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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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$118.75

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25 G
$44.40
100 G
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About This Item

Linear Formula:
CH3(CH2)11CH3
CAS Number:
629-50-5
Molecular Weight:
184.36
Beilstein/REAXYS Number:
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)

Quality Level

100

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

signalword

Danger

hcodes

H304,H413

Hazard Classifications

Aquatic Chronic 4 - Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

174.2 °F

flash_point_c

79 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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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)
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
Dorit Eliyahu et al.
Journal of chemical ecology, 38(11), 1358-1365 (2012-10-20)
One characteristic of true bugs (Heteroptera) is the presence of dorsal abdominal glands in the immature nymphal stages. These glands usually produce defensive chemicals (allomones) that vary among taxa but are still similar in closely related groups. Knowledge of the
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
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