Skip to Content
Merck
All Photos(4)

Documents

S9640

Sigma-Aldrich

Sodium tetraborate decahydrate

ACS reagent, ≥99.5%

Synonym(s):

Borax decahydrate, Sodium borate decahydrate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
Na2B4O7 · 10H2O
CAS Number:
Molecular Weight:
381.37
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Agency

suitable for SM 4500 - NH3

vapor pressure

0.213 hPa ( 20 °C)

Assay

≥99.5%

form

powder or crystals

impurities

≤0.005% Insoluble matter

pH

9.15-9.20 (25 °C, 0.01 M in solution)

density

1.73 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤0.001%
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.005%

cation traces

Ca: ≤0.005%
Fe: ≤5 ppm
heavy metals (as Pb): ≤0.001%

SMILES string

O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]B1Ob2ob([O-])ob(O1)o2

InChI

1S/B4O7.2Na.10H2O/c5-1-7-3-9-2(6)10-4(8-1)11-3;;;;;;;;;;;;/h;;;10*1H2/q-2;2*+1;;;;;;;;;;

InChI key

CDMADVZSLOHIFP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Sodium tetraborate decahydrate is a naturally occurring material used as a catalyst or additive for many organic transformations such as Nef reaction, Knoevenagel condensation, substitution, addition, selective methylation of vicinal diols, and desilylation of trimethylsilyl alkynones.

Application

Sodium tetraborate decahydrate can be used as a catalyst in the:
  • Regioselective thiolysis of 1,2-epoxides by using thiols to synthesize β-hydroxy sulfides.
  • Hetero-Michael addition of thiols with electron-deficient olefins to synthesize corresponding β-adducts.
  • Solvent-free Biginelli reaction to synthesize 3,4-dihydropyrimidin-2(1H)-ones.
It can also be used as an additive to prepare polypyrrole-borax composites with high dielectric properties.

Legal Information

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Repr. 1B

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Maxime Mivelaz et al.
Methods (San Diego, Calif.), 184, 112-124 (2020-02-01)
In eukaryotic cells, the genome is packaged into chromatin and exists in different states, ranging from open euchromatic regions to highly condensed heterochromatic regions. Chromatin states are highly dynamic and are organized by an interplay of histone post-translational modifications and
Federico Corti et al.
Nature communications, 10(1), 1562-1562 (2019-04-07)
The proteoglycan Syndecan-2 (Sdc2) has been implicated in regulation of cytoskeleton organization, integrin signaling and developmental angiogenesis in zebrafish. Here we report that mice with global and inducible endothelial-specific deletion of Sdc2 display marked angiogenic and arteriogenic defects and impaired
Jian-Feng He et al.
Journal of chromatography. A, 1218(24), 3816-3821 (2011-05-14)
The paper presents an on-line transient moving chemical reaction boundary (MCRB) method for simply but efficiently stacking analytes in capillary electrophoresis (CE). The CE technique was developed for a rapid determination of fumaric and maleic acid. Based on the theory
Sinan Ince et al.
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS), 24(3), 161-164 (2010-06-24)
The aims of this study were to clarify the effects of high dietary supplementation with boric acid and borax, called boron (B) compounds, on lipid peroxidation (LPO), antioxidant activity, some vitamin levels, and DNA damage in rats. Thirty Sprague Dawley
Uttam Manna et al.
The journal of physical chemistry. B, 113(27), 9137-9142 (2009-06-18)
We report a multilayer film of poly(vinyl alcohol) (PVA)-borate complex and chitosan by using a layer-by-layer approach. PVA is an uncharged polymer, but hydroxyl functional groups of PVA can be cross-linked by using borax as a cross-linking agent. As a

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service