85-44-9 Usage
Chemical Description
Different sources of media describe the Chemical Description of 85-44-9 differently. You can refer to the following data:
1. Phthalic anhydride is a cyclic anhydride that is used as a precursor to various chemicals, including phthalate esters, which are used as plasticizers.
2. Phthalic anhydride is an organic compound used in the production of plasticizers, dyes, and resins.
Description
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 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.
Chemical Properties
Phthalic Anhydride is moderately flammable, white solid (flake) or a clear, colorless, mobile liquid (molten) Characteristic, acrid, choking odor. It is very slightly soluble in H2O, soluble in alcohol, and slightly soluble in ether.
Physical properties
Colorless to pale cream crystals with a characteristic, choking odor. Moisture sensitive. Odor
threshold concentration is 53 ppb (quoted, Amoore and Hautala, 1983).
Uses
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: Phthalic anhydride is the cyclic dicarboxylic anhydride that is the anhydride of phthalic acid. It has a role as an allergen. It is a cyclic dicarboxylic anhydride and a member of 2-benzofurans.
Preparation
The most important modifying component used in the
manufacture of linear unsaturated polyesters is phthalic anhydride. The
anhydride is generally obtained by the oxidation of o-xylene:
The reaction is carried out in the vapour phase by passing a mixture of
o-xylene and air over a catalyst such as vanadium pentoxide supported on
silica and promoted with titanium dioxide at about 400°C. The exit gases are
cooled and the phthalic anhydride is collected and purified by distillation
under reduced pressure.
Synthesis Reference(s)
The Journal of Organic Chemistry, 25, p. 616, 1960 DOI: 10.1021/jo01074a035Synthesis, p. 612, 1973Tetrahedron Letters, 20, p. 2301, 1979 DOI: 10.1016/S0040-4039(01)93957-7
General Description
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 Reactions
Reacts, usually slowly with water to form phthalic acid and heat [Merck 11th ed. 1989]. The phthalic acid is somewhat soluble in water.
Reactivity Profile
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.
Fire Hazard
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.
Pharmaceutical Applications
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.
Contact allergens
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.
Safety Profile
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.
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.
Potential Exposure
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.
Shipping
UN2214 Phthalic anhydride with＞.05 % maleic anhydride, Hazard class: 8; Labels: 8-Corrosive material.
Purification Methods
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.]
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.
Incompatibilities
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.
Check Digit Verification of cas no
The CAS Registry Mumber 85-44-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85-44:
(4*8)+(3*5)+(2*4)+(1*4)=59
59 % 10 = 9
So 85-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H10O7/c17-13(18)9-5-1-3-7-11(9)15(21)23-16(22)12-8-4-2-6-10(12)14(19)20/h1-8H,(H,17,18)(H,19,20)
85-44-9Relevant articles and documents
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Shreve,Welborn
, p. 279,282 (1943)
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Oxidation of o-xylene to phthalic anhydride over V2O5/TiO2 catalysts: III. Study of organic residue formed on the catalyst surface
Dias, Cristina R.,Portela, M. Farinha,Bond, Geoffrey C.
, p. 284 - 294 (1996)
An organic residue is formed on V2O5/TiO2 (anatase) catalysts during the oxidation of o-xylene and o-tolualdehyde. V2O5 catalysts supported on TiO2 (0.6, 1, and 5% V2O5/TiO2), prepared by wet impregnation, were exposed to o-xylene/air and o-tolualdehyde/air mixtures under different operating conditions, and, after different times of exposure to reaction conditions, the catalysts were characterized by FTIR spectroscopy and temperature programmed oxidation. The compounds formed were also extracted and analyzed by mass spectrometry. Organic molecules containing no more than two aromatic rings, formed by dimerization of adsorbed molecules, were detected and their characteristics were found to vary with features of the catalytic surface and with operating conditions. Larger contents of residue were obtained at lower temperatures and lower contact times and, for some experimental conditions, a constant amount of such compounds was observed after l h of exposure under reaction conditions. The analysis of samples used with different reactant mixtures showed that adsorbed o-xylene can lead to the formation of a "residue" on the surface.
