cardamomum White et Maton.



It grows wild in the damp mountain forests of South India (the Cardamom Mountains) and Vietnam. Cultivated in India, Sri Lanka, Burma, Indochina, South China. Occasionally found as a weed.

Perennial herbaceous plant with large rhizome, developing several herbaceous stems 2-3 m high. Leaves broadly lanceolate, long (within 60 cm). The inflorescence is a long brush. The flowers are beautiful, irregular, with a simple white within the flower bed and a wide white lip with a yellowish edge, dotted with radiant blue veins. The fruit is a box.

Boxes are harvested unripe to avoid cracking and loss of seeds. Dry boxes – Fructus Cardamoni – straw yellow, oval-triangular, 1-2 cm long, unilocular, fragile, woody, tasteless and odorless, contain numerous seeds (within 20). Seeds within 4 mm long and 3 mm wide, angular, wrinkled, brown, fragrant, spicy-burning taste.

Seeds contain 4-8% essential oil, which is located in a special layer of the seed coat. The oil contains limonene, terpineol, borneol, their esters and cineol.

Cardamom is stored without separating the seeds from the boxes to avoid volatilization of the essential oil. Only the seeds are used as a carminative and to increase appetite, as well as to correct the taste and smell of medicines. Used as a spice. Commodity varieties of cardamom are named after the place of their collection; Malabar and Mysore cardamom are valued.

Substitutes for cardamom are plants of a close genus. The following are known.

Bengal cardamom – Amomum aromaticum Roxb. from Bengal and Assam. Cultivated in humid areas at the foot of the Himalayas. Essential oil (1-1.2%) has a high content of cineole. Doesn’t look like real cardamom.

Cardamom round Chinese – A. glogosum Lour. – from South China, cultivated there. The essential oil is close in constants to real cardamom, but with a strong smell of camphor; contains cineole.

Cardamom round Javanese – A. kepulaga Sprague et Burk. – native to the island of Java. It is cultivated in the same place and in Sumatra, in Malacca, Thailand, Kampuchea.

Corarima cardamom – A. korarima (Pereira) Engl. – from Ethiopia. It has the largest boxes, 4 cm or more long and 2 cm thick, brown, ribbed, more than 100 seeds in a box, camphor taste. In the last century, seeds replaced money.

Cardamom Melagueta – A. melegueta Rose, from tropical West Africa, from the Gulf of Guinea. The smell of seeds resembles cardamom, the taste is spicy-burning; contains 0.5% essential oil and a burning substance close to gingerol.

All substitutes for real cardamom (whose fruits are official in a number of countries) are popular in local folk medicine (stomach remedies, for the common cold, cough, rheumatism, etc.) and as spices. Many are exported.

The plant contains monocyclic terpenes.



Monocyclic terpenes are derivatives of methylisopropylcyclohexane with two (or one) double bonds. Double bonds can be both in the ring (terpenes, a-phellandrene) or one of them is in the isopropyl group (limonene) or at C 1 -C 7 ) b-phellandrene).


Of the oxygen derivatives, the most common are: alcohols – terpineol, menthol, ketones – menthone, piperitone, carvone, oxides – cineol.


Some monocyclic terpenes are often present in essential oils together with aliphatic terpenes (eg essential oils of many citrus fruits) or accompany bicyclic monoterpenes and sesquiterpenes (see below). For these reasons, the division of essential oil plants into groups of terpenes is somewhat arbitrary.


Essential oils are natural aromatic substances that are highly volatile and cause the specific smell of plants. For this reason, also due to their “oily” consistency and “greasy” stain on paper, which soon disappears, they received such a peculiar name.

Essential oils are not individual substances. These are complex mixtures of organic substances, the composition and number of which are different for each type of essential oil plants and can serve as a chemotaxonomic feature. The main group of substances that make up the essential oils of many plants are terpenes (more precisely, monoterpenes) and seseviterpenes, i.e., substances with an isoprenoid structure. However, in the essential oils of a number of plants, aromatic compounds may predominate, as well as numerous substances of the aliphatic series. There are plants with sulfur and nitrogen compounds in essential oils.

