80011
Phthalic acid
purum, ≥99.0% (T)
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
EC Number:
201-873-2
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
608199
grade
purum
assay
≥99.0% (T)
mp
210-211 °C (dec.) (lit.)
solubility
methanol: 0.1 g/mL, clear, water: soluble (hot)(lit.)
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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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
334.4 °F
flash_point_c
168 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
Russ Hauser
Seminars in reproductive medicine, 24(3), 156-167 (2006-06-29)
Scientific and public concern about the potential risk of environmental chemicals to male reproductive health has been heightened by reports of downward trends in semen quality, as well as increased rates of developmental urogenital tract anomalies and testicular cancer. Of
Paula J Lapinskas et al.
Toxicology, 207(1), 149-163 (2004-12-14)
Phthalate esters belong to a large class of compounds known as peroxisome proliferators (PP). PP include chemicals that activate different subtypes of the peroxisome proliferator-activated receptor (PPAR) family. The ability of phthalate esters and their metabolites to activate responses through
Christopher H Hurst et al.
Toxicological sciences : an official journal of the Society of Toxicology, 74(2), 297-308 (2003-06-14)
Phthalate esters are widely used as plasticizers in the manufacture of products made of polyvinyl chloride. Mono-(2-ethylhexyl)-phthalate (MEHP) induces rodent hepatocarcinogenesis by a mechanism that involves activation of the nuclear transcription factor peroxisome proliferator-activated receptor-alpha (PPARalpha). MEHP also activates PPAR-gamma
Eagleson M.
Concise Encyclopedia Chemistry, 832-832 (1994)
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