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B4059

Sigma-Aldrich

Barium hydroxide solution

0.3 N

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About This Item

Linear Formula:
Ba(OH)2
CAS Number:
Molecular Weight:
171.34
MDL number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.25

form

liquid

Quality Level

concentration

0.3 N

solubility

soluble (Clear colorless liquid, may contain some small insoluble particles.)

SMILES string

O[Ba]O

InChI

1S/Ba.2H2O/h;2*1H2/q+2;;/p-2

InChI key

RQPZNWPYLFFXCP-UHFFFAOYSA-L

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Application

Barium hydroxide may be used in the development of formulations for the purification of materials such as heteropolysaccharide-protein biopolymers and the release of long-chain bases (LCB) from biological samples. Barium hydroxide solution may be used for protein precipitation in turbid fluids such as whole blood in assays based on the Somogyi-Nelson method.
Used in conjunction with zinc sulfate to deproteinize via barium sulfate precipitation whole blood, plasma, or serum samples which are colored or turbid. The resulting supernatant or filtrate is then available for subsequent analysis of glucose by Somogi-Nelson method.

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Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Bahareh Tabatabaee Amid et al.
Molecules (Basel, Switzerland), 17(9), 10875-10892 (2012-09-12)
Natural biopolymers from plant sources contain many impurities (e.g., fat, protein, fiber, natural pigment and endogenous enzymes), therefore, an efficient purification process is recommended to minimize these impurities and consequently improve the functional properties of the biopolymer. The main objective
E Bach et al.
Analytical biochemistry, 203(2), 335-339 (1992-06-01)
A rapid, facile, and sensitive uv-spectrophotometric assay has been developed for the determination of the enzymatic degradation of polysaccharides that generates reducing sugars. The assay was carried out with 2-cyanoacetamide in a single test tube. The solution was left at
M F Byford
The Biochemical journal, 280 ( Pt 1), 261-265 (1991-11-15)
The beta-elimination of phosphoserine residues by dilute alkali is catalysed by the presence of group II metal ions. The use of 0.1 M-Ba (OH)2 catalysed the rate of beta-elimination of phosphoserine by more than two orders of magnitude compared with
T Mahendran et al.
Journal of agricultural and food chemistry, 56(19), 9269-9276 (2008-09-12)
The structural characteristics of the gum exudate of Acacia senegal (gum arabic) have been investigated by monitoring the composition and physicochemical properties before and after treatment with proteolytic enzyme and various alkaline systems. Molecular mass ( M w) and radius
T Irie et al.
Carbohydrate research, 192, 167-172 (1989-10-23)
The alkylation of cyclomalto-oligosaccharides (cyclodextrins, CDs) with dialkyl sulfate-barium hydroxide has been claimed to yield 2,6-di-O-alkyl derivatives. Re-investigation by plasma desorption-m.s. of the products of laboratory methylation of alpha CD, beta CD, or gamma CD and ethylation of beta CD

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