US20170073614A1 - Perfume Compositions - Google Patents

Perfume Compositions Download PDF

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Publication number
US20170073614A1
US20170073614A1 US15/311,366 US201515311366A US2017073614A1 US 20170073614 A1 US20170073614 A1 US 20170073614A1 US 201515311366 A US201515311366 A US 201515311366A US 2017073614 A1 US2017073614 A1 US 2017073614A1
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Prior art keywords
methyl
group
hydroxy
ingredients
perfume
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Inventor
Alain Alchenberger
Christian Quellet
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Givaudan SA
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Givaudan Sa
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0092—Heterocyclic compounds containing only N as heteroatom
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
    • B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
    • B05B11/06—Gas or vapour producing the flow, e.g. from a compressible bulb or air pump
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0007—Aliphatic compounds
    • C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0007—Aliphatic compounds
    • C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
    • C11B9/0019—Aliphatic compounds containing oxygen as the only heteroatom carbocylic acids; Salts or esters thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0007—Aliphatic compounds
    • C11B9/0023—Aliphatic compounds containing nitrogen as the only heteroatom
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
    • C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
    • C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0004—Gaseous mixtures, e.g. polluted air
    • G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
    • G01N33/0011—Sample conditioning
    • G01N33/0016—Sample conditioning by regulating a physical variable, e.g. pressure or temperature
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0004—Gaseous mixtures, e.g. polluted air
    • G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
    • G01N33/0011—Sample conditioning
    • G01N33/0021—Sample conditioning involving the use of a carrier gas for transport to the sensor
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0001—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00 by organoleptic means

Definitions

  • This disclosure relates to perfume compositions having controlled spatio-temporal olfactory profiles. More particularly, this disclosure relates to perfume compositions having coherent, fast developing and prolonged olfactory impact at a distance from the compositions' source, when submitted to convection flows. The disclosure also relates to a method of measuring said spatial-temporal olfactory profiles of said compositions.
  • Fragrance in an atmosphere or sprayed on to a substrate is often desired for a number of aesthetic and practical reasons, for example, to freshen air, to provide an attractive personal fragrance, or a particular mood or ambience in a room.
  • perfumers have developed the art of achieving the proper aesthetic effect by mixing a broad range of ingredients having various olfactive characteristics, volatilities and intensities, in a similar way as painters mix their colours to realize masterworks. This art has remained essentially empirical.
  • vapour pressure and odour detection threshold has been known for several decades.
  • Odour Value which is simply the ratio of headspace concentration of an odourant to the odour detection threshold is a convenient way to combine these two latter properties into a unique and quantitative measure of odour strength, which enables one to discriminate between odorants that are substantive, i.e. which can be perceived on a substrate for a long period of time and those which are elusive, i.e. which vanish rapidly, as well as between odorants which are impactful and those which are weak.
  • the impact of a perfume at a distance from its source is often referred to as the “volume”, or if directional convection flows are present, as “trail” or “sillage” of that perfume. Sillage has always been considered to be of interest, particularly in the fields of personal or fine fragrances. The ability of a perfume to be recognised in a space some distance from its source is an important characteristic of a perfume.
  • convection is the major driver of the transport of odorants through the air.
  • all odorants will be transported coherently through the air by convection flows, i.e. with roughly the same velocity, and that the average velocity of each odorant at any point of the space is the same as that of the convection flow itself at this point of space.
  • the perceived intensity of that odourant at distance will be proportional to its partial Odour Value, i.e. the Odour Value of the pure odourant multiplied by its effective concentration at that distance.
  • perfume ingredients may be grouped in time-dependent relationship to form perfume compositions in such a way that when placed in a directional convection flow, the nature and olfactory profile of that perfume composition can be detected at a distance from its source with a reliable and recognisable odour.
  • a method of determining the spatial-temporal olfactory profile of fragrances In a first aspect of the present invention there is provided a method of determining the spatial-temporal olfactory profile of fragrances.
  • a method of creating a perfume composition such that when placed in a directional convection flow, the nature and olfactory profile of that perfume composition can be detected at a distance from its source with a reliable and recognisable odour.
  • a perfume composition that when placed in a directional convection flow, the nature and olfactory profile of that perfume composition can be detected at a distance from its source with a reliable and recognisable odour.
  • a fine perfume, personal care composition or home care composition comprising a perfume composition defined herein.
  • the invention is based on the surprising discovery that time also plays a key role in the perception of perfume ingredients at distance.
  • the perception of ingredients at distance is characterized by two consecutive characteristic perception times, which are referred to in the following as “detection time” Td and “recognition time” Tr (i.e. the time where the smell has reached its maximum and does not change anymore, at least within the time frame of the evaluation experiment as it is defined hereunder).
  • vapour pressure and odour detection threshold Although a consideration of vapour pressure and odour detection threshold does not itself explain the concept of trail, the applicant has found that in order to be perceived at distance, a perfumery ingredient must have certain combinations of vapour pressure and odour detection threshold.
  • the plot referred to above and shown in FIG. 1 defines a straight line, having a negative slope in a log HS i 0 vs. log ODT i plot, which is referred to hereinafter as the “distance perception boundary line” (DPBL) or “isoradiance line”.
  • DPBL distance perception boundary line
  • log log in equation ( 1 ) and throughout the disclosure refers to the decimal logarithm.
