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Molecule
ID:2465
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆O₄
Molecular Mass
166.13084
Exact Mass
166.02660867
Charge
0
InChI
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
Canonic Smiles
OC(=O)c1ccccc1C(=O)O
Isomeric Smiles
OC(=O)c1ccccc1C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-4.10
LogD (pH = 5.5)
-1.53
Log P
1.29
Rotatable Bonds
2
H Donor
2
H Acceptors
4
Lipinski's Rule of Five
true
Acid pKa
2.94
Polar Surface Area
74.60
Polarizability
14.95
Molar Refractivity
40.57
LOG S
-1.61
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
•
Commercial Catalog
Names and Identifiers
•
IUPAC Traditional name
•
Synonyms
•
IUPAC name
Registration numbers
Properties
•
Physical Property
•
Product Information
•
Safety Information
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
DrugBank
DB02746
PubChem
1017
Wikipedia
Phthalic_acid
ChEBI
CHEBI:29069
Commercial Catalog
MP Biomedicals
02156246
02194877
05218496
Sigma Aldrich
80011
04924
P39303
402915
80010
442758
24-2890
24-2885
P8657
TRC
P384480
Bide Pharmatech
BD147920
Alfa Aesar
A14450
41770
Names and Identifiers
IUPAC Traditional name
phthalic acid
Synonyms
Phthalic Acid
PHTHALIC ACID ACS REAGENT GRADE
Potassium Biphthalate
Potassium Hydrogen Phthalate
PHTHALIC ACID MONOPOTASSIUM SALT
Terephthalic acid
Phthalic acid
Phthalate standard for IC
邻苯二甲酸
1,2-苯二甲酸
邻苯二甲酸
邻苯二甲酸标准溶液,用于离子色谱
p-PHTHALIC ACID
phthalic acid
1,2-Benzenedicarboxylic acid
ortho-phthalic acid
benzene-1,2-dioic acid
邻苯二甲酸, ACS
Benzene-1,2-dicarboxylic acid
Phthalic acid, ACS
o-Benzenedicarboxylic Acid
Sunftal 20
o-Dicarboxybenzene
NSC 5348
o-Carboxybenzoic Acid
M 2
PHTHALIC ACID
phthalic acid
1,2-Benzenedicarboxylic acid
Phthalic acid
o-benzenedicarboxylic acid
ortho-phthalic acid
IUPAC name
benzene-1,2-dicarboxylic acid
Registration numbers
PubChem SID
24887512
160965915
46506083
24898471
24865138
24868005
24845783
8145473
CAS Number
88-99-3
100-21-0
877-24-7
EC Number
201-873-2
231-791-2
271-676-4
202-830-0
212-889-4
MDL Number
MFCD00002467
Beilstein Number
608199
PubChem CID
1017
Merck Index
147371
Wikipedia Title
Phthalic_acid
PubMed Citation Links
10682108
16804812
15016950
9838120
BRENDA Database
1.1.99.20
1.2.1.24
1.2.1.3
1.2.1.65
1.14.12.7
4.1.1.2
4.1.1.33
1.11.1.19
3.5.1.79
1.2.1.78
6.3.5.4
7.6.2.10
1.2.3.1
4.1.1.55
4.1.1.7
3.1.1.3
3.1.1.1
2.4.2.30
4.2.1.3
3.4.15.1
5.1.1.4
1.2.3.9
2.4.2.19
MetaboLights Database
MTBLS1196
MTBLS49
MTBLS883
MTBLS804
MTBLS2291
MTBLS1040
MTBLS1191
MTBLS392
MTBLS630
MTBLS2096
MTBLS615
MTBLS4365
MTBLS3540
MTBLS212
MTBLS601
MTBLS2871
MTBLS413
MTBLS662
MTBLS872
MTBLS2349
MTBLS1302
MTBLS2224
MTBLS706
MTBLS4366
MTBLS871
MTBLS1140
MTBLS3657
MTBLS4012
MTBLS606
MTBLS2406
Patent number
EP1588707
EP1844784
EP1867318
US2005070597
US2005026981
WO2007105229
EP0897905
EP1604646
EP1857097
US2003129714
WO2007134055
EP0822189
US2007264265
US2005054632
EP1327630
EP1647543
US2004124397
US2004192623
EP0962438
EP1757583
US2007258915
WO2008135762
EP1757284
US2006058381
EP1803758
US2006135794
US2007178159
EP0998944
EP1816116
US2006111357
US2007218091
US2007269396
WO2005092392
WO2007089103
EP0962459
US2007270496
US2003069135
US2007054960
US2007244161
EP1982689
US2001021721
US2007190010
EP0850934
EP0870752
EP1149836
EP1506786
US2006035967
US2007270487
GB2081095
US2004235961
