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S8263

Sigma-Aldrich

Sodium hydroxide solution

5.0 M

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About This Item

Linear Formula:
NaOH
CAS Number:
Molecular Weight:
40.00
MDL number:
UNSPSC Code:
12352316
PubChem Substance ID:
NACRES:
NA.21

grade

for molecular biology

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Design, synthesis, and in vitro evaluation of quinolinyl analogues for α-synuclein aggregation
Yue X, et al.
Bioorganic & medicinal chemistry letters, 28, 1011-1019 (2018)
Solubility of dimethyldisulfide (DMDS) in aqueous solutions of Fe (III) complexes of trans-1, 2-cyclohexanediaminetetraacetic acid (CDTA) using the static headspace method
Iliuta MC and Larachi F
Fluid Phase Equilibria, 233, 184-189 (2005)
Richard J Travers et al.
Blood, 124(22), 3183-3190 (2014-09-10)
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
Valdeir Arantes et al.
Biotechnology for biofuels, 7, 87-87 (2014-07-01)
There is still considerable debate regarding the actual mechanism by which a "cellulase mixture" deconstructs cellulosic materials, with accessibility to the substrate at the microscopic level being one of the major restrictions that limits fast, complete cellulose hydrolysis. In the

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