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Benzol-1,2:4,5-tetracarbonsaeuredianhydrid

Pyromellitic dianhydride

HCID 6966
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Grundinformationen

CAS
89-32-7
Standard-SMILES
O=c1oc(=O)c2cc3c(=O)oc(=O)c3cc12
InChIKey
ANSXAPJVJOKRDJ-UHFFFAOYSA-N
Summenformel
C10H2O6
Durchschnittliche Molmasse
218,12 g/mol
Monoisotopische Masse
217,98513778

Überblick

See also: Polyester-10 (monomer of).

Namen und Bezeichner

Bevorzugter Name
Pyromellitic dianhydride
IUPAC
furo[3,4-f][2]benzofuran-1,3,5,7-tetrone
Lokaler Name
Benzol-1,2:4,5-tetracarbonsaeuredianhydrid
Englischer Name
Pyromellitic Dianhydride
Summenformel
C10H2O6
Molmasse
218.12

Namen und Synonyme

PYROMELLITIC DIANHYDRIDE89-32-7Pyromellitic anhydridePMDAPyromellitic acid dianhydridePyromellitic acid anhydride1,2,4,5-Benzenetetracarboxylic anhydride1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetronePyromellitic 1,2:4,5-dianhydrideDTXSID10265361H,3H-Benzo(1,2-c:4,5-c')difuran-1,3,5,7-tetroneBenzene-1,2,4,5-tetracarboxylic dianhydride
Weitere Namen anzeigen
1,2,4,5-BENZENETETRACARBOXYLIC DIANHYDRIDEDicarboxylic anhydridebenzenetetracarboxylic anhydride1,2,4,5-Benzenetetracrboxylicdianhydride1,2,3,4-Benzenetetracarboxylic dianhydride
1,2,4,5-Benzenetetracarboxylic 1,2:4,5-dianhydride2Z22T30QZQNSC-4798DTXCID9065361,2,4,5 Benzenetetracarboxylic 1,2:4,5 dianhydride1-PMDARefChem:9102201-898-9

Datenbank-Bezeichner

CAS

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,7
Polarare Oberfläche (TPSA)
86,7 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
0
Schwere Atome
16
Formalladung
0
Komplexität
349

Experimentelle und physikochemische Eigenschaften

PolymersPlastics & Rubber -> Acid Anhydrides, Cyclic
SpringerMaterials PropertiesBoiling point
LogPlog Kow = 2.14 /Estimated/
Density · 3 Einträge

1.68 g/cu cm

1.68 g/cm³

1.68 @25 °C

Color/FormWhite powder
Solubility · 3 Einträge

Soluble in some organic solvents

In water, 130 mg/L @ 25 °C /Estimated/

Solubility in water: reaction

Boiling Point · 2 Einträge

397-400 °C

397-400 °C

Melting Point · 2 Einträge

286 °C

287 °C

Vapor Pressure · 3 Einträge

0.0000048 [mmHg]

4.8X10-6 mm Hg @ 25 °C /Estimated/

0.0000048 [mm Hg] @25 °C

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

P233, P260, P261, P264+P265, P271, P272, P280, P284, P302+P352, P304+P340, P305+P354+P338, P317, P321, P333+P317, P342+P316, P362+P364, P403, and P501 (click each P-code to see the statement)

Danger

H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]

P233, P260, P261, P264+P265, P271, P272, P280, P284, P302+P352, P304+P340, P305+P354+P338, P317, P321, P333+P317, P342+P316, P362+P364, P403, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 5 Einträge

Chemical: 1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone

Hazard Traits - Respiratory Toxicity

1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: Benzene-1,2:4,5-tetracarboxylic dianhydride (EC: 201-898-9)

Pyromellitic dianhydride: Does not have an individual approval but may be used under an appropriate group standard

Fire HazardsCombustible.
Hazards Summary · 1 Eintrag

A skin irritant; [Hawley] Produces the acid on reaction with water; A skin, eye, and respiratory tract irritant; Heavy exposure may cause pulmonary hemorrhage; May cause skin sensitization and asthma; [ICSC] A mild skin sensitizer in guinea pigs; Acute exposure produces CNS depression in animals; Changes in various enzyme activity (cholinesterase, ALT, AST, cytochrome oxidase, etc.) observed in female mice administered 4.4 and 8.8 mg/kg for six months; [HSDB] An irritant that may cause serious eye injury; May cause sensitization by skin contact and inhalation; [Alfa Aesar MSDS] See ACID ANHYDRIDES.