EP0842936
EP1375468
EP1637547
EP1586569
EP1602654
US2007237810
WO2006013399
EP1918293
EP0827954
US2005019280
US2005165093
UniProt Database
P70786
Q05181
Q05183
Q46916
P33164
Q44470
P0AA76
Q44257
P42205
P0C2Y0
P0AA78
Q05184
Q8VCT4
P39398
Q79EM7
P84812
Q9AQI0
P76470
Q59727
P0AA77
Q05182
P0AA80
Q05185
P42237
P0AA81
O34456
P0AA79
P37489
NMRShiftDB Database
10021260
Protein Data Bank
3c2r
3c2v
6g74
2b7p
4r51
5ph8
7v25
4kww
1qpr
CHEBI ID
CHEBI:14832
CHEBI:29069
CHEBI:8174
CHEBI:26093
CHEBI:44902
ACToR Database
29010-86-4
88-99-3
4401-64-3
KEGG ID
C01606
BRENDA Ligand Database
108066
75896
153680
SABIO-RK Database
14371
1863
3155
DrugBank ID
DB02746
BKMS React Database
75896
108066
153680
CompTox Database
DTXSID8021484
Gmelin ID
27343
PDBeChem Database
PHT
BindingDB Database
50080272
SureChEMBL Database
SCHEMBL1808
Reaxys Registry
608199
CHEMBL
CHEMBL1045
Related Proteins
PDB Bank
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3C2R
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3C2V
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6G74
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2B7P
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4R51
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5PH8
7V25
4KWW
1QPR
Molecule Details
DrugBank
DB02746
Drug Groups
experimental
External Links
•
[Wikipedia]
MP Biomedicals
02156246
Monopotassium Salt
(Potassium hydrogen phthalate)
Purity: >99%
Crystalline
02194877
ACS Reagent Grade
Purity: >99.5%
05218496
MP Biomedicals Rare Chemical collection
Wikipedia
Phthalic_acid
Sigma Aldrich
04924
General description
filtered through a 0.45 μm membrane filter
Preparation Note
prepared with phthalic acid and H2O
P39303
Packaging
1 kg in poly bottle
100 g in poly bottle
402915
Packaging
1 kg in poly bottle
25, 250 g in poly bottle
TRC
P384480
Organic reagent used to synthesize phthalates.
ChEBI
CHEBI:29069
A benzenedicarboxylic acid cosisting of two carboxy groups at ortho positions.
References
PubChem Literature
From Data Sources
•
Lopez, Z., et al.: App. Microbiol. Biotechnol., 78, 739 (2008)
•
Duchowicz, P.R., et al.: Bioorg. Med. Chem., 16, 7944 (2008)
•
Hong, Y., et al.: Toxicol. Lett., 184, 139 (2008)
•
di Luccio, E., et al.: Biochem., 47, 4039 (2008)
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
CAS Number
•
EC Number
•
MDL Number
•
Beilstein Number
•
PubChem CID
•
Merck Index
•
Wikipedia Title
•
PubMed Citation Links
•
BRENDA Database
•
MetaboLights Database
•
Patent number
•
UniProt Database
•
NMRShiftDB Database
•
Protein Data Bank
•
CHEBI ID
•
ACToR Database
•
KEGG ID
•
BRENDA Ligand Database
•
SABIO-RK Database
•
DrugBank ID
•
BKMS React Database
•
CompTox Database
•
Gmelin ID
•
PDBeChem Database
•
BindingDB Database
•
SureChEMBL Database
•
Reaxys Registry
•
CHEMBL
Molecule Details
•
DrugBank
•
MP Biomedicals
•
Wikipedia
•
Sigma Aldrich
•
TRC
•
ChEBI
Properties
Physical Property
Hydrophobicity(logP)
0.73 [HANSCH,C ET AL. (1995)]
Source
Solubility
7.01 mg/mL at 25 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
Source
0.6 g / 100 mL in water
Source
methanol: soluble0.1 g/mL, clear
Source
DMSO
Source
Ethanol
Source
Methanol
Source
Soluble in water, alcohol and ether
Source
Melting Point
295-300°C
Source
211 °C (412 °F) decomposes; 191 °C (376 °F)
Source
211°C
Source
191-230 °C
Source
210-211 °C (dec.)(lit.)
