Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

S5006

Sigma-Aldrich

Styrene oxide

97%

Sinonimo/i:

1,2-Epoxyethylbenzene, Phenylethylene oxide, Phenyloxirane

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula empirica (notazione di Hill):
C8H8O
Numero CAS:
Peso molecolare:
120.15
Beilstein:
108582
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23

Densità del vapore

4.14 (vs air)

Tensione di vapore

<1 mmHg ( 20 °C)

Saggio

97%

Temp. autoaccensione

928 °F

Limite di esplosione

~22 %

Indice di rifrazione

n20/D 1.535 (lit.)

P. eboll.

194 °C (lit.)

Punto di fusione

−37 °C (lit.)

Densità

1.054 g/mL at 25 °C (lit.)

Stringa SMILE

C1OC1c2ccccc2

InChI

1S/C8H8O/c1-2-4-7(5-3-1)8-6-9-8/h1-5,8H,6H2
AWMVMTVKBNGEAK-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Applicazioni

  • Synthesis of poly (styrene oxide) with different molecular weights using tin catalysts: This study explores the ring-opening polymerization of styrene oxide using tin catalysts to produce homopolymers with varying molecular weights (Kayan, 2015).
  • Electrogenerated BF3 from tetrafluoroborate-based ionic liquids: theoretical and experimental studies towards selective styrene oxide isomerization: Research on using electrogenerated BF3 to selectively isomerize styrene oxide, highlighting theoretical and experimental insights (Bortolami et al., 2021).
  • Selective conversion of styrene oxide to 2-phenylethanol in cascade reactions over non-noble metal catalysts: This paper investigates the catalytic conversion of styrene oxide to 2-phenylethanol using non-noble metal catalysts (Sasu et al., 2016).
  • Laboratory blueprints for interstellar searches of aromatic chiral molecules: rotational signatures of styrene oxide: Study of the rotational spectra of styrene oxide for potential detection in interstellar space (Stahl et al., 2020).

Pittogrammi

Skull and crossbonesHealth hazard

Avvertenze

Danger

Classi di pericolo

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Carc. 1B - Eye Irrit. 2 - Muta. 1B - Skin Irrit. 2 - Skin Sens. 1

Codice della classe di stoccaggio

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

176.0 °F - closed cup

Punto d’infiammabilità (°C)

80 °C - closed cup

Dispositivi di protezione individuale

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


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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

Jan Volmer et al.
Applied and environmental microbiology, 80(20), 6539-6548 (2014-08-17)
The application of whole cells as biocatalysts is often limited by the toxicity of organic solvents, which constitute interesting substrates/products or can be used as a second phase for in situ product removal and as tools to control multistep biocatalysis.
E E McConnell et al.
Critical reviews in toxicology, 24 Suppl, S49-S55 (1994-01-01)
Eleven long-term toxicity studies were reviewed on styrene and five on styrene oxide in an effort to evaluate the potential carcinogenic activity of these chemicals in animals. The styrene studies included inhalation exposure (rats, mice, guinea pigs, and rabbits), intragastric
The genetic toxicology of styrene and styrene oxide.
R Barale
Mutation research, 257(2), 107-126 (1991-03-01)
D H Phillips et al.
Critical reviews in toxicology, 24 Suppl, S35-S46 (1994-01-01)
Styrene is metabolized to styrene oxide, a direct-acting mutagen and carcinogen. Styrene oxide reacts with DNA mainly at the N-7 position in guanine, but also at other sites and with other bases. Substitution occurs at both the alpha- and beta-positions
David M Hodgson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(35), 9731-9737 (2011-07-19)
Starting from readily available (S)-styrene oxide an asymmetric synthesis is described of the naturally occurring anti-HIV spirolactone (-)-hyperolactone C, which possesses adjacent fully substituted stereocenters. The key step involves a stereocontrolled Rh(II) -catalysed oxonium ylide formation-[2,3] sigmatropic rearrangement of an

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.