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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)

Quality Level

200

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6400
BCCL9844
BCCM5094
BCCK9572
0000206338

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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)
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
Y Suezaki et al.
Biochimica et biophysica acta, 1066(2), 225-228 (1991-07-22)
Long-chain n-alcohols decrease the main phase-transition temperature of lipid vesicle membranes at low concentrations but increase it at high concentrations. The nonlinear phenomenon is unrelated to the interdigitation and is analyzed by assuming that alcohols form solid solutions with solid
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