The international trade of essential oils accounted for more than US$ 10 billion in 2021, with a growing tendence. USA, China, India, France and Brazil are the main global players. Reliable and comprehensive market data, however, is hard to obtain. Apart from a few government databases dealing with import/export values, information regarding local (national/internal) production and consumption as well as market trends, when available, are for sale, and expensive. Data from the global and Brazilian markets in the last decade were gathered and discussed in this review, with highlights on the balance of trade and the main oils produced in Brazil. As a megadiverse country, opportunities for new essential oils from Brazil do exist, but several obstacles must be overcome, such as legislation compliance, quality, supply and safety assurance, so that the market can be conquered.

The identification of essential oils constituents has been made easier and faster by the use of automatic software search engines that compare the experimental mass spectra and calculate the retention indices with those in commercial databases. However, these search engines and databases are very expensive. Electronic sheets have been assembled in a set of linked sheets, so that after some data is inserted, linear retention indices, relative response factors, normalization, area correction and absolute quantitation are calculated automatically. The set has been applied to the analysis of essential oils and volatiles in laboratory routine and substantial reduction in time-consuming and error-prone repetitive work were observed. One specific example for the analysis of an essential oil is provided. The designed electronic sheets can be a costless alternative to commercial software for data handling and identification.

Temnadenia odorifera is an endemic species from the Brazilian Atlantic Forest. This study was developed in order to identify the volatile compounds emitted by the living flowers and nectar, to evaluate the temporal pattern of scent emission, and the sugars composition of its nectar. Analyses of the flower scent by dynamic headspace in vivo, of nectar sugar composition and studies on floral biology were performed. Twenty-three volatile compounds were identified in the flowers scent. The total amount of odor emitted by flowers varied significantly throughout anthesis, ranging from 10232.7 ng g-1 (9 to 12 h) to 620.2 ng g-1 (15 to 18 h). 2-Phenylethanol and (E)-cinnamyl alcohol were the major compounds. Concentration ratio between disaccharides and the sum of hexoses ranged from 2.3 to 3.04, which can be correlated to the physiological needs inherent to big bees, the most frequent insects in T. odorifera. Analysis of the chemical composition of T. odorifera flowers provided a broader understanding of the mechanisms responsible for plant-insect interactions.

ABSTRACT The bioavailability, toxicity, and therapeutic efficacy of a drug is directly related to its administration route. The pulmonary route can be accessed by inhalation after fumigation, vaporization or nebulization. Thus, pharmacological and toxicological evaluation accessed by an apparatus specifically designed and validated for this type of administration is extremely important. Based on pre-existing models, an inhalation chamber was developed. This presents a central structure with five animal holders. The nebulized air passes directly and continuously through these holders and subsequently to an outlet. Evaluation of its operation was performed using clove essential oil, a nebulizer, and a flow meter. The air within the chamber was collected by static headspace and analyzed by gas chromatography with a flame ionization detector. For this purpose, a 2.5 minutes chromatographic method was developed. The air flow in each of the five outputs was 0.92 liters per minute. During the first minute, the chamber became saturated with the nebulized material. Homogeneous and continuous operation of the chamber was observed without accumulation of volatile material inside it for 25 minutes. The inhalation chamber works satisfactorily for in vivo tests with medicines designed to be administrated by inhalation.

ABSTRACT Commercial antiparasitics have been the main tool to control parasites, but due to the resistance development, plant extracts have been widely investigated to find new molecules. The present study aimed to investigate the in vitro acaricide and anthelmintic activities of the essential oil from the aerial parts of Hesperozygis myrtoides (A.St.-Hil. ex Benth.) Epling, Lamiaceae. The essential oil was obtained by hydrodistillation analyzed by GC-FID and GC-MS. Four tests were conducted in vitro to screen the antiparasitic action of the essential oil. The evaluation on Rhipicephalus (Boophilus) microplus was performed with the adult immersion test at concentrations ranging from 0.391 to 25 mg/ml and the larval packet test from 3.125 to 100 mg/ml. For Haemonchus contortus the egg hatch test was performed from 0.012 to 25 mg/ml and the larval development test from 0.003 to 0.4 mg/ml. The LC50 and LC90 values were calculated by Probit. The main components identified in the essential oil were isomenthone (47.7%), pulegone (21.4%), limonene (7.7%), isomenthyl acetate (6.8%) and neoisomenthol (3.9%). In the larval packet test the LC50 and LC90 were 13.5 and 21.8 mg/ml, respectively. In egg hatch test, the LC50 and LC90 were 0.249 and 0.797 mg/ml, respectively, while in the larval development test were 0.072 and 0.167 mg/ml, respectively. This is the first report of the H. myrtoides evaluation against those parasites. The anthelmintic results proved its efficacy on H. contortus encouraging new research with a focus on their main bioactives.

