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T57401 Aldrich

Tridecane

≥99%

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Properties

Related Categories Acyclic, Alkanes, Building Blocks, Carthamus tinctorius (Safflower oil), Cell Biology,
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.)

Description

Packaging

100 g in poly bottle

25 g in glass bottle

Price and Availability


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Safety & Documentation

Safety Information

Symbol 
GHS08  GHS08
Signal word 
Danger
Hazard statements 
Precautionary statements 
Supplemental Hazard Statements 
Repeated exposure may cause skin dryness or cracking.
WGK Germany 
3
Flash Point(F) 
201.2 °F
Flash Point(C) 
94 °C

Protocols & Articles

Peer-Reviewed Papers

References

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Solvent inclusion in form II carbamazepine. Cruz Cabeza AJ, Day GM, Motherwell WD, et al. Chem. Commun. (Camb.) (16), 1600-2, (2007)

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Pseudohomogeneous kinetic study on a two-liquid-phase fermentation process. Li Y, Cao Z, and Yuan N Chin. J. Biotechnol. 10(4), 271-82, (1994)

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[Search for yeast producers of brassylic and sebacic fatty acids]. Ulezlo IV and Rogozhin IS Prikl. Biokhim. Mikrobiol. 40(5), 533-5, (2004)

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[Studies on microbial production of undecane 1, 11-dicarboxylic acid from N-tridecane]. Chen Y, Pang Y, and Hao X Wei Sheng Wu Xue Bao 39(3), 279-81, (1999)

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[Study on fermentation of 1,13-tridecanedioic acid by Candida tropicalis]. Liu S, Li S, and Fang X Wei Sheng Wu Xue Bao 40(3), 318-22, (2000)

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A chiral sex pheromone system in the pea midge, Contarinia pisi. Hillbur Y, Bengtsson M, Löfqvist J, et al. J. Chem. Ecol. 27(7), 1391-407, (2001)

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Response of the egg parasitoids Trissolcus basalis and Telenomus podisi to compounds from defensive secretions of stink bugs. Laumann RA, Aquino MF, Moraes MC, et al. J. Chem. Ecol. 35(1), 8-19, (2009)

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A photocycloaddition/fragmentation approach toward the 3,12-dioxatricyclo[8.2.1.0(6,13)]tridecane skeleton of terpenoid natural products. Hehn JP, Herdtweck E, and Bach T Org. Lett. 13(7), 1892-5, (2011)

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Investigation of high-speed gas chromatography using synchronized dual-valve injection and resistively heated temperature programming. Reid VR, McBrady AD, and Synovec RE J. Chromatogr. A 1148(2), 236-43, (2007)

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A synthetic study of atropurpuran: construction of a pentacyclic framework by an intramolecular reverse-electron-demand Diels-Alder reaction. Suzuki T, Sasaki A, Egashira N, et al. Angew. Chem. Int. Ed. Engl. 50(39), 9177-9, (2011)

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Comparative in vivo toxicity of topical JP-8 jet fuel and its individual hydrocarbon components: identification of tridecane and tetradecane as key constituents responsible for dermal irritation. Muhammad F, Monteiro-Riviere NA, and Riviere JE Toxicol. Pathol. 33(2), 258-66, (2005)

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A new bifunctional chelating agent conjugated with monoclonal antibody and labelled with technetium-99m for targeted scintigraphy: 6-(4-isothiocyanatobenzyl)-5,7-dioxo-1,11-(carboxymethyl)-1,4,8,11-tetraazacyclotridecane. Mishra AK, Panwar P, Hosono M, et al. J. Drug Target. 12(9-10), 559-67, (2004)

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Synergy versus potency in the defensive secretions from nymphs of two pentatomomorphan families (Hemiptera: Coreidae and Pentatomidae). Eliyahu D, Ceballos RA, Saeidi V, et al. J. Chem. Ecol. 38(11), 1358-65, (2012)

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Increasing the accuracy of determination of nc/nH ratios by gas chromatography-atomic emission detection. Chernetsova ES, Revelsky AI, Durst D, et al. J. Chromatogr. A 1071(1-2), 55-8, (2005)

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Pseudolarenone, an unusual nortriterpenoid lactone with a fused 5/11/5/6/5 ring system featuring an unprecedented bicyclo[8.2.1]tridecane core from Pseudolarix amabilis. Li B, Kong DY, Shen YH, et al. Chem. Commun. (Camb.) 49(12), 1187-9, (2013)

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The effect of pressure on the phase transition behavior of tridecane, pentadecane, and heptadecane: a Fourier transform infrared spectroscopy study. Yamashita M, Hirao A, and Kato M J. Chem. Phys. 134(14), 144503, (2011)

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Beil. 1,IV,512

Aldrich MSDS 1, 1746:B / Corp MSDS 1 (2), 3424:D / FT-IR 1 (1), 3:B / FT-IR 2 (1), 5:B / FT-NMR 1 (1), 3:C / IR-Spectra (2), 4:B / IR-Spectra (3), 4:B / RegBook 1 (1), 5:C / Sax 6, 2635 / Sigma FT-IR 1 (2), 942:C / Structure Index 1, 1:C:3 / Vapor Phase 3, 4:B

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