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H9892

Sigma-Aldrich

Hydrochloric acid

1.0 N, BioReagent, suitable for cell culture

Sinonimo/i:

Cloruro di idrogeno

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About This Item

Formula empirica (notazione di Hill):
HCl
Numero CAS:
7647-01-0
Peso molecolare:
36.46
Numero MDL:
MFCD00011324
Codice UNSPSC:
12352301
ID PubChem:
24895872
NACRES:
NA.71

product name

Acido cloridrico, 1.0 N, BioReagent, suitable for cell culture

Sterilità

sterile-filtered

Livello qualitativo

200

Nome Commerciale

BioReagent

Forma fisica

solution

Concentrazione

1.0 N

tecniche

cell culture | mammalian: suitable

Anioni in tracce

chloride (Cl-): passes test

Stringa SMILE

Cl

InChI

1S/ClH/h1H
VEXZGXHMUGYJMC-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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

Applicazioni

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

Azioni biochim/fisiol

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.

Pittogrammi

Corrosion
GHS05

Avvertenze

Warning

Indicazioni di pericolo

H290

Consigli di prudenza

P234 - P390

Classi di pericolo

Met. Corr. 1

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Acido cloridrico, soluzione c(HCl) = 0.1 mol/l (0.1 N), Titripur®, reag. Ph. Eur., reag. USP

Supelco

1.09060

Acido cloridrico, soluzione

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

Supelco

143007

Hydrochloric acid solution

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)
Structural analysis of photocross linkable methacryloyl-modified protein derivatives.
Yue K, et al.
Biomaterials, 139(1), 163-171 (2017)
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)
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
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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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