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H9892

Sigma-Aldrich

Hydrochloric acid

1.0 N, BioReagent, suitable for cell culture

Synonyme(s) :

Chlorure d’hydrogène solution

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About This Item

Formule empirique (notation de Hill):
HCl
Numéro CAS:
7647-01-0
Poids moléculaire :
36.46
Numéro MDL:
MFCD00011324
Code UNSPSC :
12352301
ID de substance PubChem :
24895872
Nomenclature NACRES :
NA.71

product name

Acide chlorhydrique solution, 1.0 N, BioReagent, suitable for cell culture

Stérilité

sterile-filtered

Niveau de qualité

200

Gamme de produits

BioReagent

Forme

solution

Concentration

1.0 N

Technique(s)

cell culture | mammalian: suitable

Traces d'anions

chloride (Cl-): passes test

Chaîne SMILES 

Cl

InChI

1S/ClH/h1H

Clé InChI

VEXZGXHMUGYJMC-UHFFFAOYSA-N

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Description générale

Hydrochloric acid solution, a clear colorless liquid, is a solution of hydrogen chloride gas dissolved in water. It is a strong inorganic acid.

Application

Hydrochloric acid solution (HCl solution) is mainly used to adjust the pH in cell culture medium.
It can also be used:
  • In the extraction of elderberry anthocyanins by endothelial cells.
  • To convert iron(III) perchlorate to Fe(III) ions which can then form a complex with acetohydroxamic acid (FeAHA).

The hydrochloric acid solution has been used:
  • to acidify the surface water sample and to prevent interference from carbonate concentrations up to 10 mg L-1 with organic carbon detector (OCD) detection
  • to adjust the pH of complete transfection media for transfection with chitosan/pDNA nanoparticle complexes
  • to prepare artificial tear solution (ATS) to incorporate the fluorescently tagged cholesteryl ester

Actions biochimiques/physiologiques

Hydrochloric acid (HCl) is commonly used in research and large-scale applications. Its large-scale applications include the refinement of ore to produce tin and tantalum, the cleaning of metal products, and the hydrolysis of starch and proteins in the production of food products. HCl is also used in chemical synthesis. It can also be used in hydrolyzing samples for chromatographic analysis, such as in matairesinol, in flax seed, glycopeptides, κ-carrageenan derived oligosaccharides, and syn- and anti-1,3-diols. HCl is also used as a bleaching agent to neutralize alkaline agents in the food, textile, metal, and rubber industries.

Pictogrammes

Corrosion
GHS05

Mention d'avertissement

Warning

Mentions de danger

H290

Conseils de prudence

P234 - P390

Classification des risques

Met. Corr. 1

Code de la classe de stockage

8B - Non-combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Acide chlorhydrique ACS reagent, 37%

Sigma-Aldrich

320331

Acide chlorhydrique

Solution d'acide chlorhydrique c(HCl) = 0.1 mol/l (0.1 N), Titripur®, reag. Ph. Eur., reag. USP

Supelco

1.09060

Solution d'acide chlorhydrique

Hydrochloric acid solution c(HCL) = 6.0 mol/l (6.0 N)

Supelco

143007

Hydrochloric acid solution

Incorporation of the elderberry anthocyanins by endothelial cells increases protection against oxidative stress.
Youdim KA, et al.
Free radical biology & medicine, 29(1), 51-60 (2000)
Structural analysis of photocross linkable methacryloyl-modified protein derivatives.
Yue K, et al.
Biomaterials, 139(1), 163-171 (2017)
High efficiency gene transfer using chitosan/DNA nanoparticles with specific combinations of molecular weight and degree of deacetylation.
Lavertu M, et al.
Biomaterials, 27(27), 4815-4824 (2006)
Marta Kolodziejczak et al.
ACS chemical neuroscience, 6(7), 1219-1230 (2015-04-11)
Maturation of functional neuronal circuits during central nervous system development relies on sophisticated mechanisms. First, axonal and dendritic growth should reach appropriate targets for correct synapse elaboration. Second, pruning and neuronal death are required to eliminate redundant or inappropriate neuronal
Douglas M McMillan et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 40(7), 1804-1812 (2015-01-30)
CYP2D metabolically activates codeine to morphine, which is required for codeine analgesia. Permeability across the blood-brain barrier, and active efflux, suggests that initial morphine in the brain after codeine is due to brain CYP2D metabolism. Human CYP2D is higher in
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