Chemie und Industrie

Pharmakologische Informationen

Mechanism of Action · 1 Eintrag

...Acid anhydrides are low-molecular weight, reactive chemicals that can conjugate to human proteins, rendering the chemical-protein complex immunogenic. The major clinical problem in exposed workers appears to be immune sensitization, which can induce any of three clinical syndromes-- asthma-rhinitis, /late respiratory systemic syndrome/, or /pulmonary disease anemia/. /Acid anhydrides/

Verwendung und Herstellung

Uses · 4 Einträge

Occupational asthma reported in workers using epoxy resin adhesives; [Malo] Used as a curing agent for epoxy resins (high-temperature laminates, molds, and coatings), cross-linking agent for epoxy plasticizers in vinyls and alkyd resins, and intermediate for pyromellitic acid; [Hawley]

Working with Glues and Adhesives [Category: Other]

Curing agent for epoxy resins used in high temperature laminates, molds, coatings; crosslinking agent for epoxy plasticizers in vinyls, alkyd resins; intermediate for pyromellitic acid.

Used in the manufacture of aromatic polyamides (synthetic fibers manufacture) and plasticizers.

U.S. Production2023: 700,000 - <850,000 lb
Consumer UsesNot Known or Reasonably Ascertainable
Industry UsesMonomers
Methods of Manufacturing · 3 Einträge

The oxidation of durene yields pyromellitic acid or pyromellitic dianhydride directly. The oxidation can be carried out with dilute nitric acid in solution, with air and catalyst either in the vapor phase over a solid vanadium pentoxide-based catalyst or in the liquid phase with a soluble catalyst system based on cobalt, manganese, and bromine.

Pyromellitic dianhydride is ... made from pseudocumene by carbonylation to 2,4,5-trimethylbenzaldehyde using HF-BF3 followed by oxidation to pyromellitic acid.

Oxidation of durene, either in wet process by nitric acid or a dichromate, or as direct air oxidation with catalyst.

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Weitere Aktionen
Neue NotizNeue ReaktionAnfrage stellen
89-32-7
PubChem CID
6966
DTXSID
DTXSID1026536
ChEMBL
CHEMBL3182140
UNII
2Z22T30QZQ
EC Number
201-898-9
Nikkaji
J4.301J
Food Contact Substances · 6 Einträge

FCS -> FDA Cumulative Estimated Daily Intake (CEDI)

FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR

FCS -> FDA Inventory of Effective Food Contact Substance (FCS) Notifications

FCS -> FDA Inventory of Effective Food Contact Substance (FCS) Notifications

FCS -> FDA Inventory of Effective Food Contact Substance (FCS) Notifications

FCS -> FDA Inventory of Effective Food Contact Substance (FCS) Notifications

Henry's Law ConstantHenry's Law constant = 7.5X10-9 atm-cu m/mole @ 25 °C /Estimated/
Physical Description · 3 Einträge

Large Crystals; Dry Powder

White hygroscopic solid; [ICSC] White or off-white powder; [Alfa Aesar MSDS]

WHITE HYGROSCOPIC CRYSTALLINE POWDER WITH CHARACTERISTIC ODOUR.

Physikochemische Eigenschaften

Schmelzpunkt
283 · 283-286 °C(lit.)
Siedepunkt
397 · 397-400 °C(lit.)
Dichte
1 · 1,68 g/cm3
Dampfdruck
0 Pa · 0Pa at 25℃
Brechungsindex
1.6 · 1.6000 (estimate)
Flammpunkt
380 °C · 380 °C
storage temp.
2 · 2-30°C
Löslichkeit
Soluble in dimethyl sulfoxide, acetone, chloroform, ethyl ether, n-hexane and benzene.
Aggregatzustand
Fine Powder
pka
5.45 · 5.45[at 20 ℃]
Farbe
White to pale yellow
Wasserlöslichkeit
decomposes
BRN
213583 · 213583
Henry's Law Constant
1.3 · 1.3×103 mol/(m3Pa) at 25℃, HSDB (2015)
InChI
1S/C10H2O6/c11-7-3-1-4-6(10(14)16-8(4)12)2-5(3)9(13)15-7/h1-2H
InChIKey
ANSXAPJVJOKRDJ-UHFFFAOYSA-N
SMILES
O=C1OC(=O)c2cc3C(=O)OC(=O)c3cc12
LogP
-2.03 at · -2.03 at 21.5℃
CAS Datenbank
89 · 89-32-7(CAS DataBase Reference)
NIST chemische Informationen
1 · 1,2,4,5-Benzenetetracarboxylic anhydride(89-32-7)
EPA chemische Informationen
1 H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone · 1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone (89-32-7)
EC ClassificationSymbol: Xn; R: 41-42/43; S: (2)-22-24-26-37/39
Chemical DangersReacts with water. This produces acid.
Hazard Classes and Categories · 5 Einträge

