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Merck

52209

Hexadecane

analytical standard

Synonym(s):

n-Hexadecane, Cetane

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About This Item

Linear Formula:
CH3(CH2)14CH3
CAS Number:
Molecular Weight:
226.44
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
208-878-9
Beilstein/REAXYS Number:
1736592
MDL number:
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Product Name

Hexadecane, analytical standard

InChI key

DCAYPVUWAIABOU-UHFFFAOYSA-N

InChI

1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3

SMILES string

CCCCCCCCCCCCCCCC

grade

analytical standard

vapor density

7.8 (vs air)

vapor pressure

1 mmHg ( 105.3 °C)

assay

≥99.8% (GC)

autoignition temp.

395 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.434 (lit.)
n20/D 1.435

bp

287 °C (lit.)

mp

18 °C (lit.)

transition temp

solidification point 17.5-18.5 °C

density

0.773 g/mL at 25 °C (lit.)

application(s)

petroleum

format

neat

Quality Level

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Hexadecane can find applications as a sole carbon source for the growth of canals, which are supramolecular structures observed in the cell wall of Candida maltose.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1

supp_hazards

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

233.6 °F

flash_point_c

112 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Cell wall canals formed upon growth of Candida maltosa in the presence of hexadecane are associated with polyphosphates
Zvonarev, NA
FEMS Yeast Research, 17 (2017)
Matthew A Churchward et al.
Biophysical journal, 94(10), 3976-3986 (2008-01-30)
The Ca(2+)-triggered merger of two apposed membranes is the defining step of regulated exocytosis. CHOL is required at critical levels in secretory vesicle membranes to enable efficient, native membrane fusion: CHOL-sphingomyelin enriched microdomains organize the site and regulate fusion efficiency
Ji-Quan Sun et al.
Bioresource technology, 123, 664-668 (2012-09-04)
Three phenol- and alkanes-degrading bacterial strains were isolated from a freshwater sample. Upon the 16S rRNA gene analysis, phenotype and physiological features, the three strains were designated as Acinetobacter sp. with both phenol hydroxylase gene (phe) and alkane monooxygenase gene
Hirak Chakraborty et al.
Biophysical journal, 102(12), 2751-2760 (2012-06-28)
Membrane fusion, essential to eukaryotic life, is broadly envisioned as a three-step process proceeding from contacting bilayers through two semistable, nonlamellar lipidic intermediate states to a fusion pore. Here, we introduced a new, to our knowledge, experimental approach to gain
Gibum Kwon et al.
Advanced materials (Deerfield Beach, Fla.), 24(27), 3666-3671 (2012-06-13)
In this work, the first-ever membrane-based single unit operation that enables gravity driven, on-demand separation of various oil-water mixtures is developed. Using this methodology, the on-demand separation of free oil and water, oil-in-water emulsions, and water-in-oil emulsions is demonstrated, with

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