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Phthalsureanhydrid Produkt Beschreibung

Phthalic anhydride Struktur
85-44-9
CAS-Nr.
85-44-9
Bezeichnung:
Phthalsureanhydrid
Englisch Name:
Phthalic anhydride
Synonyma:
ESEN;Ht 901;tgl6525;phthalic;Sconoc 7;TGL 6525;wiltrolp;NCI-C03601;retarderak;retarderpd
CBNumber:
CB7414905
Summenformel:
C8H4O3
Molgewicht:
148.12
MOL-Datei:
85-44-9.mol

Phthalsureanhydrid 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 below +30°C.
Löslichkeit
6g/l (slow decomposition)
Aggregatzustand
Flaky Crystals
Farbe
White
PH
2 (6g/l, H2O, 20℃)
Geruch (Odor)
Characteristic choking odor
Säure-Base-Indikators(pH-Indikatoren)
2 at 6 g/l at 20 °C
Explosionsgrenze
1.7-10.5%(V)
Wasserlöslichkeit
6 g/L (20 ºC)
Sensitive 
Moisture Sensitive
Merck 
14,7372
BRN 
118515
Henry's Law Constant
6.29 at 20 °C (approximate - calculated from water solubility and vapor pressure)
Expositionsgrenzwerte
NIOSH REL: TWA 6 mg/m3 (1 ppm), IDLH 60 mg/m3; OSHA PEL: TWA 12 mg/m3 (2 ppm); ACGIH TLV: TWA 1 ppm (adopted).
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
Phthalic anhydride (85-44-9)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22-37/38-41-42/43
S-Sätze: 23-24/25-26-37/39-46-22
RIDADR  2214
WGK Germany  1
RTECS-Nr. TI3150000
10-21
Selbstentzündungstemperatur 580 °C
TSCA  Yes
HazardClass  8
PackingGroup  III
HS Code  29173500
Giftige Stoffe Daten 85-44-9(Hazardous Substances Data)
Toxizität LD50 orally in Rabbit: 1530 mg/kg LD50 dermal Rabbit > 3160 mg/kg
Bildanzeige (GHS)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H318 Verursacht schwere Augenschäden. Schwere Augenschädigung Kategorie 1 Achtung P280, P305+P351+P338, P310
H334 Kann bei Einatmen Allergie, asthmaartige Symptome oder Atembeschwerden verursachen. Sensibilisierung der Atemwege Kategorie 1 Achtung P261, P285, P304+P341, P342+P311,P501
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P261 Einatmen von Staub vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P284 Atemschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P342+P311 Bei Symptomen der Atemwege: GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P405 Unter Verschluss aufbewahren.

Phthalsureanhydrid 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.
Phthalic anhydride
Phthalic anhydride is an important chemical intermediate in the plastics industry from which are derived numerous phthalate esters that function as plasticizers in synthetic resins. Phthalic anhydride itself is used as a monomer for synthetic resins such as glyptal, the alkyd resins, and the polyester resins.
Phthalic anhydride is also used as a precursor of anthraquinone, phthalein, rhodamine, phthalocyanine, fluorescein, and xanthene dyes.
Phthalic anhydride is used in the synthesis of primary amines, the agricultural fungicide phaltan, and thalidomide. Other reactions with phthalic anhydride yield phenolphthalein, benzoic acid, phthalylsulfathiazole (an intestinal antimicrobial agent), and orthophthalic acid.

Chemische Eigenschaften

Phthalic anhydride is very slightly soluble in H2O, soluble in alcohol, and slightly soluble in ether.

Chemische Eigenschaften

Phthalic Anhydride is moderately flammable, white solid (flake) or a clear, colorless, mobile liquid (molten) Characteristic, acrid, choking odor.

Physikalische Eigenschaften

Colorless to pale cream crystals with a characteristic, choking odor. Moisture sensitive. Odor threshold concentration is 53 ppb (quoted, Amoore and Hautala, 1983).

