Cinnamon Extract Powder 10:1, 20:1, 50:1 TLC
【Botanical source】: Cinnamomum cassia (L.) D. Don
【Part used】: Bark
【Specification】: 10:1, 20:1, 50:1 TLC
【Extraction solvents】: Water
【Appearance】: Brownish fine powder
【Particle size】: 95% pass 80 mesh size
【Main ingredients】: The main component of cinnamon is volatile oil, among which trans cinnamaldehyde (about 70-90%) is the core active substance, contributing unique aroma and pharmacological effects. It also contains eugenol, coumarin, anthocyanins, flavonoids, and various terpenoids. These ingredients endow cinnamon with antibacterial, antioxidant, anti-inflammatory, insulin sensitivity improving, and blood circulation promoting effects.
【Storage conditions】:Store at room temperature in a sealed manner, away from light, and in a ventilated, cool, and dry environment.
【Shelf life】: 24 months from the production date

Cinnamon Extract Powder Production Flowchart
Cinnamon raw materials -Coarse powder(40 mesh) -Low temperature water extraction – 1st Reflux Extraction(10 times water,2 Hrs) – 2nd Reflux Extraction8 times water,1.5 Hrs) – 3rd Reflux Extraction(6 times water,1 Hrs) – Extraction Solution-combine&Filtrate-Concentrate-Extractum-spray drying – screening – packaging – detection of physical and chemical indicators – warehousing
Specification Sheet of Cinnamon Extract Powder
| Product name: |
Cinnamon Extract |
| Specification: |
10:1 TLC |
| Part used: |
Bark of Cinnamomum cassia (L.) D. Don |
| Solvent used: |
Water |
| Process: |
Raw materials crushed, extracted, concentrated and spray-dried to powder |
| Non GMO according to regulation (EC) 1829/2003 and 1830/2003 or United States requirements. Non allergen according to Directive 2007/68 amending Annex IIIa to Directive 2000/13/EC and US Food allergen labelling and consumer protection act 2004. |
| Heavy Metals: |
|
|
|
| Lead: |
NMT 3ppm |
Cadmium: |
NMT 1ppm |
| Arsenic: |
NMT 2ppm |
Mercury: |
NMT 1ppm |
| Residual solvents: |
Comply to USP |
| Pesticides residues: |
Conform to Regulation USP<561> |
| Microbiology: |
|
|
|
| Total plate count: |
10000cfu/g Max |
Yeasts and molds: |
1000cfu/g Max |
| E.coli: |
Not detected in (g)10 |
Salmonella spp.: |
Not detected in (g)25 |
| Staphylococcus aureus: |
Not detected in (g)10 |
Clostridium spp.: |
Not Present in 0.1 g of food |
| Organoleptic quality |
Method |
Specifications |
| Aspect: |
Visual : ( CQ-MO-148) |
Powder |
| Color: |
Visual : ( CQ-MO-148) |
Brownish |
| Flavor: |
Sensory: (CQ-MO-148) |
Characteristic |
| Analytical quality |
Method |
Specifications |
| Identification: |
TLC |
Conform |
| Loss on drying: |
USP <731> |
< 10% |
| Bulk density: |
USP <616> Method I |
40 – 60 g/100mL |
| Particle size: |
Analytical sieving || USP <786> |
100% through 80meshes |
| Packaging suitable for foodstuff. |
Extended Reading
Modern Research on Cinnamon Extract
Chemical Components
Cinnamon’s composition varies significantly by species, with Cinnamomum verum (Ceylon/”true” cinnamon) and Cinnamomum cassia (Chinese cinnamon) being most common. Modern analytical techniques (GC-MS, HPLC) have characterized key bioactive compounds:
- Phenolic Compounds & Volatile Oils:
- Cinnamaldehyde: (65-80% in cassia, 50-75% in verum) – Primary bioactive, responsible for aroma and major effects.
- Eugenol: Higher in C. verum (up to 75% in leaf oil), significant in C. zeylanicum bark.
- Cinnamic Acid and its derivatives.
- Coumarin: A hepatotoxic compound; Cassia cinnamon contains high levels (~1%), while Ceylon cinnamon contains only trace amounts.
- Polyphenols & Proanthocyanidins (Type-A Polymers):
- Unique water-soluble, doubly-linked Type-A Proanthocyanidins – identified as key insulin-mimetic agents.
- Catechins and Epicatechins.
- Mucilage/Gums: Polysaccharides.
- Other: Trace amounts of safrole (carcinogen), minerals (manganese, calcium), and fiber.
Health Benefits (Evidence-Based)
- Glycemic Control & Diabetes Management
- Mechanism: Mimics insulin by activating insulin receptor kinase, autophosphorylation of the receptor, and inhibiting PTP-1E (phosphatase that inactivates insulin receptors). Increases GLUT4 translocation. The Type-A polymers are primarily responsible.
- Clinical Evidence: Multiple meta-analyses confirm that cinnamon (1-6 g/day) significantly reduces fasting blood glucose (by 10-29 mg/dL), HbA1c (by 0.5-0.8%), and insulin resistance (HOMA-IR) in type 2 diabetics and prediabetics. Effects are modest but consistent.
- Antioxidant & Anti-inflammatory
- High ORAC Value: Cinnamaldehyde and polyphenols are potent free radical scavengers.
- NF-κB Inhibition: Suppresses pro-inflammatory cytokines (TNF-α, IL-6, IL-1β). Demonstrated in models of arthritis, colitis, and neuroinflammation.
- Antimicrobial & Antifungal
- Broad-spectrum activity: Cinnamaldehyde disrupts microbial cell membranes and inhibits quorum sensing. Effective against Candida spp. (including biofilms), H. pylori, E. coli, S. aureus (including MRSA), and oral pathogens.
