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244414

Sigma-Aldrich

1-Heptyne

98%

Sinonimo/i:

1-n-Heptyne, Amylacetylene, Pentylacetylene

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About This Item

Formula condensata:
CH3(CH2)4C≡CH
Numero CAS:
628-71-7
Peso molecolare:
96.17
Beilstein:
1733518
Numero CE:
211-051-5
Numero MDL:
MFCD00009529
Codice UNSPSC:
12352100
eCl@ss:
39010410
ID PubChem:
24854674
NACRES:
NA.22

Tensione di vapore

93.1 mmHg ( 37.7 °C)

Livello qualitativo

100

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.408 (lit.)

P. eboll.

99-100 °C (lit.)

Punto di fusione

−81 °C (lit.)

Densità

0.733 g/mL at 25 °C (lit.)

Stringa SMILE

CCCCCC#C

InChI

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

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Categorie correlate

Descrizione generale

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

Applicazioni

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.

Pittogrammi

Flame
GHS02

Avvertenze

Danger

Indicazioni di pericolo

H225

Classi di pericolo

Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

14.0 °F

Punto d’infiammabilità (°C)

-10 °C

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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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.
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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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