Phthalsureanhydrid Produkt Beschreibung

Phthalic anhydride Struktur
85-44-9
  • CAS-Nr.85-44-9
  • Bezeichnung:Phthalsureanhydrid
  • Englisch Name:Phthalic anhydride
  • Synonyma:Phthalsureanhydrid;1,2-Benzoldicarbonsäureanhydrid<BR>1,3-Isobenzofurandion
    ESEN;Ht 901;tgl6525;wiltrolp;phthalic;Sconoc 7;TGL 6525;NCI-C03601;retarderak;retarderpd
  • CBNumber:CB7414905
  • Summenformel:C8H4O3
  • Molgewicht:148.12
  • MOL-Datei:85-44-9.mol
Phthalsureanhydrid physikalisch-chemischer Eigenschaften
  • Schmelzpunkt: :131-134 °C(lit.)
  • Siedepunkt: :284 °C(lit.)
  • Dichte :1,53 g/cm3
  • Dampfdichte :5.1 (vs air)
  • Dampfdruck :<0.01 mm Hg ( 20 °C)
  • Brechungsindex :1.4500 (estimate)
  • Flammpunkt: :152 °C
  • storage temp.  :Store at RT.
  • Löslichkeit :6g/l (slow decomposition)
  • Aggregatzustand :Flaky Crystals
  • Farbe :White
  • PH :2 (6g/l, H2O, 20℃)
  • Explosionsgrenze :1.7-10.5%(V)
  • Wasserlöslichkeit :6 g/L (20 ºC)
  • Sensitive  :Moisture Sensitive
  • Merck  :14,7372
  • BRN  :118515
  • Stabilität: :Stable. Combustible. Incompatible with strong oxidizing agents, strong bases, moisture, strong acids. Dust may form an explosive mixture with air.
  • CAS Datenbank :85-44-9(CAS DataBase Reference)
  • NIST chemische Informationen :Phthalic anhydride(85-44-9)
  • EPA chemische Informationen :1,3-Isobenzofurandione(85-44-9)
Sicherheit

Phthalic anhydride Chemische Eigenschaften,Einsatz,Produktion Methoden

  • ERSCHEINUNGSBILD WEISSE GLäNZENDE KRISTALLE MIT CHARAKTERISTISCHEM GERUCH.
  • PHYSIKALISCHE GEFAHREN Staubexplosion der pulverisierten oder granulierten Substanz in Gemischen mit Luft möglich.
  • CHEMISCHE GEFAHREN Zersetzung bei Kontakt mitheißem Wasser unter Bildung von Phthalsäure. Reagiert mit starken Oxidationsmitteln, starken Säuren, starken Basen und Reduktionsmitteln. Reagiert sehr heftig beim Erhitzen mit Kupferoxid oder Natriumnitrit unter Explosionsgefahr. Greift viele Metalle in Gegenwart von Wasser an.
  • ARBEITSPLATZGRENZWERTE TLV: 1 ppm; Sensibilisierung; Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); (ACGIH 2005).
    MAK: IIb (nicht festgelegt, aber Informationen vorhanden); Sensibilisierung der Atemwege; (DFG 2005).
  • AUFNAHMEWEGE Aufnahme in den Körper durch Inhalation des Aerosols und durch Verschlucken.
  • INHALATIONSGEFAHREN Eine gesundheitsschädliche Partikelkonzentration in der Luft kann beim Dispergieren schnell erreicht werden, vor allem als Pulver.
  • WIRKUNGEN BEI KURZZEITEXPOSITION WIRKUNGEN BEI KURZZEITEXPOSITION:
    Die Substanz reizt stark die Augen, die Haut und die Atemwege.
  • WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION Wiederholter oder andauernder Kontakt kann zu Hautsensibilisierung führen. Wiederholte oder andauernde Inhalation kann asthmatische Beschwerden (s. Anm.) hervorrufen.
  • LECKAGE Verschüttetes Material in abgedeckten Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. Persönliche Schutzausrüstung: Chemikalienschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.
  • R-Sätze Betriebsanweisung: R22:Gesundheitsschädlich beim Verschlucken.
    R37/38:Reizt die Atmungsorgane und die Haut.
    R41:Gefahr ernster Augenschäden.
    R42/43:Sensibilisierung durch Einatmen und Hautkontakt möglich.
  • S-Sätze Betriebsanweisung: S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
    S24/25:Berührung mit den Augen und der Haut vermeiden.
