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244414

Sigma-Aldrich

1-Heptyne

98%

Sinónimos:

1-n-Heptyne, Amylacetylene, Pentylacetylene

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About This Item

Fórmula lineal:
CH3(CH2)4C≡CH
Número de CAS:
628-71-7
Peso molecular:
96.17
Beilstein/REAXYS Number:
1733518
EC Number:
211-051-5
MDL number:
MFCD00009529
UNSPSC Code:
12352100
eCl@ss:
39010410
PubChem Substance ID:
24854674
NACRES:
NA.22

vapor pressure

93.1 mmHg ( 37.7 °C)

Quality Level

100

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.)

SMILES string

CCCCCC#C

InChI

1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3

InChI key

YVXHZKKCZYLQOP-UHFFFAOYSA-N

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General description

The hydrogenation of 1-heptyne with palladium, platinum and ruthenium supported on activated carbon as catalysts, was studied.

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.

pictograms

Flame
GHS02

signalword

Danger

hcodes

H225

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

14.0 °F

flash_point_c

-10 °C

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
STBK1870
STBJ6395
STBJ0351
STBH4973
STBH2229

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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
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
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)
Florian Birk et al.
Journal of agricultural and food chemistry, 67(49), 13460-13469 (2019-04-19)
Fermentation broths of Ashbya gossypii from the industrial production of riboflavin emit an intense floral, fruity, and nutty smell. Typical Ehrlich pathway products, such as 2-phenylethan-1-ol and 2-/3-methylbutan-1-ol, were detected in large amounts as well as some intensely smelling saturated

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