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676780

Sigma-Aldrich

Metanolo

≥99.8%, ACS reagent, suitable for HPLC

Sinonimo/i:

Alcol metilico

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About This Item

Formula condensata:
CH3OH
Numero CAS:
Peso molecolare:
32.04
Beilstein:
1098229
Numero CE:
Numero MDL:
Codice UNSPSC:
12352104
ID PubChem:
NACRES:
NA.05

product name

Metanolo, ACS reagent, ≥99.8%

Grado

ACS reagent

Densità del vapore

1.11 (vs air)

Tensione di vapore

410 mmHg ( 50 °C)
97.68 mmHg ( 20 °C)

Saggio

≥99.8%

Forma fisica

liquid

Temp. autoaccensione

725 °F

Limite di esplosione

36 %

tecniche

HPLC: suitable

Impurezze

H2SO4, passes test (darkened)
MnO4- reducers, passes test
≤0.0002 meq/g Titr. base
≤0.0003 meq/g Titr. acid
≤0.001% acetaldehyde
≤0.001% acetone
≤0.001% formaldehyde
≤0.1% Water

Residuo dopo evaporazione

≤0.001%

Colore

clear
APHA: ≤10

Indice di rifrazione

n20/D 1.329 (lit.)

P. eboll.

64.7 °C (lit.)

Punto di fusione

−98 °C (lit.)

Solubilità

benzene: miscible(lit.)
ethanol: miscible(lit.)
water: miscible(lit.)

Densità

0.791 g/mL at 25 °C (lit.)

Formato

neat

Stringa SMILE

CO

InChI

1S/CH4O/c1-2/h2H,1H3
OKKJLVBELUTLKV-UHFFFAOYSA-N

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Descrizione generale

Methanol (MeOH) is an organic solvent with a wide range of industrial applications. It is the main component of lithium batteries. It can be prepared by hydrogenation of CO2 under various conditions. MeOH is a toxic alcohol employed for denaturing ethyl alcohol. A study reports the preparation of biodiesel from canola oil using methanol under supercritical conditions.
Methanol is an alcohol. Its thermochemical conversion to C2-C10 hydrocarbons in the presence of shape-selective zeolites has been reported. Its oxidation on Ru-Pt catalyst system by ruthenium ad-atoms has been proposed.

Applicazioni

Methanol has been used during colony-forming unit (CFU) assay and histochemical staining.
Methanol may be used as:
  • A solvent for cleaning the coverslips before silanization for DNA combing.
  • An additive to improve the octane number of gasoline.
  • A liquid fuel in direct methanol fuel cells (DMFCs).
  • A solvent to synthesize methyl levulinate by acid catalyzed conversion of 5-hydroxymethylfurfural (HMF) and furfuryl alcohol (FA).
  • A reactant to prepare dimethylcarbonate by reacting with CO2 in the presence of graphene oxide-bound octahedral molybdenum cluster (GO-Cs2Mo6Bri8Bra6).
Methanol may be used for the sodium dodecyl sulfate-polyacrylamide gel electrophoretic (SDS-PAGE) analysis of alkaline protease isoforms isolated from larva of the spotted sand bass (Paralabrax maculatofasciatus). It may be used in the isolation and quantitative determination of carotenes and xanthophylls from Capsicum annum pericarp extracts by HPLC.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Organi bersaglio

Eyes,Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

49.5 °F - closed cup

Punto d’infiammabilità (°C)

9.7 °C - closed cup


Certificati d'analisi (COA)

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Metanolo

Subodh Kumar et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(8), 3488-3494 (2014-12-30)
The octahedral molybdenum cluster-based compound, Cs2 Mo6 Br(i) 8 Br(a) 6 was immobilized on graphene oxide (GO) by using a facile approach. High resolution transmission electron microscopy results revealed that molybdenum clusters were uniformly distributed on the GO nanosheets. Cs2
Upgrading biomass-derived furans via acid-catalysis/hydrogenation: the remarkable difference between water and methanol as the solvent.
Hu X, et al.
Green Chemistry, 17(1), 219-224 (2015)
Octane Rating of Gasoline and Octane Booster Additives.
Demirbas A, et al.
Petroleum Science and Technology, 33(11), 1190-1197 (2015)
Silanization of coverslips for DNA combing.
Labit H, et al.
Biotechniques, 11, 50-50 (2009)
Development of digestive enzyme activity in larvae of spotted sand bass Paralabrax maculatofasciatus II: electrophoretic analysis.
Alvarez-Gonzalez CA, et al.
Fish Physiology and Biochemistry, 36(1), 29-37 (2010)

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