Orthoamides and iminium salts, LXXXIX. Reactions of N,N,N',N',N'',N'',N''',N'''-octamethylacetylene-bis(carboxamidinium) tetrafluoroborate with nucleophilic reagents - New methods for the preparation of amidinium salts and ketene aminals
Drandarov, Konstantin,Tiritiris, Ioannis,Kantlehner, Willi
, p. 225 - 241 (2015)
The acetylene-bis(carboxamidinium) salt 4 dehydrates carboxylic acids to the corresponding anhydrides, as the byproduct 2-oxo-but-2-en-amidinium salt 6b was isolated. Aromatic hydroxy compounds and 2-furyl-methylmercaptan add to the triple bond of the salt 4 to give 2-aryloxy- and 2-alkylmercapto-but-2-enebis( amidinium) salts 7-9. According to this reaction principle, 2-organoamino-buten-2-ene-bis(amidinium) salts 10 and 11 were prepared from 4 and primary and secondary amines, whereas 4-chlorobenzhydrazide reacted with 4 to give the imidazole-3-carboxamidinium salt 13. The reaction of CH2-acidic compounds as malononitrile or ethyl cyanoacetate with the bis(amidinium) salt 4 affords 2-cyanomethylene-but-3-enamidinium salts 15. With the CH-acidic diethyl 2-bromomalonate, compound 4 undergoes a Michael-initiated ring closure cyclopropenation reaction with further ring opening by the released Br- to the corresponding 2-diethoxycarbonylmethylene- 3-bromo-but-3-enamidinium salt 18. Unlike cyclopentadiene and furane, the reaction of N-methylpyrrole and bis(amidinium) salt 4 does not lead to Diels-Alder [4 + 2] cycloadduct but to the Michaeltype 1:1 adduct 20. Pyrrole- and thiophene-2-carboxamidinium salts 23-25 can be prepared from compound 4 and esters of glycine, N-methylglycine (sarcosine), and mercaptoacetic acid, respectively. The derivatives of quinoxaline-2-carboxamidinium salts 29 are accessible from aromatic 1,2-diamines and compound 4. The reaction of the CH2/NH-acidic cyanoacetamide with the bis(amidinium) salt 4 produced the 3-pyrroline-2-on derivatives 33.
The Decisive Cooperation of Metal and Oxygen Ions of Nickel Oxide During the Oxidation of o-Xylene
Hauffe, K.,Buss, D. H.,Glemser, O.
, p. 109 - 112 (1995)
As can be concluded from the experimental results at 450 deg C in the reaction mixtures consisting of N2-O2-o-Xylene, both nickel oxide pure and doped with Li2O or In2O3 is unsuited as catalyst for the oxidation of o-xylene to phthalic anhydride.In contrast to NiO which ionosorbs both oxygen and o-xylene, NiO-Li2O, a strong ionosorbent for o-xylene, prevents the ionosorption of oxygen because of the large concentration of holes.Since gaseous oxygen does not react with ionosorbed o-xylene but a reduction of nickel oxide to metallic nickel has been observed in spite of t he fact of enough oxygen in the gas phase it can be assumed that o-xylene is forced to remove oxygen ions from the NiO lattice under generation of oxygen-ion vacanxies and nickel atoms.The predominant portions of the reaction products are H2O and CO2.With undoped nickel oxide and NiO-In2O3 which were not reduced under the same experimental conditions, the reaction products had roughly the same composition. The reduction of NiO-LiO2 however will be prevented in a gas mixture with a high oxygen pressure which oxidizes the formed nickel atoms on the surface of NiO-Li2O to nickel oxide making possible the entrance of oxygen from the gas phase and, therefore, the oxidation of o-xylene. A turbulent motion of a 2-component catalyst powder from NiO-1molepercent Li2O covered with ionosorbed 0-xylene and ZnO-1molpercent In2O3 covered with ionosorbed oxygen in the same gas mixture resulted in the same reaction products as in the presence of sole NiO-Li2O under simultaneous reduction of nickel oxide.From that we can conclude that the oxidation of o-xylene by oxygen ions of NiO occurs more easily than the reaction with ionosorbed oxygen on ZnO-In2O3 which obviously seems to be bounded too strongly.This result is also confirmed by the prevention of the oxidation of gaseous o-xylene in the presence of only ZnO-In2O3. Finally, the operation of the carrier catalyst V2O5/TiO2 which is employed for the oxidation of o-xylene to phthalic anhydride will be prevented to a large extent in simultaneous presence of nickel oxide either pure or doped with Li2O and In2O3 in roughly the same amount.This result can be mentioned as a proof for the interaction of a 2-component catalyst the mechanism of which is at present not satisfactorily understood.
