|
Product name |
Evodiamine |
|
CAS No. |
518-17-2 |
|
Molecular formula |
C19H17N3O |
|
Molecular weight |
303.36 |
|
Purity |
98.0% |
|
Appearance |
Light yellow crystalline powder |
|
Packing |
1kg/ pack |
|
Application |
Pharmaceutical raw material |
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Evodiamine is a bioactive alkaloid extracted from the dried, unripe fruit of Evodia rutaecarpa (also known as Tetradium ruticarpum), a plant used in Traditional Chinese Medicine for centuries. It is the primary active compound responsible for the thermogenic and metabolic effects of the herb.
Evodiamine has become a popular ingredient in weight management and thermogenic formulas due to its ability to increase energy expenditure, reduce appetite, and modulate fat metabolism. It is often positioned as a “non-stimulant thermogenic” alternative to caffeine-based fat burners.
|
Other name |
EVODIAMINE10% PLANTEXTRACT;EVODIAMINE98%; EVODIAMINE20%PLANTEXTRACT; EVODIAMINE5%PLANTEXTRACT; Evodiaminestd ; EVODIAMINE; 8,13,13b,14-Tetrahydro-14-mChemicalbookethylindolo[2’3′-3,4]pyrido[2,1-b]quinazolin-5-[7H]-one; Indol(2′,3′:3,4)pyrido(2,1-b)quinazolin-5(7H)-one,8,13,13b,14-tetrahydro-14-methyl-,(S)- |

| Effect | Mechanism |
|---|---|
| Thermogenesis | Activates TRPV1 → increases intracellular calcium → upregulates uncoupling protein 1 (UCP1) in brown adipose tissue |
| Energy expenditure | Increases body temperature and metabolic rate |
| Appetite suppression | Reduces ghrelin (hunger hormone) and food intake (animal studies) |
| Fat oxidation | Enhances lipolysis and fatty acid utilization |
| Application | Typical Dosage | Key Claims |
|---|---|---|
| Thermogenic fat burner | 50–150 mg/day | Increases metabolic rate, calorie burning |
| Weight management formula | 50–100 mg/day | Supports healthy weight loss |
| Non-stimulant fat burner | 50–150 mg/day | Thermogenesis without jitters |
| Application | Typical Dosage | Mechanism |
|---|---|---|
| Glucose metabolism support | 50–100 mg/day | AMPK activation, insulin sensitivity (preclinical) |
| Lipid profile support | 50–100 mg/day | May reduce triglycerides, LDL (preclinical) |
| Application | Typical Dosage | Timing |
|---|---|---|
| Pre-cardio thermogenic | 50–100 mg | 30–45 min before cardio |
| Cutting cycle support | 50–150 mg/day | Daily during fat loss phase |

Evodia rutaecarpa (Juss.)Benth
LyvBio Co., Ltd. is a GMP-certified supplier of top purity Evodiamine for the nutraceutical, weight management, and sports nutrition industries.
Supply capabilities:
Purity: ≥98.0% (standard), ≥99.0% (pharmaceutical grade)
Source: Evodia rutaecarpa fruit (standardized extract)
Monthly capacity: 500+ kg
Bulk quantities: 100g – 5,000kg
Lead time: 3–5 days (samples), 10–15 days (bulk)
Documentation: COA, MSDS, HPLC chromatogram, stability data, allergen statement
| Parameter | Standard Grade | Test Method |
|---|---|---|
| Assay (HPLC) | ≥ 98.0% | HPLC-UV |
| Appearance | White to off-white powder | Visual |
| Identification | HPLC retention time, IR | HPLC/IR |
| Melting Point | 263–266°C | USP <741> |
| Loss on Drying | ≤ 0.5% | USP <731> |
| Residue on Ignition | ≤ 0.1% | USP <281> |
| Heavy Metals | ≤ 10 ppm | ICP-MS |
| Related Substances | Single ≤ 0.5%; Total ≤ 2.0% | HPLC-UV |
| Residual Solvents | Meet USP <467> | GC |
| Particle Size | 95% through 80 mesh | Sieve Analysis |
Q: Is Evodiamine a stimulant?
A: No. Evodiamine is non-stimulant. It works through TRPV1 activation (calcium signaling), not adrenergic pathways. It does not cause jitters, anxiety, or sleep disruption.
Q: Does Evodiamine cause a burning sensation like capsaicin?
A: No. Despite both activating TRPV1, evodiamine produces thermogenesis (warmth) without the burning/pain sensation of capsaicin. This makes it much more suitable for oral supplements.
Q: How does Evodiamine promote weight loss?
A: Multiple mechanisms: (1) Increases thermogenesis (UCP1 upregulation), (2) Enhances fat oxidation, (3) Reduces appetite (ghrelin suppression – animal data), (4) Inhibits fat cell formation (adipogenesis).
Q: Is Evodiamine safe for long-term use?
A: Human long-term safety data are limited. Typical usage cycles are 8–12 weeks followed by a break. At recommended doses (50–150 mg/day), it is generally well-tolerated.
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