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 | [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. | [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.] |
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