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Key Documents

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:
Molecular Weight:
212.41
Beilstein:
1698194
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Asp. Tox. 1

Supplementary Hazards

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

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Biosynthesis of phomactins: common intermediate phomactatriene and taxadiene.
Tetsuo Tokiwano et al.
Chemical communications (Cambridge, England), (11)(11), 1324-1325 (2004-05-22)
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.
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)
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)
Thembelani E Nomkoko et al.
Dalton transactions (Cambridge, England : 2003), (33)(33), 4029-4038 (2006-10-10)
The equilibrium constants of Cu(II), Zn(II), Ca(II) and Gd(III) with 1,15-bis(N,N-dimethyl)-5,11-dioxo-8-(N-benzyl)-1,4,8,12,15-pentaazapentadecane (La) have been studied at 25 degrees C and an ionic strength of 0.15 mol dm-3. Copper forms more stable complexes with La than the other metal ions investigated.

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