  • standard equilibrium headspace concentration refers to the concentration of the ingredient in equilibrium with the condensed form, that is, solid or liquid form of this ingredient at a temperature of 25° C. and under a pressure of 1 atmosphere. It can be measured by using any of the known quantitative headspace analysis techniques, see for example Mueller and Lamparsky in Perfumes: Art, Science and Technology, Chapter 6 “The Measurement of Odors” at pages 176-179 (Elsevier 1991).
  • Odour Detection Threshold used herein above refers to the average concentration above which an odourant i can be perceived by a panellist and can be measured by olfactometry, as described, for example in Mueller and Lamparsky (op. cit).
  • the equilibrium headspace concentration may be measured as follows: 500 mg of the test compound is added to a headspace container which is then sealed. The container is then incubated at constant 25° C. until the compound reached equilibrium between the gas and the liquid phase. A defined volume of this saturated headspace (usually 0.5-1lt) is trapped on a micro filter using Porapak Q as sorbent. After filter extraction with an appropriate solvent (usually 30-100 microliters methyl tert. butyl ether), an aliquot of the extract is analyzed by GC. Quantification is performed by the external standard calibration method. The concentration in the original headspace can be calculated (in terms of microgram/l) from the headspace volume sucked through the micro filter and the aliquot of the filter extract injected into the gas chromatograph.
  • the final headspace concentration value of a given test compound is obtained as the mean value of three independent measurements each. Further information of the technique hereinabove described may be found in the article of Etzweiler, F.; Senn E. and Neuner-Jehle N., Ber. Bunsen - Ges. Phys. Chem. 1984, 88, 578-583.
  • the Odour Detection Threshold may be measured by using an olfactometer.
  • the olfactometer functions on the principle of a linear dilution of an odorant in a carrier gas. The quantity of odorant displaced depends on its vapor pressure and the carrier gas flow.
  • a constant flow of nitrogen regulated by a flow regulator, carries the odorant from a sample container to a mixing chamber. There, the carrier gas-odor mixture is diluted with odorless air. From the mixing chamber one part of the diluted odorous air is allowed to flow via a fused silica capillary to the sniffing funnel.
  • the flow rate through the capillary which determines the dosage of odorous air from the mixing chamber into the sniffing funnel, depends on the opening the valve which can be regulated via PC from 1 to 256 ml in binary steps.
  • the final dilution of the odorous air sample occurs in the glass funnel by flushing them permanently with odorless air at a flow rate of 8 lt/min.
  • Forced-choice triangle presentation is achieved by a special automated channel setting device where only one position of a switch the odorant delivering capillary enter in the sniffing funnel, whereas in two other positions the capillary is positioned outside the funnel and where the effluent is sucked away. After each trial the channel setting is changed automatically and in a random order.
  • the concentration is calculated from the odorants vapor pressure and from the dilution ratios that were applied in the olfactometer, assuming that vapor pressure saturation is achieved in the sample generator. As a control the concentration is determined analytically by sampling a known volume from the capillary effluent into a headspace filter and by subsequent gas chromatographic quantitation of the odorant in the desorption solution.
  • Each panelist (panel of 15 persons) starts sniffing at the olfactometer at a concentration level at which he perceives the odorant at medium intensity. After three correct answers in three consecutive trials (or four correct ones of five trials) at the same level, stimulus concentration is decreased by a factor of two to the next lower level, and so on, until the panelist has reached his threshold level. The final threshold value of a given odorant is obtained as the mean value of all individual threshold levels.
  • the coordinates A and B are complex functions of the amount of ingredient at a source at the time olfactory performance is assessed; of the distance at which the olfactory performance is assessed; and of the dilution taking place between the source and the point of assessment due to convection flows.
  • the amount of ingredient at a source depends on the amount of time the perfume has been allowed to evaporate after having been placed on a substrate. It is indeed well known, that once a perfume is deposited on a substrate, its composition will vary in time, as evaporation proceeds. It is also well known that the amount of each ingredient on the substrate will decrease and that the rate of decrease of any given ingredient will be proportional to the vapour pressure of the ingredient.
  • the term “coherent olfactory impact” in relation to a perfume composition is taken to mean that the olfactory impact of all perfume ingredients are perceived within a period of time at some distance from the source such that the olfactory characteristics of the impact will be homogeneous and remain qualitatively unchanged as time evolves.
  • a perfume composition exhibits an incoherent olfactory impact when it is characterized by successive smells having different olfactory characteristics.
  • a fragrance composition having an incoherent olfactory impact may develop in a first step a powdery smell, followed by a floral smell and evolving step by step until it becomes perceived as a full perfume.
  • a perfume composition exhibiting a “fast developing olfactory impact” is characterised by an olfactory impact that increases sharply with time.
  • a fragrance composition having such sharp olfactory profile may be rapidly noticed at some distance of a source and, provided it has a coherent olfactory impact, it may be immediately recognized.
  • a perfume composition exhibits a “long-lasting olfactory impact” if its olfactory impact remains perceivable over a prolonged period of time, for example for a period of 30 seconds or more at the location the perfume is perceived.
  • the present disclosure provides a method directed to the characterization of the spatio-temporal attributes of fragrances under controlled conditions.
  • the method characterises spatio-temporal attributes of fragrances under convection flows having controlled spatial distribution and velocity.
  • a schematic representation of a device capable of generating and emitting directional air flow is shown in FIG. 2 .
  • a device ( 1 ) consists of a hollow body ( 3 ), comprising a broader part ( 3 a ) housing a fan (not shown) for generating an air flow, which can be flushed out of the housing via an elongate conduit ( 5 ), hosted in a narrower part ( 3 b ) of the body, whereas the direction of the flow is represented schematically by the black arrow ( 8 ).