- Application: Studied as a natural food preservative and in dental products.
- Neuroprotection
- Inhibits tau aggregation and Aβ oligomerization in Alzheimer’s models. Enhances brain-derived neurotrophic factor (BDNF) and improves cognitive function in animal studies.
- Cardiovascular Health
- Improves lipid profile (reduces LDL-C, triglycerides; increases HDL-C) in meta-analyses.
- Mild antihypertensive effects via vasodilation (NO pathway).
- Anti-platelet aggregation activity (caution with blood thinners).
- Potential Anti-cancer Effects
- In vitro studies show cinnamaldehyde induces apoptosis, inhibits proliferation, and suppresses angiogenesis in various cancer cell lines (colon, gastric, leukemia, melanoma). Human data lacking.
Interactions
- Antidiabetic Drugs (Insulin, Metformin, Sulfonylureas): HIGH RISK – Additive hypoglycemic effect. Can cause dangerously low blood sugar. Requires close glucose monitoring and possible medication adjustment.
- Anticoagulant/Antiplatelet Drugs (Warfarin, Aspirin, Clopidogrel): MODERATE RISK. Cinnamon (especially coumarin-rich cassia) may potentiate effects, increasing bleeding risk. Multiple case reports of altered INR with warfarin.
- Hepatotoxic Drugs (Acetaminophen, Statins, Amiodarone): MODERATE RISK. High-dose cassia cinnamon (due to coumarin) may exacerbate liver damage. Monitor liver enzymes.
- Cytochrome P450: In vitro, cinnamaldehyde inhibits CYP1A2, 2B1, 2C11, 2E1. Clinical significance unclear but potential for drug interactions exists.
Taboos & Warnings
- Pregnancy: High doses may be emmenagogue (stimulate menstruation) or uterine stimulant; avoid therapeutic doses.
- Liver Disease: Contraindicated for high-dose/long-term Cassia cinnamon use due to coumarin content (can cause hepatotoxicity at >0.1 mg/kg/day). Ceylon cinnamon is preferred for supplements.
- Peptic Ulcers/Gastritis: May irritate GI mucosa. Use with caution.
- Allergy: Not uncommon; can cause contact dermatitis or oral inflammation (“cinnamon stomatitis”).
- Surgery: Discontinue at least 2 weeks prior due to blood sugar and bleeding risks.
- Cassia vs. Ceylon: Critical distinction. For therapeutic use (>1 tsp/day), Ceylon cinnamon (C. verum) is recommended to avoid cumulative coumarin toxicity.
Applications
- Nutraceuticals: Standardized extracts (often for cinnamaldehyde or Type-A polymers) in capsules for blood sugar support.
- Functional Foods: Added to beverages, cereals, and snacks for flavor and potential metabolic benefits.
- Essential Oils: Used in aromatherapy, dentistry (mouthwashes), and topical antimicrobial preparations.
- Natural Preservatives: In food packaging and edible films to extend shelf life.
- Cosmeceuticals: In anti-aging and anti-acne formulations for antioxidant/anti-inflammatory effects.
References
- Allen, R. W., et al. (2013). Cinnamon use in type 2 diabetes: an updated systematic review and meta-analysis. Annals of Family Medicine, 11(5), 452-459. (Key clinical meta-analysis)
- Rao, P. V., & Gan, S. H. (2014). Cinnamon: A multifaceted medicinal plant. *Evidence-Based Complementary and Alternative Medicine, 2014*, 642942.
- Gruenwald, J., et al. (2010). Cinnamon and health. Critical Reviews in Food Science and Nutrition, 50(9), 822-834.
- Qin, B., et al. (2010). Cinnamon extract (traditional herb) potentiates in vivo insulin-regulated glucose utilization via enhancing insulin signaling in skeletal muscle. Endocrine Research, 35(2), 59-70. (Mechanistic study)
- Wang, Y. H., et al. (2013). Antibacterial effects of cinnamon (Cinnamomum cassia) bark essential oil on Porphyromonas gingivalis. *Microbial Pathogenesis, 59-60*, 52-57.
- Hlebowicz, J., et al. (2007). Effect of cinnamon on postprandial blood glucose, gastric emptying, and satiety in healthy subjects. The American Journal of Clinical Nutrition, 85(6), 1552-1556.
- Mollazadeh, H., & Hosseinzadeh, H. (2016). Cinnamon effects on metabolic syndrome: a review based on its mechanisms. Iranian Journal of Basic Medical Sciences, 19(12), 1258–1270. (Comprehensive mechanism review)
- Woehrlin, F., et al. (2010). Quantification of flavoring constituents in cinnamon: high variation of coumarin in cassia bark from the German retail market and in authentic samples from Indonesia. Journal of Agricultural and Food Chemistry, 58(19), 10568–10575. (Important coumarin analysis)
- Kawatra, P., & Rajagopalan, R. (2015). Cinnamon: Mystic powers of a minute ingredient. Pharmacognosy Research, 7(Suppl 1), S1–S6.
- Singletary, K. (2019). Cinnamon: update of potential health benefits. Nutrition Today, 54(1), 42-52.
- European Food Safety Authority (EFSA). (2008). Coumarin in flavourings and other food ingredients with flavouring properties – Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (AFC). EFSA Journal, 6(10), 793. (Regulatory safety assessment)
- Clinical Trial: Zare, R., et al. (2019). Effect of cinnamon supplementation on blood pressure and anthropometric parameters in patients with type 2 diabetes: A systematic review and meta-analysis of clinical trials. Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 13(1), 578-585.
Note: This summary is for informational purposes. It may interact with medications and is contraindicated in certain conditions. Consult a healthcare professional before therapeutic use, particularly regarding its estrogenic activity.