Sunanda Marketing Combine

Linalool (/lɪˈnæloʊɒl, laɪ-, -loʊoʊl, -ˈluːl/) refers to two enantiomers of a naturally occurring terpene alcohol found in many flowers and spice plants.^[1] Linalool has multiple commercial applications, the majority of which are based on its pleasant scent (floral, with a touch of spiciness).^[2][3] A colorless oil, linalool is classified as an acyclic monoterpenoid.^[1] In plants, it is a metabolite, a volatile oil component, an antimicrobial agent, and an aroma compound.^[1] Linalool has uses in manufacturing of soaps, fragrances, food additives as flavors, household products, and insecticides.^[1] Esters of linalool are referred to as linalyl, e.g. linalyl pyrophosphate, an isomer of geranyl pyrophosphate.^[4]

Odor Strength:medium Substantivity:400 hour(s) at 100.00 % sweet floral jasmin cocoa rose Odor Description:at 100.00 %. sweet floral jasmin cocoa Luebke, William tgsc, (1984)

Cyclohexanol, 4- (1, 1-dimethyl ethyl) acetate OR 4- (1, 1-dimethyl ethyl) Cyclohexyl acetate OR p-tert-Butylcyclohexyl Acetate OR Vertenex OR Oryclone OR Woody Acetate :Sweet almost creamy, woody with soft floral undertone.Application PTBCHA is widely used in perfumeries along with ionones, cedarwood products, floral and non-floral perfume chemicals.

Iso Camphyl Cyclo (Hexanol (Main constituent) CAS No) 66068-84-6               

Galaxolide (trade name; also known as Abbalide, Pearlide, Astrolide, Musk 50, Polarlide; chemical name 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8,-hexamethyl-cyclopenta[g]benzopyran or HHCB, hexamethylindanopyran) is a synthetic musk with a clean sweet musky floral woody odor used in fragrances. It is one of the musk components that perfume and cologne manufacturers use to add a musk odor to their products. Galaxolide was first synthesized in 1965, and used in the late 1960s in some fabric softeners and detergents.^[1] High concentrations were also incorporated in fine fragrances.

Hydroxymethylpentylcyclohexenecarboxaldehyde is a synthetic fragrance known by the trade names Lyral, Kovanol, Mugonal, Landolal. It is found in some soaps, eau de toilettes, aftershaves and deodorants.

Hydroxycitronellal ( 7-hydroxy-3,7-dimethyloctanal) is an odorant used in perfumery. Its molecular formula is C 10 H 20 O 2. It derives from a citronellal. 7-Hydroxy-3, 7-dimethyloctanal, also known as 3, 7-dimethyl-7-hydroxyoctan-1-al or 7-hydroxycitronellal, belongs to the class of organic compounds known as medium-chain aldehydes.

Isobutyl salicylate has an orchid, wintergreen-like odor similar to amyl salicylate and a bitter taste. May be synthesized by esterification of isobutyl alcohol and salicylic acid.

Isobutyl Phenyl Acetate, Natural is a colorless to pale yellow liquid that has a honeylike, rose aroma. It is used as a natural flavorant.

Cyclogalbanate® is synthesized by esterification of cyclohexyloxyacetic acid (prepared from phenoxyacetic acid) with allyl alcohol, catalysed by a strong acid. Synthesis precursor : Cyclogalbanate® is not a precursor to the synthesis of another compound of olfactory interest.

The terpinenes are a group of isomeric hydrocarbons that are classified as monoterpenes. They each have the same molecular formula and carbon framework, but they differ in the position of carbon-carbon double bonds. α-Terpinene has been isolated from cardamom and marjoram oils, and from other natural sources. β-Terpinene has no known natural source but has been prepared from sabinene. γ-Terpinene and δ-terpinene (also known as terpinolene) have been isolated from a variety of plant sources. They are all colorless liquids with a turpentine-like odor.^[1]

Description Geranyl propionate has a fruity, somewhat flowery odor and a bitter taste. Prepared by esterificaiton of geraniol with propionic acid in the presence of a catalyst.