    S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
    S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
    S46:Bei Verschlucken sofort ärztlichen Rat einholen und Verpackung oder Etikett vorzeigen.
    S22:Staub nicht einatmen.
  • Aussehen Eigenschaften C8H4O3; 1,2-Benzoldicarbonsäureanhydrid. Farblose Kristalle mit schwach aromatischem Geruch.
  • Gefahren für Mensch und Umwelt Reizt die Atmungsorgane, Augen und die Haut.
    Verursacht beim Einatmen Husten und Atemnot.
    Nicht mit Wasser, Alkalihydroxiden und Salpetersäure in Verbindung bringen.
    LD50 (oral, Ratte): 4020 mg/kg
  • Schutzmaßnahmen und Verhaltensregeln Geeignete Schutzhandschuhe als kurzzeitiger Staubschutz.
  • Verhalten im Gefahrfall Vorsichtig trocken aufnehmen. Der Entsorgung zuführen.
    Wasser, Kohlendioxid, Pulver.
    Brennbar. Gefahr einer Staubexplosion.
  • Erste Hilfe Nach Hautkontakt: Mit reichlich Wasser abwaschen.
    Nach Augenkontakt: Mit reichlich Wasser bei geöffnetem Lidspalt mindestens 10 Minuten ausspülen. Sofort Augenarzt hinzuziehen.
    Nach Einatmen: Frischluft.
    Nach Verschlucken: Reichlich Wasser trinken lassen. Erbrechen auslösen. Sofort Arzt hinzuziehen.
    Nach Kleidungskontakt: Kontaminierte Kleidung entfernen.
    Ersthelfer: siehe gesonderten Anschlag

  • Sachgerechte Entsorgung Als feste Laborchemikalienabfälle.
  • Beschreibung Phthalic anhydride is the organic compound with the formula C6H4(CO)2O. It is the anhydride of phthalic acid. This colourless solid is an important industrial chemical, especially for the large-scale production of plasticizers for plastics. In 2000, the world wide production volume of phthalic anhydride is estimated to be about 3 232 000 tones per year.
  • Chemische Eigenschaften Phthalic Anhydride is moderately flammable, white solid (flake) or a clear, colorless, mobile liquid (molten) Characteristic, acrid, choking odor
  • Chemische Eigenschaften white crystalline solid with choking odour
  • Verwenden Phthalic Anhydride is an organic compound and the anhydride of phthalic acid (P384480). Phthalic Anhydride is an important industrial chemical commonly used in large-scale production of plasticizers f or plastics. Recent research have also evaluated Phthalic Anhydride as potential antibacterial agent.
  • Verwenden manufacture of phthaleins, phthalates, benzoic acid, synthetic indigo, artificial resins (glyptal).
  • Definition ChEBI: The cyclic dicarboxylic anhydride that is the anhydride of phthalic acid.
  • Allgemeine Beschreibung A colorless to white lustrous solid in the form of needles with a mild distinctive odor. Moderately toxic by inhalation or ingestion and a skin irritant. Melting point 64°F Flash point 305°F. Forms a corrosive solution when mixed with water. Used in the manufacture of materials such as artificial resins.
  • Air & Water Reaktionen Reacts, usually slowly with water to form phthalic acid and heat [Merck 11th ed. 1989]. The phthalic acid is somewhat soluble in water.
  • Reaktivität anzeigen Phthalic anhydride reacts exothermically with water. The reactions are sometimes slow, but can become violent when local heating accelerates their rate. Acids accelerate the reaction with water. Incompatible with acids, strong oxidizing agents, alcohols, amines, and bases. Undergoes exothmeric nitration with fuming nitric acid-sulfuric acid and may give mixtures of the potentially explosive phthaloyl nitrates or nitrites or their nitro derivatives [Chem. & Ind. 20:790. 1972]. Phthalic anhydride reacts violently with CuO at elevated temperatures [Park, Chang-Man, Richard J. Sheehan. hthalic Acids and Other Benzenepolycarboxylic Acids Kirk-Othmer Encyclopedia of Chemical Technology. John Wiley & Sons, Inc. 2005]. Mixtures of Phthalic anhydride and anhydrous CO2 explode violently if heated [eaflet No. 5, Inst. of Chem., London, 1940].
  • Health Hazard Solid irritates skin and eyes, causing coughing and sneezing. Liquid causes severe thermal burns.
