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Key Documents

402915

Sigma-Aldrich

Phthalic acid

ACS reagent, ≥99.5%

Sinônimo(s):

1,2-Benzenedicarboxylic acid

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About This Item

Fórmula linear:
C6H4-1,2-(CO2H)2
Número CAS:
Peso molecular:
166.13
Beilstein:
608199
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.21

grau

ACS reagent

Nível de qualidade

Ensaio

≥99.5%

forma

powder or crystals

Impurezas

≤0.05% insolubles
≤0.5% water

resíduo de ignição

≤0.02%

pf

210-211 °C (dec.) (lit.)

traços de ânion

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

traços de cátion

Fe: ≤0.001%
heavy metals: ≤0.001%

cadeia de caracteres SMILES

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)

chave InChI

XNGIFLGASWRNHJ-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Eye Dam. 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

334.4 °F

Ponto de fulgor (°C)

168 °C

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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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)
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)
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)
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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