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Merck
CN

84431

Hydrogen chloride solution

4.0 M in dioxane

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About This Item

Empirical Formula (Hill Notation):
HCl
CAS Number:
Molecular Weight:
36.46
UNSPSC Code:
12352106
PubChem Substance ID:
MDL number:
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Product Name

Hydrogen chloride solution, 4.0 M in dioxane

InChI

1S/ClH/h1H

SMILES string

Cl

InChI key

VEXZGXHMUGYJMC-UHFFFAOYSA-N

quality

ampule

concentration

4.0 M in dioxane
4.0 M±0.1 M in dioxane (T)

storage temp.

2-8°C

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signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

62.6 °F - closed cup

flash_point_c

17.0 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Zhaorui Sun et al.
Journal of cellular physiology, 229(2), 213-224 (2013-07-25)
We sought to explore the treatment effects and the repair mechanisms of bone marrow derived mesenchymal stem cells (MSCs) during HCl-induced acute lung injury (ALI). MSCs were delivered through the tail veins of rats 24 h after intranasal instillation of
Q Miao et al.
Physical review letters, 109(23), 233905-233905 (2013-02-02)
X-ray lasing is predicted to ensue when molecules are pumped into dissociative core-excited states by a free-electron-laser pulse. The lasing is due to the population inversion created in the neutral dissociation product, and the process features self-trapping of the x-ray
Woo Seok Yang et al.
Journal of ethnopharmacology, 146(2), 637-644 (2013-02-16)
Archidendron clypearia Jack. (Fabaceae) is a representative ethnomedicinal herbal plant prescribed for various inflammatory diseases such as pharyngolaryngitis and tonsillitis. However, the pharmacology behind this plant's anti-inflammatory properties has not been fully understood. Therefore, in this study, the anti-inflammatory mechanism
Elena N Makarova et al.
Carbohydrate polymers, 92(2), 1817-1826 (2013-02-13)
The pectic polysaccharide named abienan AS-A was isolated from the wood greenery of Abies sibirica using dilute hydrochloric acid (pH 4.0) at 70°C. The structure of abienan AS-A was elucidated using sugar composition analysis, ion-exchange chromatography and partial acid hydrolysis
Rajarethinam Solaiselvi et al.
Organic letters, 15(6), 1186-1189 (2013-03-07)
A facile method utilizing RCOX/K2CO3 as a novel reagent for conjugate addition of hydrogen halide, in addition to tertiary (3°)-hydroxyl protection that leads to the synthesis of functionalized β-halo Morita-Baylis-Hillman ester appended oxindoles, has been developed. The diastereoselective one-pot O-acylation-hydrohalogenation

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