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Molecule
ID:108233
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₈O₂
Molecular Mass
124.13722
Exact Mass
124.0524295
Charge
0
InChI
InChI=1S/C7H8O2/c8-5-6-2-1-3-7(9)4-6/h1-4,8-9H,5H2
InChIKey
OKVJCVWFVRATSG-UHFFFAOYSA-N
Canonic Smiles
OCc1cccc(c1)O
Isomeric Smiles
OCc1cccc(O)c1
Calculated Properties
JChem
LogD (pH = 7.4)
0.90
LogD (pH = 5.5)
0.90
Log P
0.90
Rotatable Bonds
1
H Donor
2
H Acceptors
2
Lipinski's Rule of Five
true
Acid pKa
9.38
Polar Surface Area
40.46
Polarizability
12.83
Molar Refractivity
34.85
LOG S
-0.48
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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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
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PDB Bank
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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ChEBI
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
05206599
Sigma Aldrich
H20601
54850
Chemik
CHB83121
Bide Pharmatech
BD34341
Alfa Aesar
A15981
Academic Data
PubChem
102
ChEBI
CHEBI:17069
Names and Identifiers
IUPAC name
3-(hydroxymethyl)phenol
Synonyms
M-HYDROXYBENZYL ALCOHOL
3-羟基苯甲醇
3-Hydroxybenzyl alcohol
3-Hydroxybenzyl alcohol
3-(Hydroxymethyl)phenol
3-hydroxybenzyl alcohol
3-Hydroxybenzenemethanol
3-hydroxybenzyl alcohol
3-Hydroxybenzyl alcohol
IUPAC Traditional name
3-hydroxybenzyl alcohol
Registration numbers
CAS Number
620-24-6
PubChem CID
102
PubChem SID
162093944
24895498
24879038
8144636
EC Number
210-633-6
Beilstein Number
2041500
MDL Number
MFCD00004643
Reaxys Registry
2041500
MetaboLights Database
MTBLS1903
MTBLS1861
MTBLS404
MTBLS4012
MTBLS20
MTBLS615
MTBLS2406
MTBLS3487
MTBLS601
NMRShiftDB Database
20035582
CHEBI ID
CHEBI:17069
CHEBI:1540
CHEBI:20066
CHEBI:11830
PubMed Citation Links
22770225
ACToR Database
620-24-6
BRENDA Database
1.1.1.97
1.1.3.7
3.5.1.58
2.3.1.196
1.1.1.91
1.14.18.1
1.1.1.90
1.1.1.184
SureChEMBL Database
SCHEMBL96097
KEGG ID
C03351
BRENDA Ligand Database
106491
IntEnz Database
EC 1.1.1.97
KNApSAcK Database
C00000776
Protein Data Bank
4msf
GeneOntology Database
GO:0018921
CompTox Database
DTXSID20211035
Rhea Database
RHEA:62212
RHEA:64832
RHEA:64828
RHEA:62208
RHEA:22340
BKMS React Database
106491
SABIO-RK Database
3857
CHEMBL
CHEMBL3337531
UM-BBD compID
c0054
Related Proteins
PDB Bank
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4MSF
Molecule Details
MP Biomedicals
05206599
MP Biomedicals Rare Chemical collection
Sigma Aldrich
H20601
Packaging
25, 100 g in poly bottle
5 g in glass bottle
ChEBI
CHEBI:17069
A hydroxybenzyl alcohol that is phenol substituted at position C-3 by a hydroxymethyl group.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
PubChem CID
•
PubChem SID
•
EC Number
•
Beilstein Number
•
MDL Number
•
Reaxys Registry
•
MetaboLights Database
•
NMRShiftDB Database
•
CHEBI ID
•
PubMed Citation Links
•
ACToR Database
•
BRENDA Database
•
SureChEMBL Database
•
KEGG ID
•
BRENDA Ligand Database
•
IntEnz Database
•
KNApSAcK Database
•
Protein Data Bank
•
GeneOntology Database
•
CompTox Database
•
Rhea Database
•
BKMS React Database
•
SABIO-RK Database
•
CHEMBL
•
UM-BBD compID
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Hazard statements
H315
-
H318
-
H335
Source
H315
-
H319
-
H335
Source
German water hazard class
3
Source
GHS Signal Word
Danger
Source
Risk Statements
36/37/38
-
41
Source
36/37/38
Source
GHS Pictograms
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
Safety Statements
26
-
36/39
Source
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
TSCA Listed
否
Source
RTECS
DA4796700
Source
Product Information
Certificate of Analysis
Download link
Source
Linear Formula
HOC6H4CH2OH
Source
Purity
99%
Source
≥98.0% (GC)
Source
98%
Source
Grade
purum
Source
Physical Property
Melting Point
69-72 °C(lit.)
Source
69-72 °C
Source
69-72°C
Source
Boiling Point
ca 300°C dec.
Source
Density
1.16
Source
Source