Skin Sens. 1 (100%)

Eye damage - category 1

Serious eye damage/eye irritation - Category 1

Skin corrosion/irritation - Category 2

Eye Dam. 1

Skin, Eye, and Respiratory Irritations · 2 Einträge

The physiological effects generally resemble those of the corresponding acids, but they are more potent eye irritants in the vapor phase, and may produce chronic conjunctivitis. They are slowly hydrolyzed on contact with body tissue and may occasionally cause sensitization. /acid anhydrides/

The substance is irritating to the eyes, the skin and the respiratory tract. Exposure at high levels may result in pulmonary hemorrhage.

Sicherheit und Schutzausrüstung

Fire FightingUse water spray, powder, foam, carbon dioxide.
First Aid Measures · 4 Einträge

Fresh air, rest. Half-upright position. Refer for medical attention.

Remove contaminated clothes. Rinse skin with plenty of water or shower.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Do NOT induce vomiting.

Safe StorageDry. Well closed.
Fire Fighting Procedures/To fight fire use:/ Powder, water spray, foam, carbon dioxide.
Storage ConditionsDry. Well closed.
Cleanup MethodsSweep spilled substance into containers; if appropriate, moisten first to prevent dusting. Wash away remainder with plenty of water. (Extra personal protection: P2 filter respirator for harmful particles.)
Disposal Methods · 1 Eintrag

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material=s impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Spillage Disposal · 1 Eintrag

Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Wash away remainder with plenty of water.

Preventive Measures · 2 Einträge

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

SRP: Contaminated protective clothing should be segregated in such a manner so that there is no direct personal contact by personnel who handle, dispose, or clean the clothing. Quality assurance to ascertain the completeness of the cleaning procedures should be implemented before the decontaminated protective clothing is returned for reuse by the workers. Contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.

Eye PreventionWear safety goggles or eye protection in combination with breathing protection.
Fire PreventionNO open flames.
Inhalation RiskEvaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.

Toxikologische Informationen

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 178(SRC), determined from a structure estimation method(2), indicates that pyromellitic dianhydride is expected to have moderate mobility in soil(SRC). Volatilization of pyromellitic dianhydride from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 7.5X10-9 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Pyromellitic dianhydride is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 4.8X10-6 mm Hg(SRC), determined from a fragment constant method(4). No biodegradation data for pyromellitic dianhydride were located(SRC); however, this compound is expected to hydrolyze in moist environments including soils producing the monohydride and subsequently pyromellitic acid(5).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 178(SRC), determined from a structure estimation method(2), indicates that pyromellitic dianhydride is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 7.5X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 9(SRC), from an estimated log Kow of 2.14(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). No biodegradation data for pyromellitic dianhydride were located(SRC); however, this compound is expected to hydrolyze in water producing the monohydride and subsequently pyromellitic acid(8). The hydrolysis half-life of pyromellitic dianhydride at pH 8 is estimated as about 9 days using an estimation method based on perturbed molecular orbital theory and linear free energy relationship (LFER) methods(9).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), pyromellitic dianhydride, which has an estimated vapor pressure of 4.8X10-6 mm Hg at 25 °C (SRC), determined from a fragment constant method(2), is expected to exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase pyromellitic dianhydride is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 56 days(SRC), calculated from its rate constant of 2.9X10-13 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Pyromellitic dianhydride is a hygroscopic substance that undergoes hydrolysis when contacted by moisture in the atmosphere resulting in the formation of pyromellitic acid(4). Unreacted particulate-phase pyromellitic dianhydride may be removed from the air by wet and dry deposition(SRC). Pyromellitic dianhydride absorbs light greater than 290 nm and is susceptible to direct photolysis in the environment(5), but the kinetics of this reaction are not known.

