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About This Item
Linear Formula:
NaOH
CAS Number:
Molecular Weight:
40.00
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352316
MDL number:
Concentration:
5.0 M
Form:
liquid
Grade:
Molecular Biology
grade
Molecular Biology
Quality Level
agency
suitable for SM 4500 - NH3
vapor pressure
3 mmHg ( 37 °C)
form
liquid
concentration
5.0 M
pH
14
solubility
water: miscible
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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.
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)
