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W510505 Aldrich

Undecane

≥99%

Synonym: n-Undecane, Hendecane

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Properties

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biological source   synthetic
grade   NI
vapor density   5.4 (vs air)
vapor pressure   <0.4 mmHg ( 20 °C)
assay   ≥99%
refractive index   n20/D 1.417(lit.)
bp   196 °C(lit.)
mp   −26 °C(lit.)
density   0.74 g/mL at 25 °C(lit.)
Organoleptic   faint
allergen   no known allergens

Description

Packaging

1 kg in glass bottle

4, 8 kg in steel drum

Other Notes

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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.
Hazard Codes (Europe) 
Xn
Risk Statements (Europe) 
Safety Statements (Europe) 
62
RIDADR 
UN 2330 3 / PGIII
WGK Germany 
3
RTECS 
YQ1525000

Protocols & Articles

Peer-Reviewed Papers

References

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A molecular half-wave rectifier. Nijhuis CA, Reus WF, Siegel AC, et al. J. Am. Chem. Soc. 133(39), 15397-411, (2011)

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Quantification of F2-isoprostanes as a reliable index of oxidative stress in vivo using gas chromatography-mass spectrometry (GC-MS) method. Wei Liu et al Free Radic. Biol. Med. 47, 1101-7, (2009)

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Closely stacked oligo(phenylene ethynylene)s: effect of π-stacking on the electronic properties of conjugated chromophores. Jagtap SP, Mukhopadhyay S, Coropceanu V, et al. J. Am. Chem. Soc. 134(16), 7176-85, (2012)

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Pentacycloundecane-based inhibitors of wild-type C-South African HIV-protease. Makatini MM, Petzold K, Sriharsha SN, et al. Bioorg. Med. Chem. Lett. 21(8), 2274-7, (2011)

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Pentacycloundecane-diol-based HIV-1 protease inhibitors: biological screening, 2D NMR, and molecular simulation studies. Honarparvar B, Makatini MM, Pawar SA, et al. ChemMedChem 7(6), 1009-19, (2012)

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A concise approach to the polycyclic scaffold of frondosin D. Masters KS and Flynn BL J. Org. Chem. 73(20), 8081-4, (2008)

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Trishomocubane as a scaffold for the development of selective dopamine transporter (DAT) ligands. Banister SD, Moussa IA, Beinat C, et al. Bioorg. Med. Chem. Lett. 21(1), 38-41, (2011)

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New binuclear Mn(II) and Fe(II) complexes supported by 1,4,8-triazacycloundecane. Pawlak PL, Panda M, Loloee R, et al. Dalton Trans. 40(12), 2926-31, (2011)

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Production of high-quality diesel from biomass waste products. Corma A, de la Torre O, Renz M, et al. Angew. Chem. Int. Ed. Engl. 50(10), 2375-8, (2011)

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On the determination of a detector response enhancement factor for flow modulated comprehensive two-dimensional gas chromatography. Krupčík J, Májek P, Gorovenko R, et al. J. Chromatogr. A 1286, 235-40, (2013)

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Pentacyclo-undecane derived cyclic tetra-amines: synthesis and evaluation as potent anti-tuberculosis agents. Oluseye K Onajole et al Eur. J. Med. Chem. 44, 4297-305, (2009)

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A new domino autocatalytic reaction leading to polyfunctionalized spiro[5.5]undecanes and dispiro[4.2.5.2]pentadecanes. Jiang B, Hao WJ, Zhang JP, et al. Org. Biomol. Chem. 7(10), 2195-201, (2009)

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Dummies versus air puffs: efficient stimulus delivery for low-volatile odors. Brandstaetter AS, Rössler W, and Kleineidam CJ Chem. Senses 35(4), 323-33, (2010)

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Increasing selectivity of CC chemokine receptor 8 antagonists by engineering nondesolvation related interactions with the intended and off-target binding sites. Shamovsky I, de Graaf C, Alderin L, et al. J. Med. Chem. 52(23), 7706-23, (2009)

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Synthesis and NMR elucidation of novel pentacycloundecane-based peptides. Altaib MS, Arvidsson PI, Govender T, et al. Magn. Reson. Chem. 48(6), 435-42, (2010)

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Quantum chemical DFT study of 4-azatricyclo [5.2.2.0(2,6)] undecane-3,5,8-trione. Panicker CY, Varghese HT, Pillai KM, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 75(5), 1559-65, (2010)

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QSPR modeling of octanol/water partition coefficient for vitamins by optimal descriptors calculated with SMILES. A A Toropov et al Eur. J. Med. Chem. 43, 714-40, (2008)

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Discovery of a potent, selective and orally bioavailable 3,9-diazaspiro[5.5]undeca-2-one CCR5 antagonist. Yang H, Lin XF, Padilla F, et al. Bioorg. Med. Chem. Lett. 19(1), 209-13, (2009)

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In vitro anthelmintic activity of the essential oils of Zanthoxylum zanthoxyloides and Newbouldia laevis against Strongyloides ratti. Olounladé PA, Azando EV, Hounzangbé-Adoté MS, et al. Parasitol. Res. 110(4), 1427-33, (2012)

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Presence of psychrotolerant phenanthrene-mineralizing bacterial populations in contaminated soils from the Greenland High Arctic. Sørensen SR, Johnsen AR, Jensen A, et al. FEMS Microbiol. Lett. 305(2), 148-54, (2010)

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Spectroscopic investigations and computational study of 4-(3-bromopropyl)-4-azatricyclo [5.2.2.0(2,6)]undecane-3,5,8-trione. Varghese HT, Panicker CY, Pillai KM, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 76(5), 513-22, (2010)

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NMR elucidation of a novel (S)-pentacyclo-undecane bis-(4-phenyloxazoline) ligand and related derivatives. Boyle GA, Govender T, Kruger HG, et al. Magn. Reson. Chem. 46(12), 1089-95, (2008)

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In vitro antifungal and antibacterial activities of pentacycloundecane tetra-amines. Onajole OK, Coovadia Y, Govender T, et al. Chem. Biol. Drug Des. 77(4), 295-9, (2011)

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Light scattering and sum rules of three coexisting phases for quasiternary solutions near the tricritical point. Wang N, An X, Wang J, et al. J. Chem. Phys. 132(7), 074501, (2010)

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Synthesis and structure of new 3,3,9,9-tetrasubstituted-2,4,8,10-tetraoxaspiro[5.5]undecane derivatives. Mihiş A, Condamine E, Bogdan E, et al. Molecules 13(11), 2848-58, (2008)

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Novel polycyclic 'cage'-1,2-diamines as potential anti-tuberculosis agents. Onajole OK, Coovadia Y, Kruger HG, et al. Eur. J. Med. Chem. 54, 1-9, (2012)

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Selective olfactory attention of a specialised predator to intraspecific chemical signals of its prey. Cárdenas M, Jiroš P, and Pekár S Naturwissenschaften 99(8), 597-605, (2012)

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Beil. 1,IV,487

Aldrich MSDS 1, 1821:D / Corp MSDS 1 (2), 3571:C / FT-IR 2 (1), 4:D / FT-IR 1 (1), 2:D / FT-IR 1 (2), 2:D / FT-NMR 1 (1), 3:A / IR-Spectra (2), 3:H / IR-Spectra (3), 3:H / NMR-Reference 2 (1), 10:D / RegBook 1 (1), 5:A / Sax 6, 2709 / Sigma FT-IR 1 (2), 968:C / Structure Index 1, 1:A:3 / Vapor Phase 3, 3:D

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