Essigsure Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
FARBLOSE FLüSSIGKEIT MIT STECHENDEM GERUCH.
CHEMISCHE GEFAHREN
Schwache S?ure. Reagiert sehr heftig mit Oxidationsmitteln und Basen. Greift viele Metalle an unter Bildung brennbarer/explosionsf?higer Gase (z.B. Wasserstoff, ICSC-Nr. 0001). Greift einige Kunststoff-, Gummi- und Beschichtungsarten an.
ARBEITSPLATZGRENZWERTE
TLV: 10 ppm (als TWA); 15 ppm (als STEL); (ACGIH 2005).
MAK: IIb (nicht festgelegt, aber Informationen vorhanden); (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den K?rper durch Inhalation der D?mpfe und durch Verschlucken.
INHALATIONSGEFAHREN
Beim Verdampfen bei 20°C kann schnell eine gesundheitssch?dliche Kontamination der Luft eintreten.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Substanz und Dampf ver?tzen die Augen, die Haut und die Atemwege. ?tzend beim Verschlucken. Inhalation des Dampfes kann zu Lungen?dem führen (s.Anm.). Die Auswirkungen treten u.U. verz?gert ein. ?rztliche Beobachtung notwendig.
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Wiederholter oder andauernder Hautkontakt kann Dermatitis hervorrufen. M?glich sind Auswirkungen auf den Magendarmtrakt mit nachfolgenden Verdauungsst?rungen einschlie?lich Sodbrennen und Verstopfung.
LECKAGE
Ausgelaufene Flüssigkeit in abdichtbaren Beh?ltern sammeln. Ausgelaufene Flüssigkeit vorsichtig mit Natriumcarbonat nur unter Aufsicht eines Fachmanns neutralisieren. Reste mit viel Wasser wegspülen. Pers?nliche Schutzausrüstung: Chemikalienschutzanzug mit umgebungsluftunabh?ngigem Atemschutzger?t.
R-S?tze Betriebsanweisung:
R34:Verursacht Ver?tzungen.
R42:Sensibilisierung durch Einatmen m?glich.
R35:Verursacht schwere Ver?tzungen.
R10:Entzündlich.
R36/38:Reizt die Augen und die Haut.
S-S?tze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
S24/25:Berührung mit den Augen und der Haut vermeiden.
Beschreibung
Acetic acid is a colourless liquid or crystal with a sour, vinegar-like odour and is one of the
simplest carboxylic acids and is an extensively used chemical reagent. Acetic acid has wide
application as a laboratory reagent, in the production of cellulose acetate mainly for photographic
film and polyvinyl acetate for wood glue, synthetic fibres, and fabric materials. Acetic
acid has also been of large use as a descaling agent and acidity regulator in food industries.
Physikalische Eigenschaften
Acetic acid is a weak carboxylic acid with a pungent odor that exists as a liquid at room temperature. It was probably the first acid to be produced in large quantities. The name acetic comes from acetum, which is the Latin word for “sour” and relates to the fact that acetic acid is responsible for the bitter taste of fermented juices.
Occurrence
Reported found in vinegar, bergamot, cornmint oil, bitter orange oil, lemon petitgrain, various dairy products
History
Vinegar is a dilute aqueous solution of acetic acid. The use of vinegar is well documented in ancient history, dating back at least 10,000 years. Egyptians used vinegar as an antibiotic and made apple vinegar. Babylonians produced vinegar from wine for use in medicines and as a preservative as early as 5000 b.c.e. Hippocrates (ca. 460–377 b.c.e.), known as the “father of medicine,” used vinegar as an antiseptic and in remedies for numerous conditions including fever, constipation, ulcers, and pleurisy. Oxymel, which was an ancient remedy for coughs, was made by mixing honey and vinegar. A story recorded by the Roman writer Pliny the Elder (ca. 23–79 c.e.) describes how Cleopatra, in an attempt to stage the most expensive meal ever, dissolved pearls from an earring in vinegar wine and drank the solution to win a wager.
Verwenden
Acetic acid is used as table vinegar, as preservative and as an intermediate in the chemical industry, e.g. acetate fibers, acetates, acetonitrile, pharmaceuticals, fragrances, softening agents, dyes (indigo) etc. Product Data Sheet
Definition
ChEBI: Acetic acid is a simple monocarboxylic acid containing two carbons. It has a role as a protic solvent, a food acidity regulator, an antimicrobial food preservative and a Daphnia magna metabolite. It is a conjugate acid of an acetate.