Óleos essenciais cítricos brasileiros (mandarina, laranja, limão, bergamota e tangerina) foram analisados a fim de determinar resíduos de pesticidas organoclorados (aldrin, clordano, dieldrin e dicofol) e organofosforados (clorpirifós metílico, dimetoato, metidationa e paration metílico). Um estudo comparativo entre cromatografia gasosa acoplada a espectrometria de massas em modo de monitoramento seletivo de íons (CG-EM-MSI) e cromatografia gasosa com detector por captura de elétrons (CG-DCE) foi realizado usando extração em fase sólida (EFS) com fase Florisil® para pré-concentração dos pesticidas. A recuperação média dos pesticidas foi de 71 a 83% por CG-EM-MSI e de 99 a 104% por CG-DCE. O limite de quantificação foi de 0,93 a 3,93 mg L-1 por CG-EM-MSI e de 0,09 a 0,12 mg L-1 por CG-DCE. Quinze amostras comerciais de óleos essenciais cítricos brasileiros foram analisadas e seis amostras apresentaram contaminação com valores acima do limite máximo de resíduos (LMR) permitido pelo Codex Alimentarius.

Brazilian citrus essential oils (mandarin, orange, lemon, bergamot and tangerine) were analyzed for the determination of pesticides residues of organochlorine (aldrin, chlordane, dieldrin and dicofol) and organophosphorus (methyl chlorpyrifos, dimethoate, methidathion and methyl parathion) . A comparative study between gas chromatography-mass spectrometry in selective ion monitoring mode (GC-MS-SIM) and gas chromatography-electron capture detector (GC-ECD) was performed using solid phase extraction (SPE) with Florisil® cartridge for the pre-concentration of pesticides. The average recovery of pesticides was from 71 to 83% as determined by GC-MS-SIM analysis and 99 to 104% by GC-ECD. The limit of quantification was from 0.93 to 3.93 mg L-1 in GC-MS-SIM and 0.09 to 0.12 mg L-1 in GC-ECD. Fifteen samples of commercial Brazilian citrus essential oils were analyzed and six samples showed contamination with values above the maximum residue limit (MRL) allowed by the Codex Alimentarius.

The influence of pre-processing of arabica coffee beans on the composition of volatile precursors including sugars, chlorogenic acids, phenolics, proteins, aminoacids, trigonelline and fatty acids was assessed and correlated with volatiles formed during roasting. Reducing sugars and free aminoacids were highest for natural coffees whereas total sugars, chlorogenic acids and trigonelline were highest for washed coffees. The highest correlation was observed for total phenolics and volatile phenolics (R= 0.999). Experimental data were evaluated by Principal Components Analysis and results showed that washed coffees formed a distinct group in relation to semi-washed and natural coffees.

A fruit chemical composition reflects its maturation stage. For coffee, it is also the reflex of the post-harvesting processing type, dry, semi-wet and wet. The object of this work was to verify if headspace solid phase microextraction coupled to gas chromatography (HS-SPME-GC) could be used to discriminate between samples harvested in different maturation stages and treated by different processes. With application of principal component analysis to the area of 117 compounds extracted by SPME, using divinylbenzene/Carboxen/polydimethylsiloxane fiber, it was possible to discriminate, in the roasted and ground coffee, the maturity stage and processing type used .