  • the inner diameter of the conduit may be smaller than 10 cm, more preferably smaller than 5 cm and most preferably smaller than 2 cm.
  • the inner diameter of the broader part is not critical, but is preferably between 2 and 5 cm and most preferably between 2.5 and 3.5 cm.
  • the body contains a slot or aperture ( 4 ) for receiving a sample of a fragrance composition on a suitable support (not shown), such as a glass plate, paper strip, fabric strip, artificial skin, animal skin, hair and the like.
  • a suitable support such as a glass plate, paper strip, fabric strip, artificial skin, animal skin, hair and the like.
  • the housing may contain a thermo-regulated element (not shown) for heating the sample.
  • the housing is fixed on a holder ( 5 ) by means of an optionally flexible foot ( 6 ) allowing orientation of the conduit in all directions of space.
  • the fan In use, the fan generates a directional air flow, which passes over the sample thereby to entrain the fragrance composition and create a fragrance plume that is expressed through the conduit and emitted into a channel ( 2 ) that is delimited by panels (ABCD) and (EFGH), which suppress undesirable lateral room convection.
  • ABCD panels
  • EFGH EFGH
  • the top of the channel (ABEF) must be open to enable an evaluator to assess the fragrance plume at different distances along the channel.
  • the panels ABCD and EFGH may be parallel or not, although a parallel arrangement is preferred.
  • the segments CD and GH may have equal or different lengths, although equal lengths are preferred, and may be varied, depending on the distance where the olfactory assessment needs to be performed.
  • the length of segments CD and GH is at least 0.5 m, preferably at least 1 m and most preferably at least 1.5 m.
  • the width of the channel, as defined by the length of the segments AE, CG, BF and GH may be at least 0.1 m, preferably at least 0.3 m and most preferably at least 0.5 m.
  • the height of the channels defined by the segment AC, EG, BD and FH may be at least 0.3 m, preferably at least 0.5 m and most preferably at least 0.7 m.
  • the device ( 1 ) has a length of 20.5 cm and is fixed on a flexible foot having a height of 18 cm and which can be oriented in all direction of the space.
  • the flexible foot is fixed on a holder having a diameter of 11.5 cm and a height of 3.5 cm.
  • the diameter of the housing ( 3 ) is 3.5 cm in the broader part and 2.5 cm in the narrower part ( 3 ), the internal diameter of the broader part ( 3 a ) is 2.6 cm and the internal diameter of the narrower part ( 3 b ) is 1.4 cm.
  • the length of the broader part is 8 cm, including a hollow conical portion having a height of 1 cm (not shown in picture 1 ), allowing the progressive reduction of the inner diameter from 2.6 to 1.4 cm.
  • the length of the narrower part is 12 cm.
  • the thermo-regulated plate built in the housing has a surface of 5 by 2 cm 2 .
  • the length of the slit (or sampler port) ( 4 ) is 4.1 cm and its width is 0.3 cm.
  • thermo-regulated element may be measured by any known means, such as thermocouple, platinum probe or infra-red detector, while the air flow through the directional tube may be measured, for example, using an anemometer or a Venturi element built up in the tube and connected to a pressure gauge, or any flow sensor.
  • the amount of fragrance composition deposited on the support is typically from 0.01 to 10 microliters, preferably from 0.05 to 5 microliters, and most preferably from 0.1 to 1.5 microliters.
  • the composition may be deposited as neat oil or diluted in a hydro-alcoholic solvent, or any other suitable solvent.
  • the support is a glass plate, having a rectangular portion etched or ground, which is surrounded by an un-etched glass frame.
  • the length and width of the etched portion are typically 1.8 cm and 0.4 cm, and the width of the un-etched glass frame is typically 0.1 cm.
  • the surface of the whole glass plate is typically 2 by 0.5 cm 2 .
  • the glass plate may be inserted in a sealable sample holder, which is designed in such a way that one part of the holder comprising the glass plate can be inserted into the device ( 1 ) through the slit ( 4 ), whilst another part remains outside and serves as a gripping means allowing easy sample insertion and removal.
  • the dimensions of the sample holder are commensurate with the size of the slit ( 4 ), so that the plug is adjusted in the device in such a way that possible voids between the sample holder and the boundaries of the slit are minimized, e.g. not larger than 0.5 millimetres.
  • the typical dimensions of the sample holder are 5.3 cm ⁇ 4 cm and the thickness of the part that is introduced in the slit ( 4 ) is 0.2 cm.
  • the sample holder can be sealed by any sealing means, so that the evaporation of the perfume deposited on the glass plate is prevented. Typically, the sealing means is removed before insertion in the device ( 1 ).
  • Measurements may be performed on fresh fragrance compositions or after compositions have been allowed to evaporate for a certain time. Preferably, it compositions are left to evaporate for at least 30 minutes, preferably at least one hour and most preferably at least 2 hours, before being inserted in the device ( 1 ).
  • a typical evaporation time is 4 hours at a temperature of 32 ⁇ 2° C. Under these conditions, the state of a composition is closer to that applied to a consumer in the day-to-day life and the evaluation provides a better picture of the performance of a fragrance composition under real life conditions. In addition, the evaporation kinetics of compositions will be much slower after 4 hours evaporation time than in the early stage of the evaporation, which makes variations between samples less significant and improves the reproducibility of the evaluation.
  • the length of the channel may be arbitrarily defined, depending on the distance at which a performance assessment is desired.
