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T57630

Sigma-Aldrich

1-Tridecanol

97%

Synonym(s):

Tridecyl alcohol

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About This Item

Linear Formula:
CH3(CH2)12OH
CAS Number:
112-70-9
Molecular Weight:
200.36
Beilstein:
1739991
EC Number:
203-998-8
MDL number:
MFCD00004756
UNSPSC Code:
12352100
PubChem Substance ID:
24900312
NACRES:
NA.22

vapor density

6.9 (vs air)

Assay

97%

bp

155-156 °C/15 mmHg (lit.)

mp

29-34 °C (lit.)

density

0.822 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCO

InChI

1S/C13H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h14H,2-13H2,1H3

InChI key

XFRVVPUIAFSTFO-UHFFFAOYSA-N

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Application

1-Tridecanol is a primary alcohol which can undergo oxidative conversion to:
  • 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.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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)
Facile oxidative conversion of alcohols to esters using molecular iodine.
Mori N and Togo H.
Tetrahedron, 61(24), 5915-5925 (2005)
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
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