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Molecule
ID:103307
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₈O₄
Molecular Mass
180.15742
Exact Mass
180.04225874
Charge
0
InChI
InChI=1S/C9H8O4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)
InChIKey
ZHQLTKAVLJKSKR-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cc1ccccc1C(=O)O
Isomeric Smiles
OC(=O)Cc1ccccc1C(=O)O
Calculated Properties
JChem
Acid pKa
3.4091654
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-2.203602
LogD (pH = 7.4)
-5.2597327
Log P
1.268577
Molar Refractivity
44.6218
Polarizability
16.924608
Polar Surface Area
74.6
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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IUPAC Traditional name
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IUPAC name
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Molecular Spectra
Molecule Details
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MP Biomedicals
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References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02151264
05207635
Sigma Aldrich
H16205
53580
Bide Pharmatech
BD11649
Alfa Aesar
A14297
Academic Data
PubChem
66643
Names and Identifiers
Synonyms
HOMOPHTHALIC ACID
α-Carboxy-o-toluic acid
2-Carboxyphenylacetic acid
邻羧基苯乙酸
α-Carboxy-o-toluic acid
α-羧基邻甲苯酸
Homophthalic acid
2-羧基苯乙酸
IUPAC Traditional name
benzeneacetic acid, 2-carboxy-
IUPAC name
2-(carboxymethyl)benzoic acid
Registration numbers
EC Number
201-913-9
CAS Number
89-51-0
Beilstein Number
1872069
PubChem SID
24895468
162090393
24878103
MDL Number
MFCD00004326
PubChem CID
66643
Molecule Details
MP Biomedicals
02151264
Crystalline
Purity: ~99%
Off-white to light green powder.
05207635
MP Biomedicals Rare Chemical collection
Sigma Aldrich
H16205
Other Notes
Remainder phthalic acid
Packaging
25, 100 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
Beilstein Number
•
PubChem SID
•
MDL Number
•
PubChem CID
Properties
Safety Information
RTECS
CY1575590
Source
Storage Condition
Room Temperature (15-30°C), Avoid excess heat
Source
MSDS Link
Download link
Source
Download link
Source
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Source
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Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
36/37/38
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
是
Source
Irritant (Xi)
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
26
-
37
Source
H315
-
H319
-
H335
Source
Product Information
Download link
Source
Download link
Source
~99%
Source
98%
Source
≥99.0% (HPLC)
Source
99%
Source
Physical Property
178-182 °C(lit.)
Source
180-182 °C
Source
ca 180°C dec.
Source
Source
Source
HO2CCH2C6H4CO2H
Source
purum
Source
≤0.1%
Source
Personal Protective Equipment
German water hazard class
Risk Statements
GHS Precautionary statements
TSCA Listed
European Hazard Symbols
GHS Pictograms
Safety Statements
GHS Hazard statements
Certificate of Analysis
Purity
Melting Point
Linear Formula
Grade
Ignition Residue