Com o objetivo de avaliar o comportamento agronômico, o potencial de rendimento de óleo essencial e identificar os quimiotipos de 16 acessos de Lippa alba (erva cidreira) da coleção da Universidade de Brasília foi conduzido um experimento de campo em Latossolo Vermelho, sob irrigação por gotejamento na região do Cerrado do Distrito Federal. Foram avaliados a época de florescimento, hábito de crescimento, área foliar, comprimento da haste, massa fresca de folhas e hastes, massa foliar seca, teor e rendimento de óleo essencial e perfil aromático. O óleo essencial foi extraído por hidrodestilação em aparelho de Clevenger modificado e os constituintes identificados e quantificados através de cromatografia em fase gasosa acoplada a espectrometria de massas. O delineamento experimental utilizado foi de blocos ao acaso, com três repetições, contendo três plantas úteis por parcela. Foram identificados os quimiotipos citral-limoneno, citral-mirceno, limoneno-carvona, citral, linalol, mirceno e linalol-limoneno. Os acessos apresentaram teores máximos de linalol de 89,8% (L.16); mirceno de 47,6% (L.37); limoneno de 36,0%, carvona de 46,9% (L.27) e citral de 56,7% (L.17). Os genótipos com maiores áreas foliares e maiores comprimentos de hastes tenderam a apresentar maiores teores de óleo e maior concentração de linalol. A concentração de óleo foi inversamente proporcional à produção de massa foliar seca. Os acessos que apresentaram os maiores rendimentos dos compostos majoritários do óleo essencial foram: L.16 (0,77 g pl-1), como fonte potencial para a produção de linalol; L.17 (0,17 g pl-1), como fonte de mirceno; L. 27 (0,17 g pl-1), como fonte de limoneno e de carvona (0,21 g pl-1) e L.38 (0,24 g pl-1), como fonte de citral.

The main objective of this work was to describe the essential oil profile of 16 genotypes of Lippia alba from the germplasm collection of the Universidade de Brasília and to analyze its potential of production. A field assay was carried out in the rural area of Distrito Federal and the following parameters were analyzed: flowering period, growing habit, foliar area, length of the main branch, fresh and dry weight of the biomass (leaves and branches), essential oil content and profile of the constituent volatile oils. Essential oil was extracted using a modified Clevenger apparatus and the constituent volatile oils were analyzed by gas chromatography and GC/MS. The experimental design was randomized blocks with three plants per plot. The following chemotypes were reported: citral-limonene, citral-myrcene, limonene-carvone, citral, linalool, myrcene and linalool-limonene. Higher levels of linalool were found in genotype L.16 (89.8%); myrcene in L.37 (47.6%); limonene in L.27 (36.0%); carvone in L.27 (46.9%) and citral in L.17 (56.7%). The genotypes with the highest leaf area and leaf length of the main branch seem to be correlated with the best yield of essential oil and the higher level of linalool. The yield of essential oil was inversely proportional to the dry weight of biomass. The accessions which presented the highest average yield of the major essential constituent oils were: L.16 (0.77 g pl-1) as a source of raw material for linalool production; L.17 (0.17 g pl-1) as source of myrcene; L. 27 as source of limonene (0.17 g pl-1) and carvone (0.21 g pl-1); and L.38 (0.24 g pl-1) as a citral source.

Descreve-se a morfo-anatomia e a análise de óleo essencial das folhas de Hennecartia omphalandra J. Poisson (Monimiaceae), uma planta tóxica. A ocorrência de tricomas unicelulares, estômatos paracíticos; braquiesclereídes em grupos no pecíolo e na lâmina foliar, além de esclereídes vermiformes e ramiformes; sistema vascular em arco, com extremidades voltadas para o centro no pecíolo e na forma de arco atenuado na lâmina foliar, sendo o padrão de venação uma variação do tipo craspedódromo-semicraspedódromo, além de óleo essencial armazenado em idioblastos oleíferos não especializados no mesofilo, foram considerados caracteres importantes que podem auxiliar na sua morfo-diagnose. A análise do óleo essencial das folhas revelou a presença de monoterpenos, sesquiterpenos e álcoois sesquiterpênicos, sendo este o grupo mais significativo. Os componentes majoritários identificados foram β-felandreno (24,0%), seguido por germacreno D (10,5%), sabineno (9,3%), biciclogermacreno (8,4%) e β-elemeno (5,3%).

