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244465

Sigma-Aldrich

1-Octyne

97%

Sinônimo(s):

1-Ethynylhexane, Hexylacetylene, n-Hexylacetylene

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About This Item

Fórmula linear:
CH3(CH2)5C≡CH
Número CAS:
629-05-0
Peso molecular:
110.20
Beilstein:
1734494
Número MDL:
MFCD00009546
Código UNSPSC:
12352100
eCl@ss:
39010411
ID de substância PubChem:
24854678
NACRES:
NA.22

pressão de vapor

37.7 mmHg ( 37.7 °C)

Ensaio

97%

forma

liquid

Impurezas

≤3% 1-bromohexane

índice de refração

n20/D 1.416 (lit.)

pb

127-128 °C (lit.)

pf

−80 °C (lit.)

densidade

0.747 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCC#C

InChI

1S/C8H14/c1-3-5-7-8-6-4-2/h1H,4-8H2,2H3

chave InChI

UMIPWJGWASORKV-UHFFFAOYSA-N

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Aplicação

1-Octyne was used as a mechanism-based inhibitor of AlkB (nonheme di-iron alkane monooxygenase).

Pictogramas

FlameHealth hazard
GHS02,GHS08

Palavra indicadora

Danger

Frases de perigo

H225,H304

Classificações de perigo

Asp. Tox. 1 - Flam. Liq. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

60.8 °F - closed cup

Ponto de fulgor (°C)

16 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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D L Kline et al.
Medical and veterinary entomology, 21(4), 323-331 (2007-12-21)
Field studies were conducted at wooded wetlands in Gainesville, FL, U.S.A., to assess responses of natural populations of adult mosquitoes (Diptera: Culicidae) to American Biophysics MM-X and Coleman MD-2500 traps baited with enantiomers of 1-octen-3-ol, a naturally occurring compound, and
Alkyne-stabilized ruthenium nanoparticles: manipulation of intraparticle charge delocalization by nanoparticle charge States.
Xiongwu Kang et al.
Angewandte Chemie (International ed. in English), 49(49), 9496-9499 (2010-10-30)
Joseph J Pesek et al.
Journal of chromatography. A, 992(1-2), 57-65 (2003-05-09)
The silanization/hydrosilation method is used to bond an alkyne (1-octyne) to a silica hydride surface. The new bonded material is characterized by elemental analysis and diffuse reflectance infrared Fourier transform spectroscopy. The hydrophobic behavior of this material was determined by
Hernan Alonso et al.
Applied and environmental microbiology, 78(22), 7946-7953 (2012-09-04)
The alkane hydroxylase system of Pseudomonas putida GPo1 allows it to use alkanes as the sole source of carbon and energy. Bacterial alkane hydroxylases have tremendous potential as biocatalysts for the stereo- and regioselective transformation of a wide range of
Isaac S Marks et al.
Bioconjugate chemistry, 22(7), 1259-1263 (2011-05-05)
1,3-Dipolar [3 + 2] cycloaddition between azides and alkynes--an archetypal "click" chemistry--has been used increasingly for the functionalization of nucleic acids. Copper(I)-catalyzed 1,3-dipolar cycloaddition reactions between alkyne-tagged DNA molecules and azides work well, but they require optimization of multiple reagents
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