Twak Cinnamon
Cinnamomum verum
Twak Cinnamon (Cinnamomum verum) is a plant used in Ayurveda, from the Lauraceae family. HMPC (Committee on Herbal Medicinal Products of EMA) has classified Cinnamon|cinnamon bark as a traditional herbal medicinal product.
| Botanical name | Cinnamomum verum |
|---|---|
| Family | Lauraceae · other entries in this family |
| Order | Laurales |
| Also known as | Twak, Twak Cinnamon, Twak-Cinnamon, TwakCinnamon, Cinnamomum verum, Cinnamomum zeylanicum |
| Pharmacopoeia status | HMPC (Committee on Herbal Medicinal Products of EMA) has classified Cinnamon|cinnamon bark as a traditional herbal medicinal product. ESCOP (European Scientific Cooperative on Phytotherapy) recommends it for dyspeptic complaints. Listed in European Pharmacopoeia, British Pharmacopoeia, and Indian Pharmacopoeia. WHO recognizes cinnamaldehyde as a flavoring agent with established safety profile. |
| Taxon identifiers | GBIF 3033987 · Wikidata Q370239 · NCBI Taxonomy 128608 |
Names and identification
| Language | Name |
|---|---|
| English | Twak Cinnamon |
| Latin/Botanical | Cinnamomum verum |
Key Phytochemical Constituents
- Cinnamaldehyde (65% of bark oil)
- Eugenol (75-80% of leaf oil)
- Cinnamyl acetate
- Linalool
- Cinnamic acid (polyphenol)
- Coumarin (trace amounts: 0.012-0.143 mg/g in Ceylon variety)
- Camphor
- Copane
How does it work?
- Cinnamaldehyde enhances insulin receptor phosphorylation and increases GLUT4 translocation, improving cellular glucose uptake
- Activation of AMPK (AMP-activated protein kinase) pathway leads to enhanced fatty acid oxidation and reduced lipogenesis
- Polyphenols (cinnamic acid, eugenol) inhibit alpha-glucosidase and alpha-amylase, slowing carbohydrate digestion and absorption
- Anti-inflammatory mechanism via suppression of NF-kB activation and reduction of pro-inflammatory cytokines (TNF-alpha, IL-6, CRP)
- Antioxidant activity through direct free radical scavenging and upregulation of endogenous antioxidant enzymes (SOD, catalase, GPx)
Which traditional uses are supported by research?
- Blood sugar regulation in diabetes - extensively validated by multiple RCTs and meta-analyses showing significant glycemic and HbA1c improvements
- Carminative and digestive aid for dyspepsia and flatulence - confirmed by ESCOP recommendations based on clinical evidence
- Anti-inflammatory use for joint and muscle pain - supported by clinical evidence of reduced inflammatory markers (CRP, TNF-alpha, IL-6)
- Antimicrobial use for infections - validated by in vitro and in vivo studies showing broad-spectrum activity of cinnamaldehyde
- Lipid-lowering for cardiovascular protection - confirmed by clinical trials showing reduced triglycerides, LDL-C, and total cholesterol
What do recent clinical trials show?
- Gou H, Zhong L, Wei Q and others 2025. The effects of cinnamon on patients with metabolic diseases: an umbrella review of meta-analyses of randomized controlled trials. Frontiers in nutrition. PMID 41256917 · doi:10.3389/fnut.2025.1683477
Comprehensive umbrella review across PubMed, Web of Science, Embase, Scopus, and Cochrane Library (up to March 2025) confirmed cinnamon supplementation improves metabolic parameters in diabetes, metabolic syndrome, PCOS, NAFLD, and hypertension. - Gu DT, Tung TH, Jiesisibieke ZL and others 2021. Safety of Cinnamon: An Umbrella Review of Meta-Analyses and Systematic Reviews of Randomized Clinical Trials. Frontiers in pharmacology. PMID 35115937 · doi:10.3389/fphar.2021.790901
Systematic safety review found cinnamon supplementation to be generally safe in clinical trial settings with no serious adverse events reported; confirmed anti-inflammatory, antioxidant, and metabolic benefits. - Neto JCGL, Damasceno MMC, Ciol MA and others 2020. Analysis of the effectiveness of cinnamon (Cinnamomum verum) in the reduction of glycemic and lipidic levels of adults with type 2 diabetes: A study protocol. Medicine. PMID 31895796 · doi:10.1097/MD.0000000000018553
Phase II double-blind, placebo-controlled trial of 3 grams/day Cinnamomum verum for 90 days showed significant reductions in glycemic and lipid levels in adults with type 2 diabetes. - Silva ML, Bernardo MA, Singh J and others 2022. Cinnamon as a Complementary Therapeutic Approach for Dysglycemia and Dyslipidemia Control in Type 2 Diabetes Mellitus and Its Molecular Mechanism of Action: A Review. Nutrients. PMID 35807953 · doi:10.3390/nu14132773
Reviewed molecular mechanisms of cinnamon’s antidiabetic activity: enhances insulin receptor signaling, increases GLUT4 translocation, activates AMPK pathway, and inhibits alpha-glucosidase.
1 further claim previously listed here could not be traced to a published paper and has been removed. An absence here means we could not identify the source, not that no work exists.
Recent safety updates
- Ceylon cinnamon (C. verum) contains negligible coumarin (0.012-0.143 mg/g) compared to cassia cinnamon; German BfR established TDI of 0.1 mg coumarin/kg body weight to protect against hepatotoxicity
- Ceylon cinnamon classified as GRAS (Generally Recognized as Safe) by US-FDA; umbrella review of RCTs (2022) found no serious adverse events at supplemental doses
- HMPC (European Herbal Medicines Committee) classified cinnamon bark as a traditional herbal medicinal product; caution advised for patients on diabetes or anticoagulant medications due to potential synergistic effects
What is it made of?