Geranyl Nitrile; 3,7-Dimethyl-2,6-octadienenitrile; Geranonitrile; Geranitrile; Citralva, Citranile. ODOUR: Powerful oily green, lemony fresh odour. COLOR & APPEARANCE: Colourless to pale yellow oily liqui

Geranyl formate has a fresh, green, leafy, rose odor with a bitter taste. Geranyl formate is prepared by direct esterification of geraniol with formic acid. Chemical Properties Geranyl Formate is a liquid with a fresh, crisp, herbal, fruity rose odor. It is used as a modifier of, among others, rose, geranium, and neroli compositions.

Geranyl acetate is a monoterpene. It is a colorless liquid with a pleasant floral or fruity rose aroma. It is a colorless liquid but commercial samples can appear yellowish. Geranyl acetate is insoluble in water but soluble in organic solvents. Several hundred tons are produced annually.

Isoborneol powder is a white crystalline powder which is manufactured though the synthesis of turpentine obtained from pine trees. We source the very best quality of Isoborneol Powder

Hexyl Salicylate has been reported in carnation flower absolute. It is a colorless liquid with a green, floral, spicy odor, reminiscent of azaleas. It is used for blossom and herbal notes in perfumes, for example, in soaps, personal hygiene products, and detergents.

Vetiveryl Acetate: Arctander speaks very highly of this material: “The beauty of the odor is only fully appreciated when the material is incorporated in a suitable perfume. The peculiar dry-sweet note does not appear with a woody tone, but it gives fresh lift, yet outstanding tenacity and warmth to a fragrance.

: This super dry substantive ambery/ woody molecule can be used to accent the top, middle and dry down notes in men’s and woman’s fragrances. Normally used as a 10% solution. A woody note that gives top and middle note effects in addition to its long-lasting and substantive properties. Should be tried wherever a woody character is required but does require careful blending and dosing.

Stemone imparts a natural and fresh nuance to fragrance notes such as lily-of-the-valley, narcissus, mandarin, fig leaves, grapefruit, black currant and tomato. It is an excellent modifier that strengthens and modernises green notes.

Neryl acetate is a terpenoid found in citrus oils. It is the acetate ester of nerol, an isomer of the more common fragrance geranyl acetate.^[2] In flavors and perfumery it is used to impart floral and fruity aromas.^[3]

Lilial (a trade name for lily aldehyde, also known as lysmeral) is a chemical compound commonly used as a perfume in cosmetic preparations and laundry powders, often under the name butylphenyl methylpropional. It is a synthetic aromatic aldehyde. It was banned for use in cosmetics by the EU in March 2022 after being found to be harmful to fertility.

The ionones are a series of closely related chemical substances that are part of a group of compounds known as rose ketones, which also includes damascones and damascenones. Ionones are aroma compounds found in a variety of essential oils, including rose oil. β-Ionone is a significant contributor to the aroma of roses, despite its relatively low concentration, and is an important fragrance chemical used in perfumery.^[1] The ionones are derived from the degradation of carotenoids.

The combination of α-ionone and β-ionone is characteristic of the scent of violets and used with other components in perfumery and flavouring to recreate their scent.^[2][3]

The carotenes α-carotene, β-carotene, γ-carotene, and the xanthophyll β-cryptoxanthin, can all be metabolized to β-ionone, and thus have vitamin A activity because they can be converted by plant-eating animals to retinol and retinal. Carotenoids that do not contain the β-ionone moiety cannot be converted to retinol, and thus have no vitamin A activity.

Guaiyl acetate is obtained by acetylation and special fractioned rectification of 100% pure and natural Guaiacwood oil.A delicate, woody, fatty, green tea aroma

 Isopulegol is a monoterpene alcohol intermediate in the preparation of (-)-menthol and it is present in the essential oils of various plants.

