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1.06018

Supelco

Methanol

≥99.8% (GC), HPLC grade, suitable for HPLC, LiChrosolv®

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Synonym(s):
MeOH, Hydroxymethane, Carbinol, Methyl alcohol
Linear Formula:
CH3OH
CAS Number:
Molecular Weight:
32.04
Beilstein:
1098229
MDL number:
UNSPSC Code:
12191502
EC Index Number:
200-659-6
NACRES:
NA.03

grade

HPLC grade
isocratic

Quality Level

vapor density

1.11 (vs air)

vapor pressure

128 hPa ( 20 °C)
410 mmHg ( 50 °C)
97.68 mmHg ( 20 °C)

product line

LiChrosolv®

Assay

≥99.8% (GC)

form

liquid

autoignition temp.

725 °F

potency

5628 mg/kg LD50, oral (Rat)
17100 mg/kg LD50, skin (Rabbit)

expl. lim.

36 %

technique(s)

HPLC: suitable

impurities

≤0.0002 meq/g Acidity
≤0.0002 meq/g Alkalinity
≤0.03% Water

evapn. residue

≤3.0 mg/L

color

APHA: ≤10

transmittance

225 nm, ≥50%
240 nm, ≥80%
265 nm, ≥98%

refractive index

n20/D 1.329 (lit.)

kinematic viscosity

0.54-0.59 cSt(20 °C)

bp

64.7 °C (lit.)

mp

−98 °C (lit.)

transition temp

flash point 9.7 °C

density

0.791 g/mL at 25 °C (lit.)

format

neat

storage temp.

2-30°C

SMILES string

CO

InChI

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

InChI key

OKKJLVBELUTLKV-UHFFFAOYSA-N

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General description

LiChrosolv® solvents exhibit high degree of UV transmittance, low particle count, low acidity and alkalinity and low evaporation residue level. This makes them ideal for reproducible separations.

Application

Intended for HPLC and UHPLC-MS applications.
Featured in method development of:
  • Benazepril - USP Method Benazepril RS
  • Betamethasone - USP Method Betamethasone Valerate Assay
  • Irbesartan - USP Method Irbesartan Assay
  • Lamivudine - USP Method Lamivudine RS
  • Lansoprazole - USP Method Lansoprazole RS
  • Levofloxacin - USP Method Levofloxacin RS - USP Method Levofloxacin Assay
  • Nifedipine - USP Method Nifedipine RS - USP Method Nifedipine Assay
  • Pharmacopoeia Monograph Methods - HPLC and UHPLC methods for Regulated Drug Analysis
  • Pioglitazone - USP Method Pioglitazone HCl RS - USP Method Pioglitazone HCl Assay

Features and Benefits

  • suitability tested and specified for UHPLC-MS and UHPLC-UV: for analytical flexibility
  • specified quality in positive and negative in positive and negative electrospray ionization (ESI) and atmospheric-pressure chemical ionization-mass spectrometry (APCI-MS) for lowest detection limits and confidence in analyses for all important MS modes (test 1)
    —ESI/APCI (+) < 2 ppb
    —ESI/APCI (-) < 10 ppb
  • lowest impurity profile: for interference-free baselines (test 2)
  • microfiltered through 0.2 μm filter (test 3) to provide:
    —A long lifespan to filters and mechanical parts of HPLC systems
    ––reduced risk of column clogging
  • packaged in borosilicate glass bottles for minimized metal ion contaminations
  • lowest levels of trace metal impurities for a minimum metal ion adduct formation
    —<5 ppb
  • lowest level of polyethylene glycol (PEG) impurities in UHPLC-MS solvent lineup (PEG S/N signal-to-noise-ratio < 50)

Preparation Note

Product filtered through a 0.2 μm filter

Analysis Note

Evaporation Number: 1.9
Purity (GC): ≥ 99.8 %
Identity (IR): conforms
Evaporation residue: ≤ 3.0 mg/l
Water: ≤ 0.03 %
Color: ≤ 10 Hazen
Acidity: ≤ 0.0002 meq/g
Alkalinity: ≤ 0.0002 meq/g
Transmission (at 225 nm): ≥ 50 %
Transmission (at 240 nm): ≥ 80 %
Transmission (from 265 nm): ≥ 98 %
Filtered by 0.2 µm filter

Other Notes

Explore various lab safety accessories and equipment for safe handling of solvents to increase your safety level from the first usage.

Legal Information

LICHROSOLV is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

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

WGK

WGK 2

Regulatory Information

危险化学品

Certificates of Analysis (COA)

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