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D221104 Sigma-Aldrich

Dodecane

ReagentPlus®, ≥99%

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Properties

Related Categories ReagentPlus, ReagentPlus Solvent Grade Products, ACS and Reagent Grade Solvents, Amber Glass Bottles, Solvent Bottles,
grade   ReagentPlus®
vapor density   5.96 (vs air)
vapor pressure   1 mmHg ( 47.8 °C)
assay   ≥99%
autoignition temp.   401 °F
refractive index   n20/D 1.421(lit.)
bp   215-217 °C(lit.)
mp   −9.6 °C(lit.)
density   0.75 g/mL at 25 °C(lit.)

Description

Packaging

100, 500 mL in glass bottle

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Price and Availability

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Safety & Documentation

Safety Information

Symbol 
GHS08  GHS08
Signal word 
Danger
Hazard statements 
Precautionary statements 
Hazard Codes (Europe) 
Xn
Risk Statements (Europe) 
65
Safety Statements (Europe) 
62
WGK Germany 
1
RTECS 
JR2125000

Documents

Certificate of Analysis

Certificate of Origin

Protocols & Articles

Articles

Determination of Water Content in Dodecane Using Karl Fischer Titration

Water determination in hydrocarbons is relatively straightforward. Lower hydrocarbons dissolve in methanol, however, even if the dissolution is incomplete, the water is rapidly extracted and complete...
Keywords: Titrations

Peer-Reviewed Papers

References

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Numerical modeling of the elution peak profiles of retained solutes in supercritical fluid chromatography. Kaczmarski K, Poe DP, and Guiochon G J. Chromatogr. A 1218(37), 6531-9, (2011)

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Electrostatically gated membrane permeability in inorganic protocells. Li M, Harbron RL, Weaver JV, et al. Nature Chemistry 5(6), 529-36, (2013)

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Self-cleaning organic vapor sensor based on a nanoporous TiO₂ interferometer. Liang F, Kelly TL, Luo LB, et al. ACS Appl. Mater. Interfaces 4(8), 4177-83, (2012)

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Whole-cell bio-oxidation of n-dodecane using the alkane hydroxylase system of P. putida GPo1 expressed in E. coli. Grant C, Woodley JM, and Baganz F Enzyme Microb. Technol. 48(6-7), 480-6, (2011)

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Tailored one- and two-dimensional self-assembly of a perylene diimide derivative in organic solvents. Usowicz MT, Kelley MJ, Singer KD, et al. J. Phys. Chem. B 115(32), 9703-9, (2011)

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Transport of charged Aerosol OT inverse micelles in nonpolar liquids. Karvar M, Strubbe F, Beunis F, et al. Langmuir 27(17), 10386-91, (2011)

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Size limit for particle-stabilized emulsion droplets under gravity. Tavacoli JW, Katgert G, Kim EG, et al. Phys. Rev. Lett. 108(26), 268306, (2012)

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Facilitated transport of Pd(II) through a supported liquid membrane (SLM) containing N,N,N',N'-tetra-(2-ethylhexyl) thiodiglycolamide T(2EH)TDGA: a novel carrier. Ruhela R, Panja S, Sharma JN, et al. J. Hazard. Mater. 229-230, 66-71, (2012)

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Sonochemical proteinaceous microspheres for wound healing. Silva R, Ferreira H, Vasconcelos A, et al. Adv. Exp. Med. Biol. 733, 155-64, (2012)

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Synthesis of calcium-silica composites: a route toward an in vitro model system for calcific band keratopathy precipitates. Doostdar N, Manrique CJ, Hamill MB, et al. J. Biomed. Mater. Res. A 99(2), 173-83, (2011)

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Study of nano-emulsion formation by dilution of microemulsions. Solè I, Solans C, Maestro A, et al. J. Colloid. Interface Sci. 376(1), 133-9, (2012)