Adverse EffectsOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Exposure RoutesThe substance can be absorbed into the body by inhalation of its aerosol.
Signs and Symptoms · 4 Einträge

Cough. Sore throat. Wheezing. Shortness of breath.

Redness. Burning sensation.

Redness. Pain. Blurred vision.

Burning sensation.

Soil Adsorption/Mobility · 1 Eintrag

Using a structure estimation method based on molecular connectivity indices(1), the Koc for pyromellitic dianhydride can be estimated to be 178(SRC). According to a classification scheme(2), this estimated Koc value suggests that pyromellitic dianhydride is expected to have moderate mobility in soil(SRC).

Human Toxicity Excerpts · 5 Einträge

/HUMAN EXPOSURE STUDIES/ ...Pyromellitic dianhydride... /has/ been reported to cause occupational immune lung disease (OILD).

/HUMAN EXPOSURE STUDIES/ The most common adverse health effects of the acid anhydrides are noncardiac pulmonary edema, immune sensitization, and irritation of mucous membranes and skin. Reports of the irritant effects and pulmonary edema have been extensive; some of the reports of pulmonary edema, pulmonary hemorrhage, and chemical pneumonitis may actually represent immune sensitization that was not evaluated. Immune sensitization, which has been studied only in the last 15 years, is probably the most important problem clinically. The first cases were probably reported in the 1940s, but there was no accompanying immunologic investigation. /Acid anhydrides/

/CASE REPORTS/ A 17-yr-old man was occupationally exposed to pyromellitic acid dianhydride dust during the production of epoxy resin in a chemical factory. He was clinically diagnosed as having acute hemorrhagic alveolitis associated with anemia. The serologic analysis revealed a high concentration of IgG antibodies against pyromellitic acid dianhydride-treated human serum albumin (PMDA-HSA). Immunoblotting with PMDA-treated human serum as antigen and the patient's serum as the first antibody showed that additional PMDA-modified serum proteins other than HSA were recognized by the patient's IgG antibodies in the higher mol. mass range (>67 kDa). No specific IgG could be detected against other anhydride conjugates (maleic acid, MA; phthalic acid, PA) with the exception of a reaction with the trimellitic acid anhydride-conjugated HSA (TMA-HSA). No specific IgE antibodies could be detected against any of the above mentioned antigens, but immunoblotting of the patient's serum indicated IgG4-type autoantibodies against in vitro PMDA-treated Ig molecules of normal serum proteins.

/CASE REPORTS/ Seven workers using an epoxy adhesive cured with pyromellitic dianhydride were studied. Workers both mixed and used the adhesive. Each completed a questionnaire about previous respiratory symptoms, family or personal history of atopy, smoking history and symptoms using the adhesive. FEV1 /(forced expiratory volume in 1 second)/ was measured as a base-line and after working with the adhesive. Skin tests to common allergens were performed on all subjects. Two subjects who stated they wheezed with adhesive had falls in FEV1 of 15% and 18% from base-line. Totally symptom-free subjects had falls of less than 4% from base-line or a rise in FEV1. There was no clear relationship between smoking habits or atopic state or skin rashes with resin and a fall in FEV1. There is no simple way to identify those at risk of developing wheeze. Care should be taken with epoxy adhesives to avoid sensitization and where it occurs a simple questionnaire would provide a screening method.

For more Human Toxicity Excerpts (Complete) data for PYROMELLITIC DIANHYDRIDE (7 total), please visit the HSDB record page.

Artificial Pollution SourcesPyromellitic dianhydride's production and use as a curing agent for epoxy resins and plasticizers(1) may result in its release to the environment through various waste streams(SRC).
Environmental Bioconcentration · 1 Eintrag

An estimated BCF of 9 was calculated for pyromellitic dianhydride(SRC), using an estimated log Kow of 2.14(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Volatilization from Water/Soil · 1 Eintrag

The Henry's Law constant for pyromellitic dianhydride is estimated as 7.5X10-9 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that pyromellitic dianhydride is expected to be essentially nonvolatile from water surfaces(2). Pyromellitic dianhydride's Henry's Law constant indicates that volatilization from moist soil surfaces is not expected(SRC). Pyromellitic dianhydride is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 4.8X10-6 mm Hg(SRC), determined from a fragment constant method(3).

