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Molecule
ID:9963
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₂O₂
Molecular Mass
164.20108
Exact Mass
164.08372962
Charge
0
InChI
InChI=1S/C10H12O2/c1-8-3-2-4-9(7-8)5-6-10(11)12/h2-4,7H,5-6H2,1H3,(H,11,12)
InChIKey
VWXVTHDQAOAENP-UHFFFAOYSA-N
Canonic Smiles
OC(=O)CCc1cccc(c1)C
Isomeric Smiles
C(CC(=O)O)c1cc(ccc1)C
Calculated Properties
JChem
Acid pKa
4.8487053
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
1.8307647
LogD (pH = 7.4)
0.059893917
Log P
2.5689843
Molar Refractivity
47.0078
Polarizability
18.12346
Polar Surface Area
37.3
Rotatable Bonds
3
Lipinski's Rule of Five
true
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
No Data Available
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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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JChem
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Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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MDL Number
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CAS Number
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PubChem SID
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PubChem CID
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
138042
Commercial Catalog
Matrix Scientific
006649
Sigma Aldrich
656178
Enamine
EN300-24264
Alfa Aesar
H34395
A&J Pharmtech
AJA-O38798
Names and Identifiers
Synonyms
3-(3-Methylphenyl)propionic acid
3-(3-Methylphenyl)propionic acid
3-Methylhydrocinnamic acid
3-(3-甲基苯基)丙酸
3-甲基氢化肉桂酸
3-(3-methylphenyl)propanoic acid
3-(m-Tolyl)propionic acid
3-(3-甲苯基)丙酸
IUPAC name
3-(3-methylphenyl)propanoic acid
IUPAC Traditional name
3-(3-methylphenyl)propanoic acid
Registration numbers
MDL Number
MFCD00060326
CAS Number
3751-48-2
PubChem SID
24883708
160973270
PubChem CID
138042
Molecule Details
Sigma Aldrich
656178
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
41-44°C
Source
39-42 °C(lit.)
Source
43 - 45°C
Source
42-44°C
Source
Flash Point
>230 °F
Source
>110 °C
Source
Hydrophobicity(logP)
2.402
Source
Safety Information
Download link
Source
Download link
Source
IRRITANT
Source
false
Source
否
Source
Product Information
98%
Source
97%
Source
95%
Source
96%
Source
H3CC6H4CH2CH2CO2H
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
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
European Hazard Symbols
Harmful (Xn)
Source
Irritant (Xi)
GHS Signal Word
Danger
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Safety Statements
26
-
36/37/39
Source
26
-
37
Source
German water hazard class
2
Source
GHS Hazard statements
H302
-
H318
Source
H315
-
H319
-
H335
Source
Risk Statements
22
-
41
Source
36/37/38
Source
MSDS Link
Storage Warning
TSCA Listed
GHS Pictograms
Purity
Linear Formula
Source
Source