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Phthalic anhydride
[CAS# 85-44-9]

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Complete supplier list of Phthalic anhydride
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound >> Amine
Name Phthalic anhydride
Synonyms 2,5-Isobenzofurandione
Molecular Structure CAS # 85-44-9, Phthalic anhydride, 2,5-Isobenzofurandione
Molecular Formula C8H4O3
Molecular Weight 148.12
CAS Registry Number 85-44-9
EC Number 201-607-5
SMILES C1=CC=C2C(=C1)C(=O)OC2=O
Properties
Density 1.4±0.1 g/cm3 Calc.*, 1.53 g/mL (Expl.)
Melting point 131 - 134 ºC (Expl.)
Boiling point 295.0 ºC 760 mmHg (Calc.)*, 295 ºC (Sublimes) (Expl.)
Flash point 139.7±15.9 ºC (Calc.)*, 152 ºC (Expl.)
Solubility 0.50-0.70 g/100g (Expl.)
Index of refraction 1.613 (Calc.)*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol symbol   GHS05;GHS07;GHS08 Danger    Details
Hazard Statements H302-H315-H317-H318-H334-H335    Details
Precautionary Statements P233-P260-P261-P264-P264+P265-P270-P271-P272-P280-P284-P301+P317-P302+P352-P304+P340-P305+P354+P338-P317-P319-P321-P330-P332+P317-P333+P317-P342+P316-P362+P364-P403-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Respiratory sensitizationResp. Sens.1H334
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Skin sensitizationSkin Sens.1H317
Specific target organ toxicity - single exposureSTOT SE3H335
Specific target organ toxicity - single exposureSTOT SE3H370
Skin sensitizationSkin Sens.1AH317
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
SDS Available
up Discovory and Applicatios
Phthalic anhydride is a white crystalline organic compound that serves as an important industrial chemical intermediate. It is the anhydride form of phthalic acid and is produced primarily by the catalytic oxidation of ortho-xylene or naphthalene. This compound was first synthesized in the 19th century and has since become a key raw material in the chemical industry due to its reactivity and versatility.

The production of phthalic anhydride is carried out on a large scale using vapor-phase catalytic oxidation processes. Ortho-xylene or naphthalene is passed over a vanadium pentoxide catalyst at elevated temperatures, resulting in the formation of phthalic anhydride with high yield and purity. This manufacturing route is favored because it is efficient and cost-effective.

Phthalic anhydride is primarily used as a precursor to produce plasticizers, especially phthalate esters, which are added to polymers such as polyvinyl chloride (PVC) to increase flexibility and durability. These plasticizers improve the physical properties of plastics, making them suitable for applications in cables, flooring, automotive parts, and consumer goods.

Beyond plasticizers, phthalic anhydride is utilized in the synthesis of alkyd resins, which are widely employed in paints, coatings, and varnishes. These resins provide desirable properties such as gloss, adhesion, and chemical resistance, contributing to the durability and appearance of coated surfaces.

Phthalic anhydride is also involved in the manufacture of dyes, pigments, and pharmaceuticals. It acts as a building block for various chemical compounds, including isobenzofuranones and certain herbicides. In the pharmaceutical industry, derivatives of phthalic anhydride have been used as intermediates for producing drugs with anti-inflammatory and other therapeutic properties.

Due to its reactive anhydride group, phthalic anhydride readily undergoes hydrolysis to form phthalic acid and reacts with alcohols to produce phthalate esters. It can also react with amines to form imides, which are valuable in polymer chemistry and material science for their thermal stability and mechanical strength.

Safety and environmental considerations are important in the handling and use of phthalic anhydride. It is a respiratory irritant and can cause skin and eye irritation upon contact. Industrial processes are designed to minimize exposure and environmental release. The compound is also subject to regulations regarding its use and disposal to reduce potential health and ecological impacts.

In summary, phthalic anhydride is a white crystalline compound obtained by catalytic oxidation of ortho-xylene or naphthalene. It serves as a fundamental chemical intermediate in producing plasticizers, alkyd resins, dyes, pharmaceuticals, and other materials. Its chemical reactivity and versatility underpin its widespread industrial applications, while safety and environmental measures are integral to its production and use.

References

2016. Contact dermatitis: in pursuit of sensitizer's molecular targets through proteomics. Archives of Toxicology. 90 (8), 1849�1864.
DOI: 10.1007/s00204-016-1714-y

2000. Exposure assessment and sensitisation in workers exposed to organic acid anhydrides. International Archives of Occupational and Environmental Health. 73(3), 163�170.
DOI: 10.1007/s004200050422

2008. Nickel-Catalyzed Decarbonylative Addition of Anhydrides to Alkynes. Journal of the American Chemical Society. 130(48), 16486�16487.
DOI: 10.1021/ja806569h
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