  • the evaluation is however performed at a distance larger than 0.5 metres, more preferably at distance larger than 1 m and most preferably larger than 1.5 metres. e.g. 2 metres.
  • the device and channel may be placed in a room having constant ventilation conditions maintained at constant temperature and humidity. Convection flows in the room should be minimized and the way the air circulates in the room should be held constant, the temperature in the room should not vary by more than ⁇ 5° C. over time and the relative humidity in the room should not vary by more than ⁇ 20%. Such conditions are easily realized using standard air conditioning systems.
  • the sample temperature may take any desired value of the thermometric scale and is only limited by the thermal resistance of the materials constituting the device and of the perfume ingredients. Typically, the temperature preferably ranges from 0° C. to 150° C., more preferably from 10° C. to 100° C. and most preferably from 20° C. to 50° C. Temperatures below room temperatures are best achieved by embedding cooling elements in the thermo-regulated plate. A typical sample temperature is 32 ⁇ 2° C.
  • the evaluation procedure involves the steps of:
  • the sample is then removed from the device and the channel is flushed using the fan ( 7 ), operating in such a way that the air contained in the channel is moved in the opposite direction relatively to the flow produced by the device, as symbolized by the white arrow ( 9 ) in FIG. 2 .
  • the fan ( 7 ) operating in such a way that the air contained in the channel is moved in the opposite direction relatively to the flow produced by the device, as symbolized by the white arrow ( 9 ) in FIG. 2 .
  • the convection in the room and the flow rate at the aperture of the conduit ( 5 ) are preferably fixed in such a way that:
  • the assessment of the olfactory attributes at distance from a source may be diverse and comprise olfactory intensity or impact, and more descriptive qualifiers, such as odour description, sharpness, transparency, presence, volume and the like. Such qualifiers determine the “nature” of the olfactory profile, as discussed in more detail hereunder.
  • odour descriptors is meant a description of the smell in words according to a specific vocabulary, usually defined by convention.
  • a suitable odour descriptor vocabulary comprises, but is not limited to terms such as “citrus”, “rosy”, “hesperidic”, “green”, “woody”, “ambry”, “musky”, and the like. Odour descriptors are widely used in the art of assessing perfumery and a more detailed discussion is not merited herein. A full discussion of odour descriptors is provided in “Perfume and Flavour Chemicals”, S. Arctander, Allured Publishing Corporation, 1994, IL, USA, which is incorporated herein by reference.
  • the present method enables one to assess the trail performance of perfumes.
  • the perfume is applied onto a substrate at a concentration of 10% by weight in a solvent, such as ethanol, ethanol/water mixture, propylene glycol, dipropylene glycol, triethyl citrate and the like, or as provided by vendors, for example 5%, 10% or 15% by weight.
  • a solvent such as ethanol, ethanol/water mixture, propylene glycol, dipropylene glycol, triethyl citrate and the like, or as provided by vendors, for example 5%, 10% or 15% by weight.
  • 10 microliters of perfume solution is applied on the substrate.
  • the present method also enables one to group perfume ingredients that behave coherently with respect to each other, by which is meant, groupings of perfume ingredients can be made based on the observation that they are detected at a particular defined point in space relative to a perfume source within a given time frame, such that they display a coherent olfactory impact, as this term is defined above.
  • a first grouping of perfume ingredients is selected from those ingredients having a combination of standard equilibrium headspace concentration and odour detection threshold such that said ingredients lie on or below a Distance Perception Boundary Line (DPBL) in a log HS i 0 vs.
  • DPBL Distance Perception Boundary Line
  • Perfume ingredients of INGREDIENT GROUP I include but are not limited to (2-benzyl-1,3-dioxolan-4-yl)methanol; (2-(1-propoxyethoxy)ethyl)benzene; 1-(4-methoxyphenyl)ethanone; allyl 2-phenoxyacetate; (Z)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene; (E)-2-methoxy-4-(prop-1-en-1-yl)phenyl acetate; 1-(pyrazin-2-yl)ethanone; 4-formyl-2-methoxyphenyl acetate; 2,6,10-trimethylundec-9-enal; undecanal; decanal; dodecanal; 2-methylundecanal; tridecanal; (E)-undec-9-enal; 4-[(6,6-dimethyl-5-bicyclo[2.2.1]heptanyl)methyl]-2-
  • Perfume ingredients conforming to this definition are deemed to be coherent relative to each other according to how that term is understood in the present invention.
  • a second grouping of perfume ingredients referred to hereafter as INGREDIENT GROUP 2 is selected from those ingredients having a combination of standard equilibrium headspace concentration and odour detection threshold such that said ingredients lie on or below a distance perception boundary line in a log HS i 0 vs.
  • perfume ingredients include: allyl 2-phenoxyacetate; (E)-2-methoxy-4-(prop-1-en-1-yl)phenyl acetate; 1-(pyrazin-2-yl)ethanone; 2-methylundecanal; tridecanal; 4-[(6,6-dimethyl-5-bicyclo[2.2.1]heptanyl)methyl]-2-methylcyclohexan-1-one; 3,8,8,11a-tetramethyldodecahydro-1H-3,5a-epoxynaphtho[2,1-c]oxepine; 4-formyl-2-methoxyphenyl acetate; (2,4a,5,8a-tetramethyl-1,2,3,4,7,8-hexahydronaphthalen-1-yl) formate; (Z)-oxacycloheptadec-10-en-2-one; 2,5,5-trimethyl-1,2,3,4,4a,5,6,7-octahydron
  • Perfume ingredients conforming to this definition are deemed to be coherent relative to each other according to how that term is understood in the present invention.
