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S8263

Sigma-Aldrich

Sodium hydroxide solution

5.0 M

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Linear Formula:
NaOH
CAS Number:
Molecular Weight:
40.00
MDL number:
PubChem Substance ID:
NACRES:
NA.21

grade

for molecular biology

Quality Level

agency

suitable for SM 4500 - NH3

vapor pressure

3 mmHg ( 37 °C)

form

liquid

concentration

5.0 M

pH

14

density

1.327 g/cm3 at 25 °C

storage temp.

room temp

SMILES string

[OH-].[Na+]

InChI

1S/Na.H2O/h;1H2/q+1;/p-1

InChI key

HEMHJVSKTPXQMS-UHFFFAOYSA-M

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Application

Sodium hydroxide solution can be used:
  • As a base in the reduction of oximes, imines, and hydrazones using Raney nickel.
  • In the preparation of trans-1,2-cyclohexanediaminetetraacetic acid standard solution applicable in the synthesis of the ferric chelate complex.
  • In the synthesis of radiolabeled quinolinyl analogs for α-synuclein binding assay studies.

pictograms

Corrosion

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Storage Class

8B - Non-combustible, corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Convenient method for reduction of CN double bonds in oximes, imines, and hydrazones using sodium borohydride-Raney Ni system
Yang Y, et al.
Synthetic Communications, 42, 2540-2554 (2012)
Solubility of dimethyldisulfide (DMDS) in aqueous solutions of Fe (III) complexes of trans-1, 2-cyclohexanediaminetetraacetic acid (CDTA) using the static headspace method
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Design, synthesis, and in vitro evaluation of quinolinyl analogues for α-synuclein aggregation
Yue X, et al.
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During termination of translation in eukaryotes, a GTP-binding protein, eRF3, functions within a complex with the tRNA-mimicking protein, eRF1, to decode stop codons. It remains unclear how the tRNA-mimicking protein co-operates with the GTPase and with the functional sites on
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Polyphosphate (polyP) is secreted by activated platelets and has been shown to contribute to thrombosis, suggesting that it could be a novel antithrombotic target. Previously reported polyP inhibitors based on polycationic substances, such as polyethylenimine, polyamidoamine dendrimers, and polymyxin B

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