Cassia EO
Naturelle
Spicy > Warm Spices > Cinnamic
Crédits photo: ScenTree SAS
Latin name :
Cinnamomum cassia
Botanical profile :
Chinese Cinnamon, also called cassia, corresponds to the bark of a tree of the Lauraceae family and the genus Cinnamomum.
Geographic origin :
The major producer of cassia is China, followed by Indonesia and South Vietnam.
Chemotypes :
There are more than 250 species of cinnamon trees throughout Southeast Asia, China and Australia. The perfume industry generally uses only two of those varieties of cinnamon:
Cinnamomum zeylanicum : Ceylon cinnamon EO. Leaves are extracted.
Cinnamomum cassia : Chinese cinnamon or Cassia EO. Leaves from this tree are not extracted for perfumery.
We can also distinguish Cinnamomum burmanni : Korintje cassia SFE and Cinnamomum tamala : Indian cinnamon, much less cultivated.
The difference between the two types of cinnamon lies in the way they are dried. Cassia dries forming two spirals, whereas Ceylon cinnamon forms thin layers of wood which crumble easily. The chinese variety is also darker and harder. Ceylon cinnamon has a more zesty and terpenic smell than the Chinese cinnamon, which contains more Cinnamaldehyde.
Cinnamomum zeylanicum : Ceylon cinnamon EO. Leaves are extracted.
Cinnamomum cassia : Chinese cinnamon or Cassia EO. Leaves from this tree are not extracted for perfumery.
We can also distinguish Cinnamomum burmanni : Korintje cassia SFE and Cinnamomum tamala : Indian cinnamon, much less cultivated.
The difference between the two types of cinnamon lies in the way they are dried. Cassia dries forming two spirals, whereas Ceylon cinnamon forms thin layers of wood which crumble easily. The chinese variety is also darker and harder. Ceylon cinnamon has a more zesty and terpenic smell than the Chinese cinnamon, which contains more Cinnamaldehyde.
Extraction process :
Chinese cinnamon culture is comparable to the one of Ceylon. Wild cultivation is done in Indonesian and Chinese rainforests in majority. Many olfactive variations may occur according to the culture locations, the forests and even between trees of a same forest.
Cinnamon tree has a very easy to peel bark. Cultivators first take off the grey external bark of the tree. They peel it to remove the undesired dry parts, and keep the rest for drying and extraction. The rest of the tree is cut down to peel the internal parts of the tree. Shavings are then gathered on palets and brought to the plant for drying, using local animals. Strips are dried for a few days in the shade, to avoid the bark from burning. A double spiral is observed, making the difference with Ceylon cinnamon, for which the spiral is unique.
After drying, strips are extracted as they are, or slightly crushed to enhance the extraction yield. In a steam distillation tank, steam is injected under pressure to be condensed at the top of the column, to make the oil settle over the water. For a 5 to 8 hours extraction, the yield is in the order of 1 to 2%.
The distillation can be done on site, or directly by the companies that produces the essential oil, in Western Europe or in North America.
Cinnamon oleoresin can be obtained from the extraction of the bark with a volatile solvent. Using ethanol gives a yield of 10 to 12%, while using benzene leads to a yield of 2 to 4%.
Cassia essential oil is a major precursor for the extraction of natural Cinnamaldehyde.
Cinnamon tree has a very easy to peel bark. Cultivators first take off the grey external bark of the tree. They peel it to remove the undesired dry parts, and keep the rest for drying and extraction. The rest of the tree is cut down to peel the internal parts of the tree. Shavings are then gathered on palets and brought to the plant for drying, using local animals. Strips are dried for a few days in the shade, to avoid the bark from burning. A double spiral is observed, making the difference with Ceylon cinnamon, for which the spiral is unique.
After drying, strips are extracted as they are, or slightly crushed to enhance the extraction yield. In a steam distillation tank, steam is injected under pressure to be condensed at the top of the column, to make the oil settle over the water. For a 5 to 8 hours extraction, the yield is in the order of 1 to 2%.
The distillation can be done on site, or directly by the companies that produces the essential oil, in Western Europe or in North America.
