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Supelco

Hydrogen chloride solution

~1.25 M in 2-propanol, for GC derivatization, LiChropur™

Synonym(s):

Hydrochloric acid in 2-propanol

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About This Item

Linear Formula:
HCl · CH3CH(OH)CH3
Molecular Weight:
36.46
Beilstein:
1098214
MDL number:
MFCD00011324
UNSPSC Code:
41116105
PubChem Substance ID:
329751588
NACRES:
NA.22

product name

Hydrogen chloride – 2-propanol solution, ~1.25 M HCl (T), for GC derivatization, LiChropur™

grade

for GC derivatization

Quality Level

100

form

liquid

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

concentration

~1.25 M HCl (T)

technique(s)

gas chromatography (GC): suitable

density

0.821 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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Application

Diluted solutions of Hydrogen chloride in 2-propanol is used as a derivatizing agent for GC.
It may be used in measuring their conductance at 25°C.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

H225,H290,H319,H336

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Met. Corr. 1 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

53.6 °F

Flash Point(C)

12 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB0928
BCCH8622
BCBP9611V
BCBK4173V
BCBF5327V

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Sigma-Aldrich

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Hydrogen chloride

Effect of water on proton migration in alcoholic solvents-II. conductance of hydrogen chloride in 2-propanol at 25? C.
De Lisi, R., and M. Goffredi.
Electrochimica Acta, 17, 2001-2008 (1972)
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Nucleic acids research, 42(22), 13911-13919 (2014-11-13)
N(6)A methylation is the most abundant RNA modification occurring within messenger RNA. Impairment of methylase or demethylase functions are associated with severe phenotypes and diseases in several organisms. Beside writer and eraser enzymes of this dynamic RNA epigenetic modification, reader
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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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