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Continuous production of carotenoids from Dunaliella salina. Kleinegris DM, Janssen M, Brandenburg WA, et al. Enzyme Microb. Technol. 48(3), 253-9, (2011)

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Three-phase hollow fiber microextraction based on two immiscible organic solvents for determination of tricyclic antidepressant drugs: comparison with conventional three-phase hollow fiber microextraction. Ghambarian M, Yamini Y, and Esrafili A J. Chromatogr. A 1222, 5-12, (2012)

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The biodegradation of cable oil components: impact of oil concentration, nutrient addition and bioaugmentation. Towell MG, Paton GI, and Semple KT Environ. Pollut. 159(12), 3777-83, (2011)

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Concentration dependent refractive index of a binary mixture at high pressure. Croccolo F, Arnaud MA, Bégué D, et al. J. Chem. Phys. 135(3), 034901, (2011)

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Concentrations of bisphenol A in the composite food samples from the 2008 Canadian total diet study in Quebec City and dietary intake estimates. Cao XL, Perez-Locas C, Dufresne G, et al. Food Addit. Contam. Part A. Chem. Anal. Control. Expo. Risk Assess. 28(6), 791-8, (2011)

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Combination of corona discharge ion mobility spectrometry with a novel reagent gas and two immiscible organic solvent liquid-liquid-liquid microextraction for analysis of clomipramine in biological samples. Saraji M, Bidgoli AA, Khayamian T, et al. J. Chromatogr. A 1218(48), 8600-7, (2011)

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Influence of interfacial properties on Ostwald ripening in crosslinked multilayered oil-in-water emulsions. Zeeb B, Gibis M, Fischer L, et al. J. Colloid. Interface Sci. 387(1), 65-73, (2012)

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Retinoid production using metabolically engineered Escherichia coli with a two-phase culture system. Jang HJ, Yoon SH, Ryu HK, et al. Microb. Cell Fact. 10, 59, (2011)

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Predicting the wetting dynamics of a two-liquid system. Seveno D, Blake TD, Goossens S, et al. Langmuir 27(24), 14958-67, (2011)

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Hydroconversion of n-dodecane over nanoporous catalysts. Park YK, Lee HW, Jeon JK, et al. J. Nanosci. Nanotechnol. 13(1), 714-7, (2013)

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Extending the Total Pore Blocking method to normal phase high performance liquid chromatography. Liekens A, Denayer J, and Desmet G J. Chromatogr. A 1218(43), 7781-7, (2011)

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Detoxifying emulsion for overdosed aspirin intoxication. Zhang W, Stambouli M, and Pareau D Int. J. Pharm. 441(1-2), 598-602, (2013)

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Gibbs free energy of liquid drops on conical fibers. Michielsen S, Zhang J, Du J, et al. Langmuir 27(19), 11867-72, (2011)

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Competition of hydrophobic steroids with sodium dodecyl sulfate, dodecyltrimethylammonium bromide, or dodecyl β-D-maltoside for the dodecane/water interface. Feng S and Bummer PM Langmuir 28(49), 16927-32, (2012)

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Biosynthesis of high molecular weight hyaluronic acid by Streptococcus zooepidemicus using oxygen vector and optimum impeller tip speed. Lai ZW, Rahim RA, Ariff AB, et al. J. Biosci. Bioeng. 114(3), 286-91, (2012)

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Beil. 1,IV,498

Aldrich MSDS 1, 843:C / Corp MSDS 1 (1), 1488:B / FT-IR 2 (1), 5:A / FT-IR 1 (1), 3:A / FT-NMR 1 (1), 3:B / IR-Spectra (2), 4:A / IR-Spectra (3), 4:A / NMR-Reference 2 (1), 11:A / RegBook 1 (1), 5:B / Sax 6, 1261 / Sigma FT-IR 1 (2), 535:D / Structure Index 1, 1:B:3 / Vapor Phase 3, 4:A

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