Cinnamon oleoresin can be obtained from the extraction of the bark with a volatile solvent. Using ethanol gives a yield of 10 to 12%, while using benzene leads to a yield of 2 to 4%.
Cassia essential oil is a major precursor for the extraction of natural Cinnamaldehyde.
Major Components :
Cinnamaldehyde (75-85%)
Ortho-Methoxycinnamaldehyde (5-10%)
Cinnamyl Acetate (≈2%)
Anisic Aldehyde (≈1%)
Benzaldehyde (≈1%)
Ortho-Methoxycinnamaldehyde (5-10%)
Cinnamyl Acetate (≈2%)
Anisic Aldehyde (≈1%)
Benzaldehyde (≈1%)
- Uses in perfumery :
- Cassia EO is used similarly as Ceylon Cinnamon EO although it is more used for resinous, smoky and honey notes and to bring richness in floral, spicy and oriental perfumes. It is also used because it is less costly than Ceylon cinnamon.
- Other comments :
- The quality of a cinnamon bark is measured by its appearance, the constitution of its essential oil and the fineness of its chips.
A quality cinnamon contains 0.9 to 2.3% of essential oil in its bark.
Possible adulteration of the products from the barks of the different varieties of Cinnamomum by adding synthetic Cinnamaldehyde
The smell of cinnamon roots is more camphoric, earthy and floral than the bark. - Volatility :
- Heart/Base
- Appearance :
- Pale yellow liquid
- Stability :
- Aldehydes can form diethylacetals in stability tests, without modifying the raw material’s smell
- Price Range :
- €€
- Aromatherapy :
Informations provided below are taken from reference works in aromatherapy. They are given for information purposes only and can not constitute medical information, nor engage the responsibility of ScenTree.
The consumption of essential oil of cassia, although limited for its toxicity, is recommended in case of bronchitis, angina, warts, and for its antioxidant virtues.
Crédits photo: ScenTree SAS
- EINECS number :
- 84961-46-6
- FEMA number :
- 2258
- Allergens :
- Cinnamaldehyde - Cinnamyl Alcohol - Cinnamyl Acetate - Benzyl Benzoate - Eugenol - Coumarin
- IFRA :
- This ingredient is restricted by IFRA
- Annexe I :
- Some regulated synthetic ingredients are found in nature and in certain proportions in natural ingredients. This presence in nature has to be taken into account when calculating limits of use recommended by the IFRA. In case you do not know these concentrations, you can use the ones estimated by the IFRA. Here they are :
- Annexe I :
- Some regulated synthetic ingredients are found in nature and in certain proportions in natural ingredients. This presence in nature has to be taken into account when calculating limits of use recommended by the IFRA. In case you do not know these concentrations, you can use the ones estimated by the IFRA. Here they are :
List of regulated compounds contained in this ingredient | ||
---|---|---|
Regulated ingredient name | CAS N° | Estimated Concentration |
Benzaldehyde | 100-52-7 | 1 |
Cinnamyl acetate | 103-54-8 | 3 |
Cinnamic alcohol | 104-54-1 | 0,2 |
Cinnamic aldehyde | 104-55-2 | 80 |
Benzyl benzoate | 120-51-4 | 0,1 |
o-Methoxycinnamaldehyde | 1504-74-1 | 9 |
Coumarin | 91-64-5 | 2 |
Eugenol | 97-53-0 | 0,1 |
Isoeugenol | 97-54-1 | 0,1 |
List of regulated compounds contained in this ingredient | ||
---|---|---|
Regulated ingredient name | CAS N° | Estimated Concentration |
Benzaldehyde | 100-52-7 | 1 |
Cinnamyl acetate | 103-54-8 | 3 |
Cinnamic alcohol | 104-54-1 | 0,2 |
Cinnamic aldehyde | 104-55-2 | 80 |
Benzyl benzoate | 120-51-4 | 0,1 |
o-Methoxycinnamaldehyde | 1504-74-1 | 9 |
Coumarin | 91-64-5 | 2 |
Eugenol | 97-53-0 | 0,1 |
Isoeugenol | 97-54-1 | 0,1 |
To learn more about IFRA's standards : https://ifrafragrance.org/safe-use/library
ScenTree is solely responsible for the information provided here.