Passa al contenuto
Merck
Tutte le immagini(2)

Key Documents

View All Documentation

161241

Sigma-Aldrich

1-Phenyl-1-propyne

99%

Sinonimo/i:

(2-Methylethynyl)benzene, 1-Methyl-2-phenylacetylene, 1-Propyn-1-ylbenzene, 1-Propynylbenzene, 3-Phenyl-2-propyne, Methylphenylacetylene, Methylphenylethyne, Phenylmethylacetylene

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(2)

About This Item

Formula condensata:
C6H5C≡CCH3
Numero CAS:
673-32-5
Peso molecolare:
116.16
Numero CE:
211-607-7
Numero MDL:
MFCD00009272
Codice UNSPSC:
12352100
ID PubChem:
24849915
NACRES:
NA.22

Livello qualitativo

100

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.564 (lit.)

P. eboll.

185 °C (lit.)

Densità

0.928 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

CC#Cc1ccccc1

InChI

1S/C9H8/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,1H3
GHUURDQYRGVEHX-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

Co-catalyzed reaction between cyclopentene and 1-phenyl-1-propyne has been reported. Bonding properties of 1-phenyl-1-propyne on Cu(111) at 100K have been studied using temperature-programmed desorption and X-ray, ultraviolet and two-photon photoemission spectroscopies. 1-Phenyl-1-propyne is an inhibitor of dopamine beta-hydroxylase. Polymerization of 1-phenyl-1-propyne by TaCl5 and NbCl5 has been reported.

1-Phenyl-1-propyne serves as a starting material for various chemical reactions, such as addition reactions and polymerization.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

143.6 °F - closed cup

Punto d’infiammabilità (°C)

62 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
SHBL0550
SHBJ6624
SHBH2813V
SHBF0997V
SHBD8775V

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 4

1 of 4

4′-(Phenylethynyl)acetophenone AldrichCPR

Sigma-Aldrich

CDS000680

4′-(Phenylethynyl)acetophenone

3-Hexyne 99%

Sigma-Aldrich

306894

3-Hexyne

Propyne ≥97%

Sigma-Aldrich

480983

Propyne

1-Phenyl-2-propyn-1-ol 98%

Sigma-Aldrich

226610

1-Phenyl-2-propyn-1-ol

Youngku Sohn et al.
Langmuir : the ACS journal of surfaces and colloids, 23(24), 12185-12191 (2007-10-31)
The bonding properties of 1-phenyl-1-propyne (PP, C6H5CCCH3) on Cu(111) at 100 K have been studied using temperature-programmed desorption (TPD), and X-ray, ultraviolet, and two-photon photoemission spectroscopies (XPS, UPS, and 2PPE). In TPD, there is no evidence for dissociation. Multilayer desorption
Effect of organometallic cocatalysts on the polymerization of 1-phenyl-1-propyne by tantalum pentachloride (TaCl5) and niobium pentachloride (NbCl5).
Masuda T, et al.
Macromolecules, 18(11), 2109-2113 (1985)
Shuhuai Xiang et al.
Journal of the American Chemical Society, 136(16), 5832-5835 (2014-04-12)
Here we report a general method for the measurement of (13)C kinetic isotope effects at natural abundance for reactions that yield two or more products concurrently. We use, as an example, a recently reported Co-catalyzed reaction between cyclopentene and 1-phenyl-1-propyne.
Ekaterina V Pokochueva et al.
Physical chemistry chemical physics : PCCP, 21(48), 26477-26482 (2019-11-30)
Parahydrogen-induced polarization (PHIP) is a powerful technique for studying hydrogenation reactions in gas and liquid phases. Pairwise addition of parahydrogen to the hydrogenation substrate imparts nuclear spin order to reaction products, manifested as enhanced 1H NMR signals from the nascent
G Colombo et al.
The Journal of biological chemistry, 259(24), 15017-15020 (1984-12-25)
The catalytic action of dopamine beta-hydroxylase on 1-phenyl-1-propyne results in concomitant loss of enzyme activity. At pH 5.5 and 25 degrees C, 1-phenyl-1-propyne inactivates dopamine beta-hydroxylase in a mechanism-based fashion. The inactivation rate is first-order, follows saturation kinetics, and is
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.