16-Dehydropregnenolone acetate Cas 979-02-2
Specification
Items | Specification |
Product name | 16-Dehydropregnenolone acetate |
CAS# | 979-02-2 |
Appearance | White crystalline powder |
Purity | ≥98.5% |
Molecular Formula | C23H32O3 |
Molecular weight | 356.5 |
EINECS | 213-558-7 |
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16-Dehydropregnenolone acetate (16-DPA) is a critically important synthetic steroid intermediate. It is not a drug or medication itself but a key starting material, or "building block," used in the industrial-scale pharmaceutical synthesis of a wide range of medically essential steroid hormones, particularly corticosteroids and progestogens.
Its significance lies in its unique molecular structure, which provides an ideal foundation for chemical modifications that allow efficient production of complex steroid molecules that would otherwise be difficult and expensive to obtain.
Chemical Structure and Significance
To understand its role, it helps to break down its name and structure:
Pregnenolone Backbone: It is derived from pregnenolone, a natural prohormone produced in the body from cholesterol. This means it has the fundamental four-ring carbon skeleton common to all steroid hormones.
Acetate Group: The "acetate" refers to an acetyl group attached to the oxygen at the 3-position of the steroid. This group protects the molecule during chemical reactions, making it more stable and easier to work with.
The Key Feature - 16-Dehydro: The most crucial part of its name is "16-Dehydro." This indicates a double bond between carbon atoms 16 and 17 in the steroid's D-ring. This double bond is the key reactive site that unlocks its utility. It makes the molecule highly receptive to chemical reactions that are fundamental to building more complex structures.
Historical and Industrial Role
The importance of 16-DPA exploded in the mid-20th century with the discovery of cortisone's powerful anti-inflammatory effects. There was an urgent need to produce large quantities of cortisone and related corticosteroids, but isolating them from natural sources was incredibly inefficient.
16-DPA, which could be semi-synthesized in large quantities from readily available plant sterols like diosgenin (found in Mexican yams), became the solution. It served as the launchpad for the Marker Degradation and Partial Synthesis pathways, which revolutionized steroid manufacturing.
Primary Uses as a Synthetic Intermediate
16-DPA's structure is strategically modified to produce various classes of steroid drugs:
Corticosteroids (Anti-inflammatories): This is its most significant application. The 16-Double bond allows for a crucial microbial step using specific bacteria or fungi (e.g., Rhizopus species) that easily add oxygen atoms to the 11-position of the steroid ring. An oxygen at C-11 is a mandatory structural feature for potent glucocorticoid activity (anti-inflammatory and immunosuppressive effects). From 16-DPA, manufacturers can efficiently produce:
Progestogens (Sex Hormones): 16-DPA is also a key intermediate in synthesizing various progestins (synthetic progesterone). It can be chemically converted into hormones like:
Summary
In essence, 16-Dehydropregnenolone acetate is a workhorse of steroid chemistry. While unknown to patients, it is a foundational pillar of the modern pharmaceutical industry. Its cleverly designed structure, featuring the reactive 16-double bond, provides an efficient and cost-effective pathway for the large-scale synthesis of life-saving anti-inflammatory steroids and essential sex hormones, making it one of the most important intermediates in the history of steroid drug production.
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