Allgemeine Beschreibung
A colorless aqueous solution. Smells like vinegar. Density 8.8 lb / gal. Corrosive to metals and tissue.
Air & Water Reaktionen
Dilution with water releases some heat.
Reaktivit?t anzeigen
ACETIC ACID, [AQUEOUS SOLUTION] reacts exothermically with chemical bases. Subject to oxidation (with heating) by strong oxidizing agents. Dissolution in water moderates the chemical reactivity of acetic acid, A 5% solution of acetic acid is ordinary vinegar. Acetic acid forms explosive mixtures with p-xylene and air (Shraer, B.I. 1970. Khim. Prom. 46(10):747-750.).
Hazard
Corrosive; exposure of small amounts can
severely erode the lining of the gastrointestinal
tract; may cause vomiting, diarrhea, bloody feces
and urine; cardiovascular failure and death.
Health Hazard
Glacial acetic acid is a highly corrosive liquid. Contact with the eyes can produce mild to moderate irritation in humans. Contact with the skin may produce burns. Ingestion of this acid may cause corrosion of the mouth and gastrointestinal tract. The acute toxic effects are vomiting, diarrhea, ulceration, or bleeding from intestines and circulatory collapse. Death may occur from a high dose (20–30 mL), and toxic effects in humans may be felt from ingestion of 0.1–0.2 mL. An oral LD50 value in rats is 3530 mg/kg (Smyth 1956).
Glacial acetic acid is toxic to humans andanimals by inhalation and skin contact. Inhumans, exposure to 1000 ppm for a fewminutes may cause eye and respiratory tractirritation. Rabbits died from 4-hour exposureto a concentration of 16,000 ppm in air.
Flammability and Explosibility
Acetic acid is a combustible substance (NFPA rating = 2). Heating can release
vapors that can be ignited. Vapors or gases may travel considerable distances to
ignition source and "flash back." Acetic acid vapor forms explosive mixtures with
air at concentrations of 4 to 16% (by volume). Carbon dioxide or dry chemical
extinguishers should be used for acetic acid fires.
Landwirtschaftliche Anwendung
Herbicide, Fungicide, Microbiocide; Metabolite,
Veterinary Medicine: A herbicide used to control grasses, woody plants
and broad-leaf weeds on hard surface and in areas where
crops are not normally grown; as a veterinary medicine.
Pharmazeutische Anwendungen
Glacial and diluted acetic acid solutions are widely used as
acidifying agents in a variety of pharmaceutical formulations and
food preparations. Acetic acid is used in pharmaceutical products as
a buffer system when combined with an acetate salt such as sodium
acetate. Acetic acid is also claimed to have some antibacterial and
antifungal properties.
Handelsname
ACETUM®; ACI-JEL®; ECOCLEAR®;
NATURAL WEED SPRAY® No. One; VOSOL®
Sicherheitsprofil
A human poison by an unspecified route. Moderately toxic by various routes. A severe eye and skin irritant. Can cause burns, lachrymation, and conjunctivitis. Human systemic effects by ingestion: changes in the esophagus, ulceration, or bleeding from the small and large intestines. Human systemic irritant effects and mucous membrane irritant. Experimental reproductive effects. Mutation data reported. A common air contaminant. A flammable liquid. A fire and explosion hazard when exposed to heat or flame; can react vigorously with oxidizing materials. To fight fire, use CO2, dry chemical, alcohol foam, foam and mist. When heated to decomposition it emits irritating fumes. Potentially explosive reaction with 5azidotetrazole, bromine pentafluoride, chromium trioxide, hydrogen peroxide, potassium permanganate, sodium peroxide, and phosphorus trichloride. Potentially violent reactions with acetaldehyde and acetic anhydride. Ignites on contact with potassium tert-butoxide. Incompatible with chromic acid, nitric acid, 2-amino-ethanol, NH4NO3, ClF3, chlorosulfonic acid, (O3 + diallyl methyl carbinol), ethplenediamine, ethylene imine, (HNO3 + acetone), oleum, HClO4, permanganates, P(OCN)3, KOH, NaOH, xylene
Sicherheit(Safety)
Acetic acid is widely used in pharmaceutical applications primarily
to adjust the pH of formulations and is thus generally regarded as
relatively nontoxic and nonirritant. However, glacial acetic acid or
solutions containing over 50% w/w acetic acid in water or organic
solvents are considered corrosive and can cause damage to skin,
eyes, nose, and mouth. If swallowed glacial acetic acid causes severe
gastric irritation similar to that caused by hydrochloric acid.
