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Merck
CN

242527

1-Undecene

97%

Synonym(s):

α-Undecene, n-1-Undecene

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About This Item

Linear Formula:
CH3(CH2)8CH=CH2
CAS Number:
821-95-4
Molecular Weight:
154.29
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854564
EC Number:
212-483-7
Beilstein/REAXYS Number:
1740044
MDL number:
MFCD00008956

Key Documents

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Product Name

1-Undecene, 97%

InChI key

DCTOHCCUXLBQMS-UHFFFAOYSA-N

InChI

1S/C11H22/c1-3-5-7-9-11-10-8-6-4-2/h3H,1,4-11H2,2H3

SMILES string

CCCCCCCCCC=C

assay

97%

form

liquid

refractive index

n20/D 1.426 (lit.)

bp

192-193 °C (lit.)

mp

−49 °C (lit.)

density

0.75 g/mL at 25 °C (lit.)

functional group

allyl

Quality Level

100

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Application

1-undecene is an alkene that can be used as a reactant:
  • In the Pd-catalyzed aerobic oxidative amination reaction with nitrogen nucleophiles to produce useful amine analogs.
  • To prepare a key intermediate in the total synthesis of (+)-deoxoprosopinine.

General description

1-undecene (or α-undecene) is an organic compound, which belongs to the class of unsaturated aliphatic hydrocarbons. It is a hydrophobic molecule found in the essential oil of Farfugium japonicum and some mushroom species.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV9230
MKCW9821
MKCR7618
MKCS0106
MKCP8169

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Preparation and characterisation of luminescent alkylated-silicon quantum dots
Lie Lars H, et al.
Journal of Electroanalytical Chemistry, 538, 183-190 (2002)
Ji-Young Kim et al.
Journal of oleo science, 57(11), 623-628 (2008-10-08)
In this study, the chemical composition and anti-inflammatory activities of hydrodistilled essential oil from Farfugium japonicum were investigated for the first time. The chemical constituents of the essential oil were further analyzed by GC-MS and included 1-undecene (22.43%), 1-nonene (19.83%)
Stereoselective strategies for the construction of polysubstituted piperidinic compounds and their applications in natural products? synthesis
Kandepedu, N, et al.
Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry, 4(8), 1655-1704 (2017)
Palladium-Catalyzed Intermolecular Aerobic Oxidative Amination of Terminal Alkenes: Efficient Synthesis of Linear Allylamine Derivatives
Liu Guosheng, et al.
Angewandte Chemie (International ed. in English), 47(25), 4733-4736 (2008)
Lieuwe D J Bos et al.
PLoS pathogens, 9(5), e1003311-e1003311 (2013-05-16)
Ideally, invading bacteria are detected as early as possible in critically ill patients: the strain of morbific pathogens is identified rapidly, and antimicrobial sensitivity is known well before the start of new antimicrobial therapy. Bacteria have a distinct metabolism, part
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