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71859

Sodium (meta)periodate

BioUltra, ≥99.5% (RT)

Synonym(s):

Sodium periodate

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About This Item

Linear Formula:
NaIO4
CAS Number:
7790-28-5
Molecular Weight:
213.89
NACRES:
NA.25
PubChem Substance ID:
57652368
UNSPSC Code:
12352201
EC Number:
232-197-6
MDL number:
MFCD00003534
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product line

BioUltra

Quality Level

200

assay

≥99.5% (RT)

form

crystals

impurities

insoluble matter, passes filter test

loss

≤0.1% loss on drying, 20 °C (HV)

color

white to light yellow

pH

3.5-5.5 (25 °C, 0.5 M in H2O)

mp

270  °C ((518 °F ) at 1,013 hPa - OECD Test Guideline 102 -)

solubility

H2O: 0.5 M at 20 °C, clear, colorless

anion traces

bromide, bromate, chloride, chlorate (as Cl-): ≤100 mg/kg, sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤5 mg/kg, Ba: ≤5 mg/kg, Bi: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 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, Zn: ≤5 mg/kg

absorption

cut-off at 350 nm in H2O at 0.05 M

SMILES string

[Na+].[O-]I(=O)(=O)=O

InChI

1S/HIO4.Na/c2-1(3,4)5;/h(H,2,3,4,5);/q;+1/p-1

InChI key

JQWHASGSAFIOCM-UHFFFAOYSA-M

Application

Sodium periodate is use in molecular biology and carbohydrate research to cleave carbon-carbon bonds of carbohydrates alginates, chitosans, hyaluronan, scleroglucan/schizophyllan, cellulose nucleic acids other molecules rich in hydroxyls and ketones to prepare them for chemical and physical modifications.
Useful reagent for the oxidation of carbohydrates prior to labeling with biotin hydrazide

Other Notes

Periodate oxidation of agarose gels in enzyme immobilization; Preparation of oligonucleotide 3′-dialcohols in ribonucleoside labeling; Cleavage of cross-linked proteins.

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Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Ox. Sol. 1 - Skin Corr. 1C - STOT RE 1

target_organs

thymus gland

Storage Class

5.1A - Strongly oxidizing hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC7524
BCBV9343
BCBS5360V
BCBR8007V
BCBP4910V

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Immobilization of enzymes to agar, agarose, and Sephadex supports.
J Porath et al.
Methods in enzymology, 44, 19-45 (1976-01-01)
U Bergmann et al.
Biochemistry, 32(11), 2880-2887 (1993-03-23)
50S ribosomal subunits from the extreme halophilic archaebacterium Haloarcula marismortui were treated with the homobifunctional protein-protein cross-linking reagents diepoxybutane (4 A) and dithiobis(succinimidyl propionate) (12 A). The dominant product with both cross-linking reagents was identified on the protein level as
3H and 32P derivative methods for base composition and sequence analysis of RNA.
K Randerath et al.
Methods in enzymology, 65(1), 638-680 (1980-01-01)
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Global Trade Item Number

SKUGTIN
71859-25G04061832855172
71859-100G04061832855165