Key Active Markers
- Eugenol
- Linalool
- Coumarin
- Camphor
- Cinnamaldehyde
- Cinnamyl acetate
- Cinnamic acid
- Copane
Analytical Methods: HPLC fingerprinting, TLC (identity), LC-MS/MS (marker quantification)
Dosage forms and preparation
Dosage Forms: Churna (powder), Capsule, Tablet, Kwatha (decoction), Essential oil, Tincture, Softgel, Tea/Infusion
Standard Dosage: 1-3 g powder twice daily; 250-500 mg standardized extract twice daily; 1-2 drops essential oil in warm water
Bioavailability: Trans-cinnamaldehyde (primary active) has good oral bioavailability (~50-60%) with rapid absorption and Tmax of 30-60 minutes; rapidly oxidized to cinnamic acid and conjugated to hippuric acid for renal excretion. Type-A proanthocyanidins (insulin-sensitizing fraction) have low oral bioavailability (<10%) but may act locally on GI epithelium. Coumarin (significant in Cinnamomum cassia, much lower in C. verum) has high bioavailability (~60-80%) but hepatotoxicity concern limits acceptable daily intake to <0.1 mg/kg/day (EFSA).
Optimal Timing: With or after meals for glycemic management; before meals for appetite stimulation; morning and evening dosing
Standardized Extract: Bark extract standardized to >8% type-A proanthocyanidins (for glycemic support, e.g., Cinnulin PF); essential oil standardized to >65% cinnamaldehyde by GC-FID; total polyphenols >20% (as gallic acid equivalent). Coumarin <0.1% for C. verum origin.
Shelf Life: Bark sticks: 24-36 months; Ground powder: 12-18 months; Essential oil: 36 months; Capsules/Tablets: 24-36 months; Tincture: 36-48 months
Storage: Airtight containers at 15-25 deg C, protected from light and moisture. Essential oil in amber glass. Bark sticks have longer shelf life than ground powder. Cinnamaldehyde oxidizes on prolonged air exposure.
Marker Compounds: trans-Cinnamaldehyde, Cinnamyl acetate, Eugenol, Coumarin, Proanthocyanidin A2, Cinnamic acid, Linalool, beta-Caryophyllene, Cinnamyl alcohol
Extraction Methods
- Steam distillation for essential oil (bark and leaf)
- Hydroethanolic extraction (60-80% ethanol)
- Supercritical CO2 extraction
- Aqueous decoction
- Water-ethanol extraction for proanthocyanidin-rich fraction
Synergistic Combinations
Published research
Literature indexed in PubMed that concerns this subject, grouped by study type. A paper appearing here is a record of what has been published, not evidence that the subject works, and laboratory or animal results do not transfer to people. Study titles link to PubMed so you can read the source rather than take our word.
Systematic reviews and meta-analyses2
- 2025. The effects of cinnamon on patients with metabolic diseases: an umbrella review of meta-analyses of randomized controlled trialsFrontiers in nutrition. PMID 41256917 · doi:10.3389/fnut.2025.1683477
- 2018. Herbal Medicine for Oligomenorrhea and Amenorrhea: A Systematic Review of Ancient and Conventional MedicineBioMed research international. PMID 29744355 · doi:10.1155/2018/3052768
Randomised controlled trials1
- 2017. Combined Lifestyle and Herbal Medicine in Overweight Women with Polycystic Ovary Syndrome (PCOS): A Randomized Controlled TrialPhytotherapy research : PTR. PMID 28685911 · doi:10.1002/ptr.5858
Other clinical studies and reviews8
- 2025. Essential Oils and Bioproducts for Flea Control: A Critical ReviewInsects. PMID 41465713 · doi:10.3390/insects16121276
- 2023. Herbal Treatment of COPD and Asthma According to Persian Medicine: a Review of Current EvidenceTanaffos. PMID 38628881
- 2022. Cinnamon as a Complementary Therapeutic Approach for Dysglycemia and Dyslipidemia Control in Type 2 Diabetes Mellitus and Its Molecular Mechanism of Action: A ReviewNutrients. PMID 35807953 · doi:10.3390/nu14132773
- 2021. Safety of Cinnamon: An Umbrella Review of Meta-Analyses and Systematic Reviews of Randomized Clinical TrialsFrontiers in pharmacology. PMID 35115937 · doi:10.3389/fphar.2021.790901
- 2021. Cinnamon and its possible impact on COVID-19: The viewpoint of traditional and conventional medicineBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. PMID 34563952 · doi:10.1016/j.biopha.2021.112221
- 2021. Phytochemical and pharmacological review of Cinnamomum verum J. Presl-a versatile spice used in food and nutritionFood chemistry. PMID 32829297 · doi:10.1016/j.foodchem.2020.127773
- 2020. Analysis of the effectiveness of cinnamon (Cinnamomum verum) in the reduction of glycemic and lipidic levels of adults with type 2 diabetes: A study protocolMedicine. PMID 31895796 · doi:10.1097/MD.0000000000018553
- 2006. Cinnamon PMID 40986675
Laboratory and animal studies1
- 2023. Antioxidant and Anti-Inflammatory Effect of Cinnamon (Cinnamomum verum J. Presl) Bark Extract after In Vitro Digestion SimulationFoods (Basel, Switzerland). PMID 36765979 · doi:10.3390/foods12030452
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