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Key Documents

229946

Sigma-Aldrich

Sodium tetraborate

99.998% trace metals basis

Synonym(s):

Borax, fused

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About This Item

Linear Formula:
Na2B4O7
CAS Number:
Molecular Weight:
201.22
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99.998% trace metals basis

form

powder

mp

741 °C (lit.)

density

2.367 g/mL at 25 °C (lit.)

SMILES string

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

InChI

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

InChI key

UQGFMSUEHSUPRD-UHFFFAOYSA-N

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Application

Sodium tetraborate, also known as borax(Na2B4O7), can be employed as a catalyst:
  • In the chemoselective oxidation of alkyl and aryl sulfides to sulfoxides and sulfones using H2O2 as the oxidant.
  • In the synthesis of pyridines, dienes, anilines, and dihydropyrano[3,2-c]chromenes via Knoevenagel condensation and Michael addition pathway.
  • In thiolysis of 1,2-epoxides to β-hydroxy sulfides.

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Borax-Catalyzed and pH-Controlled Selective Oxidation of Organic Sulfides by H2O2: An Environmentally Clean Protocol
Hussain S, et al.
European Journal of Organic Chemistry, 2009(20), 3319-3322 (2009)
Borax catalyzed domino reactions: synthesis of highly functionalised pyridines, dienes, anilines and dihydropyrano [3, 2-c] chromenes
Molla A and Hussain S
Royal Society of Chemistry Advances, 4(56), 29750-29758 (2014)
Borax-catalyzed thiolysis of 1, 2-epoxides in aqueous medium
Gao P, et al.
Tetrahedron Letters, 49(46), 6536-6538 (2008)
Shuai Liu et al.
Journal of the American Heart Association, 9(8), e014757-e014757 (2020-04-21)
Background The protective effects of polyamines on cardiovascular disease have been demonstrated in many studies. However, the roles of spermidine, a natural polyamine, in abdominal aortic aneurysm (AAA) disease have not been studied. In this study, we investigated the influence
Tatiana S Fukuji et al.
Journal of pharmaceutical and biomedical analysis, 51(2), 430-438 (2009-06-24)
In this work, the separation of nine phenolic acids (benzoic, caffeic, chlorogenic, p-coumaric, ferulic, gallic, protocatechuic, syringic, and vanillic acid) was approached by a 3(2) factorial design in electrolytes consisting of sodium tetraborate buffer (STB) in the concentration range of

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