Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

292206

Sigma-Aldrich

2-Methyl-1,3-dioxolane

97%

Sinonimo/i:

Acetaldehyde ethylene acetal

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C4H8O2
Numero CAS:
497-26-7
Peso molecolare:
88.11
Beilstein:
102520
Numero CE:
207-841-4
Numero MDL:
MFCD00003210
Codice UNSPSC:
12352100
ID PubChem:
24857568
NACRES:
NA.22

Saggio

97%

Indice di rifrazione

n20/D 1.398 (lit.)

P. eboll.

82-83 °C (lit.)

Densità

0.982 g/mL at 25 °C (lit.)

Stringa SMILE

CC1OCCO1

InChI

1S/C4H8O2/c1-4-5-2-3-6-4/h4H,2-3H2,1H3
HTWIZMNMTWYQRN-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Descrizione generale

The kinetics and mechanism of the gas-phase thermal decomposition of 2-methyl-1,3-dioxolane has been studied in a static system. The infrared spectra of solid, liquid and gaseous 2-methyl-1,3-dioxolane has been studied. Low-temperature ozonation of 2-methyl-1,3-dioxolane in acetone-d6, methyl acetate and tert-butyl methyl ether has been reported.

Pittogrammi

Flame
GHS02

Avvertenze

Danger

Indicazioni di pericolo

H225

Classi di pericolo

Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

28.4 °F - closed cup

Punto d’infiammabilità (°C)

-2 °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 1

1 of 1

2-Methylaminomethyl-1,3-dioxolane 98%

Sigma-Aldrich

279749

2-Methylaminomethyl-1,3-dioxolane

Bozo Plesnicar et al.
Journal of the American Chemical Society, 124(38), 11260-11261 (2002-09-19)
Low-temperature ozonation (-78 degrees C) of 2-methyl-1,3-dioxolane (1a) in acetone-d6, methyl acetate, and tert-butyl methyl ether produced both the corresponding acetal hydrotrioxide (3a, ROOOH) and the hemiortho ester (2a, ROH) in molar ratio 1:5. Both intermediates were fully characterized by
N Watson et al.
Journal of autonomic pharmacology, 14(4), 283-293 (1994-08-01)
1. Muscarinic receptors mediating contraction of rabbit endothelium-denuded aorta have been characterized functionally, in vitro, using a range of antagonists (atropine, pirenzepine, methoctramine, himbacine, 4-diphenyl-acetoxy-N-methyl piperidine methiodide (4-DAMP) and para-fluoro-hexahydro-siladifenidol (p-F-HHSiD). 2. The non-selective muscarinic agonist, (+)cis-dioxolane, induced concentration-dependent contractions
E T Iwamoto et al.
The Journal of pharmacology and experimental therapeutics, 271(2), 601-608 (1994-11-01)
This study was designed to determine if the antinociception produced by intrathecally (i.t.) administered muscarinic agonists in male Sprague-Dawley rats is mediated by an L-arginine/nitric oxide/cyclic GMP cascade. Seven days after implantation of intrathecal catheters, antinociception was produced with graded
G Blanchet et al.
Comptes rendus des seances de la Societe de biologie et de ses filiales, 178(5), 526-534 (1984-01-01)
The radioreceptor assay for acetylcholine (ACh) is based on the ability of the ACh to compete with the specific binding of [3H] cis-methyldioxolane to muscarinic receptors of rat cerebral cortex membranes. The technique described was used to measure ACh levels
T R Ward et al.
Toxicology and applied pharmacology, 122(2), 300-307 (1993-10-01)
Some compounds that inhibit acetylcholinesterase (AChE) activity compete directly with quinuclidinyl benzilate (QNB) binding, a muscarinic antagonist which binds to all subtypes equally, and with cis-methyldioxolane (CD), an agonist that binds with high affinity to the M2 subtype of muscarinic
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.