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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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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)
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)
Xi-Ping Huang et al.
Nature, 527(7579), 477-483 (2015-11-10)
At least 120 non-olfactory G-protein-coupled receptors in the human genome are 'orphans' for which endogenous ligands are unknown, and many have no selective ligands, hindering the determination of their biological functions and clinical relevance. Among these is GPR68, a proton
Nicole von Burg et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(35), 12835-12840 (2014-08-20)
Group 3 innate lymphoid cells (ILC3s) have emerged as important cellular players in tissue repair and innate immunity. Whether these cells meaningfully regulate adaptive immune responses upon activation has yet to be explored. Here we show that upon IL-1β stimulation

Related Content

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

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