  • Brandgefahr Combustible material: may burn but does not ignite readily. Substance will react with water (some violently) releasing flammable, toxic or corrosive gases and runoff. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapors may travel to source of ignition and flash back. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.
  • Pharmazeutische Anwendungen Phthalic anhydride reacted with cellulose acetate forms cellulose acetate phthalate (CAP), a common enteric coating excipient that has also been shown to have antiviral activity. Phthalic anhydride is a degradation product of CAP.
  • Kontakt-Allergie Phthalic anhydride is used in the manufacture of unsaturated polyesters and as a curing agent for epoxy resins. When used as a pigment, it can be responsible for sensitization in ceramic workers. Phthalic anhydride per se is not responsible for the sensitization to the resin used in nail varnishes phthalic anhydride/trimellitic anhydride/ glycols copolymer.
  • Sicherheitsprofil Poison by ingestion. Experimental teratogenic effects. A corrosive eye, skin , and mucous membrane irritant. A common air contaminant. Combustible when exposed to heat or flame; can react with oxidzing materials. Moderate explosion hazard in the form of dust when exposed to flame. The production of ths material has caused many industrial explosions. Mixtures with copper oxide or sodium nitrite explode when heated. Violent reaction with nitric acid + sulfuric acid above 80℃. To fight fire, use CO2, dry chemical. Used in plasticizers, polyester resins, and alkyd resins, dyes, and drugs. See also ANHYDRIDES.
  • Chemical Synthesis Phthalic anhydride is a precursor to a variety of reagents useful in organic synthesis. Important derivatives include phthalimide and its many derivatives. Chiral alcohols form half-esters (see above), and these derivatives are often resolvable because they form diastereomeric salts with chiral amines such as brucine. A related ring - opening reaction involves peroxides to give the useful peroxy acid:
    C6H4(CO)2O + H2O2 → C6H4(CO3H)CO2H.
  • Chemical Synthesis Phthalic anhydride is a versatile intermediate in organic chemistry, in part because it is bi functional and cheaply available. It undergoes hydrolysis and alcoholysis. Hydrolysis by hot water forms ortho-phthalic acid. This process is reversible: Phthalic anhydride reforms upon heating the acid above 180 °C. Hydrolysis of anhydrides is not typically a reversible process. However, phthalic acid is easily dehydrated to form phthalic anhydride due to the creation of a thermo dynamically favorable 5-membered ring.
  • Chemical Synthesis Phthalic anhydride was first reported in 1836 by Auguste Laurent. It is presently obtained by catalytic oxidation of ortho-xylene and naphthalene ("Gibbs phthalic anhydride process"):
    C6H4(CH3)2 + 3 O2→C6H4(CO)2O + 3 H2O
    C10H8 + 4.5 O2→ C6H4(CO)2O + 2 H2O + 2 CO2 The catalyst that is used for the oxidation of xylene is a modified vanadium pent oxide (V2O5). When separating the phthalic anhydride from byproducts such as o-xylene in water, or maleic anhydride, a series of “switch condensers” is required. Phthalic anhydride can also be prepared from phthalic acid:.
  • mögliche Exposition Phthalic anhydride is used in plasticizers; in the manufacture of phthaleins; benzoic acid; alkyd and polyester resins; synthetic indigo; and phthalic acid;which is used as a plasticizer for vinyl resins. To a lesser extent, it is used in the production of alizarin, dye, anthranilic acid; anthraquinone, diethyl phthalate; dimethyl phthalate; erythrosine, isophthalic acid; methylaniline, phenolphthalein, phthalamide, sulfathalidine, and terephthalic acid. It has also found uses as a pesticide intermediate.
  • Erste Hilfe If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. If victim is conscious, administer water, or milk. Do not induce vomiting.
  • Versand/Shipping UN2214 Phthalic anhydride with>.05 % maleic anhydride, Hazard class: 8; Labels: 8-Corrosive material.
  • läuterung methode Distil the anhydride under reduced pressure. Purify it from the acid by extracting with hot CHCl3, filtering and evaporating. The residue is crystallised from CHCl3, CCl4 or *benzene, or sublimed. Fractionally crystallise it from its melt. Dry it under vacuum at 100o. [Saltiel J Am Chem Soc 108 2674 1986, Beilstein 17/11 V 253.]