Source
204-206°C
Source
205°C dec.
Source
Density
1.59 (water = 1)
Source
1.593 g/cm
3
, solid
Source
1.593
Source
Boiling Point
289 °C (552 °F); decomposes
Source
289°C
Source
Vapor Density
5.73 (air = 1)
Source
p𝘒ₐ
2.98, 5.28
Source
Apperance
white solid
Source
White Solid
Source
Powder
Source
Flash Point
168°C(334°F)
Source
Product Information
Certificate of Analysis
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Purity
>99%
Source
≥99.5%
Source
~99%
Source
≥99.0% (T)
Source
98%
Source
≥99.5%
Source
≥99.5% (T)
Source
≥99.0%
Source
95+%
Source
99%
Source
99.5+%
Source
REAGENT
Source
ACS
Source
purum
Source
analytical standard
Source
reagent grade
Source
ACS reagent
Source
puriss. p.a.
Source
SAJ first grade
Source
SAJ special grade
C6H4-1,2-(CO2H)2
Source
1.000 g/L in H2O
Source
(limited shelf life, expiry date on the label)
Source
Fe: ≤0.001%
Source
heavy metals: ≤0.001%
Source
Cr: ≤5 mg/kg
Source
Ca: ≤10 mg/kg
Source
Ni: ≤5 mg/kg
Source
Zn: ≤5 mg/kg
Source
Cu: ≤5 mg/kg
Source
Fe: ≤5 mg/kg
Source
Co: ≤5 mg/kg
≤0.05% insolubles
Source
≤0.5% water
Source
sulfate (SO42-): ≤0.005%
Source
chloride (Cl-): ≤0.001%
Source
nitrate (NO3-): ≤0.005%
Source
chloride (Cl-): ≤50 mg/kg
Source
sulfate (SO42-): ≤50 mg/kg
Source
≤0.02%
Source
≤0.02% (as SO4)
Source
ampule of 1000 mg
Source
Safety Information
Storage Condition
Room Temperature (15-30°C)
Source
Refrigerator
Source
RTECS
CZ4326000
Source
TH9625000
Source
WZ0875000
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
0
2
0
Warning
Source
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
dust mask type N95 (US), Eyeshields, Gloves
Source
Eyeshields, Gloves
Source
26
Source
26
-
37
Source
H315
-
H319
-
H335
Source
H315
-
H319
-
H335
-
H303
Source
36/37/38
Source
Irritant (Xi)
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
3
Source
Hygroscopic
Source
是
Source
Source
Source
Mn: ≤5 mg/kg
Source
Na: ≤50 mg/kg
Source
Pb: ≤5 mg/kg
Source
Mg: ≤5 mg/kg
Source
Cd: ≤5 mg/kg
Source
K: ≤50 mg/kg
Source
Source
Source
Source
Grade
Linear Formula
Concentration
Shelf Life
Cation Traces
Impurities
Antion Traces
Ignition Residue
Packaging
NFPA704
GHS Signal Word
GHS Pictograms
Personal Protective Equipment
Safety Statements
GHS Hazard statements
Risk Statements
European Hazard Symbols
GHS Precautionary statements
German water hazard class
Storage Warning
TSCA Listed