKEIT.
PHYSIKALISCHE GEFAHREN
Die Dämpfe mischen sich leicht mit Luft. Bildung explosionsfähiger Gemische.
CHEMISCHE GEFAHREN
Reagiert mit starken Oxidationsmitteln. Greift einige Kunststoffe und Gummi an.
ARBEITSPLATZGRENZWERTE
TLV: 200 ppm (als TWA); 400 ppm (als STEL); Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); (ACGIH 2005).
MAK: 200 ppm, 500 mg/m? Spitzenbegrenzung: überschreitungsfaktor II(2); Schwangerschaft: Gruppe C; (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation der Dämpfe.
INHALATIONSGEFAHREN
Beim Verdampfen bei 20°C tritt langsam eine gesundheitsschädliche Kontamination der Luft ein; viel schneller jedoch beim Versprühen oder Dispergieren.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen und die Atemwege. Möglich sind Auswirkungen auf das Zentralnervensystem mit nachfolgender Depression. Exposition weit oberhalb der Arbeitsplatzgrenzwerte kann zu Bewusstlosigkeit führen.
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Die Flüssigkeit entfettet die Haut.
LECKAGE
Ausgelaufene Flüssigkeit in abdichtbaren Behältern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. Persönliche Schutzausrüstung: Atemschutzfilter für organische Gase und Dämpfe.
R-Sätze Betriebsanweisung:
R11:Leichtentzündlich.
R36:Reizt die Augen.
R67:Dämpfe können Schläfrigkeit und Benommenheit verursachen.
R40:Verdacht auf krebserzeugende Wirkung.
R10:Entzündlich.
R36/38:Reizt die Augen und die Haut.
S-Sätze Betriebsanweisung:
S7:Behälter dicht geschlossen halten.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
Aussehen Eigenschaften
C3H8O; Isopropanol, Dimethylcarbinol, 2-Hydroxypropan. Farblose Flüssigkeit mit charakteristischem Geruch.
Gefahren für Mensch und Umwelt
Leicht entzündlich. Nicht stark erhitzen. Nicht mit Alkali-, Erdalkalimetallen, Aluminium, Oxidationsmitteln und organischen Nitroverbindungen in Berührung bringen. Gefährliche Zersetzungsprodukte sind Peroxide.
Reizt die Haut und Schleimhäute, vor allem als Dampf.
LD
50 (oral, Ratte): 5850 mg/kg.
Schutzmaßnahmen und Verhaltensregeln
Schutzhandschuhe als kurzzeitiger Spritzschutz.
Verhalten im Gefahrfall
Mit flüssigkeitsbindendem Material, z. B. Rench Rapid aufnehmen. Der Entsorgung zuführen. Nachreinigen.
Kohlendioxid, Wasser, Schaum, Pulver.
Brennbar. Dämpfe schwerer als Luft. Mit Luft Bildung explosionsfähiger Gemische möglich.
Erste Hilfe
Nach Hautkontakt: Mit reichlich Wasser abwaschen.
Nach Augenkontakt: Mit reichlich Wasser bei geöffnetem Lidspalt mindestens 10 Minuten ausspülen. Augenarzt hinzuziehen.
Nach Einatmen: Frischluft.
Nach Verschlucken: Viel Wasser trinken lassen. Erbrechen vermeiden. Sofort Arzt hinzuziehen.
Nach Kleidungskontakt: Kontaminierte Kleidung sofort entfernen.
Ersthelfer: siehe gesonderten Anschlag
Sachgerechte Entsorgung
Als halogenfreie, organische Lösemittelabfälle.
Beschreibung
Isopropanol is a clear, colorless alcohol that is used in the
production of acetone and as a solvent in the manufacture of
various industrial and commercial products. It is used by the
public for a number of different purposes and is commonly
known as rubbing alcohol. It is flammable and miscible with
both water and many different organic solvents. Isopropanol
can be prepared via three different methods: indirect hydration
of propylene (the ‘strong acid’ method), direct hydration of
propylene, and catalytic hydrogenation of acetone.
