P39303
Phthalic acid
reagent grade, 98%
Synonym(s):
1,2-Benzenedicarboxylic acid
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About This Item
Linear Formula:
C6H4-1,2-(CO2H)2
CAS Number:
Molecular Weight:
166.13
Beilstein:
608199
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
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grade
reagent grade
Quality Level
Assay
98%
form
crystalline powder
powder
mp
210-211 °C (dec.) (lit.)
functional group
carboxylic acid
SMILES string
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)
InChI key
XNGIFLGASWRNHJ-UHFFFAOYSA-N
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General description
Phthalic acid (PA) is the final metabolite of phthalic acid esters (PAEs). Its interaction with well-ordered MgO(100) (magnesium oxide) thin films has been investigated. The efficiency of activated carbon suspended in aqueous medium for the adsorption of PA has been analyzed. The degradation of PA via oxidation by electro-Fenton (EF) and solar photoelectro-Fenton (SPEF) has been reported.
Application
Phthalic acid may be used as an additive to the mobile phase to enhance the detection sensitivity of amino acids (AAs) by hydrophilic interaction liquid chromatography (HILIC) coupled with electrospray ionization tandem mass spectrometry (ESI-MS/MS).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
334.4 °F
Flash Point(C)
168 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Mineralization of phthalic acid by solar photoelectro-Fenton with a stirred boron-doped diamond/air-diffusion tank reactor: Influence of Fe3+ and Cu2+ catalysts and identification of oxidation products.
Garcia-Segura S, et al.
Electrochimica Acta, 113, 609-619 (2013)
Adsorption/bioadsorption of phthalic acid, an organic micropollutant present in landfill leachates, on activated carbons.
Mendez-Diaz JD, et al.
Journal of Colloid and Interface Science, 369(1), 358-365 (2012)
Benzoic Acid and Phthalic Acid on Atomically Well-Defined MgO(100) Thin Films: Adsorption, Interface Reaction, and Thin Film Growth.
Xu T, et al.
The Journal of Physical Chemistry C, 119(48), 26968-26979 (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
Wanshu Qi et al.
Analytica chimica acta, 870, 75-82 (2015-03-31)
In this work, 0.08 mmol L(-1) of phthalic acid was introduced as a mobile phase additive to quantify free amino acids (AAs) by hydrophilic interaction liquid chromatography (HILIC) coupled with electrospray ionization tandem mass spectrometry (ESI-MS/MS). The addition of phthalic
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