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Merck

24229

Methanol

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

Synonym(s):

Methyl alcohol

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About This Item

Linear Formula:
CH3OH
CAS Number:
67-56-1
Molecular Weight:
32.04
NACRES:
NA.05
PubChem Substance ID:
329752606
eCl@ss:
39020101
UNSPSC Code:
12352104
EC Number:
200-659-6
MDL number:
MFCD00004595
Beilstein/REAXYS Number:
1098229
Assay:
≥99.7% (GC)
Technique(s):
immunofluorescence: suitable
Bp:
64.7 °C (lit.)
Vapor pressure:
410 mmHg ( 50 °C), 97.68 mmHg ( 20 °C)

Key Documents

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Product Name

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

SMILES string

CO

InChI key

OKKJLVBELUTLKV-UHFFFAOYSA-N

InChI

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

vapor density

1.11 (vs air)

vapor pressure

410 mmHg ( 50 °C), 97.68 mmHg ( 20 °C)

grade

puriss.

assay

≥99.7% (GC)

form

liquid

autoignition temp.

725 °F

quality

meets analytical specification of Ph Eur

expl. lim.

36 %

technique(s)

immunofluorescence: suitable

impurities

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)

refractive index

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

bp

64.7 °C (lit.)

mp

−98 °C (lit.)

density

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

anion traces

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

cation traces

Fe: ≤1 mg/kg

suitability

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

format

neat

Quality Level

200

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General description

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

Application

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

Packaging

This product is also available in glass bottles.

Other Notes

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.

signalword

Danger

Hazard Classifications

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

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB2030
STBL2845
STBL2124
STBL1902
STBK8278

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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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