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T57401

Sigma-Aldrich

Tridecane

≥99%

Synonym(s):

Cactus Normal Paraffin N 13, Cetiol iSAN, Paraffin N 13, n-Tridecane

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About This Item

Linear Formula:
CH3(CH2)11CH3
CAS Number:
629-50-5
Molecular Weight:
184.36
Beilstein:
1733089
EC Number:
211-093-4
MDL number:
MFCD00008979
UNSPSC Code:
12352100
PubChem Substance ID:
24900311
NACRES:
NA.22
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vapor density

6.4 (vs air)

vapor pressure

1 mmHg ( 59.4 °C)

Assay

≥99%

refractive index

n20/D 1.425 (lit.)

bp

110-112 °C/12 mmHg (lit.)
234 °C (lit.)

mp

−6-−4 °C (lit.)

density

0.756 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCC

InChI

1S/C13H28/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3-13H2,1-2H3

InChI key

IIYFAKIEWZDVMP-UHFFFAOYSA-N

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Application

Tridecane can be used as a:
  • Reagent for the hydrodechlorination of 4‑chlorophenol in the presence of bimetallic nanocrystals as a catalyst.[1]
  • Reactant to synthesize α, ω-dicarboxylic acids through terminal oxygenation in the presence of an inorganic-biohybrid catalyst.[2]

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H304,H413

Hazard Classifications

Aquatic Chronic 4 - Asp. Tox. 1

Supplementary Hazards

EUH066

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

174.2 °F

Flash Point(C)

79 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW6785
MKCV4738
MKCS4909
MKCQ4764
MKCP8312

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An unexpected mixture of substances in the defensive secretions of the tubuliferan thrips, Callococcithrips fuscipennis (Moulton)
Tschuch G, et al.
Journal of Chemical Ecology, 34(6), 742-747 (2008)
Chemical composition and biological activities of essential oil from the leaves of Sesuvium portulacastrum
Magwa ML, et al.
Journal of Ethnopharmacology, 103(1), 85-89 (2006)
Raúl A Laumann et al.
Journal of chemical ecology, 35(1), 8-19 (2009-01-08)
We tested the hypotheses that host-searching behavior of the egg parasitoids Telenomus podisi and Trissolcus basalis may be differentially influenced by the different blends of volatiles released from the metathoracic glands of adult stink bug host species. We further studied
Anil Kumar Mishra et al.
Journal of drug targeting, 12(9-10), 559-567 (2004-12-29)
The purpose of this study was to obtain the convenient, synthetically useful bifunctional chelating agent, 6-(4-isothiocyanatobenzyl)-5,7-dioxo-1,11-(carboxymethyl)-1,4,8,11-tetraazacyclotridecane, and to apply it to stable (99m)Tc-labelling of monoclonal antibodies (mAbs). The chelate was synthesised by reaction of nitrobenzyl malonate and triethylenetetramine followed by
Jörg P Hehn et al.
Organic letters, 13(7), 1892-1895 (2011-03-09)
Starting from tetronate 1 (R = CH(2)OH), a short photochemical access to the 3,12-dioxatricyclo[8.2.1.0(6,13)]tridecane-skeleton 2 of briarellin and asbestinin diterpenes has been explored. In the course of these studies, a number of surprising observations were made. For example, a two-step
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