Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH3IO3S |
| Molecular Weight | 222.002 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(=O)(=O)CI
InChI
InChIKey=RDFJFVXMRYVOAC-UHFFFAOYSA-N
InChI=1S/CH3IO3S/c2-1-6(3,4)5/h1H2,(H,3,4,5)
| Molecular Formula | CH3IO3S |
| Molecular Weight | 222.002 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/4377903
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4377903
Methiodal is used in lumbar myelography as a contrast agent.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Displacement of protein-bound thiopental by sodium methiodal may contribute to anesthetic complications during canine myelography. | 1981-09 |
|
| Effects of intramedullary injection of methiodal and lidocaine on spinal cords of dogs. | 1975-10 |
|
| [Complications of myelography with methiodal]. | 1969-12-18 |
|
| [New technic of radiooculography with Methiodal with simultaneous anesthesia and injection of the contrast medium]. | 1967-10 |
Patents
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 18:06:16 GMT 2025
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Mon Mar 31 18:06:16 GMT 2025
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| Record UNII |
H20847G0I0
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| Record Status |
Validated (UNII)
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| Record Version |
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WHO-ATC |
V08AA09
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WHO-VATC |
QV08AA09
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C100285
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H20847G0I0
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31346
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143-47-5
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DB13321
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3346
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100000085951
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DTXSID60162274
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METHIODAL
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SUB03220MIG
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PRIMARY |
| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |