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Merck
CN

3951

Periodic Acid Solution

1 g/dL in deionized water

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About This Item

NACRES:
NA.47
PubChem Substance ID:
24864643
UNSPSC Code:
12352106
MDL number:
MFCD00011344

Key Documents

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Product Name

Periodic Acid Solution, 1 g/dL in deionized water

InChI

1S/H5IO6/c2-1(3,4,5,6)7/h(H5,2,3,4,5,6,7)

SMILES string

OI(O)(O)(O)(O)=O

InChI key

TWLXDPFBEPBAQB-UHFFFAOYSA-N

form

solution

shelf life

expiry date on label

reaction suitability

reagent type: oxidant

IVD

for in vitro diagnostic use

concentration

1 g/dL in deionized water

pH

1.77

application(s)

hematology
histology

shipped in

wet ice

storage temp.

2-8°C

Quality Level

500

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Related Categories

Application

For use in procedure no. 395 for Periodic Acid-Schiff (PAS) and Silver Stain Procedure No. HT100.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

监管及禁止进口产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000361262
0000361268
0000361268
0000361262
SLCQ7089

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Robert W Morton et al.
The Journal of physiology, 597(17), 4601-4613 (2019-07-12)
Performing resistance exercise with heavier loads is often proposed to be necessary for the recruitment of larger motor units and activation of type II muscle fibres, leading to type II fibre hypertrophy. Indirect measures [surface electromyography (EMG)] have been used
Sonja Frimmel et al.
Journal of ophthalmic & vision research, 12(2), 175-182 (2017-05-26)
Diabetic retinopathy is a leading cause of vision loss. There is a great need for early diagnosis prior to the occurrence of irreversible structural damages. Expression of endothelial adhesion molecules is observed before the onset of diabetic vascular damage; however
Allison M Bradbury et al.
Human gene therapy, 29(7), 785-801 (2018-01-11)
Globoid cell leukodystrophy (GLD), or Krabbe disease, is an inherited, neurologic disorder that results from deficiency of a lysosomal enzyme, galactosylceramidase. Most commonly, deficits of galactosylceramidase result in widespread central and peripheral nervous system demyelination and death in affected infants
Allison M Bradbury et al.
Journal of neuroscience research, 94(11), 1007-1017 (2016-09-18)
Globoid cell leukodystrophy (GLD), or Krabbe's disease, is a debilitating and always fatal pediatric neurodegenerative disease caused by a mutation in the gene encoding the hydrolytic enzyme galactosylceramidase (GALC). In the absence of GALC, progressive loss of myelin and accumulation
Daniela Rovito et al.
Nucleic acids research, 49(8), 4472-4492 (2021-04-10)
Skeletal muscle is a dynamic tissue the size of which can be remodeled through the concerted actions of various cues. Here, we investigated the skeletal muscle transcriptional program and identified key tissue-specific regulatory genetic elements. Our results show that Myod1
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