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Merck
CN

03378

Chloride atomic spectroscopy standard concentrate 10.00 g Cl-

10.00 g/L, for 1 l standard solution, analytical standard

Synonym(s):

Hydrochloric acid solution, Hydrogen chloride solution

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About This Item

Empirical Formula (Hill Notation):
HCl
CAS Number:
Molecular Weight:
36.46
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
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InChI

1S/ClH/h1H

SMILES string

Cl

InChI key

VEXZGXHMUGYJMC-UHFFFAOYSA-N

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

packaging

ampule of

concentration

10.00 g/L

solubility

H2O: soluble

format

single component solution

General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Preparation Note

prepared with HCl and H2O

pictograms

Corrosion

signalword

Warning

hcodes

Hazard Classifications

Met. Corr. 1

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Synaptic degeneration is an early pathogenic event in Alzheimer's disease, associated with cognitive impairment and disease progression. Cerebrospinal fluid biomarkers reflecting synaptic integrity would be highly valuable tools to monitor synaptic degeneration directly in patients. We previously showed that synaptic
Thomas Krohn et al.
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To determine the frequency of seemingly pathological retroperitoneal uptake in the location of the coeliac ganglia in patients undergoing [(68)Ga]PSMA-HBED PET/CT. The study included 85 men with prostate cancer referred for [(68)Ga]PSMA-HBED PET/CT. The PET/CT scans were evaluated for the
Dominik Theler et al.
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
Sandra Donkervoort et al.
Human mutation, 36(1), 48-56 (2014-09-11)
Collagen 6-related dystrophies and myopathies (COL6-RD) are a group of disorders that form a wide phenotypic spectrum, ranging from severe Ullrich congenital muscular dystrophy, intermediate phenotypes, to the milder Bethlem myopathy. Both inter- and intrafamilial variable expressivity are commonly observed.

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