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24229

Sigma-Aldrich

Metanol

≥99.7% (GC), suitable for immunofluorescence, meets analytical specification of Ph Eur

Sinônimo(s):

Álcool metílico

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About This Item

Fórmula linear:
CH3OH
Número CAS:
Peso molecular:
32.04
Beilstein:
1098229
Número CE:
Número MDL:
Código UNSPSC:
12352104
eCl@ss:
39020101
ID de substância PubChem:
NACRES:
NA.05
Ensaio:
≥99.7% (GC)
técnica(s):
immunofluorescence: suitable
p.e.:
64.7 °C (lit.)
pressão de vapor:
410 mmHg ( 50 °C)
97.68 mmHg ( 20 °C)
Preço e disponibilidade não estão disponíveis no momento.

Nome do produto

Metanol, puriss., meets analytical specification of Ph Eur, ≥99.7% (GC)

densidade de vapor

1.11 (vs air)

Nível de qualidade

pressão de vapor

410 mmHg ( 50 °C)
97.68 mmHg ( 20 °C)

grau

puriss.

Ensaio

≥99.7% (GC)

Formulário

liquid

temperatura de autoignição

725 °F

qualidade

meets analytical specification of Ph Eur

Lim. expl.

36 %

técnica(s)

immunofluorescence: suitable

Impurezas

impurities A, complies (GC)
reducing substances, complies
related substances, complies (GC)
residual solvents, complies
≤0.0002% benzene
≤0.0003% free alkali (as NH3)
≤0.001% acetone (GC)
≤0.001% non-volatile matter
≤0.003% aldehydes and ketones (as CH3COCH3)
≤0.003% free acid (as HCOOH)
≤0.1% water (Karl Fischer)

índice de refração

n20/D 1.328-1.330
n20/D 1.329 (lit.)

p.e.

64.7 °C (lit.)

pf

−98 °C (lit.)

densidade

0.791-0.793 g/mL at 20 °C
0.791 g/mL at 25 °C (lit.)

traços de ânion

chloride (Cl-): ≤1 mg/kg
sulfate (SO42-): ≤5 mg/kg

traços de cátion

Fe: ≤1 mg/kg

adequação

complies for UV absorption
complies for appearance
complies for identity (IR)
complies for reaction against H2SO4

Formato

neat

cadeia de caracteres SMILES

CO

InChI

1S/CH4O/c1-2/h2H,1H3

chave InChI

OKKJLVBELUTLKV-UHFFFAOYSA-N

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Descrição geral

Methanol is an alcohol. Its conversion to C2-C10 hydrocarbons by employing a new class of shape-selective zeolites has been reported.[1] Its oxidation on Ru-Pt catalyst system by ruthenium ad-atoms has been proposed.[2]

Aplicação

Methanol was used in the following studies:
  • Colony forming unit-fibroblast assay of bone marrow mononuclear cells.[3]
  • As solvent for the preparation of extracts of hyphae of Aspergillus for the estimation of gliotoxin by reversed phase-HPLC.[4]
  • Immunofluorescence studies.[5]

Embalagem

This product is also available in glass bottles.

Outras notas

The article number 24229-4X2.5L-R will be discontinued. Please order the single bottle 24229-2.5L-R which is physically identical with the same exact specifications.

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Eyes,Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

49.5 °F - closed cup

Ponto de fulgor (°C)

9.7 °C - closed cup


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Emer P Reeves et al.
Mycopathologia, 158(1), 73-79 (2004-10-19)
Aspergillus fumigatus is a pathogenic fungus capable of causing both allergic lung disease and invasive aspergillosis, a serious, life-threatening condition in neutropenic patients. Aspergilli express an array of mycotoxins and enzymes which may facilitate fungal colonisation of host tissue. In
Robert E Schwartz et al.
The Journal of clinical investigation, 109(10), 1291-1302 (2002-05-22)
We have derived from normal human, mouse, and rat postnatal bone marrow primitive, multipotent adult progenitor cells (MAPCs) that can differentiate into most mesodermal cells and neuroectodermal cells in vitro and into all embryonic lineages in vivo. Here, we show
The conversion of methanol and other O-compounds to hydrocarbons over zeolite catalysts.
Chang CD and Silvestri AJ.
J. Catal., 47(2), 249-259 (1977)
Electrocatalysis by ad-atoms: Part II. Enhancement of the oxidation of methanol on platinum by ruthenium ad-atoms.
Watanabe MA and Motoo S.
J. Electroanal. Chem. Interfac. Electrochem., 60(3), 267-273 (1975)
Venkata Lokesh Battula et al.
Haematologica, 94(2), 173-184 (2008-12-11)
Conventionally, mesenchymal stem cells are functionally isolated from primary tissue based on their capacity to adhere to a plastic surface. This isolation procedure is hampered by the unpredictable influence of co-cultured hematopoietic and/or other unrelated cells and/or by the elimination

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