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Merck
CN

S9640

Sigma-Aldrich

Sodium tetraborate decahydrate

ACS reagent, ≥99.5%

Synonym(s):

Borax decahydrate, Sodium borate decahydrate

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1 L
CN¥951.34

CN¥951.34


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1 L
CN¥951.34

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
form:
powder or crystals

CN¥951.34


Available to ship onApril 25, 2025Details


Request a Bulk Order

grade

ACS reagent

Quality Level

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%

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1 of 4

This Item
SAB1412536SAB1412591SAB1412560
species reactivity

mouse

species reactivity

human

species reactivity

human

species reactivity

human

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

clone

6E8, monoclonal

clone

6A10, monoclonal

clone

1F5, monoclonal

clone

4G7, monoclonal

Gene Information

human ... EGR1(1958)

Gene Information

human ... EGR1(1958)

Gene Information

human ... EGR1(1958)

Gene Information

human ... EGR1(1958)

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

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


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