Phthalic anhydride, 99%, Thermo Scientific Chemicals

Catalog Number	Quantity
ALFA14955.0B	1000 g

Catalog number ALFA14955.0B

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1000 g

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Chemical Identifiers

CAS9085-42-1

MDL NumberMFCD00132715

Specifications

Water retention capacity65 to 75 % (Cl)

Particle size=<5 % (< 100 µm)

Appearance (Form)Beads

Particle size100 to 200 mesh

Particle size=<10 % (> 300 µm)

Phthalic anhydride is used in the preparation of primary amines. It is used as a precursor to prepare anthraquinone, phthalein, rhodamine, phthalocyanine, fluorescein and xanthene dyes. It serves as an important intermediate in the plastics industry, dyes, resins and pigments. It is used as a monomer for synthetic resins such as glyptal, alkyd resins and polyester resins. It plays a vital role in the large-scale production of plasticizers for plastics. Further, it acts as a curing agent for epoxy resins, anti-scaling agents, plating agents, surface treating agents, ion exchange agents, paint additives, adhesives, sealant chemicals and potential antibacterial agent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Phthalic anhydride is used in the preparation of primary amines. It is used as a precursor to prepare anthraquinone, phthalein, rhodamine, phthalocyanine, fluorescein and xanthene dyes. It serves as an important intermediate in the plastics industry, dyes, resins and pigments. It is used as a monomer for synthetic resins such as glyptal, alkyd resins and polyester resins. It plays a vital role in the large-scale production of plasticizers for plastics. Further, it acts as a curing agent for epoxy resins, anti-scaling agents, plating agents, surface treating agents, ion exchange agents, paint additives, adhesives, sealant chemicals and potential antibacterial agent.

Solubility
Soluble in water, carbon disulfide, ethanol, acetone and benzene. Slightly soluble in ethyl ether.

Notes
Moisture sensitive. Incompatible with strong oxidizing agents, strong bases, strong reducing agents and strong acids.

RUO – Research Use Only

General References:

For examples of formation of phthalimides from amines, see: Org. Synth. Coll., 4, 106 (1963); 5, 973 (1973). As an alternative to hydrazinolysis, ɑ-amino acids can also be quantitatively recovered from their phthaloyl derivatives by prolonged reaction with aqueous methylamine at room temperature: Can. J. Chem., 48, 3572 (1970).
Can be used for the dehydration of nitro aldols to nitroalkenes; see, e.g.: Org. Synth. Coll., 7, 396 (1990).
Reaction with H₂O₂ gives monoperphthalic acid, useful in peroxidation reactions; see, e.g.: Org. Synth. Coll., 3, 619 (1955); 5, 805 (1973). With urea hydrogen peroxide, provides a superior system for converting N-heteroaromatics and tert-amines to their N-oxides: Chem. Ber., 125, 1965 (1992)
Liu, Y.; Gu, Y.; Hou, Y.; Yang, Y.; Deng, S.; Wei, Z. Hydrophobic activated carbon supported Ni-based acid-resistant catalyst for selective hydrogenation of phthalic anhydride to phthalide. Chem. Eng. J. 2015, 275, 271-280.
Lin, Z.; Ierapetritou, M.; Nikolakis, V. Phthalic anhydride production from hemicellulose solutions: Technoeconomic analysis and life cycle assessment. AlChE J. 2015, 61 (11), 3708-3718.