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442700

Supelco

Pentadecane

analytical standard

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About This Item

Linear Formula:
CH3(CH2)13CH3
CAS Number:
629-62-9
Molecular Weight:
212.41
Beilstein/REAXYS Number:
1698194
EC Number:
211-098-1
MDL number:
MFCD00008990
UNSPSC Code:
12000000
PubChem Substance ID:
24867969

grade

analytical standard

vapor density

7.4 (vs air)

vapor pressure

1 mmHg ( 91.6 °C)

description

This product has been discontinued. It has been replaced by product 76509.

expl. lim.

6.5 %

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

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.)

application(s)

environmental
petroleum

format

neat

storage temp.

room temp

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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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

signalword

Danger

hcodes

H304

Hazard Classifications

Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
LRAB9325
LRAB7732
LC27155V
LC23800V
LC19911V

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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)
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)
Nao Fujiwara-Tsujii et al.
Zoological science, 23(4), 353-358 (2006-05-17)
The alarm pheromone of the ant Camponotus obscuripes (Formicinae) was identified and quantified by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). Comparisons between alarm pheromone components and extracts from the major exocrine gland of this ant species revealed that
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.
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