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Merck
CN

87189

1-Tetradecene

≥97.0% (GC)

Synonym(s):

1-Butadecene, n-Tetradec-1-ene, alpha-Tetradecene

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About This Item

Linear Formula:
CH3(CH2)11CH=CH2
CAS Number:
1120-36-1
Molecular Weight:
196.37
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57653175
EC Number:
214-306-9
Beilstein/REAXYS Number:
1701156
MDL number:
MFCD00008981

Key Documents

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Product Name

1-Tetradecene, ≥97.0% (GC)

InChI key

HFDVRLIODXPAHB-UHFFFAOYSA-N

InChI

1S/C14H28/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3H,1,4-14H2,2H3

SMILES string

CCCCCCCCCCCCC=C

vapor density

6.8 (vs air)

assay

≥97.0% (GC)

form

liquid

autoignition temp.

455 °F

refractive index

n20/D 1.436 (lit.)
n20/D 1.436

bp

251 °C (lit.)

mp

−13-−11 °C (lit.)

density

0.775 g/mL at 25 °C (lit.)

functional group

allyl

Quality Level

100

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Application

1-Tetradecene can be used as a reactant to synthesize:
  • 2-Tetradecanone via PdCl2/CrO3 catalyzed oxidation reaction.
  • (E)-ethyl pentadec-2-enoate, which is used as a key intermediate in the diastereoselective synthesis of (+)-nephrosterinic acid and (+)-protolichesterinic acid via Johnson-Claisen rearrangement.

It can also be used as a monomer unit to synthesize high molecular weight polymer [poly(1- tetradecene)] by titanium complex catalyzed polymerization reaction.

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H304

Hazard Classifications

Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F

flash_point_c

110 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL9659
BCCF3862
BCCG0935
BCBW7637
BCBX4247

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Diastereoselective synthesis of (+)-nephrosterinic acid and (+)-protolichesterinic acid
Fernandes RA, et al.
Tetrahedron Asymmetry, 23(1), 60-66 (2012)
Synthesis of ultrahigh molecular weight polymers with low PDIs by polymerizations of 1-decene, 1-dodecene, and 1-tetradecene by Cp* TiMe2 (O-2, 6-iPr2C6H3)-borate catalyst
Nomura K, et al.
Molecules (Basel), 24(8), 1634-1634 (2019)
Synthesis of methyl ketones from terminal olefins using PdCl2/CrO3 system mimicking the Wacker process
Fernandes RA and Bethi V
Tetrahedron, 70(32), 4760-4767 (2014)
Marta Krasny et al.
Cell and tissue banking, 16(4), 631-638 (2015-07-15)
Increasingly dental surgeons face the challenge of reconstruction of the height and/or thickness of the alveolar ridge as more and more patients wish to have permanent restoration of their dental defects based on intraosseous implants. Evaluation of human allogeneic bone
Lucas A Lane et al.
The journal of physical chemistry. B, 118(49), 14140-14147 (2014-08-27)
Quantum dots (QDs) offer distinct advantages over organic dyes and fluorescent proteins for biological imaging applications because of their brightness, photostability, and tunability. However, a major limitation is that single QDs emit fluorescent light in an intermittent on-and-off fashion called

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