Choline Bitartrate
Quick Summary
- Category: Amino Acid (site classification) · Sourcing Origin: China · Form: Powder · Standard Pack Size: 25 kg
- Choline is an essential nutrient — not strictly a vitamin, but officially classified as such by NIH and EFSA
- NIH AI: 550 mg/day (men), 425 mg/day (women); EFSA AI: 400 mg/day; NIH UL: 3,500 mg/day
- Bitartrate is a salt form — cost-effective, widely used; provides less choline per gram than alpha-GPC or CDP-choline (not in YNP catalogue), but significantly more affordable
What Is Choline Bitartrate?
Choline is an essential nutrient required for the synthesis of phosphatidylcholine (a major structural component of cell membranes), the neurotransmitter acetylcholine (critical for muscle control and cognitive function), and betaine (via choline oxidase — linking choline metabolism to the homocysteine methylation pathway). The NIH classifies choline as an essential nutrient that most healthy adults do not consume in adequate amounts from diet alone, with eggs, liver, and meat being the primary dietary sources.
Choline Bitartrate is one of the most commercially available and affordable supplemental forms of choline — a salt of choline with bitartaric acid. It provides approximately 41% choline by molecular weight, compared to approximately 40% for choline chloride, ~28% for lecithin, ~19% for CDP-choline (citicoline), and ~40% for alpha-GPC (though alpha-GPC is claimed to have superior brain bioavailability in some research).
Specification & Form
| Attribute | Detail |
|---|---|
| Form | White to off-white crystalline powder |
| Choline content (approx.) | ~41% choline by molecular weight |
| Solubility | Freely soluble in water |
| Standard pack size | 25 kg |
| Sourcing origin | China |
How It's Sourced
YNP Ingredients sources Choline Bitartrate from certified manufacturers in China, supplied with FSSAI-compliant documentation.
Reference Values
| Body | Adequate Intake (AI) | Tolerable Upper Intake Level (UL) |
|---|---|---|
| NIH (USA) | 550 mg/day (men); 425 mg/day (women) | 3,500 mg/day |
| EFSA (EU) | 400 mg/day | Not formally established by EFSA |
Applications
- Cognitive health and focus supplements
- Pre-workout formulations (as a focus/alertness ingredient)
- Liver health and detoxification products
- Prenatal and maternal nutrition (choline is important for foetal brain development)
- General wellness multivitamin formulations
Industries Served
Sports Nutrition · Nutraceuticals/Dietary Supplements · Functional Food/Beverage
Buyer Checklist
- Confirmed choline bitartrate is the appropriate form for the product (vs CDP-choline or alpha-GPC for higher-end cognitive positioning)
- Dose calculated in terms of choline equivalents (~41% choline per gram of bitartrate salt)
- COA confirming assay/purity
- FSSAI-compliant documentation confirmed
- 25 kg pack size and MOQ confirmed
Common Mistakes
Dosing in terms of "choline bitartrate" rather than "choline equivalents." The AI values (550 mg, 425 mg) refer to choline itself, not the bitartrate salt. A 550 mg choline target requires approximately 1,340 mg choline bitartrate — a meaningful difference for label accuracy.
Claiming cognitive performance benefits equivalent to CDP-choline or alpha-GPC evidence. The cognitive research base for choline is strongest for CDP-choline and alpha-GPC formulations. Choline bitartrate is a more cost-effective general-purpose form; its specific nootropic evidence is less developed.
Frequently Asked Questions
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References
Company Information
- YNP Ingredients, Choline Bitartrate product page, ynpingredients.com (China sourcing, 25 kg, FSSAI documentation)
Industry Information
- NIH Office of Dietary Supplements. *Choline — Fact Sheet for Health Professionals.* ods.od.nih.gov/factsheets/Choline-HealthProfessional/ — AI, UL, functions, and pregnancy requirements.
- EFSA Panel on Dietetic Products, Nutrition and Allergies. *Scientific Opinion on Choline.* EFSA Journal. 2016;14(8):4484 — AI of 400 mg/day.
- Zeisel SH, da Costa KA. *Choline: an essential nutrient for public health.* Nutr Rev. 2009;67(11):615–623. doi:10.1111/j.1753-4887.2009.00246.x
