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76510

Sigma-Aldrich

Pentadecane

≥98.0% (GC)

Synonym(s):

n-Pentadecane

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About This Item

Linear Formula:
CH3(CH2)13CH3
CAS Number:
629-62-9
Molecular Weight:
212.41
Beilstein:
1698194
EC Number:
211-098-1
MDL number:
MFCD00008990
UNSPSC Code:
12352100
PubChem Substance ID:
57652646
NACRES:
NA.22

vapor density

7.4 (vs air)

vapor pressure

1 mmHg ( 91.6 °C)

Assay

≥98.0% (GC)

form

liquid

expl. lim.

6.5 %

refractive index

n20/D 1.431 (lit.)

bp

270 °C (lit.)

mp

8-10 °C (lit.)

density

0.769 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCC

InChI

1S/C15H32/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3-15H2,1-2H3

InChI key

YCOZIPAWZNQLMR-UHFFFAOYSA-N

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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)

219.2 °F - closed cup

Flash Point(C)

104 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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From 2,2'-methylenedifuran to all stereomeric pentadecane-1,3,5,7,9,11,13,15-octols.
M E Schwenter et al.
The Journal of organic chemistry, 66(23), 7869-7872 (2001-11-10)
Keith D Schwartz et al.
Organic letters, 13(2), 248-251 (2010-12-18)
Conjugate reduction of an enone accompanied by in situ intramolecular aldol condensation was used to construct the tetrasubstituted cyclohexane nucleus of phomactins. Subsequent relay ring-closing metathesis completed the nine-membered ansa bridge of the diterpenoid framework.
Synthesis of homogeneous FePt nanoparticles using a nitrile ligand.
Virginie Monnier et al.
Small (Weinheim an der Bergstrasse, Germany), 4(8), 1139-1142 (2008-07-16)
Biosynthesis of phomactins: common intermediate phomactatriene and taxadiene.
Tetsuo Tokiwano et al.
Chemical communications (Cambridge, England), (11)(11), 1324-1325 (2004-05-22)
Kevin M Foote et al.
Organic & biomolecular chemistry, 1(22), 3917-3948 (2003-12-11)
A concise synthesis of the tricyclic furanochroman unit 3 found in the PAF antagonist phomactin A (1) isolated from the marine fungus Phoma sp., is described. In complementary studies, a variety of synthetic routes towards the bicyclo[9.3.1]pentadecane ring system 4
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