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Molecule
ID:83005
Structure
Similarity
Functional Group
Text
General Information
Structure
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Molecular Formula
C₂₁H₂₁P
Molecular Mass
304.365201
Exact Mass
304.1380873
Charge
0
InChI
InChI=1S/C21H21P/c1-16-4-10-19(11-5-16)22(20-12-6-17(2)7-13-20)21-14-8-18(3)9-15-21/h4-15H,1-3H3
InChIKey
WXAZIUYTQHYBFW-UHFFFAOYSA-N
Canonic Smiles
Cc1ccc(cc1)P(c1ccc(cc1)C)c1ccc(cc1)C
Isomeric Smiles
P(c1ccc(cc1)C)(c1ccc(cc1)C)c1ccc(cc1)C
Calculated Properties
JChem
H Acceptors
0
H Donor
0
LogD (pH = 5.5)
6.5082
LogD (pH = 7.4)
6.5082
Log P
6.5082
Molar Refractivity
96.7465
Polarizability
37.638176
Polar Surface Area
0.0
Rotatable Bonds
3
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
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
Properties
•
Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR25774
MP Biomedicals
05223176
Sigma Aldrich
287830
93414
Bide Pharmatech
BD155761
Alfa Aesar
A14021
Academic Data
PubChem
13956
Names and Identifiers
IUPAC name
tris(4-methylphenyl)phosphane
IUPAC Traditional name
tris(4-methylphenyl)phosphane
Synonyms
PHOSPHORUS TRI-p-TOLYL
tris(4-methylphenyl)phosphine
Tri-p-tolylphosphine
三(对甲苯基)膦
TPTP
Tri(p-tolyl)phosphine
Tris(p-tolyl)phosphine
Tris(4-methylphenyl)phosphine
Registration numbers
MDL Number
MFCD00008542
PubChem SID
24857296
162070124
CAS Number
1038-95-5
EC Number
213-863-5
Beilstein Number
651045
PubChem CID
13956
Properties
Safety Information
RTECS
SZ3880000
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Safety Statements
S:
20
-
25
-
26
-
37/39
Source
26
-
36
Source
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
R:
36/37/38
Source
36/37/38
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Storage Warning
Air Sensitive
Source
TSCA Listed
是
Source
Product Information
Certificate of Analysis
Download link
Source
Linear Formula
(CH3C6H4)3P
Source
Purity
98%
Source
≥97.0% (GC)
Source
Grade
purum
Source
Physical Property
Melting Point
144-148 °C(lit.)
Source
144-148 °C
Source
144-146°C
Source
Molecule Details
MP Biomedicals
05223176
MP Biomedicals Rare Chemical collection
Sigma Aldrich
287830
Packaging
5 g in glass bottle
93414
Other Notes
Ligand used in organometallic chemistry1,2,3,4
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
•
MDL Number
•
PubChem SID
•
CAS Number
•
EC Number
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Beilstein Number
•
PubChem CID