  • a third grouping of perfume ingredients referred to hereafter as INGREDIENT GROUP 3, is characterised in that they belong to INGREDIENT GROUP 1 and are further characterised in that they are crystalline at room temperature (20° C.).
  • This third group of ingredients comprises: (E)-2-methoxy-4-(prop-1-en-1-yl)phenyl acetate; 4-formyl-2-methoxyphenyl acetate; 1-((2-(tert-butyl)cyclohexyl)oxy)butan-2-ol; 3,8,8,11a-tetramethyldodecahydro-1H-3,5a-epoxynaphtho[2,1-c]oxepine1,3,4,5,6,7-hexahydro-.beta.,1,1,5,5-pentamethyl-2H-2,4a-methanonaphthalene-8-ethanol; (4aR,5R,7aS,9R)-octahydro-2,2,5,8,8,9a-hexamethyl-4h-4a,9-methanoazuleno(5,6-d)-1,3-dioxole; 3a,6,6,9a-tetramethyldodecahydronaph
  • Preferred INGREDIENT GROUP 3 are 3,8,8,11a-tetramethyldodecahydro-1H-3,5a-epoxynaphtho[2,1-c]oxepine; 1,3,4,5,6,7-hexahydro-.beta.,1,1,5,5-pentamethyl-2H-2,4a-methanonaphthalene-8-ethanol; (4aR,5R,7aS,9R)-octahydro-2,2,5,8,8,9a-hexamethyl-4h-4a,9-methanoazuleno(5,6-d)-1,3-dioxole; 3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan; 7-isopentyl-2H-benzo[b][1,4]dioxepin-3(4H)-one; 7-methyl-2H-benzo[b][1,4]dioxepin
  • Perfume ingredients conforming to this definition are deemed to be coherent relative to each other according to how that term is understood in the present invention.
  • a fourth grouping of perfume ingredients referred to hereafter as INGREDIENT GROUP 4, are characterised in that they belong to INGREDIENT GROUP 2, but are characterized by a superior performance in terms of intensity at distance, and are not crystalline in their pure state at room temperature (20° C.).
  • This fourth group of ingredients comprises:
  • Preferred INGREDIENT GROUP 4 are (Z)-oxacycloheptadec-10-en-2-one; 4-methoxybenzaldehyde; 3-(4-(tert-butyl)phenyl)propanal; 2-(2-mercaptopropan-2-yl)-5-methylcyclohexanone; (Z)-3-methylcyclotetradec-5-enone; 4-(4-hydroxy-4-methylpentyl)cyclohex-3-enecarbaldehyde; (E)-1-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)but-2-en-1-one; (E)-1-(2,6,6-trimethylcyclohex-3-en-1-yl)but-2-en-1-one; 8-ethyl -1-oxaspiro[4.5]decan-2-one; 4-allyl-2-methoxyphenol; (E)-2-methoxy-4-(prop-1-en-1-yl)
  • Perfume ingredients conforming to this definition are deemed to be coherent relative to each other according to how that term is understood in the present invention.
  • a fifth grouping of perfume ingredients referred to hereafter as INGREDIENT GROUP 5, are characterised in that they belong to INGREDIENT GROUP 2 and are crystalline at room temperature (20° C.).
  • This fifth group ingredients comprise: 3,8,8,11a-tetramethyldodecahydro-1H-3,5a-epoxynaphtho[2,1-c]oxepine; (2,4a,5,8a-tetramethyl-1,2,3,4,7,8-hexahydronaphthalen-1-yl) formate; (4aR,5R,7aS,9R)-octahydro-2,2,5,8, 8,9a-hexamethyl-4h-4a,9-methanoazuleno(5,6-d)-1,3-dioxole; 3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan; 7-isopentyl-2H-benzo[b][1,4]dioxepin-3(4H)-one; 7-methyl-2H-benzo[b][1,4]dioxepin-3(4H)-one; 3-hydroxy-4,5-d
  • Perfume ingredients conforming to this definition are deemed to be coherent relative to each other according to how that term is understood in the present invention.
  • Perfume compositions comprising mixtures of the INGREDIENT GROUP 2, 3, 4 and 5 will exhibit a coherent, fast developing and prolonged olfactory impact at a distance from the compositions' source, when submitted to convection flows, and to a skilled evaluator the composition will have a readily recognisable olfactory profile.
  • perfumers will be able to design new perfumery products that will have, with use, an instantly memorable signature recognisable by consumers that will lead to greater consumer acceptance.
  • Such coherent perfume compositions are to be contrasted with perfume compositions that have an incoherent olfactory impact, which exhibit sequentially different fragrance impressions, e.g. floral, powdery etc. before the full perfume impact evolves over time.
  • a perfume composition comprising two or more perfume ingredients selected from those ingredients belonging to GROUP 2, 3, 4 and 5 according to the following rules:
  • Perfume compositions according to the present invention need not be limited to a mixture of those perfume ingredients mentioned above. Other ingredients commonly used in perfumery may be employed to form the balance of perfume ingredients. Any of those ingredients described in “Perfume and Flavour Chemicals”, S. Arctander, Allured Publishing Corporation, 1994, IL, USA, which is incorporated herein by reference.
  • Perfume compositions of the present invention and consumer products containing same may also contain commonly employed adjuvants.
  • adjuvants refers to ingredients that may affect the performance of a composition, other than its hedonic performance.
