Details
Stereochemistry | ACHIRAL |
Molecular Formula | 3CNS.Fe |
Molecular Weight | 230.092 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Fe+3].[S-]C#N.[S-]C#N.[S-]C#N
InChI
InChIKey=SUBFIBLJQMMKBK-UHFFFAOYSA-K
InChI=1S/3CHNS.Fe/c3*2-1-3;/h3*3H;/q;;;+3/p-3
Molecular Formula | Fe |
Molecular Weight | 55.845 |
Charge | 3 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | CHNS |
Molecular Weight | 59.09 |
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/10660469
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10660469
Ferric thiocyanate is a complex of Fe3+ with [SCN]- ions. Solution of ferric thiocyanate has a blood red color, and its formation is used to detect Fe3+ ions. Oxidation of ferrous to ferric ion and subsequent complexation of the latter by thiocyanate is known as ferric thiocyanate assay and is used for determination of presence of various oxidizers, such as lipid hydroperoxides, and evaluation of effects of antioxidants.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The reevaluation of the ferric thiocyanate assay for lipid hydroperoxides with special considerations of the mechanistic aspects of the response. | 1996 |
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Choosing the proper organic solvent for the determination of lipid hydroperoxides by the ferric thiocyanate assay. | 2000 Feb 15 |
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Evaluation of the anti-oxidative effect (in vitro) of tea polyphenols. | 2003 Feb |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8791093
Ammonium thiocyanate (7.5 g) was dissolved in 25 ml distilled deionized water (thiocyanate solution). Barium chloride dihydrate (0.2 g) was dissolved in 25 ml of 0.4 N HCl (solution A). Ferrous sulfate heptahydrate (0.1 g) was dissolved in 10 ml distilled deionized water (solution B). Six milliliters of solution A was mixed with 6 ml of solution B by vortexing for 1 min, followed by centrifugation for 3 min. The clear solution of Fe(II) chloride was used immediately after preparation. Cumene hydroperoxide was dissolved in nonpolar solvent prior to mixing with methanol. To 10 ml of the nonpolar solvent/methanol (2:1) mixture, 50 ml of ammonium thiocyanate solution was added and vortexed for 2–4 s. Then 50 ml of iron(II) chloride solution was added and vortexed for 2–4 s. After a 20-min incubation period at room temperature, the absorbance was determined at 500 nm.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:43:47 GMT 2023
by
admin
on
Fri Dec 15 19:43:47 GMT 2023
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Record UNII |
46CC1IS9BT
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Record Status |
Validated (UNII)
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Record Version |
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46CC1IS9BT
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DTXSID60194111
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223-913-8
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m5331
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165185
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C103724
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PARENT -> SALT/SOLVATE |