Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

T57630

Sigma-Aldrich

1-Tridecanol

97%

Synonym(s):

Tridecyl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Looking for similar products? Visit Product Comparison Guide

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

1-Octadecanol ReagentPlus®, 99%

Sigma-Aldrich

258768

1-Octadecanol

1-Bromotridecane 98%

Sigma-Aldrich

192422

1-Bromotridecane

2-Undecanol ≥98.0% (GC)

Sigma-Aldrich

94070

2-Undecanol

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)
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)
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service