Chemical Modifications Induced by Phthalic Anhydride, a Respiratory Sensitizer, in Reconstructed Human Epidermis: A Combined HRMAS NMR and LC-MS/MS Proteomic Approach
Khong, Minh-Thuong,Berl, Valérie,Kuhn, Lauriane,Hammann, Philippe,Lepoittevin, Jean-Pierre
, p. 2087 - 2099 (2021/08/30)
Chemical skin and respiratory allergies are becoming a major health problem. To date our knowledge on the process of protein haptenation is still limited and mainly derived from studies performed in solution using model nucleophiles. In order to better understand chemical interactions between chemical allergens and the skin, we have investigated the reactivity of phthalic anhydride 1 (PA), a chemical respiratory sensitizer, toward reconstructed human epidermis (RHE). This study was performed using a new approach combining HRMAS NMR to investigate the in situ chemical reactivity and LC-MS/MS to identify modified epidermal proteins. In RHE, the reaction of PA appeared to be quite fast and the major product formed was phthalic acid. Two amide type adducts on lysine residues were observed and after 8h of incubation, we also observed the formation of an imide type cyclized adducts with lysine. In parallel, RHE samples topically exposed to phthalic anhydride (13C)-1 were analyzed using the shotgun proteomics method. Thus, 948 different proteins were extracted and identified, 135 of which being modified by PA, i.e., 14.2% of the extracted proteome. A total of 211 amino acids were modified by PA and validated by fragmentation spectra. We thus identified 154 modified lysines, 22 modified histidines, 30 modified tyrosines, and 5 modified arginines. The rate of modified residues, as a proportion of the total number of modifiable nucleophilic residues in RHE, was rather low (1%). At the protein level, modified proteins were mainly type I and type II keratins and other proteins which are abundant in the epidermis such as protein S100A, Caspase 14, annexin A2, serpin B3, fatty-acid binding protein 5, histone H2, H3, H4, etc. However, the most modified protein, mainly on histidine residues, was filaggrin, a protein that is of low abundance (0.0266 mol %) and rich in histidine.
Photo-induced deep aerobic oxidation of alkyl aromatics
Wang, Chang-Cheng,Zhang, Guo-Xiang,Zuo, Zhi-Wei,Zeng, Rong,Zhai, Dan-Dan,Liu, Feng,Shi, Zhang-Jie
, p. 1487 - 1492 (2021/07/10)
Oxidation is a major chemical process to produce oxygenated chemicals in both nature and the chemical industry. Presently, the industrial manufacture of benzoic acids and benzene polycarboxylic acids (BPCAs) is mainly based on the deep oxidation of polyalkyl benzene, which is somewhat suffering from environmental and economical disadvantage due to the formation of ozone-depleting MeBr and corrosion hazards of production equipment. In this report, photo-induced deep aerobic oxidation of (poly)alkyl benzene to benzene (poly)carboxylic acids was developed. CeCl3 was proved to be an efficient HAT (hydrogen atom transfer) catalyst in the presence of alcohol as both hydrogen and electron shuttle. Dioxygen (O2) was found as a sole terminal oxidant. In most cases, pure products were easily isolated by simple filtration, implying large-scale implementation advantages. The reaction provides an ideal protocol to produce valuable fine chemicals from naturally abundant petroleum feedstocks. [Figure not available: see fulltext.].