Dilute acetic acid solutions containing up to 10% w/w of acetic
acid have been used topically following jellyfish stings.Dilute
acetic acid solutions containing up to 5% w/w of acetic acid have
also been applied topically to treat wounds and burns infected with
Pseudomonas aeruginosa.
The lowest lethal oral dose of glacial acetic acid in humans is
reported to be 1470 mg/kg.The lowest lethal concentration on
inhalation in humans is reported to be 816 ppm.Humans, are,
however, estimated to consume approximately 1 g/day of acetic acid
from the diet.
LD
50 (mouse, IV): 0.525 g/kg
LD
50 (rabbit, skin): 1.06 g/kg
LD
50 (rat, oral): 3.31 g/kg
m?gliche Exposition
Acetic acid is widely used as a chemical feedstock for the production of vinyl plastics, acetic anhydride, acetone, acetanilide, acetyl chloride, ethyl alcohol, ketene, methyl ethyl ketone, acetate esters, and cellulose acetates. It is also used alone in the dye, rubber, pharmaceutical, food preserving, textile, and laundry industries. It is utilized, too; in the manufacture of Paris green, white lead, tint rinse, photographic chemicals, stain removers, insecticides, and plastics.
Carcinogenicity
Acetic acid is a very weak tumor
promoter in a multistage mouse skin model for chemical
carcinogenesis, but was very effective in enhancing cancer
development when applied during the progression phase of
the model. Female SENCAR mice were initiated with
a topical application of 7,12-dimethylbenzanthracene and
2 weeks later were promoted with 12-O-tetradecanoylphorbol-
13-acetate, twice weekly for 16 weeks. Topical treatment
with acetic acid started 4 weeks later (40 mg glacial acetic
acid in 200mL acetone, twice weekly) and continued for
30 weeks. Before treatment with acetic acid, each group of
mice had approximately the same number of papillomas at
the exposure site. After 30 weeks of treatment, mice treated
with acetic acid had a 55% greater conversion of skin
papillomas to carcinomas than vehicle-treated mice. Selective
cytotoxicity to certain cells within the papilloma and a
compensatory increase in cell proliferation were considered
the most probable mechanism.
Environmental Fate
Biological. Near Wilmington, NC, organic wastes containing acetic acid (representing 52.6% of
total dissolved organic carbon) were injected into an aquifer containing saline water to a depth of
approximately 1,000 feet below ground surface. The generation of gaseous components
(hydrogen, nitrogen, hydrogen sulfide, carbon dioxide, and methane) suggests acetic acid and
possibly other waste constituents, were anaerobically degraded by microorganisms (Leenheer et
al., 1976).
Plant. Based on data collected during a 2-h fumigation period, EC50 values for alfalfa, soybean,
wheat, tobacco, and corn were 7.8, 20.1, 23.3, 41.2, and 50.1 mg/m
3, respectively (Thompson et
al., 1979).
Photolytic. A photooxidation half-life of 26.7 d was based on an experimentally determined rate
constant of 6 x 10
-13 cm
3/molecule?sec at 25 °C for the vapor-phase reaction of acetic acid with
OH radicals in air (Atkinson, 1985). In an aqueous solution, the rate constant for the reaction of
acetic acid with OH radicals was determined to be 2.70 x 10
-17 cm
3/molecule?sec (Dagaut et al.,
1988).
Chemical/Physical. Ozonolysis of acetic acid in distilled water at 25 °C yielded glyoxylic acid
which oxidized readily to oxalic acid before undergoing additional oxidation producing carbon
dioxide. Ozonolysis accompanied by UV irradiation enhanced the removal of acetic acid (Kuo et
al., 1977).
Lager
Acetic acid should be used only in areas free
of ignition sources, and quantities greater than 1 liter should be stored in tightly
sealed metal containers in areas separate from oxidizers.