Chemische Eigenschaften
Isopropyl alcohol is a clear, colorless, mobile, volatile, flammable liquid with a characteristic, spirituous odor resembling that of a mixture of ethanol and acetone; it has a slightly bitter taste.It is miscible with water, ethyl ether, and ethyl alcohol. Isopropyl alcohol is incompatible with strong oxidizers, acetaldehyde, chlorine, ethylene oxide, acids, and isocyanates.
Occurrence
Reported found in apple and cognac aromas (esterified). Also found in apple, banana, grapefruit and lime
juice, melon, papaya, pear, onion, peas, rutabaga, tomato, wheat bread, cheeses, milk, boiled egg, cooked beef, pork and mutton, hop
oil beer, rum, cocoa, coffee, scotch whiskey, grape wines, peanut, pecan, soybean, honey, beans, plum brandy, walnut, crab, clam,
prickly pear and clary sage.
synthetische
Isopropyl alcohol may be prepared from propylene; by the catalytic reduction of acetone, or by fermentation of certain carbohydrates.
Definition
ChEBI: Isopropyl Alcohol is a secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group. It is an isomer of propyl alcohol with antibacterial properties.
Application
Isopropyl Alcohol is used in a variety of applications including as a solvent for industrial processes and coating; as a component in cleaning, car care and deicing products; as a wetting agent for printing inks and as a feedstock in the manufacture of ester and Mogas/Luboil additives.
isopropyl alcohol is a carrier, anti-bacterial, and solvent for skin care lotions. Isopropyl alcohol is made from propylene, a petroleum derivative.
When compared to ethanol, 50% less is required for nucleic acid precipitation, thus minimizing the total volume to be centrifuged for DNA or RNA recovery.
Isopropyl alcohol 70% is used as an ingredient in alcohol swabs and alcohol wipes for wound cleaning, it is found in hand sanitizers, and in ear drops to prevent swimmer's ear.
Allgemeine Beschreibung
Volatile, colorless liquid with a sharp musty odor like rubbing alcohol. Flash point of 53°F. Vapors are heavier than air and mildly irritating to the eyes, nose, and throat. Density approximately 6.5 lb / gal. Used in making cosmetics, skin and hair preparations, pharmaceuticals, perfumes, lacquer formulations, dye solutions, antifreezes, soaps, window cleaners. Sold in 70% aqueous solution as rubbing alcohol.
Air & Water Reaktionen
Highly flammable. Water soluble.
Reaktivität anzeigen
Isopropyl Alcohol can react with AIR and OXYGEN over time to form unstable peroxides that can explode. Contact with 2-butanone increases the rate of peroxide formation. An explosive reaction occurs when Isopropanol is heated with (aluminum isopropoxide + crotonaldehyde). Forms explosive mixtures with trinitromethane and hydrogen peroxide. Reacts with barium perchlorate to form a highly explosive compound. Ignites on contact with dioxygenyl tetrafluoroborate, chromium trioxide and potassium-tert-butoxide. Vigorous reactions occur with (hydrogen + palladium), nitroform, oleum, COCl2, aluminum triisopropoxide and oxidizing agents. Reacts explosively with phosgene in the presence of iron salts. Incompatible with acids, acid anhydrides, halogens and aluminum . Isopropanol can react with PCl3, forming toxic HCl gas. (Logsdon, John E., Richard A. Loke., sopropyl Alcohol. Kirk-Othmer Encyclopedia of Chemical Technology. John Wiley & Sons, Inc. 1996.).
Health Hazard
Exposures to isopropyl alcohol cause irritation to the eyes and mucous membranes. Exposures to isopropyl alcohol for 3–5 min (400 ppm) caused mild irritation of the eyes, nose, and throat, and at 800 ppm these symptoms became severe. Ingestion or an oral dose of 25 mL in 100 mL of water produced hypotension, facial flushing, bradycardia, and dizziness. Ingestion in large quantities caused extensive hemorrhagic tracheobronchitis, bronchopneumonia, and hemorrhagic pulmonary edema. Prolonged skin contact with isopropyl alcohol caused eczema and sensitivity. Delayed dermal absorption is attributed to a number of pediatric poisonings that have occurred following repeated or prolonged sponge bathing with isopropyl alcohol to reduce fever. In several cases, symptoms included respiratory distress, stupor, and coma. Laboratory animals exposed to isopropyl alcohol develop poisoning with symptoms of hind leg paralysis, unsteadiness, lack of muscular coordination, respiratory depression, and stupor. Isopropyl alcohol is a potent CNS depressant, and in large doses causes cardiovascular depression.