This paper describes the morphological and anatomical aspects and the essential oil analysis of the leaves from Hennecartia omphalandra J. Poisson (Monimiaceae), a toxic plant. The presence of trichomes formed by a single cell, paracitic stomata, groups of braquisclereids in the petiole and leaf blade; vermiform and ramiform sclereids, vascular system in arc softly invaginated at ends in the petiole, and in a flat arc in the middle vein, being the venation pattern a variation of craspedodromous-semicraspedodromous type, and essential oil stored in oil idioblasts in the mesophyll were the most important characters that can help the morphological diagnosis. The analysis of essential oil of the leaves showed the presence of monoterpenes, as well as sesquiterpenes hydrocarbons and alcohols, being the latter the most significant group. The major identified compounds were β-phelandrene (24.0%), germacrene D (10.5%), sabinene (9.3%), bicyclogermacrene (8.4%) and β-elemene (5.3%).

A habilidade da técnica de espectrometria de massas com infusão direta e ionização por eletronebulização (IES-EM), nos modos de íons positivos e negativos, foi avaliada na diferenciação de cafés Arábica verdes e torrados e com diferentes estágios de amadurecimento (verde, maduro e passado), processo pós-colheita (seco, úmido e semi-úmido) e cafés classificados por prova de xícara. No modo negativo, a análise dos cafés verdes mostrou que os íons correspondentes aos ácidos graxos e ácidos clorogênicos desprotonados são os mais importantes para a discriminação da maturidade. No modo positivo, a maturidade é diferenciada através de íons correspondentes a cafeína, ácidos clorogênicos protonados e adutos de K+ de ácidos graxos. Na diferenciação da pós-colheita, em ambos os modos de ionização, são mais importantes os íons correspondentes aos ácidos graxos, ácidos clorogênicos, açúcares e ácidos carboxílicos formados da fermentação. Cafés Arábica torrados também são discriminados com eficiência. No modo negativo, são importantes os íons correspondentes aos ácidos clorogênicos e ácidos orgânicos de cadeia curta, derivados de açúcares. No modo positivo, a discriminação é realizada por íons de baixa m/z tais como piridina e alquil piridinas protonadas, formadas através da degradação da trigonelina. Ambos os IES(+)-EM e IES(-)-EM são capazes de discriminar diferentes cafés Arábica torrados classificados por prova de xícara e os íons que permitem esta diferenciação são os mesmos descritos para a maturidade e processos pós-colheita.

Direct infusion electrospray ionization mass spectrometry in both the negative ESI(-)-MS and positive ESI(+)-MS ion modes are investigated to differentiate green and roasted Arabica coffees with different stages of ripeness (green, ripe and overripe), post-harvesting process (dry, wet and semi-wet) and coffees with different cup qualities. In the ESI(-)-MS of green coffees, ions from deprotonated fatty acids and chlorogenic acids are the most important for ripeness discrimination. In the ESI(+)-MS, maturity is differentiated by ions from protonated caffeine, chlorogenic acids and K+ adducts of fatty acids. To differentiate between post-harvesting process in both ionization modes, ions from fatty acids, chlorogenic acids, sugars and carboxylic acids generated in the fermentation process are the most representative. Roasted Arabica coffees are also well discriminated: in the ESI(-)-MS, ions from chlorogenic acids and short-chain organic acids derived from sugars are important. In the ESI(+)-MS, discrimination are mainly performed by low m/z ions such as protonated pyridine and alkylpiridines formed via trigonelline degradation. Both ESI(+)-MS and ESI(-)-MS are able to differentiate cup quality for Arabica roasted coffees and the ions used to perform discrimination are the same ones described in ripeness and post-harvesting processes.

Essential oils are extracted by steam distillation of plants or cold pressing of citrus fruit pericarp. They are used in food, cosmetic, personal care and pharmaceutical industries. In Brazil, oils from orange and related products contribute to near 97% to the positive commercial performance of the sector. Predatory exploitation and the availability of new sources of raw materials, with more attracting prices, changed the paradigm. Prospective studies, sustainable use of Brazilian biodiversity, domestication of exotic species with commercial relevance, the use of breeding techniques and the development of new applications for essential oils are thematic lines, usually multidisciplinary, which have been prompting the expansion of the research on essential oils. This paper presents an analysis on essential oils balance trade from 2005 to 2008 and some historical data on research and production of essential oils in Brazil.

