161306

Sigma-Aldrich

1,8-Nonadiyne

98%

Linear Formula:
HC≡C(CH2)5C≡CH
CAS Number:
Molecular Weight:
120.19
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

refractive index

n20/D 1.449 (lit.)

bp

55-55.5 °C/13 mmHg (lit.)

mp

−21 °C (lit.)

density

0.799 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C#CCCCCCC#C

InChI

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

InChI key

DMOVPHYFYSASTC-UHFFFAOYSA-N

Related Categories

General description

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.

Packaging

10 g in glass bottle

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

UN 3295C 3 / PGIII

WGK Germany

WGK 3

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42 °C - closed cup

Certificate of Analysis

Certificate of Origin

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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