Brandgefahr
Isopropyl Alcohol(IPA) is highly flammable in its liquid and vapor forms and flammable atmospheres can be created at temperatures as low as 540°F /120℃ . This means that any environment where IPA is being used needs to be well ventilated. It should be kept away from heat and open flame. As the vapour is heavier than air, it may spread along the ground, so care needs to be taken that the vapour is not ignited by a distant source.
Pharmazeutische Anwendungen
Isopropyl alcohol (propan-2-ol) is used in cosmetics and pharmaceutical
formulations, primarily as a solvent in topical formulations.( It is not recommended for oral use owing to its toxicity.
Although it is used in lotions, the marked degreasing properties
of isopropyl alcohol may limit its usefulness in preparations used
repeatedly. Isopropyl alcohol is also used as a solvent both for tablet
film-coating and for tablet granulation, where the isopropyl
alcohol is subsequently removed by evaporation. It has also been
shown to significantly increase the skin permeability of nimesulide
from carbomer 934.
Isopropyl alcohol has some antimicrobial activity and a 70% v/v aqueous solution is used as a topical disinfectant.
Therapeutically, isopropyl alcohol has been investigated for the
treatment of postoperative nausea or vomiting.
Carcinogenicity
CD-1 mice were exposed by inhalation
to 0, 500, 2500, or 5000 ppm of isopropanol vapor for
6 h/day, 5 days/week for 18 months. An additional group of
mice (all exposure levels) were assigned to a recovery group
that were exposed to isopropanol for 12 months and then
retained until study termination at 18 months. There was
no increased frequency of neoplastic lesions in any of the
isopropanol-exposed animals. Nonneoplastic lesions were
limited to the testes (males) and the kidney. In the testes,
enlargement of the seminal vesicles occurred in the absence
of associated inflammatory or degenerative changes. The
kidney effects included tubular proteinosis and/or tubular
dilatation. The incidence of testicular and kidney effects
was not increased in the isopropanol-exposed recovery
animals.
Environmental Fate
The vast majority of isopropanol in the environment originates
from manufacturing processes. Small amounts are
produced by certain microbes, fungi, and yeast. The high
volatility of isopropanol ensures that when it is released
into the environment in any state, it eventually ends up in
the atmosphere. There, it can be degraded by hydroxyl radicals
or it can return to soil or water through precipitation. Its
half-life in the environment is approximately 3.2 days and is
highly biodegradable; bioaccumulation in plants and animals
does not occur.
Lager
Isopropyl alcohol should be stored in a cool, dry, well-ventilated area in tightly sealed containers with a proper label. Outside or detached storage is preferable. Inside storage should be a flammable liquids storage room or cabinet. Workers should not store isopropyl alcohol above 37°C (100°F). Containers of isopropyl alcohol should be protected from physical damage and contact with air, and should be stored separately from strong oxidizers, acetaldehyde, chlorine, ethylene oxide, acids, and isocyanates. Isopropyl alcohol should be transported to the nearest laboratory as quickly as possible in cool containers.
Inkompatibilitäten
Incompatible with oxidizing agents such as hydrogen peroxide and
nitric acid, which cause decomposition. Isopropyl alcohol may be
salted out from aqueous mixtures by the addition of sodium
chloride, sodium sulfate, and other salts, or by the addition of
sodium hydroxide.
Vorsichtsmaßnahmen
Workers should wash hands and face thoroughly after handling isopropyl alcohol. Workers should wear gloves, safety glasses and a face shield, boots, apron, and a full impermeable suit is recommended if exposure is possible to a large portion of the body.
Regulatory Status
Included in the FDA Inactive Ingredients Database (oral capsules,
tablets, and topical preparations). Included in nonparenteral
medicines licensed in the UK. Included in the Canadian List of
Acceptable Non-medicinal Ingredients.
Propan-2-ol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
