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Sigma-Aldrich

Methanol

≥99.9%, HPLC Plus, suitable for HPLC, poly-coated bottles

Synonym(s):

Methyl alcohol

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About This Item

Linear Formula:
CH3OH
CAS Number:
Molecular Weight:
32.04
Beilstein/REAXYS Number:
1098229
EC Number:
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:
NACRES:
NA.21

product name

Methanol, HPLC Plus, ≥99.9%, poly-coated bottles

grade

HPLC Plus

Quality Level

vapor density

1.11 (vs air)

vapor pressure

410 mmHg ( 50 °C)
97.68 mmHg ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

725 °F

expl. lim.

36 %

technique(s)

HPLC: suitable

impurities

≤0.0002 meq/g Titr. base
≤0.0003 meq/g Titr. acid
≤0.001% Carbonyl Compounds
≤1.0 ppb Fluorescence (quinine) at 254 nm
≤1.0 ppb Fluorescence (quinine) at 365 nm
<0.05% water

evapn. residue

≤0.0001%

color

APHA: ≤10

refractive index

n20/D 1.329 (lit.)

bp

64.7 °C (lit.)

mp

−98 °C (lit.)

solubility

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

density

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

HPLC-gradient

≤2 mAU at 230 nm
≤5 mAU at 254 nm

λ

H2O reference

UV absorption

λ: 205 nm Amax: 1.0
λ: 210 nm Amax: 0.80
λ: 220 nm Amax: 0.20
λ: 230 nm Amax: 0.10
λ: 250 nm Amax: 0.02
λ: 400 nm Amax: 0.005

format

neat

SMILES string

CO

InChI

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

InChI key

OKKJLVBELUTLKV-UHFFFAOYSA-N

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General description

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.

Application

Methanol (MeOH) may be 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.
  • To compose eluent for the ion-pair reverse-phase HPLC isolation of nucleotides and their decomposition products.
  • As eluent in the HPLC estimation of malondialdehyde in plasma, which is an indicator of oxidative stress.
Suitable for HPLC, spectrophotometry, and some LC-MS applications

Preparation Note

Product filtered through a 0.2 μm filter

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_germany

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


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Nomaan M Rezayee et al.
Journal of the American Chemical Society, 137(3), 1028-1031 (2015-01-17)
This Communication describes the hydrogenation of carbon dioxide to methanol via tandem catalysis with dimethylamine and a homogeneous ruthenium complex. Unlike previous examples with homogeneous catalysts, this CO2-to-CH3OH process proceeds under basic reaction conditions. The dimethylamine is proposed to play
Methanol.
R Von Burg
Journal of applied toxicology : JAT, 14(4), 309-313 (1994-07-01)
Combining Low-Pressure CO2 Capture and Hydrogenation To Form Methanol.
Khusnutdinova JR, et al.
ACS Catalysis, 5(4), 2416-2422 (2015)
Ufuk Cobanoglu et al.
Asian Pacific journal of cancer prevention : APJCP, 12(6), 1399-1403 (2011-12-01)
Early diagnosis and prevention is very important for lung cancer patients. Previous studies have emphasized that the level of coenzyme Q10 (CoQ10), present primarily in mitochondria, decreases with age and is low in patients with chronic diseases. Our goal was
R A Cunha et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 18(6), 1987-1995 (1998-05-15)
ATP analogs substituted in the gamma-phosphorus (ATPgammaS, beta, gamma-imido-ATP, and beta,gamma-methylene-ATP) were used to probe the involvement of P2 receptors in the modulation of synaptic transmission in the hippocampus, because their extracellular catabolism was virtually not detected in CA1 slices.

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