What molecule am I?
Adrenochrome is a biomolecule produced in the body by the oxidation of the hormone adrenaline1鈥攈ence its name. The 鈥渃hrome鈥� in its name indicates that it is deeply colored, compared with white adrenaline.
Adrenochrome was known as long ago as 1856, when French neurologist Alfred Vulpian (who also discovered adrenaline) observed that when exposed to air. But it was not until 1937 that David Ezra Green and Derek Richter at the University of Cambridge (UK) named the compound and described its .
The structure of adrenochrome is chiral at the position of the hydroxyl group2. Little information is available on the individual enantiomers. Adrenochrome is an unstable molecule with no practical uses. Its monosemicarbazone (carbazochrome3), however, is stable; it is said to promote blood clotting and can be . From the 1950s through the 1970s, adrenochrome was thought to cause schizophrenia, but this theory was eventually debunked.
In recent years, adrenochrome has been implicated in far-right conspiracy theories, such as QAnon and Pizzagate reports of satanic ritual abuse, as described in a . It has also been touted as a .
1. CAS Reg. No. 51-43-4; also known as epinephrine.
2. CAS Reg. Nos.: (R)-enantiomer, 7506-92-5; (S)-enantiomer, 5181-82-8.
3. CAS Reg. No. 69-81-8.
Adrenochrome hazard information
| Hazard class* | GHS code and hazard statement | |
|---|---|---|
| Acute toxicity, oral, category 4 | H302鈥擧armful if swallowed |  |
| Acute toxicity, dermal, category 4 | H312鈥擧armful in contact with skin | |
Serious eye damage/eye irritation, category 2A | H319鈥擟auses serious eye irritation | |
Acute toxicity, inhalation (dusts/mists), category 4 | H332鈥擧armful if inhaled | |
| Specific target organ toxicity, single exposure, respiratory tract irritation, category 3 | H335鈥擬ay cause respiratory irritation | |
*Globally Harmonized System (GHS) of Classification and Labeling of Chemicals.听.
MOTW updates
Heme1 was the Molecule of the Week for January 17, 2011. It is a porphyrin derivative and the color component of hemoglobin, which transports oxygen in blood.
Last month, Frances H. Arnold, Kendall N. Houk, and colleagues at Caltech (Pasadena, CA) and the University of California, Los Angeles, described a potential use for heme in organic synthesis. They used computational chemistry to determine the mechanism of to synthesize cyclopropane derivatives. The advantage of this method is that the carbene precursors are diazirines, which are air-stable, user-friendly alternatives to traditionally used diazo compounds.
Testosterone2 was the Molecule of the Week for June 14, 2005. It is the primary male sex hormone, the shortness of which in older men can cause fatigue, low energy, and loss of libido.
In January, Martha E. Stone, Max B. Kelz, and Alex Proekt at the University of Pennsylvania (Philadelphia) and collaborators there and at the University of Michigan (Ann Arbor) and Washington University (St. Louis) reported that testosterone is primarily responsible for the . In a mouse study, the researchers found that, at equal brain concentrations of the inhaled anesthetic isoflurane3, females are more resistant to the anesthetic than males, and that the difference results from testosterone modulation in males.
1. CAS Reg. No. 14875-96-8.
2. CAS Reg. No. 58-22-0.
3. CAS Reg. No. 26675-46-7.
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Adrenochrome fast facts
| CAS Reg. No. | 54-06-8 |
| SciFinder nomenclature | 1H-Indole-5,6-dione, 2,3-dihydro-3-hydroxy-1-methyl- |
| Empirical formula | C9H9NO3 |
| Molar mass | 179.17 g/mol |
| Appearance | Deep violet crystals or powder |
| Melting point | 125 掳C (dec.) |
| Water solubility | 0.3 g/L |
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