Versand/Shipping
UN2789 Acetic acid, glacial or Acetic acid solution, with .80 % acid, by mass, hazard class: 8; labels: 8-Corrosive material, 3-flammable liquid. UN2790 acetic acid solution, not ,50% but not .80% acid, by mass, hazard class: 8; labels: 8-Corrosive material; acetic acid solution, with .10% and ,50%, by mass, hazard class: 8; labels: 8-Corrosive material
l?uterung methode
Usual impurities are traces of acetaldehyde and other oxidisable substances and water. (Glacial acetic acid is very hygroscopic. The presence of 0.1% water lowers its m by 0.2o.) Purify it by adding some acetic anhydride to react with water present, heat it for 1hour to just below boiling in the presence of 2g CrO3 per 100mL and then fractionally distil it [Orton & Bradfield J Chem Soc 960 1924, Orton & Bradfield J Chem Soc 983 1927]. Instead of CrO3, use 2-5% (w/w) of KMnO4, and boil under reflux for 2-6hours. Traces of water have been removed by refluxing with tetraacetyl diborate (prepared by warming 1 part of boric acid with 5 parts (w/w) of acetic anhydride at 60o, cooling, and filtering off, followed by distillation [Eichelberger & La Mer J Am Chem Soc 55 3633 1933]. Refluxing with acetic anhydride in the presence of 0.2g % of 2-naphthalenesulfonic acid as catalyst has also been used [Orton & Bradfield J Chem Soc 983 1927]. Other suitable drying agents include anhydrous CuSO4 and chromium triacetate: P2O5 converts some acetic acid to the anhydride. Azeotropic removal of water by distillation with thiophene-free *benzene or with butyl acetate has been used [Birdwhistell & Griswold J Am Chem Soc 77 873 1955]. An alternative purification uses fractional freezing. [Beilstein 2 H 96, 2 IV 94.] Rapid procedure: Add 5% acetic anhydride, and 2% of CrO3. Reflux and fractionally distil.
Inkompatibilit?ten
Acetic acid reacts with alkaline substances.
Waste disposal
Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed
Regulatory Status
GRAS listed. Accepted as a food additive in Europe. Included in the
FDA Inactive Ingredients Database (injections, nasal, ophthalmic,
and oral preparations). Included in parenteral and nonparenteral
preparations licensed in the UK.
Essigsure Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
2-Amino-5-bromo-4-methylpyridine
Isochinolin-N-oxyd
2-ACETYLAMINO-5-BROMO-6-METHYLPYRIDINE
Chromtriacetat
Hydroxy silicone oil emulsion
5-Nitrothiophene-2-carboxylic acid
4-(1H-PYRROL-1-YL)BENZOIC ACID
4-(DIMETHYLAMINO)PHENYL THIOCYANATE
Dye-fixing agent G
Cellulose diacetate plastifier
4-Brombrenzcatechin
6-Nitropiperonal
Zirconiumacetat
1,1,2,2-Tetraphenylethan-1,2-diol
10-Nitroanthrone
Levothyroxinnatrium
γ-L-glutamyl-1-naphthylamide
4-BROMOPHENYLUREA
5-BROMO-2-HYDROXY-3-METHOXYBENZALDEHYDE
3,5-Dibromsalicylsaeure
Ethyltrichloracetat
1,3-Dithian
ETHYLENEDIAMINE DIACETATE
7-Nitro-1H-indazol
1H-Indazol-7-amin
2-Bromo-2′-hydroxyacetophenone
ALLOXAN MONOHYDRATE
4-CHLORO-3-METHYL-1H-PYRAZOLE
4,5-Dichloronaphthalene-1,8-dicarboxylic anhydride
METHYL-(3-PHENYL-PROPYL)-AMINE
6-Nitroindazol
1,3-Dihydro-3,3-bis(4-hydroxy-m-tolyl)-2H-indol-2-on
DL-Glyceraldehyd
3-Hydroxy-2,4,6-tribromobenzoic acid
(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate
2-Bromcinnamaldehyd
2,3-Dimethylpyridine-N-oxide
Ethyltriphenylphosphoniumacetat
N-(6-CHLORO-3-NITROPYRIDIN-2-YL)ACETAMIDE
3-Amino-4-bromopyrazole
