210021
Hydriodic acid
57 wt. % in H2O, distilled, stabilized, 99.95%
Synonyme(s) :
Hydriotic acid
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A propos de cet article
Formule empirique (notation de Hill) :
HI
Numéro CAS:
Poids moléculaire :
127.91
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
Assay:
99.95%
Concentration:
57 wt. % in H2O
Form:
liquid
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Laissez-nous vous aiderQuality Level
assay
99.95%
form
liquid
contains
<1.5% hypophosphorous acid as stabilizer
concentration
57 wt. % in H2O
solubility
water: soluble
density
1.701 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
I
InChI
1S/HI/h1H
InChI key
XMBWDFGMSWQBCA-UHFFFAOYSA-N
General description
Hydriodic acid (HI) along with red phosphorus (HI/red P) plays the role of a reducing agent for the preparation of methamphetamine. HI/Phosphorous causes the reduction of various polycyclic quinones. HI also participates as a reducing agent for the conversion of various polyarene quinones, hydroquinones and phenols to the corresponding aromatic hydrocarbons.
Hydriodic acid is hydrogen iodide gas dissolved in water. It is a strong acid generally used as a reducing agent.
Application
Hydriodic acid may be used as a reagent for the conversion of fatty alcohols and glyceryl ethers to alkyl iodides.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Classe de stockage
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Studies on the composition of glyceryl ethers and their preparation from diacyl glyceryl ethers in liver oils.
Guyer KE, et al.
Journal of Lipid Research, 4(4), 385-391 (1963)
Chao Chen et al.
Nature communications, 10(1), 1927-1927 (2019-04-28)
Circularly polarized light (CPL) detection is required in various fields such as drug screening, security surveillance and quantum optics. Conventionally, CPL photodetector needs the installation of optical elements, imposing difficulties for integrated and flexible devices. The established CPL detectors without
Efficient reduction of polycyclic quinones, hydroquinones, and phenols with hydriodic acid.
Konieczny M and Harvey RG.
The Journal of Organic Chemistry, 44(26), 4813-4816 (1979)