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402915

Sigma-Aldrich

Phthalic acid

ACS reagent, ≥99.5%

Sinonimo/i:

1,2-Benzenedicarboxylic acid

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About This Item

Formula condensata:
C6H4-1,2-(CO2H)2
Numero CAS:
Peso molecolare:
166.13
Beilstein:
608199
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.21

Grado

ACS reagent

Livello qualitativo

Saggio

≥99.5%

Forma fisica

powder or crystals

Impurezze

≤0.05% insolubles
≤0.5% water

Residuo alla calcinazione

≤0.02%

Punto di fusione

210-211 °C (dec.) (lit.)

Anioni in tracce

chloride (Cl-): ≤0.001%
nitrate (NO3-): ≤0.005%
sulfate (SO42-): ≤0.005%

Cationi in tracce

Fe: ≤0.001%
heavy metals: ≤0.001%

Stringa SMILE

OC(C1=C(C(O)=O)C=CC=C1)=O

InChI

1S/C8H6O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H,(H,9,10)(H,11,12)
XNGIFLGASWRNHJ-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Phthalic acid (PA, PTA), also called as 1,2-benzenedicarboxylic acid is an aromatic carboxylic acid. It is the ortho form of the three phthalic acid isomers, the other two being isophthalic acid (meta form) and terephthalic acid (para form). PA is the starting material in the synthesis of plasticizers. A study on toxicity reveals that PA shows in vitro and in vivo toxicity. Its mineralization by photocatalysis using TiO2/UV system has been studied. It also is used as a potential tyrosinase inhibitor.

Applicazioni

Phthalic acid may be used as a catalyst for the thiocyanation of aromatics and heteroaromatics and as an interfacial protector for the preparation of ordered mesoporous γ-alumina. It may be used as a model compound in understanding the adsorption of aromatic carboxylic acids on gold surfaces.

Pittogrammi

Corrosion

Avvertenze

Danger

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Eye Dam. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

334.4 °F

Punto d’infiammabilità (°C)

168 °C

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Modeling of photocatalytic mineralization of phthalic acid in TiO2 suspension using response surface methodology (RSM).
Abaamrane A, et al.
Desalination and Water Treatment, 53(1), 249-256 (2015)
Phthalic acid as a di-functional organocatalyst for the regioselective thiocyanation of aromatic compounds.
Sajjadifar S, et al.
Scientia Iranica. Transaction C, Chemistry, Chemical Engineering, 21(6), 2005-2005 (2014)
Shang-Jun Yin et al.
Enzyme research, 2011, 294724-294724 (2011-06-04)
Tyrosinase inhibition studies are needed due to the medicinal applications such as hyperpigmentation. For probing effective inhibitors of tyrosinase, a combination of computational prediction and enzymatic assay via kinetics was important. We predicted the 3D structure of tyrosinase, used a
A new synthetic procedure for ordered mesoporous γ-alumina using phthalic acid as an interfacial protector.
Huang F, et al.
Materials Letters, 65(2), 244-246 (2011)
Du Yeon Bang et al.
Toxicological research, 27(4), 191-203 (2011-12-01)
There has been growing concern about the toxicity of phthalate esters. Phthalate esters are being used widely for the production of perfume, nail varnish, hairsprays and other personal/cosmetic uses. Recently, exposure to phthalates has been assessed by analyzing urine for

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