Passa al contenuto
Merck
Tutte le immagini(2)

Documenti

534102

Sigma-Aldrich

Methylamine solution

greener alternative

33 wt. % in absolute ethanol ((denatured with 1% toluene))

Sinonimo/i:

Monomethylamine

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

About This Item

Formula condensata:
CH3NH2
Numero CAS:
74-89-5
Peso molecolare:
31.06
Beilstein:
741851
Numero MDL:
MFCD00008104
Codice UNSPSC:
12352302
ID PubChem:
24878015
NACRES:
NA.22

Livello qualitativo

200

Caratteristiche più verdi

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Concentrazione

33 wt. % in absolute ethanol ((denatured with 1% toluene))

Impurezze

≤1.0% water

Indice di rifrazione

n20/D 1.360-1.372

Densità

0.756 g/mL at 25 °C

Categoria alternativa più verde

, Enabling

Temperatura di conservazione

2-8°C

Stringa SMILE

CN

InChI

1S/CH5N/c1-2/h2H2,1H3
BAVYZALUXZFZLV-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Descrizione generale

Methylamine solution is a 33wt.% solution of methylamine in absolute ethanol. Methylamine is an aliphatic primary amine. It participates in the synthesis of isothiazolium salts. Chemical degradation of methylamine solution of γ-irradiated poly(ε-caprolactone) has been described. Maillard reaction of D-glucose and methylamine in aqueous acetic acid has been reported.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Applicazioni

Methylamine solution in absolute ethanol can be used as a precursor that facilitates the synthesis of perovskite based materials. It can also be used as a deactivating agent to study the catalytic performance of acidic macroporous ion exchange resins. It can be annealed to reduce impurity in the grain boundaries, improve the stability and efficiency of the perovskite solar cells.

Avvertenze

Danger

Indicazioni di pericolo

H225,H314,H335

Classi di pericolo

Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

-9.0 °F - closed cup

Punto d’infiammabilità (°C)

-22.8 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, 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 2

1 of 2

Formamidine acetate salt 99%

Sigma-Aldrich

F15803

Formamidine acetate salt

Hydrobromic acid 48 wt. % in H2O, ≥99.99%

Sigma-Aldrich

339245

Hydrobromic acid

Bianca-Maria Bresolin et al.
Nanomaterials (Basel, Switzerland), 10(1) (2020-01-16)
The development of visible-light active photocatalysts is a current challenge especially energy and environmental-related fields. Herein, methylammonium lead iodide perovskite (MAIPb) was chosen as the novel semiconductor material for its ability of absorbing visible-light. An easily reproducible and efficient method
Preparation of the MacMillan imidazolidinones.
Samulis L and Tomkinson NCO.
Tetrahedron, 67(23), 4263-4267 (2011)
Formation of aromatic compounds from carbohydrates. V. Reaction of d-glucose and methylamine in slightly acidic, aqueous solution.
Olsson KJELL, et al.
Acta Chemica Scandinavica. Series B, 31(6), 469-469 (1977)
Nucleophilic Attack on Some Isothiazolium Salts.
Mckinnon DM and Hassan ME.
Canadian Journal of Chemistry, 51(18), 3081-3086 (1973)
Five-membered rings. II. Inter and intramolecular reactions of simple amines with N-substituted phthalimides. Methylamine as a reagent for removal of a phthaloyl group from nitrogen.
Wolfe S and Hasan SK.
Canadian Journal of Chemistry, 48(22), 3572-3579 (1970)
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.