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Sigma-Aldrich

Borax Anhydrous

puriss. p.a., anhydrous, ≥98.0% (T)

Synonym(s):

Sodium tetraborate

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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

grade

puriss. p.a.

Assay

≥98.0% (T)

form

crystals

anion traces

chloride (Cl-): ≤10 mg/kg
phosphate (PO43-): ≤20 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Ag: ≤5 mg/kg
Al: ≤5 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤50 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤10 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Tl: ≤5 mg/kg
Zn: ≤5 mg/kg

application(s)

forensics and toxicology

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

Borax Anhydrous can be used as a boron source to synthesize phase pure ZrB2 powder via a novel green silicothermic reduction method using ZrO2 and Si as raw materials. It is also used to prepare sodium borohydride, nano-sized titanium diboride, and alkali-activated borosilicate inorganic polymers.

Other Notes

Reagent for the decomposition of oxides and silicates by fusion

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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R. Bock
Aufschlussmethoden der anorg. & org. Chemie (1972)
Z. Sulcek et al.
Methods of Decomposition in Inorganic Analysis (1989)
Danyue Zhao et al.
Electrophoresis, 33(15), 2424-2432 (2012-08-14)
An efficient and sensitive method for the separation and determination of three essential amino acids and three B vitamins by CE-LIF with a simultaneous derivatization procedure was developed. The conditions for derivatization and separation of these micronutrients were investigated. FITC
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
Shao-Qiang Hu et al.
Electrophoresis, 34(2), 260-268 (2012-11-20)
Based on the investigation of the effect of microemulsion charge on the chiral separation, a new chiral separation method with MEEKC employing neutral microemulsion was established. The method used a microemulsion containing 3.0% (w/v) neutral surfactant Tween 20 and 0.8%

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