  • Precursor to dyestuffs Phthalic anhydride is widely used in industry for the production of certain dyes. A well-known application of this reactivity is the preparation of the anthroquinone dye quinizarin by reaction with parachloro phenol followed by hydrolysis of the chloride.
  • Preparation of phthalate esters As with other anhydrides, the alcoholysis reaction is the basis of the manufacture of phthalate esters, which are widely used (and controversial - see endocrine disruptor) plasticizers. In the 1980s, approximately 6.5×109 kg of these esters were produced annually, and the scale of production was increasing each year, all from phthalic anhydride. The process begins with the reaction of phthalic anhydride with alcohols, giving the monoesters:
    C6H4(CO)2O + ROH → C6H4(CO2H)CO2R
    The second esterification is more difficult and requires removal of water:
    C6H4(CO2H)CO2R + ROHC6H4(CO2R)2 + H2O
    The most important di ester is bis (2-ethyl hexyl) phthalate ("DEHP"), used in the manufacture of polyvinyl chloride.
  • Inkompatibilitäten Dust forms an explosive mixture with air. Phthalic anhydride reacts exothermically with water. The reactions are sometimes slow, but can become violent when local heating accelerates their rate. Acids accelerate the reaction with water. Incompatible with acids, strong oxidizing agents, alcohols, amines, and bases. Converted to phthalic acid in hot water. 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. caustics, ammonia, amines, water. Reacts violently with copper oxide or sodium nitrite 1 heat.
  • Waste disposal Use a licensed professional waste disposal service to dispose of this material. 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. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.
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85-44-9, Phthalic anhydride Verwandte Suche:
  • wiltrolp
  • O-PHTHALIC ANHYDRIDE
  • PHTHALANDIONE
  • PHTHALIC ACID ANHYDRIDE
  • PHTHALIC ANHYDRIDE
  • 2,5-Isobenzofurandione
  • Phthalic anhydride 99+ %
  • PTHALIC ANHUDRIDE
  • PHTHALIC ANHYDRIDE MIN 99.5%
  • PHATHALIC ANHYDRIDE
  • PTHALIC ANHYDRIDE
  • PHTHALIC ANHYDRIDE, REAGENTPLUS, 99%
  • PHTHALIC ANHYDRIDE, ACS
  • PHTHALIC ANHYDRIDE, 99+%, A.C.S. REAGENT
  • PhthalicAnhydrideForSynthesis
  • PhthalicAnhydrideC8H4O3
  • o-phthalic anhydrie
  • Phthalic anhydride, reagent ACS
  • PHTHALATEANHYDRIDE
  • ISOBENZOICFURANODIONE
  • ORTHO-PHTHALICANHYDRIDE
  • Phthalsureanhydrid
  • Phthalic anyhdride
  • BENZENE-1,2-DICARBOXYLIC ANHYDRIDE
  • Phthalic anhyd
  • Phthalic anhydride ACS reagent, >=99%
  • Phthalic anhydride anhydrous, free-flowing, Redi-Dri(TM), ACS reagent, >=99%
  • Phthalic acid anhydride 1,3-iso-Benzofurandione
  • Phthalic anhydride Manufacturer
  • Phthalic anhydride manufacturer CAS NO.85-44-9 CAS NO.85-44-9
  • anhydridephtaliquesolide
  • anhydridkyselinyftalove
  • Anidride ftalica
  • anidrideftalica
  • Araldite HT 901
  • ESEN
  • Ftaalzuuranhydride
  • Ftalanhydrid
  • Ftalowy bezwodnik
  • ftalowybezwodnik
  • AKOS BBS-00004337
  • 1,3-ISOBENZOFURANDIONE
  • 1,3-ISOBENZOFURANIDONE
  • 1,3-DIOXOPHTHALAN
  • 1,3-DIOXOPHTHALANE
  • 1,2-BENZENEDICARBONIC ACID, ANHYDRIDE
  • 1,2-BENZENE DICARBOXYLIC ACID ANHYDRIDE
  • 1,2-Benzenedicarboxylic Anhydride
  • 1,2-benzenedicarboxylicanhydride
  • 1,3-dihydro-1,3-dioxo-isobenzofura
  • 1,3-dihydro-1,3-dioxoisobenzofuran
  • 1,3-phthalandion
  • 1,3-Phthalandione
  • 2-Benzofuran-1,3-dione
  • Anhydrid kyseliny ftalove
  • Anhydride phtalique
  • anhydridephtalique
  • anhydridephtalique(etatvitreux)