  • an adjuvant may be an ingredient that acts as an aid to processing a perfume composition or consumer product containing said composition, or it may improve handling or storage of a perfume composition or consumer product. It might also be an ingredient that provides additional benefits such as imparting colour or texture. It might also be an ingredient that imparts light resistance or chemical stability to one or more ingredients contained in a perfume composition or consumer product.
  • adjuvants include solvents and co-solvents; surfactants and emulsifiers; viscosity and rheology modifiers; thickening and gelling agents; preservative materials; pigments, dyestuffs and colouring matters; extenders, fillers and reinforcing agents; stabilisers against the detrimental effects of heat and light, bulking agents, acidulants, buffering agents and antioxidants.
  • One or more of the perfume ingredients or adjuvants employed in perfume compositions or consumer products may be formulated in a delivery vehicle to provide a desired effect.
  • Delivery vehicles may include capsule technologies.
  • the delivery vehicle may be in the form of a solid support, e.g. a polymeric support material onto which one or more perfume ingredients may be chemically or physically bound.
  • one or more perfume ingredients may be dissolved or dispersed in a matrix material, which serves to control the rate at which said ingredient or ingredients emanates.
  • one or more ingredients may be supported on a porous substrate, such as a cyclodextrin or a zeolite or other inorganic material.
  • one or more ingredients may be provided in the form of a pro-perfume, which will react in a suitable environment to release the perfume ingredient in a controlled manner.
  • Perfume compositions of the present invention may be employed in all manner of personal and home care consumer products known in the art.
  • a non-limiting list of applications include a textile treatment product, an ironing aid, a cleaning cloth, a laundry detergent, a cleaning product, in particular, for hard and/or soft surfaces, a household cleaner, a care product, a wash care product, a laundry care product, a room fragrancer, and air freshener, a conditioner, a colorant, a fabric conditioner, a conditioning substrate, a pharmaceutical, a crop protection product, a polish, a food, a cosmetic product, a fertilizer, a building material, an adhesive, a bleach, a decalcifier, an auto care product, floor care product, cooker care product, leather care product or furniture care product, a scourer, a disinfectant, a fragrancer, a mould remover, fine fragrance, body lotion, skin care preparations, candles, air fresheners, plug ins and toilet soaps.
  • cleaning products include the toilet cleaners or lavatory cleaners, these products being supplied in the form of powders, blocks, tablets or liquids, or gels, pipe-cleaning products or drain cleaners, universal or all-purpose or general-purpose cleaners, such as those used universally for all hard surfaces in the household and in commerce that can be wiped down wet or damp, sanitary cleaners, oven cleaners or grill cleaners which may be presented in the form of gels or foam sprays, metal polishes, including those supplied as polishing cloths, dipping baths, pastes, and liquids; glass cleaners and window cleaners; all special-purpose cleaning products, for example those for glass-ceramic hobs; carpet cleaners and stain removers.
  • toilet cleaners or lavatory cleaners these products being supplied in the form of powders, blocks, tablets or liquids, or gels, pipe-cleaning products or drain cleaners, universal or all-purpose or general-purpose cleaners, such as those used universally for all hard surfaces in the household and in commerce that can be wiped down we
  • auto care products include paint preservers, paint polishes, paint cleaners, wash preservers, shampoos for auto washing, auto-wash and wax products, polishes for trim metals, protective films for trim metals, plastics cleaners, tar removers, screen cleaners, engine cleaners and the like.
  • cosmetic products include cosmetic skincare products, e.g. bath products, skin washing and cleansing products, skincare products, eye makeup, lip care products, nail care products, intimate care products, foot care products; cosmetic products with specific effects, such as sunscreens, tanning products, de-pigmenting products, deodorants, antiperspirants, hair removers, shaving products; cosmetic dental-care products, such as dental and oral care products, toothcare products, cleaners for dental prostheses, adhesives for dental prostheses; cosmetic hair care products, e.g. hair shampoos, hair care products, hair setting products, hair-shaping products, and hair colouring products.
  • cosmetic skincare products e.g. bath products, skin washing and cleansing products, skincare products, eye makeup, lip care products, nail care products, intimate care products, foot care products
  • cosmetic products with specific effects such as sunscreens, tanning products, de-pigmenting products, deodorants, antiperspirants, hair removers, shaving products
  • cosmetic dental-care products such as dental and oral care products, toothcare products, cleaners for dental pros
  • textile treatment products include detergents or fabric conditioners.
  • air fresheners and room fragrancers include fragrancers for spaces such as autos, cupboards, dishwashers, refrigerators or shoes, and vacuum cleaners.
  • the perfume composition is employed in a fine fragrance composition. More particularly, in a fine fragrance application said perfume composition may be diluted in a hydroalcoholic base, comprising 0 to 50 wt %, more particularly 0.5 to 30 wt %, still more particularly 1 to 25 wt % water. Alternatively, in a fine fragrance application the perfume composition may be presented in the form of a microemulsion, wherein said perfume composition is present in an amount of 1 to 50 wt %, more particularly 3 to 40 wt %, and still more particularly between 5 and 30 wt % based on the total weight of the composition.
  • 0.24% by weight of the following perfumery ingredients are dissolved in 99.76% of a mixture comprising 76.4% ethanol, 10% tri-ethyl citrate and 3.6% water; and 10 microliters of this solution are placed on a etched glass plates having a etched surface of 0.4 ⁇ 1.8 cm 2 and a total surface of 0.5 ⁇ 2 cm 2 and let to evaporate for 4 hours at a temperature of 32° C.+/ ⁇ 2° C.
