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Molecule
ID:25233
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₈N₂
Molecular Mass
190.28472
Exact Mass
190.14699859
Charge
0
InChI
InChI=1S/C12H18N2/c1-11-2-4-12(5-3-11)10-14-8-6-13-7-9-14/h2-5,13H,6-10H2,1H3
InChIKey
RNAXUUAJNMDESG-UHFFFAOYSA-N
Canonic Smiles
Cc1ccc(cc1)CN1CCNCC1
Isomeric Smiles
N1(Cc2ccc(cc2)C)CCNCC1
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-1.3725039
LogD (pH = 7.4)
-0.020557147
Log P
1.8921356
Molar Refractivity
60.3973
Polarizability
23.671999
Polar Surface Area
15.27
Rotatable Bonds
2
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
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
•
RDKit
•
JChem
Data Source
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Commercial Catalog
•
Academic Data
Names and Identifiers
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IUPAC Traditional name
•
IUPAC name
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Synonyms
Registration numbers
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MDL Number
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PubChem CID
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PubChem SID
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CAS Number
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
027768
Life Chemicals
F2169-0414
Sigma Aldrich
646172
Alfa Aesar
H55548
ChemBridge
3002628
Academic Data
PubChem
764723
Names and Identifiers
IUPAC Traditional name
1-[(4-methylphenyl)methyl]piperazine
IUPAC name
1-[(4-methylphenyl)methyl]piperazine
Synonyms
1-(4-Methylbenzyl)piperazine
1-(4-Methyl-benzyl)-piperazine
1-(4-Methylbenzyl)piperazine
1-(4-甲基苄基)哌嗪
Registration numbers
MDL Number
MFCD01075235
PubChem CID
764723
PubChem SID
160988540
24883438
CAS Number
23173-57-1
Molecule Details
Sigma Aldrich
646172
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
Danger
Source
26
-
39
Source
26
-
37/39
-
60
Source
H315
-
H318
-
H335
Source
H318
-
H315
-
H335
Source
P261
-
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
37/38
-
41
Source
2
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Irritant (Xi)
dust mask type N95 (US), Eyeshields, Gloves
Source
Product Information
95+%
Source
97%
Source
C12H18N2
Source
Physical Property
1.51
Source
204.8 °F
Source
96 °C
Source
96°C(205°F)
Source
37-41 °C(lit.)
Source
37-41°C
Source
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
Source
GHS Signal Word
Safety Statements
GHS Hazard statements
GHS Precautionary statements
Risk Statements
German water hazard class
GHS Pictograms
European Hazard Symbols
Personal Protective Equipment
Purity
Empirical Formula (Hill Notation)
Partition Coefficient
Flash Point
Melting Point