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17935

Supelco

Hydrogen chloride – methanol solution

~1.25 m HCl (T), for GC derivatization, LiChropur

Sinónimos:
Hydrochloric acid in methanol
Fórmula lineal:
HCl · CH3OH
Número de CAS:
Peso molecular:
36.46
Beilstein:
1098214
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

grade

for GC derivatization

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

concentration

~1.25 m HCl (T)

application(s)

gas chromatography (GC): suitable

density

0.831 g/mL at 20 °C

storage temp.

2-8°C

SMILES string

Cl

InChI

1S/ClH/h1H

InChI key

VEXZGXHMUGYJMC-UHFFFAOYSA-N

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK Germany

WGK 2

Flash Point F

51.8 °F - closed cup

Flash Point C

11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificado de Análisis

Certificado de origen

Esterification of galacturonic acid and polyuronides with methanol-hydrogen chloride.
E F JANSEN et al.
Journal of the American Chemical Society, 68, 1475-1477 (1946-08-01)
A REACTION TUBE FOR METHANOLYSIS; INSTABILITY OF HYDROGEN CHLORIDE IN METHANOL.
Y KISHIMOTO et al.
Journal of lipid research, 6, 435-436 (1965-07-01)
Michael F. L'Annunziata
Handbook of Radioactivity Analysis, 400-400 (2012)
Jay G Hosking et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 40(4), 1005-1015 (2014-10-21)
Successful decision making often requires weighing a given option's costs against its associated benefits, an ability that appears perturbed in virtually every severe mental illness. Animal models of such cost/benefit decision making overwhelmingly implicate mesolimbic dopamine in our willingness to...
Mahsa Sadeghi et al.
British journal of pharmacology, 172(2), 460-468 (2014-01-01)
Tapentadol is a novel analgesic that combines moderate μ-opioid receptor agonism and noradrenaline reuptake inhibition in a single molecule. Both mechanisms of action are involved in producing analgesia; however, the potency and efficacy of tapentadol in individual neurons has not...

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