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.
manufacture of phthaleins, phthalates, benzoic acid, synthetic indigo, artificial resins (glyptal).
Intermediate for Plastizers, Paints, Dyes and Pigments, Polyester Resins.

Verwenden

The compound is a high-tonnage chemical and is widely used in a variety of industrial organic syntheses.

Verwenden

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.

Definition

ChEBI: The cyclic dicarboxylic anhydride that is the anhydride of phthalic acid.

Synthesis Reference(s)

The Journal of Organic Chemistry, 25, p. 616, 1960 DOI: 10.1021/jo01074a035
Synthesis, p. 612, 1973
Tetrahedron Letters, 20, p. 2301, 1979 DOI: 10.1016/S0040-4039(01)93957-7

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.

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.

Environmental Fate

Chemical/Physical. Reacts with water to form o-phthalic acid (Kollig, 1993; Windholz et al., 1983). Based on an observed rate constant of 7.9 x 10-9/sec, the hydrolysis half-life is 88 sec (Hawkins, 1975).
Pyrolysis of phthalic anhydride in the presence of polyvinyl chloride at 600 °C for 10 min gave the following compounds: biphenyl, fluorene, benzophenone, 9-fluorenone, o-terphenyl, 9-phenylfluorene, and three unidentified compounds (Bove and Dalven, 1984).

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.

Toxicity evaluation

Phthalic anhydride modulates lipid mediator release and cytokine formation and has sensitizing effects on the respiratory tract. The local irritating effect particularly on the mucous membranes probably depends on the hydrolysis to phthalic acid.

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.

Phthalsureanhydrid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Phthalsureanhydrid Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 404)Lieferanten
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BAODING STORD IMPORT AND EXPORT CO.,LTD
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Springchem New Material Technology Co.,Limited
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85-44-9(Phthalsureanhydrid)Verwandte Suche:


  • AKOS BBS-00004337
  • 2-Benzofuran-1,3-dione
  • Anhydrid kyseliny ftalove
  • Anhydride phtalique
  • anhydridephtalique
  • anhydridephtalique(etatvitreux)
  • anhydridephtalique(french)
  • 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
  • 1,3-ISOBENZOFURANDIONE
  • 1,3-ISOBENZOFURANIDONE
  • 1,3-DIOXOPHTHALAN
  • 1,3-DIOXOPHTHALANE
  • 1,2-BENZENEDICARBONIC ACID, ANHYDRIDE
  • 1,2-BENZENE DICARBOXYLIC ACID ANHYDRIDE
  • Phthalic Anhydride, Reagent
  • Phthalic anhydride, ACS, 99.0-100.2%
  • PHTHALIC ANHYDRIDE pure
  • phthalic anhydride, unregulated
  • Phthlandione
  • PHTHALIC ANHYDRIDE ACS REAGENT
  • Phthalic anhydride, synthesis grade
  • Phthalic anhydride 5g [85-44-9]
  • Phthalic Anhydride Flake
  • Phthalic anhydride, 99% 1KG
  • Phthalic anhydride, 99% 2.5KG
  • Phthalic anhydride, reagent ACS 500GR
  • Phthalicanhydridetwo
  • Twophthalicanhydride
  • o-PhthalMic acid anhydride
  • Phthalic anhydride, ACS, 99.0-100.2%, 99.0-100%
  • anhydridephtaliquesolide
  • anhydridkyselinyftalove
  • Anidride ftalica
  • anidrideftalica
  • Araldite HT 901
  • ESEN
  • Ftaalzuuranhydride
  • Ftalanhydrid
  • Ftalowy bezwodnik
  • ftalowybezwodnik
  • ftalowybezwodnik(polish)
  • Ht 901
  • Isobenzofuran, 1,3-dihydro-1,3-dioxo-
  • Isobenzofuran-1,3-dione
  • NCI-C03601
  • o-Phthalic acid anhydride
  • o-phthalicacidanhydride
  • Phthalanhydride
  • phthalic
  • phthalicanhydride(non-specificname)
  • phthalicanhydridemoltenliquid
  • phthalicanhydridesolid
  • Phthalsaeureanhydrid
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