76510
Pentadecane
≥98.0% (GC)
Synonym(s):
n-Pentadecane
Sign Into View Organizational & Contract Pricing
All Photos(1)
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
Pricing and availability is not currently available.
Recommended Products
vapor density
7.4 (vs air)
Quality Level
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
Looking for similar products? Visit Product Comparison Guide
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
