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Merck
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Key Documents

244414

Sigma-Aldrich

1-Heptyne

98%

동의어(들):

1-n-Heptyne, Amylacetylene, Pentylacetylene

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About This Item

Linear Formula:
CH3(CH2)4C≡CH
CAS Number:
Molecular Weight:
96.17
Beilstein:
1733518
EC Number:
MDL number:
UNSPSC 코드:
12352100
eCl@ss:
39010410
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

93.1 mmHg ( 37.7 °C)

Quality Level

분석

98%

형태

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

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

애플리케이션

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.

픽토그램

Flame

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

14.0 °F

Flash Point (°C)

-10 °C

개인 보호 장비

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


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시험 성적서(COA)

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문서 라이브러리 방문

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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