Non-Human Toxicity Excerpts · 3 Einträge

/LABORATORY ANIMALS: Acute Exposure/ Poisoning /in animals/ is accompanied by CNS depression including behavioral changes (ataxia, somnolence, adynamia, muscle weakness, etc.). Death within the first three days.

/LABORATORY ANIMALS: Acute Exposure/ /1,2,4,5-Benzenetetracarboxylic, 1,2:4,5 dianhydride/ exhibits mild sensitizing properties on skin application of 0.2 mg/kg bw to guinea pigs.

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Female rats exposed to 4.4 and 8.8 mg/kg bw for 6 months developed changes in the activities of a number of enzymes (cholinesterase, AST and ALT, cytochrome oxidase, etc.). Gross pathology and histology changes were evident.

Environmental Abiotic Degradation · 1 Eintrag

The rate constant for the vapor-phase reaction of pyromellitic dianhydride with photochemically-produced hydroxyl radicals has been estimated as 2.9X10-13 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 56 days at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). Pyromellitic dianhydride is a hygroscopic substance that undergoes hydrolysis initially forming the monohydride and subsequently pyromellitic acid when contacted by moist air(2); however the rate of this reaction was not quantified. The second order base catalyzed rate constant of pyromellitic dianhydride was estimated as 0.868 l/mol-sec using an estimation method based on perturbed molecular orbital theory and linear free energy relationship (LFER) methods(3). This corresponds to a half-life of about 9 days at pH 8(SRC). Pyromellitic dianhydride absorbs light greater than 290 nm and is susceptible to direct photolysis in the environment(4), but the kinetics of this reaction are not known.

Probable Routes of Human Exposure · 1 Eintrag

NIOSH (NOES Survey 1981-1983) has statistically estimated that 286 workers (16 of these are female) are potentially exposed to pyromellitic dianhydride in the US(1). Occupational exposure to pyromellitic dianhydride may occur through inhalation of dust and dermal contact with this compound at workplaces where pyromellitic dianhydride is produced or used(SRC).

Sicherheitsdaten

F
10-21
wgk
1
tsca
TSCA listed
hs_code
29173980
RTECS-Nr.
DB9300000
risk_code
41-42/43
hazard_code
Xn
safety_code
22-24-26-37/39
Speicherklasse
11 - Combustible Solids
Giftige Stoffe Daten
89-32-7(Hazardous Substances Data)
Hazard Classifications
Eye Dam. 1Resp. Sens. 1Skin Sens. 1
Selbstentzündungstemperatur
630°C
Formulations/Preparations98 +% purity
General Manufacturing Information · 2 Einträge

Paint and Coating Manufacturing

1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone: ACTIVE

Anwendungen

VerwendenPyromellitic dianhydride (PMDA) is employed as a curing agent for epoxy agent resins used for casting, laminating, the manufacture of moulding powders, adhesives and coatings.

Darstellung · 1 Eintrag

synthetischePyromellitic Dianhydride is prepared by gas-phase oxidation of 1,2,4,5-tetramethylbenzene (or related tetrasubstituted benzene derivatives). An idealized equation is:C6H2(CH3)4 + 6 O2 &rarr; C6H2(C2O3)2 + 6 H2OIn the laboratory, it can be prepared by dehydration of pyromellitic acid using acetic anhydride.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

1,2,4-TrimethylbenzolPropylbenzolp-Xylolm-XylolChromsureAnthracentetramethylbenzene1,2,4,5-Tetramethylbenzol

Nachgelagerte Produkte

Benzol-1,2:4,5-tetracarboxydiimidPolyimide film1,2,4,5-Benzenetetracarboxamide1,2,4,5-Tetracyanobenzene1,2,4,5-Cyclohexanetetracarboxylic Dianhydride2,6-Bis(2-pyridinyl)benzo[1,2-c:4,5-c']dipyrrole-1,3,5,7-tetrone2,6-Bis(3-hydroxyphenyl)-1,3,5,7-tetraoxo-1,2,3,5,6,7-hexahydrobenzo[1,2-c:4,5-c']dipyrrole1,2,4,5-Benzenetetrakis(carbonyl chloride)4-pmpmd2,2-(1,3,5,7-tetraoxo-5,7-dihydropyrrolo(3,4-f)isoindole-2,6(1H,3H)diyl)dibenzoic acid