752851
Hydriodic acid
57 wt. %, distilled, 99.999% trace metals basis
Synonym(s):
Hydriotic acid
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
HI
CAS Number:
Molecular Weight:
127.91
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352300
MDL number:
Assay:
99.999% trace metals basis
Concentration:
57 wt. %
Form:
liquid
Quality Level
assay
99.999% trace metals basis
form
liquid
concentration
57 wt. %
bp
127 °C (lit.)
storage temp.
2-8°C
SMILES string
I
InChI
1S/HI/h1H
InChI key
XMBWDFGMSWQBCA-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under Hydriodic acid
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Daniel J Weisenberger et al.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 24(3), 512-519 (2015-01-15)
The CpG island methylator phenotype (CIMP) represents a subset of colorectal cancers characterized by widespread aberrant DNA hypermethylation at select CpG islands. The risk factors and environmental exposures contributing to etiologic heterogeneity between CIMP and non-CIMP tumors are not known.
Hailong Li et al.
Journal of agricultural and food chemistry, 60(21), 5307-5310 (2012-05-15)
The paper reports on a headspace gas chromatographic (HS-GC) method for the determination of methoxyl in lignin. The method involves the quantitive cleavage of methoxyl with hydroiodic acid (HI) to form methyl iodide in a closed headspace sample vial at
Kazumasa Wakamatsu et al.
Pigment cell & melanoma research, 22(4), 474-486 (2009-06-06)
Pheomelanogenesis is a complex pathway that starts with the oxidation of tyrosine (or DOPA, 3,4-dihydroxyphenylalanine) by tyrosinase in the presence of cysteine, which results in the production of 5-S-cysteinyldopa and its isomers. Beyond that step, relatively little has been clarified