| Identification | Back Directory | [Name]
ADRENOCHROME | [CAS]
54-06-8 | [Synonyms]
adraxone
usafuctl-7
ADRENOCHROME
D,L-ADRENOCHROME
adrenochrome free base
L-Adrenochrome, free base
3-hydroxy-1-methyl-6-indolinedione
3-hydroxy-1-methylindoline-5,6-dione
1-Methyl-3-hydroxyindoline-5,6-dione
3-HYDROXY-1-METHYL-5,6-INDOLINE-DIONE
5,6-Dihydro-3-hydroxy-1-methyl-5,6-indolinedione
2,3-dihydro-3-hydroxy-1-methyl-1h-indole-6-dione
2,3-DIHYDRO-3-HYDROXY-1-METHYL-1H-INDOLE-5,6-DIONE
3-Hydroxy-1-methyl-5,6-indolinedione, 2,3-Dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione | [EINECS(EC#)]
200-192-8 | [Molecular Formula]
C9H9NO3 | [MDL Number]
MFCD00069732 | [MOL File]
54-06-8.mol | [Molecular Weight]
179.17 |
| Chemical Properties | Back Directory | [Appearance]
Red Crystalline Solid | [Melting point ]
115-120°C | [Boiling point ]
311.69°C (rough estimate) | [density ]
1.2822 (rough estimate) | [refractive index ]
1.5600 (estimate) | [storage temp. ]
−20°C
| [solubility ]
Methanol (Slightly), Water | [form ]
Solid | [pka]
13.31±0.20(Predicted) | [color ]
Red to Black | [Stability:]
Air Sensitive, Light Sensitive | [Major Application]
diagnostic assay manufacturing
hematology
histology | [InChI]
InChI=1S/C9H9NO3/c1-10-4-9(13)5-2-7(11)8(12)3-6(5)10/h2-3,9,13H,4H2,1H3 | [InChIKey]
RPHLQSHHTJORHI-UHFFFAOYSA-N | [SMILES]
N1(C)C2C(=CC(=O)C(=O)C=2)C(O)C1 | [Uses]
Adrenochrome is a derivative of epinephrine. When complexed with a salicylate, its stability is increased (carbazochrome). It was claimed to reduce blood loss, but the evidence is sparse. |
| Hazard Information | Back Directory | [Chemical Properties]
Red Crystalline Solid | [Uses]
The substance mainly responsible for the red colours produced during the mild oxidation of adrenaline | [Definition]
ChEBI: Adrenochrome is a member of indoles. | [Biological Activity]
Adrenochrome is an oxidation product of adrenaline. It has been implicated in cardiotoxicity. It is a short-lived cytotoxic molecule and is part of the leukocyte response used to kill bacteria. Adrenochrome is also suggested to exhibit psychotomimetic effects. It is used to determine superoxide dismutase activity. | [Purification Methods]
It was crystallised from MeOH/formic acid, as red crystals of the hemihydrate, and stored in a vacuum desiccator. The mono-semicarbazone (Carbazochrome) [69-81-8] M 236.2, crystallises as orange-red crystals from dilute EtOH with m ~203o (dec) and is haemostatic. [Heacock Chem Rev 59 181 1959, Beilstein 21 III/IV 6434.] |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
|