Niacin (Nicotinic Acid) vs Niacinamide (Nicotinamide): The Vitamin B3 Difference Explained
Niacin vs Niacinamide in skincare: what each form of vitamin B3 is, how they differ, and why niacinamide is the one you see most often.
Niacin vs Niacinamide in skincare: what each form of vitamin B3 is, how they differ, and why niacinamide is the one you see most often.
As different as chalk and cheese. That is perhaps the most apt description for nicotinic acid (niacin) and nicotinamide (niacinamide). While both are called Vitamin B3, they act very differently in the body.
One can make your skin turn beetroot red, while the other is a gentle ingredient in skincare products that helps repair cells.
This is a simple overview of what separates Niacin (nicotinic acid) from Niacinamide (nicotinamide): their chemistry, historical context, specific effects on the skin, and the reason for the skin-flushing effect of one but not the other.
To see why these compounds act differently, it helps to look at their structure.
Vitamin B3 refers to a group of related compounds, mainly nicotinic acid (niacin) and nicotinamide (niacinamide). Another form, nicotinamide riboside (NR), is being studied for its possible role in promoting longevity, but this article does not cover it.
All forms of B3 serve one main purpose: they are precursors to nicotinamide adenine dinucleotide (NAD⁺) and its phosphorylated partner, NADP⁺. These are coenzymes involved in over 400 reactions in the body. They cover energy metabolism, DNA repair, cell signalling, and antioxidant defence.
The story begins, rather unexpectedly, with tobacco. In 1867, nicotinic acid was first synthesised through the oxidative degradation of nicotine using potassium chromate and sulphuric acid. The chemist Hugo Weidel described the compound more formally in 1873 during his studies of nicotine, though no one yet understood it had anything to do with nutrition.
It took decades to link nicotinic acid to human health. In 1937, biochemist Conrad Elvehjem at the University of Wisconsin isolated nicotinic acid from liver extract. He showed it could cure black tongue in dogs – a disease similar to pellagra in humans. Elvehjem and his team also found that nicotinamide was a cure factor. Both were designated as vitamin B3.
When vitamins began to be marketed directly to consumers in the 1940s, a problem arose. The name “nicotinic acid” was too close to “nicotine,” and the public understandably made unfortunate associations. The U.S. Food and Drug Administration allowed renaming: nicotinic acid became niacin (a contraction of nicotinic acid + vitamin), and nicotinamide became niacinamide.
Now look more closely at each molecule’s structure and role, starting with Niacin (nicotinic acid).
Niacin, also called nicotinic acid, is a molecule built on a six-sided ring structure (called pyridine) with an acidic group (carboxyl, -COOH) attached to it.
| Property | Detail |
|---|---|
| Name | Nicotinic acid |
| Molecular formula | C₆H₅NO₂ |
| Molecular weight | 123.11 g/mol |
| CAS number | 59-67-6 |
| Functional group | Carboxyl (-COOH) |
| Melting point | 236.6 °C |
| State | Solid (white crystalline powder) |
Nicotinic acid is found in foods such as meat, fish, legumes, and fortified cereals. Nicotinic acid has even been found in carbonaceous chondrite meteorites and in sample returns from the asteroids Ryugu and Bennu.
Niacinamide is the amide form of vitamin B3. It is almost the same as nicotinic acid, except it has a carboxamide group (-CONH₂) instead of a carboxyl group (-COOH).
| Property | Detail |
|---|---|
| Name | Niacinamide |
| Molecular formula | C₆H₆N₂O |
| Molecular weight | 122.12 g/mol |
| CAS number | 98-92-0 |
| Functional group | Carboxamide (-CONH₂) |
| Melting point | 130 °C |
| State | Solid (white crystalline powder) |
Niacinamide works as a vitamin just like nicotinic acid, but its effects and side effects are different. It does not cause flushing and is the main form used in skincare products.
The main difference between these two molecules is one functional group on the pyridine ring:
| Feature | Niacin | Niacinamide |
|---|---|---|
| Core structure | Pyridine ring | Pyridine ring |
| Position-3 group | -COOH (carboxyl) | -CONH₂ (carboxamide) |
| Molecular formula | C₆H₅NO₂ | C₆H₆N₂O |
| Molecular weight | 123.11 g/mol | 122.12 g/mol |
| Charge at physiological pH | Anionic | Neutral |
This substitution, swapping an oxygen for an amine, changes how the molecules bind to receptors. Niacin activates the GPR109A receptor, but niacinamide does not. This difference explains the flushing response and most of their other effects.
The most well-known difference between these two compounds is the flush caused by niacin, and its mechanism is well understood.
When nicotinic acid enters the body:
This usually starts 20–30 minutes after taking niacin and fades within 1–2 hours. Most people develop tolerance after a few weeks, and the flushing becomes less intense or stops altogether.
Niacinamide does not bind to the GPR109A receptor, so it does not trigger this cascade of events. No prostaglandins, no flushing. This is why niacinamide replaced niacin in most skincare products where the flush is undesirable.
Niacinamide is one of the most well-studied ingredients in cosmetic science. It is usually used in products at concentrations between 2% and 5%, but some products contain up to 10%.
Clinical trials have shown that niacinamide can:
Niacinamide is easy to use in products because it is pH-neutral and dissolves in water. It is usually well tolerated by all skin types.
Nicotinic acid is rarely used in skincare products because it causes flushing. When applied to the skin, it activates the same receptor (GPR109A), leading to redness and irritation, which is not desirable in products meant to improve skin appearance.
Here is a table that shows the main differences in properties and uses between niacin and niacinamide.
| Category | Niacin (Nicotinic Acid) | Niacinamide (Nicotinamide) |
|---|---|---|
| Chemical class | Pyridinecarboxylic acid | Pyridinecarboxamide |
| Chemical formula | C₆H₅NO₂ | C₆H₆N₂O |
| Causes flushing | Yes (GPR109A activation) | No |
| Used in skincare | Rarely (causes redness) | Very common (2–5%) |
Niacin and niacinamide are two forms of the same vitamin, but a small structural difference leads to big differences in how they work. Niacin is used as a medicine and can cause flushing, while niacinamide is gentle and widely used in skincare. Although they share a vitamin name and similar roles in the body, they should be seen as separate ingredients with different uses. For best results, it’s important to use the right form in the right way, not just the highest amount.