24-1090
Periodic acid
SAJ special grade, ≥98.5%
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About This Item
Empirical Formula (Hill Notation):
H5IO6
CAS Number:
Molecular Weight:
227.94
UNSPSC Code:
12352106
PubChem Substance ID:
EC Number:
233-937-0
MDL number:
Assay:
≥98.5%
Form:
crystalline
Grade:
SAJ special grade
grade
SAJ special grade
assay
≥98.5%
form
crystalline
reaction suitability
reagent type: oxidant
availability
available only in Japan
mp
122 °C (lit.)
solubility
water: soluble
SMILES string
OI(O)(O)(O)(O)=O
InChI
1S/H5IO6/c2-1(3,4,5,6)7/h(H5,2,3,4,5,6,7)
InChI key
TWLXDPFBEPBAQB-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Ox. Sol. 1 - Skin Corr. 1B - STOT RE 1 Oral
target_organs
Thyroid
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
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Murad Alturkustani et al.
Journal of neuropathology and experimental neurology, 74(3), 233-240 (2015-02-11)
The pathologic features of adult-onset leukoencephalopathy/leukodystrophy with axonal spheroids (ALAS) are variable, and this has led to different hypotheses as to whether primarily demyelination or axonopathy may underlie this disorder. Typical ALAS pathology is rarely accompanied by focal multiple sclerosis
Vered Padler-Karavani et al.
The Journal of biological chemistry, 287(27), 22593-22608 (2012-05-03)
DNA and protein arrays are commonly accepted as powerful exploratory tools in research. This has mainly been achieved by the establishment of proper guidelines for quality control, allowing cross-comparison between different array platforms. As a natural extension, glycan microarrays were
Karen Mollet et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(10), 3383-3396 (2013-01-26)
The reactivity of 3-hydroxy-4-(1,2-dihydroxyethyl)-β-lactams with regard to the oxidant sodium periodate was evaluated, unexpectedly resulting in the exclusive formation of new 2-hydroxy-1,4-oxazin-3-ones through a C3C4 bond cleavage of the intermediate 4-formyl-3-hydroxy-β-lactams followed by a ring expansion. This peculiar transformation stands