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Merck
CN

T57630

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900312
EC Number:
203-998-8
Beilstein/REAXYS Number:
1739991
MDL number:
MFCD00004756

Key Documents

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Product Name

1-Tridecanol, 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.)

mp

29-34 °C (lit.)

density

0.822 g/mL at 25 °C (lit.)

Quality Level

200

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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

signalword

Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2384
BCCM8185
BCCL6400
BCCL9844
BCCM5094

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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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