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Molecule
ID:69784
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₃N
Molecular Mass
183.24902
Exact Mass
183.10479942
Charge
0
InChI
InChI=1S/C13H13N/c1-11-6-5-9-13(10-11)14-12-7-3-2-4-8-12/h2-10,14H,1H3
InChIKey
TWPMMLHBHPYSMT-UHFFFAOYSA-N
Canonic Smiles
Cc1cccc(c1)Nc1ccccc1
Isomeric Smiles
N(c1cc(ccc1)C)c1ccccc1
Calculated Properties
JChem
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
3.926582
LogD (pH = 7.4)
3.9265928
Log P
3.926593
Molar Refractivity
59.5854
Polarizability
22.904295
Polar Surface Area
12.03
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
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RDKit
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Synonyms
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IUPAC Traditional name
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IUPAC name
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Product Information
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Safety Information
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Physical Property
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
•
PubChem BioAssay
Data Source
Academic Data
PubChem
14569
Commercial Catalog
Sigma Aldrich
183512
Matrix Scientific
075291
Bide Pharmatech
BD14651
Alfa Aesar
B25441
Names and Identifiers
Synonyms
3-Methyldiphenylamine
3-Methyldiphenylamine
3-甲基二苯胺
N-Phenyl-m-toluidine
3-甲基二苯基胺
IUPAC Traditional name
3-methyl diphenyl amine
IUPAC name
3-methyl-N-phenylaniline
Registration numbers
PubChem CID
14569
PubChem SID
162035509
24851060
EC Number
214-885-8
CAS Number
1205-64-7
MDL Number
MFCD00008530
Molecule Details
Sigma Aldrich
183512
Packaging
10, 50 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem CID
•
PubChem SID
•
EC Number
•
CAS Number
•
MDL Number
Properties
Product Information
Purity
95+%
Source
98%
Source
99%
Source
Linear Formula
CH3C6H4NHC6H5
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
IRRITANT
Source
false
Source
是
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
Warning
Source
H315
-
H319
-
H335
Source
H302
-
H312
-
H315
-
H319
Source
36/37/38
Source
21/22
-
36/38
Source
3
Source
P261
-
P305+P351+P338
Source
P280H-
P305+P351+P338
Source
Irritant (Xi)
26
-
37/39
Source
26
-
36/37
Source
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Physical Property
235.4 °F
Source
113 °C
Source
147°C(297°F)
Source
1.066 g/mL at 25 °C(lit.)
Source
1.066
Source
315 °C/724 mmHg(lit.)
Source
317°C
Source
Source
Source
Harmful (X)
Source
Refractive Index
n20/D 1.635(lit.)
Source
1.6350
Source
Melting Point
25-27°C
Source
Storage Warning
TSCA Listed
GHS Pictograms
GHS Signal Word
GHS Hazard statements
Risk Statements
German water hazard class
GHS Precautionary statements
European Hazard Symbols
Safety Statements
Personal Protective Equipment
Flash Point
Density
Boiling Point