  • Each plate is then inserted in the device as described above and submitted to aforementioned flow and room convection conditions, whereas the optimal measurement conditions for said room were obtained by setting the air flow at 20 ml/min.
  • the odour intensity is then measured at the outlet of the channel at least 5 trained panellists and reported in Table 1. All ingredients are detected within 60 seconds in average. The scores obtained by panellists deemed anosmic to a particular ingredient are removed.
  • Ingredients having an average intensity higher than 7 were given a Score Class A; ingredients having an average intensity ranging from 6 to 7 were given a Score Class B; ingredients having an average intensity ranging from 5 to 6 were given a Score Class C; ingredients having an average intensity ranging from 3 to 5 were given a Score Class D and ingredients having an average intensity ranging from 1 to 3 were given a Score Class E and the ingredients having an average intensity lower than 1 were given a Score Class F.
  • the formulations of a series of perfumes are reported in Table 2 as illustrative but not limitative examples.
  • the sums of the concentrations of the ingredients in each GROUP are also reported in Table 2.
  • the intensity at distance was measured according to the following procedures: 10 microliters of a solution of 10% perfume in solvent comprising 96% ethanol and 4% water (hydro-alcoholic solution)_are placed on a etched glass plates having a etched surface of 0.4 ⁇ 1.8 cm 2 and a total surface of 0.5 ⁇ 2 cm 2 and let to evaporate for 4 hours at a temperature of of 32° C.+/ ⁇ 2° C.
  • Each plate is then inserted in the device as described above and submitted to aforementioned flow and room convection conditions, whereas the optimal measurement conditions for said room were obtained by setting the air flow at 20 ml/min.
  • the odour intensity is then measured at the outlet of the channel (i.e. 2 m away from the source) by at least 5 trained panellists and reported in Table 2.
  • Perfumes having an average intensity higher than 7 were given a score “+++”; perfumes having an average intensity ranging from 4 to 7 were given a score “++”; perfumes having an average intensity ranging from 1 to 4 were given a score “+”and perfumes having substantially no trail (i.e. an average intensity lower than 1) were given a score “ ⁇ ”.
  • perfumes C, D, E, F, G and H were detected within 60 seconds in average and found to produce a coherent, fast developing and prolonged olfactory impact at a distance of 2 m, whereas the coherence and development speed were found to increase with increasing intensity.
  • perfumes A and B which were not obeying the composition rules according to the present invention were found to produce an incoherent olfactory impact at a distance of 2 m, i.e. the perfume did not reach a maximum odour intensity could not be recognized by the skilled panellists within the time frame of the measurement. Only perfumes C, D, E, F, G and H can be considered as having coherent, fast developing and prolonged olfactory impact at a distance from the compositions' source, when submitted to convection flows

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10407644B2 (en) 2016-03-14 2019-09-10 Givaudan S.A. Perfume compositions
WO2019238680A1 (fr) * 2018-06-11 2019-12-19 Givaudan Sa Procédé associé à des compositions organiques
US11636870B2 (en) 2020-08-20 2023-04-25 Denso International America, Inc. Smoking cessation systems and methods
US11760170B2 (en) 2020-08-20 2023-09-19 Denso International America, Inc. Olfaction sensor preservation systems and methods
US11760169B2 (en) 2020-08-20 2023-09-19 Denso International America, Inc. Particulate control systems and methods for olfaction sensors
US11813926B2 (en) 2020-08-20 2023-11-14 Denso International America, Inc. Binding agent and olfaction sensor
US11828210B2 (en) 2020-08-20 2023-11-28 Denso International America, Inc. Diagnostic systems and methods of vehicles using olfaction
US11881093B2 (en) 2020-08-20 2024-01-23 Denso International America, Inc. Systems and methods for identifying smoking in vehicles
US11932080B2 (en) 2020-08-20 2024-03-19 Denso International America, Inc. Diagnostic and recirculation control systems and methods
US12017506B2 (en) 2020-08-20 2024-06-25 Denso International America, Inc. Passenger cabin air control systems and methods

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2515128B (en) * 2013-06-10 2015-05-27 Givaudan Sa Improvements in or relating to organic compounds
JP6487042B2 (ja) * 2014-11-10 2019-03-20 ジボダン エス エー 有機化合物におけるまたは関連する改善
GB201421838D0 (en) 2014-12-09 2015-01-21 Givaudan Sa Improvements in or relating to organic compounds
GB201421855D0 (en) 2014-12-09 2015-01-21 Givaudan Sa Improvements in or relating to organic compounds
WO2017100426A1 (fr) * 2015-12-11 2017-06-15 Bedoukian Research, Inc. Composition aromatisée ou parfumée contenant des alcadiénals isomères ou des alcadiènenitriles isomères
US10794798B2 (en) 2016-03-31 2020-10-06 Symrise Ag Device for assessing the sillage of fragrance materials
WO2018071897A1 (fr) * 2016-10-14 2018-04-19 International Flavors & Fragrances Inc. Accord de fleurs à impact élevé et à haute performance
WO2018153499A1 (fr) 2017-02-27 2018-08-30 Symrise Ag Procédé pour produire des mélanges contenant de la rotundone
CN107157292B (zh) * 2017-05-24 2018-10-26 方军 一种家用盘香及制备方法
FR3104720B1 (fr) 2019-12-16 2024-03-15 Aryballe Tech Procédé et dispositif pour obtenir la signature olfactive temporelle d’un échantillon et utilisations dudit procédé
EP3862027A1 (fr) 2020-02-07 2021-08-11 International Flavors & Fragrances Inc. Dispositif portable et procédés de mesure de la diffusion de parfums et de matières premières de parfums
WO2022069634A1 (fr) 2020-09-30 2022-04-07 Firmenich Sa Procédés de prédiction d'aptitude à la reconnaissance spatiale d'ingrédient de parfum et procédés de prédiction d'aptitude à la reconnaissance spatiale de composition de parfum
WO2023247599A1 (fr) * 2022-06-22 2023-12-28 Firmenich Sa Compositions de parfum ayant des performances de sillage de longue durée

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5948812A (en) * 1997-06-09 1999-09-07 Givaudan Roure (International) Sa 1,7-dioxacycloalkan-8-one compounds
US6184419B1 (en) * 1999-05-27 2001-02-06 Givaudan Roure (International) Sa α, β-unsaturated ketones

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2976327A (en) * 1959-06-09 1961-03-21 Givaudan Corp Alpha-methylhydrocinnamic aldehyde dimethyl acetal
CH577797A5 (fr) * 1973-08-01 1976-07-30 Firmenich & Cie
CH648015A5 (de) * 1977-03-28 1985-02-28 Givaudan & Cie Sa Cyclohexenonderivate mit riech- und/oder geschmackstoffeigenschaften.
