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Molecule
ID:90303
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₈O₃
Molecular Mass
152.14732
Exact Mass
152.04734412
Charge
0
InChI
InChI=1S/C8H8O3/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChIKey
XQXPVVBIMDBYFF-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cc1ccc(cc1)O
Isomeric Smiles
OC(=O)Cc1ccc(cc1)O
Calculated Properties
JChem
LogD (pH = 7.4)
-1.86
LogD (pH = 5.5)
-0.20
Log P
1.31
Rotatable Bonds
2
H Donor
2
H Acceptors
3
Lipinski's Rule of Five
true
Acid pKa
4.00
Polar Surface Area
57.53
Polarizability
14.78
Molar Refractivity
39.35
LOG S
-0.65
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
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC name
•
Synonyms
•
IUPAC Traditional name
Registration numbers
Properties
•
Physical Property
•
Safety Information
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Product Information
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5988
MP Biomedicals
02151303
05208583
InterBioScreen
BB_NC-2267
STOCK1N-74030
Sigma Aldrich
H50004
56140
TRC
H949060
Chemik
CHB15312
Enamine
EN300-18714
Alfa Aesar
A15018
BioBioPha
BBP02607
A&J Pharmtech
AJA-O1552
Academic Data
Wikipedia
4-Hydroxyphenylacetic_acid
PubChem
127
ChEBI
CHEBI:18101
Names and Identifiers
IUPAC name
2-(4-hydroxyphenyl)acetic acid
Synonyms
4-(Carboxymethyl)phenol
4-Hydroxyphenylacetic acid 98%
4-Hydroxyphenylacetic acid
p-HYDROXYPHENYLACETIC ACID
2-(4-hydroxyphenyl)acetic acid
p-Hydroxyphenylacetic acid
4-Hydroxyphenylacetic acid
4-Hydroxyphenylacetic acid
对羟基苯乙酸
(4-hydroxyphenyl)acetic acid
p-Hydroxybenzeneacetic Acid
(p-Hydroxyphenyl)acetic Acid
4-Hydroxybenzeneacetic Acid
2-[4-(Hydroxy)phenyl]acetic Acid
(4-Hydroxyphenyl)acetic Acid
4-羟基苯乙酸
4-Hydroxyphenylacetic acid
4-carboxymethylphenol
4-Hydroxyphenylacetate
4-hydroxybenzeneacetic acid
4-hydroxyphenylacetic acid
(p-hydroxyphenyl)acetic acid
p-hydroxyphenylacetic acid
IUPAC Traditional name
4-hydroxyphenylacetic acid
Registration numbers
MDL Number
MFCD00004347
CAS Number
156-38-7
EC Number
205-851-3
PubChem SID
24895664
24879945
162077124
8143891
Beilstein Number
1448766
CHEMBL
1772
CHEMBL1772
CHEBI ID
18101
CHEBI:40091
CHEBI:1874
CHEBI:18101
CHEBI:20419
CHEBI:12014
Chemspider ID
124
Wikipedia Title
4-Hydroxyphenylacetic_acid
4-hydroxyphenylacetic_acid
PubChem CID
127
BRENDA Database
1.4.3.3
1.14.16.1
4.2.1.1
1.13.11.15
1.2.1.39
1.14.13.18
1.14.14.9
2.6.1.24
1.13.11.3
1.14.13.63
1.4.3.4
7.6.2.1
6.2.1.30
1.5.1.34
1.13.11.27
1.14.13.39
3.1.1.73
1.13.11.80
1.2.1.3
1.2.1.53
1.13.11.5
1.14.99.15
1.3.1.43
4.1.1.119
4.1.1.83
6.2.1.B11
1.2.3.13
1.14.18.1
3.1.2.B5
1.14.13.5
3.5.1.11
3.1.2.20
1.10.3.2
1.14.13.2
2.6.1.5
1.14.14.8
3.5.5.1
3.5.5.5
2.7.11.4
1.14.12.9
BRENDA Ligand Database
1708
15421
45931
48087
3471
198050
8425
10446
5492
175167
49766
15905
47301
MetaboLights Database
MTBLS615
MTBLS726
MTBLS751
MTBLS873
MTBLS763
MTBLS407
MTBLS2224
MTBLS673
MTBLS1326
MTBLS4099
MTBLS205
MTBLS345
MTBLS804
MTBLS136
MTBLS296
MTBLS404
MTBLS675
MTBLS2550
MTBLS1196
MTBLS220
MTBLS2633
MTBLS670
MTBLS2017
MTBLS545
MTBLS71
MTBLS926
MTBLS2384
MTBLS198
MTBLS1437
MTBLS440
MTBLS627
MTBLS2406
MTBLS138
MTBLS20
MTBLS2267
MTBLS4012
MTBLS413
MTBLS1866
MTBLS2615
MTBLS312
MTBLS697
MTBLS204
MTBLS530
MTBLS135
MTBLS612
MTBLS1677
MTBLS560
MTBLS841
MTBLS2096
MTBLS3750
MTBLS309
MTBLS179
MTBLS1918
MTBLS4820
MTBLS1906
MTBLS580
MTBLS3540
MTBLS406
BKMS React Database
175167
15421
3471
47301
48087
5492
198050
1708
49766
10446
8425
45931
15905
Golm Database
f8e6f6c2-fd53-4e52-8439-239bfc5436d1
71e23b2f-c005-4521-b94c-6cc0c3b348ea
810bec85-b379-4779-8563-ac8262ee9167
626fec26-5afb-4029-938b-086425fac54d
NMRShiftDB Database
20040753
UniProt Database
P42270
A8A876
