Thiamine | Thiamin
Supports energy metabolism*
Supports metabolic health*
Supports cognitive function*
Thiamine (vitamin B1) is part of the B complex—a group of water-soluble vitamins that play important roles in cellular metabolism and energy production. It was the first of the B complex vitamins to be isolated, which is why it’s called B1. Thiamine is on the World Health Organization's List of Essential Medicines, the most effective and safe compounds needed in a health system, because of its essential role in preventing thiamine deficiency disorders. The body concentrates thiamine in metabolically active tissues, including skeletal muscle, heart, brain, liver, and kidneys. But the body only stores a small amount of thiamine (about 20-30 mg), so it needs to be consumed consistently in the diet. Thiamine is involved in many cellular processes. It is essential for the metabolism of sugars, proteins, and fats, and is instrumental in several important processes needed to make cellular energy.
Thiamine is supplied as thiamine HCL (hydrochloride) because oral supplementation with this form of vitamin B1 can rapidly increase blood levels of thiamine .
Thiamine HCl is NON-GMO, gluten-free and vegan.
Thiamine has a wide dosing range that varies from about the daily value amount of 1.2 mg to several hundred milligrams. We consider it to be subject to a dosing threshold (see Neurohacker Dosing Principles), which means, while more might be better within a range, increasing amounts beyond that range is unlikely to add significant additional nutritional or functional benefits for most people. Depending on the goal of a formulation, the dose of thiamine used can vary. If we are using it in combination with the rest of the B-complex family of vitamins to complement this family’s functional activities, especially for energy production, a low-to-modest dose will be used. If we are using thiamine for a more specific purpose—as a nootropic for example—a higher dose may be used.
Supports energy generation (ATP) from carbohydrate and sugar metabolism 
Cofactor in the pyruvate dehydrogenase complex
Thiamine pyrophosphate (TPP) is required as a cofactor in the E1 subunit of the pyruvate dehydrogenase (PDH) complex 
TPP is essential for the generation by the PDH complex of acetyl-CoA, used in the citric acid cycle to generate ATP 
TPP is essential for the generation by the PDH complex of nicotinamide adenine dinucleotide (NADH), required for the production of ATP 
Cofactor in the citric acid cycle 
TPP is required as a cofactor in the alpha-ketoglutarate dehydrogenase reaction of the citric acid cycle (conversion of alpha-ketoglutarate to succinyl-CoA) 
TPP is essential in propagating the citric acid cycle to generate ATP 
Cofactor in the pentose phosphate pathway
TPP is required as a cofactor in the transketolase reaction of the pentose phosphate pathway (PPP) 
The PPP provides nicotinamide adenine dinucleotide phosphate (NADPH), used in several biochemical pathways such as in steroid, fatty acid, amino acid, neurotransmitter, and glutathione synthesis 
The PPP provides ribose-5-phosphate, an essential building block in nucleic acids 
Ribose-5-phosphate can enter the non-oxidative phase of the PPP where transketolase and TPP help transform ribose-5-phosphate back into glycolysis intermediates (such as glucose-6-phosphate) 
Participates in the synthesis of NADPH to be used in the recycling of the antioxidant glutathione (GSH) 
Essential for the production by the pyruvate dehydrogenase complex of acetyl-CoA used for the production of acetylcholine 
The alpha-ketoglutarate dehydrogenase reaction of the citric acid cycle reaction has a role in maintaining glutamate and gamma-aminobutyric acid (GABA) levels 
May help counter the production of advanced glycation end-products (AGEs) [3,4]
Supports healthy blood pressure 
Supports healthy blood glucose levels 
Supports healthy insulin sensitivity 
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 D. A. Bender, in Nutritional Biochemistry of the Vitamins (Cambridge University Press, 2003), pp. 148–171.
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 N. Karachalias, R. Babaei-Jadidi, C. Kupich, N. Ahmed, P. J. Thornalley, Ann. N. Y. Acad. Sci. 1043, 777–783 (2005).
 F. Alaei-Shahmiri, M. J. Soares, Y. Zhao, J. Sherriff, Diabetes Metab. Syndr. 9, 213–217 (2015).
 F. Alaei Shahmiri, M. J. Soares, Y. Zhao, J. Sherriff, Eur. J. Nutr. 52, 1821–1824 (2013).