244414
1-Heptyne
98%
Synonym(s):
1-n-Heptyne, Amylacetylene, Pentylacetylene
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About This Item
Linear Formula:
CH3(CH2)4C≡CH
CAS Number:
Molecular Weight:
96.17
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39010410
UNSPSC Code:
12352100
EC Number:
211-051-5
MDL number:
Beilstein/REAXYS Number:
1733518
Product Name
1-Heptyne, 98%
InChI
1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3
InChI key
YVXHZKKCZYLQOP-UHFFFAOYSA-N
SMILES string
CCCCCC#C
vapor pressure
93.1 mmHg ( 37.7 °C)
assay
98%
form
liquid
refractive index
n20/D 1.408 (lit.)
bp
99-100 °C (lit.)
mp
−81 °C (lit.)
density
0.733 g/mL at 25 °C (lit.)
Quality Level
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Application
1-Heptyne was used in the synthesis of (6Z,10E,12Z)-octadeca-6,10,12-trienoic acid and (8Z,12E,14Z)-eicosa-8,12,14-trienoic acid.
General description
The hydrogenation of 1-heptyne with palladium, platinum and ruthenium supported on activated carbon as catalysts, was studied.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
14.0 °F
flash_point_c
-10 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Cecilia R Lederhos et al.
TheScientificWorldJournal, 2013, 528453-528453 (2013-12-19)
Palladium, platinum, and ruthenium supported on activated carbon were used as catalysts for the selective hydrogenation of 1-heptyne, a terminal alkyne. All catalysts were characterized by temperature programmed reduction, X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. TPR and
O Loreau et al.
Chemistry and physics of lipids, 124(2), 135-145 (2003-06-24)
To study the metabolic fate of conjugated linoleic acid isomers, we synthesized, in seven steps, from 1-heptyne, (6Z,10E,12Z)-octadeca-6,10,12-trienoic acid, (8Z,12E,14Z)-eicosa-8,12,14-trienoic acid, and their [1-(14)C]-analogs. In the case of (6Z,10E,12Z)-octadecatrienoic acid, a series of palladium-catalyzed cross-coupling reactions between 1-heptyne and (E)-1,2-dichloro-ethene
Chloë L Wright et al.
Applied and environmental microbiology, 86(9) (2020-02-23)
Ammonia monooxygenase (AMO) is a key nitrogen-transforming enzyme belonging to the same copper-dependent membrane monooxygenase family (CuMMO) as the particulate methane monooxygenase (pMMO). The AMO from ammonia-oxidizing archaea (AOA) is very divergent from both the AMO of ammonia-oxidizing bacteria (AOB)
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