B4T2T9
C9YHW1
Q18CP4
B2TZN1
B5R6F7
A9N6T0
C9YHW3
B4TSL7
Q8ZQ47
A4IT51
Q83P19
P42269
Q84F15
Q6Q271
Q18CP3
C9YHW2
Q05354
Q47098
B5R043
Q38HX2
Q5PG96
B6I2N1
Q84F14
B5FR34
Q8Z7P9
Q38HX3
Q31SY8
Q48441
A9MH59
B5Y2D2
P76149
A6THU5
Q05353
Q6Q272
Q5SJP8
Q8ZQ51
Q4L1M7
Q46978
C9XIS6
B5F1Y9
Q48440
Q38HX4
Q9RPV0
Q18CP5
Q5SJP7
B5BBH8
Q57501
Q8Z7Q5
C0SPC0
C0Q8A0
Q078T0
B4TEM9
C9XIS5
P37352
Q9RPU5
B1IS70
C9XIS7
Q57160
Q57QP9
Q84F16
P81594
Q9RPU2
Q3YU43
PubMed Citation Links
11339992
977696
24636068
24831010
22296160
7126379
21476434
Protein Data Bank
2jbt
6wh8
2yym
7e0x
3pcg
2yaj
1ai6
2yyj
5aip
7e7l
7nqg
Patent number
US2007178123
WO2006020234
EP1876169
SABIO-RK Database
8613
9071
12803
11663
BindingDB Database
50339586
UM-BBD compID
c0271
ACToR Database
156-38-7
Reaxys Registry
1448766
CompTox Database
DTXSID5059745
KEGG ID
C00642
SureChEMBL Database
SCHEMBL75700
HMDB Database
HMDB0000020
MetaCyc Database
4-HYDROXYPHENYLACETATE
PDBeChem Database
4HP
Related Proteins
PDB Bank
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2JBT
Loading...
6WH8
Loading...
2YYM
Loading...
7E0X
Loading...
3PCG
Loading...
2YAJ
1AI6
2YYJ
5AIP
7E7L
7NQG
Molecule Details
MP Biomedicals
02151303
Crystalline
Purity: 99+%
For fluorometric determination of oxidative enzymes.
05208583
MP Biomedicals Rare Chemical collection
Wikipedia
4-Hydroxyphenylacetic_acid
Sigma Aldrich
H50004
Packaging
25, 100 g in poly bottle
5 g in glass bottle
Application
Reagent used in the acylation of phenols1 and amines.2
TRC
H949060
A compound present in olive oil. An important fine chemical intermediate with broad prospects for application development.
ChEBI
CHEBI:18101
A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is substituted by a 4-hydroxyphenyl group.
References
PubChem Literature
From Data Sources
•
Papadopoulos, G., et al.: J Am Oil Chem Soc, 68, 669 (2010)
•
Shu, Y., et al.: Guangdong Huagong, 37, 108 (2010)
Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
CAS Number
•
EC Number
•
PubChem SID
•
Beilstein Number
•
CHEMBL
•
CHEBI ID
•
Chemspider ID
•
Wikipedia Title
•
PubChem CID
•
BRENDA Database
•
BRENDA Ligand Database
•
MetaboLights Database
•
BKMS React Database
•
Golm Database
•
NMRShiftDB Database
•
UniProt Database
•
PubMed Citation Links
•
Protein Data Bank
•
Patent number
•
SABIO-RK Database
•
BindingDB Database
•
UM-BBD compID
•
ACToR Database
•
Reaxys Registry
•
CompTox Database
•
KEGG ID
•
SureChEMBL Database
•
HMDB Database
•
MetaCyc Database
•
PDBeChem Database
Molecule Details
•
MP Biomedicals
•
Wikipedia
•
Sigma Aldrich
•
TRC
•
ChEBI
Properties
Physical Property
Melting Point
149-151°C
Source
148-151°C
Source
148-151 °C(lit.)
Source
148-151 °C
Source
149 - 151°C
Source
148-150°C
Source
Hydrophobicity(logP)
0.747
Source
Apperance
Powder
Source
Safety Information
Storage Warning
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
AI2680000
Source
Room Temperature (15-30°C)
Source
3
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
26
-
36
Source
26
-
37
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
H315
-
H319
-
H335
Source
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Irritant (Xi)
Warning
Source
36/37/38
Source
是
Source
Product Information
Certificate of Analysis
Download link
Source
Download link
Source
Download link
Source
Purity
≥99%
Source
98%
Source
≥98.0% (T)
Source
95%
Source
99%
Source
HOC6H4CH2CO2H
Source
for fluorescence
Source
purum
Source
Genuine Natural Compounds
Source
Source
Source
RTECS
Storage Condition
German water hazard class
GHS Pictograms
Safety Statements
Personal Protective Equipment
GHS Hazard statements
GHS Precautionary statements
European Hazard Symbols
GHS Signal Word
Risk Statements
TSCA Listed
Linear Formula
Grade
Classification