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161306

Sigma-Aldrich

1,8-Nonadiyne

98%

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About This Item

Formule linéaire :
HC≡C(CH2)5C≡CH
Numéro CAS:
2396-65-8
Poids moléculaire :
120.19
Numéro CE :
219-254-0
Numéro MDL:
MFCD00008581
Code UNSPSC :
12352100
ID de substance PubChem :
24849920
Nomenclature NACRES :
NA.22

Pureté

98%

Forme

liquid

Indice de réfraction

n20/D 1.449 (lit.)

Point d'ébullition

55-55.5 °C/13 mmHg (lit.)

Pf

−21 °C (lit.)

Densité

0.799 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

C#CCCCCCC#C

InChI

1S/C9H12/c1-3-5-7-9-8-6-4-2/h1-2H,5-9H2

Clé InChI

DMOVPHYFYSASTC-UHFFFAOYSA-N

Description générale

1,8-Nonadiyne undergoes one-step hydrosilylation reaction for attaching acetylene-terminated alkyl monolayers to nonoxidized crystalline silicon surfaces.

Application

1,8-Nonadiyne was used as starting reagent in the synthesis of 2,6-hexadecadiynoic acid, 2,6-nonadecadiynoic acid and 2,9-hexadecadiynoic acid.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H226,H315,H319,H335

Classification des risques

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

107.6 °F - closed cup

Point d'éclair (°C)

42 °C - closed cup

Équipement de protection individuelle

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

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Néstor M Carballeira et al.
Lipids, 41(5), 507-511 (2006-08-29)
The hitherto unknown 2,6-hexadecadiynoic acid, 2,6-nonadecadiynoic acid, and 2,9-hexadecadiynoic acid were synthesized in two steps and in 11-18% overall yields starting from either 1,5-hexadiyne or 1,8-nonadiyne. Among all the compounds 2,6-hexadecadiynoic acid displayed the best overall antifungal activity against both
Stephen G Parker et al.
Nature communications, 9(1), 2288-2288 (2018-06-14)
For many normal and aberrant cell behaviours, it is important to understand the origin of cellular heterogeneity. Although powerful methods for studying cell heterogeneity have emerged, they are more suitable for common rather than rare cells. Exploring the heterogeneity of
Benjamin S Flavel et al.
Langmuir : the ACS journal of surfaces and colloids, 29(26), 8355-8362 (2013-06-25)
Poly(ethylene glycol) (PEG) is one of the most extensively studied antifouling coatings due to its ability to reduce protein adsorption and improve biocompatibility. Although the use of PEG for antifouling coatings is well established, the stability and density of PEG
Yan B Vogel et al.
Nature communications, 8(1), 2066-2066 (2017-12-14)
Predicting or manipulating charge-transfer at semiconductor interfaces, from molecular electronics to energy conversion, relies on knowledge generated from a kinetic analysis of the electrode process, as provided by cyclic voltammetry. Scientists and engineers encountering non-ideal shapes and positions in voltammograms
Janneke Veerbeek et al.
ACS applied materials & interfaces, 9(1), 413-421 (2016-12-10)
Silicon-based solar fuel devices require passivation for optimal performance yet at the same time need functionalization with (photo)catalysts for efficient solar fuel production. Here, we use molecular monolayers to enable electrical passivation and simultaneous functionalization of silicon-based solar cells. Organic

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