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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:
Molecular Weight:
184.36
Beilstein:
1733089
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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 is generally used as an analytical standard in studying the composition of alkanes in food, biological and industrial samples.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Chronic 4 - Asp. Tox. 1

Supplementary Hazards

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

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’.

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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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