DE3242042C1 (de) * 1982-11-13 1983-11-17 Dragoco Gerberding & Co Gmbh, 3450 Holzminden Gemisch von Dimethyl-tricyclo[5.2.1.0?]decan-Derivaten sowie dessen Herstellung und Verwendung als Riech- und Aromastoff
EP0294746A1 (fr) * 1987-06-12 1988-12-14 L. GIVAUDAN & CIE Société Anonyme Composés nitrobicycliques
EP1098195A3 (fr) * 1999-11-04 2001-06-13 Givaudan SA Appareil pour la formation d'un jugement olfactif d'une substance odorante, utilisation de celui-ci, et méthode pour la mise en oeuvre de cet appareil
ATE349997T1 (de) * 2000-03-20 2007-01-15 Firmenich & Cie Optisch aktive, sauerstoffhaltige, alizyklische verbindungen und ihre verwendung als duftstoffe
EP1281406A1 (fr) * 2001-08-01 2003-02-05 Givaudan SA Bougie èlectronique desodorisante
CA2589089A1 (fr) * 2004-11-29 2006-06-01 Givaudan Sa Produit de soin de substrat
GB0521119D0 (en) * 2005-10-18 2005-11-23 Ici Plc Evaluation of the fragrance characteristrics of a substance
DE102006034899A1 (de) * 2006-07-25 2008-01-31 Henkel Kgaa OH-gruppenhaltige Esterquats zur verbesserten Duftstoffausbeute
EP2100589B1 (fr) * 2008-11-27 2017-07-26 Symrise AG Pyridine substituée par 4-alkyl en tant que parfum
DE102009052267A1 (de) * 2009-11-06 2011-05-12 Georg Ortner Verfahren und Vorrichtung zur Erzeugung eines Duftluftstroms
US9021860B2 (en) * 2011-03-29 2015-05-05 Q Research Solutions, Inc. Mobile scent tester
WO2013053102A1 (fr) * 2011-10-11 2013-04-18 Givaudan Sa Améliorations à ou relatives à des composés organiques
US20150284660A1 (en) * 2012-08-21 2015-10-08 Firmenich Sa Method to improve the performance of encapsulated fragrances

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5948812A (en) * 1997-06-09 1999-09-07 Givaudan Roure (International) Sa 1,7-dioxacycloalkan-8-one compounds
US6184419B1 (en) * 1999-05-27 2001-02-06 Givaudan Roure (International) Sa α, β-unsaturated ketones

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10407644B2 (en) 2016-03-14 2019-09-10 Givaudan S.A. Perfume compositions
US10899995B2 (en) 2016-03-14 2021-01-26 Givaudan S.A. Perfume compositions
US11434448B2 (en) 2016-03-14 2022-09-06 Givaudan S.A. Perfume compositions
WO2019238680A1 (fr) * 2018-06-11 2019-12-19 Givaudan Sa Procédé associé à des compositions organiques
US12002550B2 (en) 2018-06-11 2024-06-04 Givaudan Sa Method related to organic compositions
US11760169B2 (en) 2020-08-20 2023-09-19 Denso International America, Inc. Particulate control systems and methods for olfaction sensors
US11760170B2 (en) 2020-08-20 2023-09-19 Denso International America, Inc. Olfaction sensor preservation systems and methods
US11813926B2 (en) 2020-08-20 2023-11-14 Denso International America, Inc. Binding agent and olfaction sensor
US11828210B2 (en) 2020-08-20 2023-11-28 Denso International America, Inc. Diagnostic systems and methods of vehicles using olfaction
US11881093B2 (en) 2020-08-20 2024-01-23 Denso International America, Inc. Systems and methods for identifying smoking in vehicles
US11932080B2 (en) 2020-08-20 2024-03-19 Denso International America, Inc. Diagnostic and recirculation control systems and methods
US11636870B2 (en) 2020-08-20 2023-04-25 Denso International America, Inc. Smoking cessation systems and methods
US12017506B2 (en) 2020-08-20 2024-06-25 Denso International America, Inc. Passenger cabin air control systems and methods

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