79255
Phthalsäure
analytical standard
Synonym(e):
1,2-Benzoldicarbonsäure
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Alle Fotos(2)
About This Item
Lineare Formel:
C6H4-1,2-(CO2H)2
CAS-Nummer:
Molekulargewicht:
166.13
Beilstein:
608199
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
NACRES:
NA.24
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Qualität
analytical standard
Qualitätsniveau
Assay
≥99.5% (GC)
≥99.5% (T)
Haltbarkeit
limited shelf life, expiry date on the label
Methode(n)
HPLC: suitable
gas chromatography (GC): suitable
Verunreinigungen
≤0.5% water
mp (Schmelzpunkt)
210-211 °C (dec.) (lit.)
Anwendung(en)
cleaning products
cosmetics
food and beverages
personal care
Format
neat
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)
InChIKey
XNGIFLGASWRNHJ-UHFFFAOYSA-N
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Allgemeine Beschreibung
Phthalic acid is an organic acid and a major bioactive component, reportedly identified in the extracts of Solanum nigrum, Nigella sativa, Angelicae Radix and Ligustici Rhizoma, utilized as Chinese herbal medicines.
Anwendung
Phthalic acid may be used as an analytical reference standard for the quantification of the analyte in the following:
- Angelicae Radix and Ligustici Rhizoma using high performance liquid chromatography with photodiode array detection (HPLC-PDA) followed by liquid chromatography coupled to mass spectrometry (LC-MS) and capillary electrophoresis (CE) analyses.
- Nigella sativa and Solanum nigrum using gas chromatography-mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Signalwort
Danger
H-Sätze
P-Sätze
Gefahreneinstufungen
Eye Dam. 1
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 1
Flammpunkt (°F)
334.4 °F
Flammpunkt (°C)
168 °C
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Separation and identification of the organic acids in Angelicae Radix and Ligustici Rhizoma by HPLC and CE
Huang Y-W and Sheu J-S
Journal of Separation Science, 29(17), 2616-2624 (2006)
Characterization of alkaloid constitution and evaluation of antimicrobial activity of Solanum nigrum using gas chromatography mass spectrometry (GC-MS)
Jasim H, et al.
Journal of pharmacognosy and phytotherapy, 7(4), 56-72 (2015)
En-Cui Yang et al.
Dalton transactions (Cambridge, England : 2003), 44(7), 3190-3199 (2015-01-13)
Four new 4-amino-1,2,4-triazole (atr)-based coordination polymers, {[Cu2(atr)(H2O)(μ-OH)2(pa)]·H2O}n (), {[Cu3(atr)2(H2O)2(μ-OH)2(npa)2]·2H2O}n (), {[Cu3(atr)5(dca)(μ-OH)(ClO4)2](ClO4)2}n () and {[Cu3(atr)2(H2O)(μ3-OH)(μ-OH)2(spa)]·1.5H2O}n () (pa(2-) = phthalate, npa(2-) = 3-nitrophthalate, dca(-) = dicyanamide and spa(3-) = 4-sulfophthalate), were successfully obtained by varying the carboxylate- and cyanide-modified magnetic bridges. Structural
Xiao-Yan Zhang et al.
Applied and environmental microbiology, 80(22), 6870-6878 (2014-08-26)
EstS1, a newly identified thermostable esterase from Sulfobacillus acidophilus DSM10332, was heterologously expressed in Escherichia coli and shown to enzymatically degrade phthalate esters (PAEs) to their corresponding monoalkyl PAEs. The optimal pH and temperature of the esterase were found to
Wenli Liu et al.
Bulletin of environmental contamination and toxicology, 92(5), 621-624 (2014-02-19)
Effects of di-(2-ethylhexyl) phthalate and di-n-butyl phthalate on seed germination rate and antioxidant enzymes activities of mung bean (Phaseolus radiatus L.) were investigated. Results showed that under the treatment with 10 mg/kg of phthalate esters (PAEs), superoxide dismutase (SOD), peroxidase and
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