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341797

Sigma-Aldrich

1-Phenyl-1-butyne

99%

Synonym(s):

1-Butynylbenzene

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About This Item

Linear Formula:
C6H5C≡CC2H5
CAS Number:
Molecular Weight:
130.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Quality Level

assay

99%

form

solid

refractive index

n20/D 1.551 (lit.)

bp

73-75 °C/4 mmHg (lit.)

density

0.916 g/mL at 25 °C (lit.)

SMILES string

CCC#Cc1ccccc1

InChI

1S/C10H10/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2H2,1H3

InChI key

FFFMSANAQQVUJA-UHFFFAOYSA-N

General description

1-Phenyl-1-butyne is a phenyl alkyl acetylenic compound.[1] It′s reaction with alkali metals (sodium, potassium) in various solvents is reported.[2] Palladium particles incorporated into organophilic montmorillonite catalyzed liquid-phase hydrogenation of 1-phenyl-1-butyne is reported.[3] Copolymerization of C60 and 1-phenyl-1-butyne is reported.[4]

Application

1-Phenyl-1-butyne was used to investigate the liquid-phase stereoselective hydrogenation of phenyl alkyl acetylenics at 298K and atmospheric pressure on Pd-supported catalysts.[1]

pictograms

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Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Customers Also Viewed

Synthesis and light-emitting properties of C< sub> 60</sub>-containing poly (1-phenyl-1-butyne) s.
Xu H, et al.
Thin Solid Films, 363(1), 143-145 (2000)
Alkynes hydrogenation over Pd-supported catalysts.
Marin-Astorga N, et al.
Catalysis Letters, 91(1-2), 115-121 (2003)
Competitive pathways in the reaction of 1-phenyl-1-butyne with alkali metals in various solvents.
Derocque JL and Sundermann FB.
The Journal of Organic Chemistry, 39(12), 1736-1744 (1974)
Preparation of organophilic Pd-montmorillonite, an efficient catalyst in alkyne semihydrogenation.
Mastalir A, et al.
J. Catal., 194(1), 146-152 (2000)

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