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Molecule
ID:70952
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₃₈H₃₂N₂
Molecular Mass
516.67408
Exact Mass
516.25654903
Charge
0
InChI
InChI=1S/C38H32N2/c1-29-11-9-17-37(27-29)39(33-13-5-3-6-14-33)35-23-19-31(20-24-35)32-21-25-36(26-22-32)40(34-15-7-4-8-16-34)38-18-10-12-30(2)28-38/h3-28H,1-2H3
InChIKey
OGGKVJMNFFSDEV-UHFFFAOYSA-N
Canonic Smiles
Cc1cccc(c1)N(c1ccccc1)c1ccc(cc1)c1ccc(cc1)N(c1cccc(c1)C)c1ccccc1
Isomeric Smiles
N(c1ccc(cc1)c1ccc(N(c2ccccc2)c2cc(ccc2)C)cc1)(c1ccccc1)c1cc(ccc1)C
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
11.290435
LogD (pH = 7.4)
11.290435
Log P
11.290435
Molar Refractivity
167.5976
Polarizability
65.76112
Polar Surface Area
6.48
Rotatable Bonds
7
Lipinski's Rule of Five
false
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
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
•
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
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
076526
Sigma Aldrich
443263
Bide Pharmatech
BD22028
Academic Data
PubChem
103315
Names and Identifiers
Synonyms
N,N'-Bis(3-methylphenyl)-N,N'-bis(phenyl)benzidine
TPD
N,N′-Bis(3-methylphenyl)-N,N′-diphenylbenzidine
N,N′-双(3-甲基苯基)-N,N′-二苯基-1,1′-联苯-4,4′-二胺
IUPAC name
N-(3-methylphenyl)-4-{4-[(3-methylphenyl)(phenyl)amino]phenyl}-N-phenylaniline
IUPAC Traditional name
N-(3-methylphenyl)-4-{4-[(3-methylphenyl)(phenyl)amino]phenyl}-N-phenylaniline
Registration numbers
CAS Number
65181-78-4
MDL Number
MFCD00144965
PubChem CID
103315
PubChem SID
162036660
24868055
EC Number
413-810-8
Molecule Details
Sigma Aldrich
443263
Application
Organic photoconductor. Hole transporter.
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem CID
•
PubChem SID
•
EC Number
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Source
European Hazard Symbols
Nature polluting (N)
Source
Personal Protective Equipment
Eyeshields, Gloves
Source
German water hazard class
2
Source
UN Number
3077
Source
GHS Hazard statements
H411
Source
Risk Statements
51/53
Source
GHS Precautionary statements
P273
Source
Hazard Class
9
Source
Packing Group
3
Source
RID/ADR
UN 3077 9/PG 3
Source
Safety Statements
61
Source
Product Information
Purity
95+%
Source
99%
Source
OLED Device Performance
ITO/2-TNATA/TPD/Alq3/Mg:Ag1• Color: green• Max. Luminance: 22200 Cd/m2• Turn-On Voltage: 5.5 V
Source
ITO/TPD/Alq3:DCM (10%)/Alq3/Mg:Ag2• Color: red• Max. Luminance: 150 Cd/m2
Source
ITO/m-MTDATA/TPD/TTPhPhB/Alq3/LiF/Al4• Color: blue• Max. Luminance: 2600 Cd/m2• Max. EQE: 1.5 %• Turn-On Voltage: 3.4 V
Source
ITO/TPD/Znq/Mg:In3• Color: yellow• Max. Luminance: 16200 Cd/m2
Source
[-C6H4-4-N(C6H4CH3)C6H5]2
Source
Physical Property
Melting Point
175-177 °C(lit.)
Source
Orbital energy
LUMO 2.3 eV
Source
HOMO 5.5 eV
Source
Linear Formula