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Molecule
ID:74459
Structure
Similarity
Functional Group
Text
General Information
Structure
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Molecular Formula
C₂₄H₅₁N
Molecular Mass
353.66844
Exact Mass
353.40215064
Charge
0
InChI
InChI=1S/C24H51N/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3
InChIKey
XTAZYLNFDRKIHJ-UHFFFAOYSA-N
Canonic Smiles
CCCCCCCCN(CCCCCCCC)CCCCCCCC
Isomeric Smiles
N(CCCCCCCC)(CCCCCCCC)CCCCCCCC
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
6.00179
LogD (pH = 7.4)
6.336945
Log P
9.496691
Molar Refractivity
116.8209
Polarizability
46.588814
Polar Surface Area
3.24
Rotatable Bonds
21
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
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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MP Biomedicals
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References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02157109
05219007
Apollo Scientific
OR10063
Sigma Aldrich
T81000
92828
92830
30-4700
Alfa Aesar
A15067
Academic Data
PubChem
14227
Names and Identifiers
Synonyms
Tri-n-octylamine
TRICAPRYLYLAMINE PRACTICAL GRADE
Trioctylamine
TOA
三辛胺
三正辛胺
Tri-n-octylamine
IUPAC Traditional name
tri(N-octyl)amine
IUPAC name
trioctylamine
Registration numbers
EC Number
214-242-1
CAS Number
1116-76-3
PubChem SID
24889736
24900500
162039378
24889735
Beilstein Number
1210618
MDL Number
MFCD00009560
PubChem CID
14227
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Storage Condition
Room Temperature (15-30°C)
Source
RTECS
RG8225000
Source
GHS Signal Word
Warning
Source
German water hazard class
2
Source
Risk Statements
36/37/38
Source
36/38
-
51/53
Source
European Hazard Symbols
Irritant (Xi)
Source
Nature polluting (N)
Source
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Safety Statements
26
Source
26
-
37
-
61
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
H315
-
H319
-
H411
-
H401
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
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P280G-
P273
-
P305+P351+P338
Source
TSCA Listed
是
Source
Packing Group
III
Source
Hazard Class
9
Source
UN Number
UN3082
Source
Storage Warning
Air Sensitive
Source
Product Information
Purity
>90%
Source
98%
Source
≥99.0% (NT)
Source
≥98.0% (GC)
Source
≥99.0%
Source
95%
Source
Certificate of Analysis
Download link
Source
Download link
Source
Grade
PRACTICAL
Source
puriss.
Source
purum
Source
SAJ first grade
Source
Linear Formula
[CH3(CH2)7]3N
Source
Physical Property
Density
0.82 g/ml
Source
0.809 g/mL at 25 °C(lit.)
Source
0.810 g/mL at 20 °C
Source
0.810
Source
Boiling Point
365-367 °C(lit.)
Source
164-168 °C/0.7 mmHg(lit.)
Source
164-168°C/0.7mm
Source
Flash Point
163 °C
Source
325.4 °F
Source
158°C(316°F)
Source
Refractive Index
n20/D 1.449(lit.)
Source
n20/D 1.450
Source
n20/D 1.449
Source
1.4485
Source
Solubility
chloroform: soluble0.1 g/mL, clear, colorless
Source
Melting Point
-39°C
Source
Molecule Details
MP Biomedicals
02157109
Purity: >90%
1 ml = approx. 0.82 g
05219007
MP Biomedicals Rare Chemical collection
Sigma Aldrich
T81000
Application
Trioctylamine is used as an extractant for organic acids (such as TCA, succinic acid, and acetic acid), and precious metals.
Packaging
25, 100, 500 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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EC Number
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CAS Number
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PubChem SID
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Beilstein Number
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MDL Number
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PubChem CID