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Supelco

Hexadecane

analytical standard

Synonym(s):

n-Hexadecane, Cetane

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About This Item

Linear Formula:
CH3(CH2)14CH3
CAS Number:
544-76-3
Molecular Weight:
226.44
Beilstein:
1736592
EC Number:
208-878-9
MDL number:
MFCD00008998
UNSPSC Code:
41116107
PubChem Substance ID:
329757798
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

CCCCCCCCCCCCCCCC

InChI

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

InChI key

DCAYPVUWAIABOU-UHFFFAOYSA-N

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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.

Application

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

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H304

Precautionary Statements

P301 + P310 - P331 - P405 - P501

Hazard Classifications

Asp. Tox. 1

Supplementary Hazards

EUH066

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

233.6 °F

Flash Point(C)

112 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6153
BCCJ7030
BCCJ7115
BCCD9129
BCCB5830

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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
Shweta Mishra et al.
Bioresource technology, 111, 148-154 (2012-03-13)
In the present study, n-hexadecane degradation in MSM was investigated by three bacteria identified as Pseudomonas aeruginosa PSA5, Rhodococcus sp. NJ2 and Ochrobactrum intermedium P2, isolated from petroleum sludge. During 10 days of incubation, n-hexadecane was degraded to 99% by
Yanpeng Dong et al.
Applied microbiology and biotechnology, 94(4), 1019-1029 (2012-04-25)
LadA, a monooxygenase catalyzing the oxidation of n-alkanes to 1-alkanols, is the key enzyme for the degradation of long-chain alkanes (C(15)-C(36)) in Geobacillus thermodenitrificans NG80-2. In this study, random- and site-directed mutagenesis were performed to enhance the activity of the
Homeira Ebrahimzadeh et al.
Talanta, 94, 77-83 (2012-05-23)
A simple and high sensitive technique based on three phase hollow fiber liquid phase microextraction (HF-LPME), optimized by using a four-variable experimental design and response surface methodology was performed to evaluate dextromethorphan hydrobromide (DEX) and chloropheniramine maleate (CLP) simultaneously in
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Protocols

US EPA Method 8015 (modified): GC Analysis of Diesel Range Organics (DRO) on SLB®-5ms (20 m x 0.18 mm I.D., 0.18 µm), Fast GC Analysis

Separation of Decane; Dodecane; Tetradecane; Hexadecane; Octadecane; Eicosane; Docosane; Tetracosane; Hexacosane; Octacosane

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