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94000 Fluka

Undecane

analytical standard

Synonym: n-Undecane, Hendecane

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Properties

Related Categories Additional Standards, Alkan, All Alphabetically Sorted, Analytical Standards, Analytical/Chromatography,
grade   analytical standard
vapor density   5.4 (vs air)
vapor pressure   <0.4 mmHg ( 20 °C)
assay   ≥99.8% (GC)
form   neat
shelf life   limited shelf life, expiry date on the label
impurities   cycloparaffins
  isoparaffin
refractive index   n20/D 1.417(lit.)
  n20/D 1.418
bp   196 °C(lit.)
mp   −26 °C(lit.)
density   0.74 g/mL at 25 °C(lit.)

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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
Flash Point(F) 
143.6 °F
Flash Point(C) 
62 °C

Protocols & Articles

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Peer-Reviewed Papers

References

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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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