Essential oils in plants are mostly in a free state. However, some plants contain them in the form of glycosides and are released during enzymatic cleavage. Essential oils are formed in all parts of plants, but quantitatively they accumulate in them traditionally unequally.

They can be in a plant organism in a diffuse diffuse state (ie, emulsified or dissolved in cells) or accumulate, localize in special anatomical and morphological formations that are easily detected under a microscope. These excretory formations can be exogenous and endogenous.

Exogenous formations develop in the epidermal tissue and are:

– glandular “spots” – small-drop accumulations of essential oils immediately under the cuticle of the epidermis;

– glandular hairs – cylindrical epidermal outgrowths, consisting of a unicellular or multicellular pedicle and a head with cells that secrete essential oil;

– glands – epidermal outgrowths that have received the most

the highest specialization in the extraction and accumulation of essential oils. They have a different structure and can serve as a systematic feature. For example, in yasnotkovye (labial) 8 excretory cells are arranged in a rosette on a short stalk; in aster (composite) glandular cells have a vertical arrangement – 2 in 4 rows, etc.

Endogenous formations develop in parenchymal tissues and are:

– secretory cells – single (for example, in the air parenchyma of calamus rhizome) or form layers of such cells (for example, in valerian roots);

– receptacles – rounded cavities formed in the mesophyll of the leaf, peel of citrus fruits, in the bark and wood of a number of plants and filled with essential oil;

– tubules and passages – strongly elongated excretory formations found in the fruits of umbellate, bark and wood of a number of plants.

Essential oils accumulate in plants in all possible quantities: from hundredths and thousandths of a percent (for example, in violet flowers – 0.004%) to 20% or more (for example, in flower buds of carnations – up to 23%).

Essential oils are obtained: 1) by steam distillation; 2) extraction with some extractants; 3) enfleurage; 4) mechanically.

Steam distillation is the most common method. It is carried out in installations consisting of a double-jacketed still (in which steam circulates to prevent the still from cooling), a condenser and a receiver. Steam is fed into the cube loaded with raw materials from below through a perforated coil, entraining the essential oil. A mixture of cooled vapors of water and essential oil enters the receiver, where the mixture separates and excess water is removed through a tube at the bottom of the receiver (if oil is lighter than water) or through a drain tube at the top (if oil is heavier than water).

The extraction of essential oils from raw materials is carried out with volatile organic solvents in Soxhlet-type apparatuses or in column apparatuses. Subsequently, the raw material is lifted by the screw from the bottom up, and the extractant enters towards it. After distillation of the solvent, the residue is either pure essential oil or its mixture with other extracted substances (resins, waxes, etc.); in the latter case, additional cleaning is required.

Enfleurage is based on the fact that essential oil from raw materials (mainly from flowers) is absorbed by sorbents (solid fats, activated carbon, etc.) in special frame installations.

The mechanical method is used to extract essential oils from citrus fruits by pressing or scraping.

Although essential oils are very common in the plant world, their role for the plant organism and the reasons for their formation have not yet been reliably established. It was assumed that essential oils serve to protect plants from diseases and pests, to attract the smell of insects, which contributes to the pollination of flowers, to protect plants from excessive heating during the day and hypothermia at night, etc. Currently, most scientists believe that essential oils (or rather, their components) are actively involved in the metabolic processes of plant organisms.

Essential oils find a wide and varied application for medicinal, cosmetic, food (spices) and other chains.

Essential oils are classified according to the substances that make up their bulk, or substances that determine their medicinal and industrial value. There are the following groups (and subgroups) of components of essential oils:

Monoterpenes (terpenes), including:

1. Acyclic terpenes.

2. Monocyclic terpenes.

3. Bicyclic terpenes.

Sesquiterpenes, including:

1. Acyclic sesquiterpenes.

2. Cyclic sesquiterpenes.

Aromatic and phenolic compounds.

Sulfur and nitrogen-containing compounds.

The listed compounds, especially terpenoids, in essential oils can occur in the form of numerous oxygen derivatives: alcohols, aldehydes, ketones, phenols, acids, esters, lactones, oxides, quinones. The number of terpenoids also increases due to the tendency of many of these compounds to various forms of isomerism (optical, geometric, etc.).

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