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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)
William R Gunther et al.
Nature communications, 3, 1109-1109 (2012-10-11)
Carbohydrate epimerization is an essential technology for the widespread production of rare sugars. In contrast to other enzymes, most epimerases are only active on sugars substituted with phosphate or nucleotide groups, thus drastically restricting their use. Here we show that
Shridhar K Sathe et al.
Journal of agricultural and food chemistry, 57(17), 7846-7856 (2009-08-07)
The solubility of almond, Brazil nut, cashew nut, hazelnut, macadamia, pecan, pine nut, pistachio, walnut, and peanut proteins in several aqueous solvents was qualitatively and quantitatively assessed. In addition, the effects of extraction time and ionic strength on protein solubility
Qianqian Zhu et al.
Journal of chromatography. A, 1246, 35-39 (2012-03-03)
A technique known as field enhancement sample stacking (FESS) and capillary electrophoresis (CE) separation has been developed to analyze and detect organic acids in the three traditional Chinese medicines (such as Portulaca oleracea L., Crataegus pinnatifida and Aloe vera L.).

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