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Molecule
ID:69631
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/c1-11-7-4-2-3-6(5-9)8(7)10/h2-5,10H,1H3
InChIKey
JJVNINGBHGBWJH-UHFFFAOYSA-N
Canonic Smiles
COc1cccc(c1O)C=O
Isomeric Smiles
C(=O)c1c(O)c(ccc1)OC
Calculated Properties
JChem
LogD (pH = 7.4)
1.87
LogD (pH = 5.5)
1.87
Log P
1.87
Rotatable Bonds
2
H Donor
1
H Acceptors
3
Lipinski's Rule of Five
true
Acid pKa
9.54
Polar Surface Area
46.53
Polarizability
14.80
Molar Refractivity
41.09
LOG S
-0.95
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
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
Properties
Related Proteins
Molecular Spectra
Molecule Details
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02158286
05202206
InterBioScreen
BB_NC-0156
STOCK1N-72413
Sigma Aldrich
120804
94760
94762
Matrix Scientific
075125
TRC
V097400
Bide Pharmatech
BD75552
Alfa Aesar
A15672
Academic Data
Wikipedia
Ortho-Vanillin
PubChem
8991
ChEBI
CHEBI:78339
Names and Identifiers
IUPAC Traditional name
O-vanillin
IUPAC name
2-hydroxy-3-methoxybenzaldehyde
Synonyms
3-Methoxysalicylaldehyde
2-HYDROXY-3-METHOXYBENZALDEHYDE
o-VANILLIN
2-Hydroxy-3-methoxybenzaldehyde
o-Vanillin
3-Methoxysalicylaldehyde
3-甲氧基水杨醛
邻香草醛
2-Hydroxy-m-anisaldehyde
2-羟基-3-甲氧基苯甲醛
2-香草醛
o
-Vanillin
Ortho-Vanillin
NSC 2150
6-Formylguaiacol
6-Formyl-2-methoxyphenol
2-Vanillin
3-Methoxysalicyladehyde
2-Vanillin
o-Vanillin
NC 005
3-Methoxy-2-hydroxybenzaldehyde
2-Hydroxy-3-methoxybenzaldehyde
2-羟基-3-甲氧基苯甲醛
2-Vanillin
Oxy-2 methoxy-3 benzaldehyde
6-Formyl-2-methoxyphenol
6-Formylguaiacol
ortho-vanillin
3-methoxysalicylaldehyde
2-Hydroxy-m-anisaldehyde
Registration numbers
CAS Number
148-53-8
MDL Number
MFCD00003322
CHEMBL
13859
CHEMBL13859
Wikipedia Title
Ortho-Vanillin
Chemspider ID
21105848
EC Number
205-715-3
PubChem SID
24890054
162035357
24847429
24890053
223443696
Beilstein Number
471913
PubChem CID
8991
PubMed Citation Links
2671704
23625436
22904806
20292487
BRENDA Ligand Database
123549
152488
Reaxys Registry
471913
CHEBI ID
CHEBI:78339
SureChEMBL Database
SCHEMBL16004
NMRShiftDB Database
10008647
BRENDA Database
4.1.2.45
1.1.1.71
BKMS React Database
152488
123549
CompTox Database
DTXSID5022011
ACToR Database
148-53-8
BindingDB Database
111024
Molecule Details
MP Biomedicals
02158286
Crystalline
05202206
MP Biomedicals Rare Chemical collection
Wikipedia
Ortho-Vanillin
Sigma Aldrich
120804
Packaging
10, 100, 500 g in glass bottle
TRC
V097400
A positional isomer of Vanillin. o-Vanillin is a more potent antioxidant than Vanillin. Used in the synthesis of Veralipride (V122500).
ChEBI
CHEBI:78339
A member of the class of benzaldehydes that is salicylaldehyde substituted by a methoxy group at position 3.
References
PubChem Literature
From Data Sources
•
Tamai, K., et al.: Mutat. Res., 268, 231 (1988)
•
Davies, M., et al.: Biochem. J., 255, 513 (1988)
•
Wang, M., et al.: J. Agric. Food Chem., 47, 3974 (1988)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
CHEMBL
•
Wikipedia Title
•
Chemspider ID
•
EC Number
•
PubChem SID
•
Beilstein Number
•
PubChem CID
•
PubMed Citation Links
•
BRENDA Ligand Database
•
Reaxys Registry
•
CHEBI ID
•
SureChEMBL Database
•
NMRShiftDB Database
•
BRENDA Database
•
BKMS React Database
•
CompTox Database
•
ACToR Database
•
BindingDB Database
Molecule Details
•
MP Biomedicals
•
Wikipedia
•
Sigma Aldrich
•
TRC
•
ChEBI
Properties
•
Product Information
•
Safety Information
•
Physical Property
Properties
Product Information
Purity
95+%
Source
99%
Source
≥97.0% (HPLC)
Source
≥98.5% (HPLC)
Source
98%
Source
Certificate of Analysis
Download link
Source
Download link
Source
Download link
Source
CH3OC6H3-2-(OH)CHO
Source
purum
Source
puriss.
Source
Genuine Natural Compounds
Source
Safety Information
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Physical Property
265-266°C
Source
265°C
Source
265–266 °C (458–459 K)
Source
265-266 °C(lit.)
Source
265-266°C
Source
40-42°C
Source
40°C
Source
40–42 °C (313–315 K)
Source
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Air Sensitive
Source
TSCA Listed
false
Source
是
Source
Safety Statements
S:
20
-
25
-
26
-
37/39
Source
S26 36 37 39
Source
23
-
36
Source
26
-
36/37
Source
RTECS
CU6530000
Source
European Hazard Symbols
Irritant (Xi)
Source
Harmful (Xn)
Harmful (X)
Risk Statements
R:
36/37/38
Source
R20 21 22 36 37 38
Source
22
-
36/37/38
Source
Storage Condition
Room Temperature (15-30°C)
Source
Main Hazard
May cause irritation to skin,
eyes, and respiratory tract
Source
GHS Signal Word
Warning
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Hazard statements
H302
-
H315
-
H319
-
H335
Source
German water hazard class
3
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
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Source
40-42 °C(lit.)
Source
41-45 °C
Source
43-45 °C
Source
40-42°C
Source
Apperance
Yellow, fibrous solid
Source
Flash Point
>110 °C
Source
113 °C
Source
235.4 °F
Source
Linear Formula
Grade
Classification
MSDS Link
Boiling Point
Melting Point
Source
Source