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71996

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:
1330-43-4
Molecular Weight:
201.22
NACRES:
NA.22
PubChem Substance ID:
329763685
UNSPSC Code:
12352302
EC Number:
215-540-4
MDL number:
MFCD00081185
Assay:
≥98.0% (T)
Form:
crystals
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Quality Level

200

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

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

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Repr. 1B

Storage Class

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

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2680
BCCM7989
BCCL3393
BCCL7413
BCCM3357

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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
View All Related Papers

Global Trade Item Number

SKUGTIN
71996-1KG04061826715253
71996-250G04061832855530