T57630
1-Tridecanol
97%
Synonym(s):
Tridecyl alcohol
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About This Item
Linear Formula:
CH3(CH2)12OH
CAS Number:
Molecular Weight:
200.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-998-8
Beilstein/REAXYS Number:
1739991
MDL number:
Assay:
97%
InChI key
XFRVVPUIAFSTFO-UHFFFAOYSA-N
InChI
1S/C13H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h14H,2-13H2,1H3
SMILES string
CCCCCCCCCCCCCO
vapor density
6.9 (vs air)
assay
97%
bp
155-156 °C/15 mmHg (lit.)
Quality Level
mp
29-34 °C (lit.)
density
0.822 g/mL at 25 °C (lit.)
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Application
1-Tridecanol is a primary alcohol which can undergo oxidative conversion to:
It can also be used as a phase modifier for protonated trioctylamine in n-dodecane to study the speciation of vanadium (V) extracted from acidic sulfate media.
- 2,2,2-trifluoroethyl tridecanoate.
- Dodecanenitrile in the presence of molecular iodine in aq NH3.
It can also be used as a phase modifier for protonated trioctylamine in n-dodecane to study the speciation of vanadium (V) extracted from acidic sulfate media.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Speciation of vanadium (V) extracted from acidic sulfate media by trioctylamine in n-dodecane modified with 1-tridecanol.
Chagnes A, et al.
Hydrometallurgy, 104(1), 20-24 (2010)
Chemical degradation of trioctylamine and 1-tridecanol phase modifier in acidic sulfate media in the presence of vanadium (V).
Chagnes A, et al.
Hydrometallurgy, 105(3-4), 328-333 (2011)
Direct oxidative conversion of alcohols and amines to nitriles with molecular iodine and DIH in aq NH3.
Iida S and Togo H
Tetrahedron, 63(34), 8274-8281 (2007)
D A Haydon et al.
Biochimica et biophysica acta, 863(2), 337-340 (1986-12-16)
The effects of 0.09 saturated solutions of the n-alkanols n-hexanol to n-tridecanol on the surface (compensation) potential of lipid monolayers have been examined. Actions on monolayers spread from pure egg phosphatidylcholine have been compared with effects on a system containing
Facile oxidative conversion of alcohols to esters using molecular iodine.
Mori N and Togo H.
Tetrahedron, 61(24), 5915-5925 (2005)
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