Descreve-se o estudo morfo-anatômico e a análise de óleo essencial do fruto de Hennecartia omphalandra J. Poisson (Monimiaceae), uma planta tóxica. A ocorrência de feixes recurrentes e de um anel descontínuo de braquiesclereides no hipanto; assim como a presença de células oleíferas no mesocarpo, de "idioesclereídes" formando o endocarpo e de células com espessamento parietal em rede, constituindo a testa da semente, foram considerados caracteres importantes que podem auxiliar na sua morfo-diagnose. A análise do óleo essencial dos frutos revelou a presença de monoterpenos, sesquiterpenos e álcoois sesquiterpênicos, sendo este o grupo mais significativo. Os componentes majoritários identificados foram o biciclogermacreno (19,6%) e o β-felandreno (8,7%), além do germacreno D (5,3%), α-bulneseno (5,1%) e valerianol (4,9%).

The morphological and anatomical aspects of flower and fruit and the essential oil analysis of fruits of Hennecartia omphalandra J. Poisson (Monimiaceae), a toxic plant, are described in this paper. The presence of vascular recurrent bundles and of a ring of brachysclereids in the hypanthium; the oil cells in the mesocarp, the "idiosclereids" that constitutes the endocarp and cells with reticulated thick walls, shaping the seed coat were described as characters that may help in its diagnosis. The analysis of the essential oil of fruits showed the presence of monoterpenes, as well as sesquiterpenes hydrocarbons and alcohols, being the latter the most significant group. The major identified compounds were bicyclogermacrene (19.6%); β-felandrene (8.7%); germacrene D (5.3%); α - bulnesene (5.1%) and valerianol (4.9%).

Lippia lacunosa e L. rotundifolia são duas espécies brasileiras que formam um complexo de difícil delimitação taxonômica. A composição química do óleo essencial das folhas e flores dessas plantas foi investigada por cromatografia com fase gasosa (CG) e por cromatografia com fase gasosa acoplada à espectrometria de massas (CG-EM). Principais constituintes dos óleos essenciais de L. lacunosa (flores e folhas): mirceno (14,7% e 11,9%), mircenona (45,2% e 64,2%), Z-ocimenona (5,7% e 5,2%), e E-ocimenona (14,7% e 4,1%), respectivamente; L. rotundifolia (flores e folhas): a-pineno (8,7% e 1,8%), mirceno (5,1% e 3,6%), limoneno (26,0% e 7,9 %), cis-pinocanfona (4,5% e 3,1%) e mirtenal (22,3% e 16,7%), respectivamente. Os óleos essenciais de L. lacunosa apresentaram um forte e agradável aroma de manga, que foi relacionado à presença de mirceno e mircenona. Diferenças fundamentais na composição química de seus óleos essenciais podem representar uma poderosa ferramenta na classificação botânica das espécies.

Lippia lacunosa and L. rotundifolia (Verbenaceae) are two Brazilian species of complex taxonomic delimitation. The composition of the essential oils from leaves and flowers of these plants was investigated by gas chromatography (GC) and gas chromatography coupled with mass spectrometry (GC-MS) analysis. The major components of the essential oils of flowers and leaves of L. lacunosa were: myrcene (14.7% and 11.9%), myrcenone (45.2% and 64.2%), Z-ocimenone (5.7% and 5.2%), and E-ocimenone (14.7% and 4.1%), respectively; whereas in L. rotundifolia (flowers and leaves) were a-pinene (8.7% and 1.8%), myrcene (5.1% and 3.6%), limonene (26.0% and 7.9 %), cis-pinocamphone (4.5% and 3.1%) and myrtenal (22.3% and 16.7%), respectively. The essential oils from L. lacunosa exhibited a strong and pleasant mango aroma, which was related to the presence of myrcene and myrcenone. The marked differences in the chemical composition of their essential oils may represent a powerful tool for the botanical classification.