Menthone is a monoterpene with a minty flavor^[1] that occurs naturally in a number of essential oils. l-Menthone (or (2S,5R)-trans-2-isopropyl-5-methylcyclohexanone), shown at right, is the most abundant in nature of the four possible stereoisomers.^[2] It is structurally related to menthol, which has a secondary alcohol in place of the carbonyl. Menthone is used in flavoring, perfume and cosmetics for its characteristic aromatic and minty odor.

Isobornyl acetate is a kind of acetate ester. It can be manufactured through the esterification between acetate and camphene. It is a kind of flavoring agent with fragrance.

Ethylvanillin is the organic compound with the formula (C2H5O)(HO)C6H3CHO. This colorless solid consists of a benzene ring with hydroxyl, ethoxy, and formyl groups on the 4, 3, and 1 positions, respectively. It is a homologue of vanillin, differing on the 3 position.

Indole is an aromatic, heterocyclic, organic compound with the formula C8H7N. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered pyrrole ring. Indole is widely distributed in the natural environment and can be produced by a variety of bacteria. As an intercellular signal molecule, indole regulates various aspects of bacterial physiology, including spore formation, plasmid stability, resistance to drugs, biofilm formation, and virulence.^[2] The amino acid tryptophan is an indole derivative and the precursor of the neurotransmitter serotonin.^[3]

The chemical compound isobutyl acetate, also known as 2-methylpropyl ethanoate (IUPAC name) or β-methylpropyl acetate, is a common solvent. It is produced from the esterification of isobutanol with acetic acid. It is used as a solvent for lacquer and nitrocellulose. Like many esters it has a fruity or floral smell at low concentrations and occurs naturally in raspberries, pears and other plants. At higher concentrations the odor can be unpleasant and may cause symptoms of central nervous system depression such as nausea, dizziness and headache.

Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers.^[1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an alpha-CH2-containing aldehyde and a member of phenylacetaldehydes.^[2]

Geraniol is a monoterpenoid and an alcohol. It is the primary component of citronella oil and is a primary component of rose oil, palmarosa oil. It is a colorless oil, although commercial samples can appear yellow. It has low solubility in water, but it is soluble in common organic solvents. The functional group derived from geraniol (in essence, geraniol lacking the terminal −OH) is called geranyl

Benzyl acetate is an organic ester with the molecular formula CH3C(O)OCH2C6H5. It is formed by the condensation of benzyl alcohol and acetic acid.

Similar to most other esters, it possesses a sweet and pleasant aroma, owing to which, it finds applications in personal hygiene and health care products. It is a constituent of jasmin and of the essential oils of ylang-ylang and neroli. It has pleasant sweet aroma reminiscent of jasmine. Further as a flavoring agent it is also used to impart jasmine or apple flavors to various cosmetics and personal care products like lotions, hair creams etc..^[1]

It is one of many compounds that is attractive to males of various species of orchid bees. It is collected and used by the bees as an intra-specific pheromone; In apiculture benzyl acetate is used as a bait to collect bees. Natural sources of benzyl acetate include varieties of flowers like jasmine (Jasminum), and fruits like pear, apple, etc.

Rose oxide^[1] is a fragrance chemical found in roses and rose oil. It also contributes to the flavor of some fruits, such as lychee, and wines, such as Gewürztraminer.

Musk ketone dates to 1888, when German chemist Albert Baur made it serendipitously while he was trying to find a better way to produce the explosive TNT. In the perfume industry, musk ketone is called a fixative because it stabilizes the volatility and improves the tenacity of perfume aromas.

Dihydromyrcenol is a monoterpenoid that is oct-7-en-2-ol substituted by methyl groups at positions 2 and 6 respectively. It has a role as a fragrance and a metabolite.

Tolu balsam^[1] or balsam of Tolu^[2] is a balsam that originates from South America (Colombia, Peru, Venezuela). It is similar to (and frequently confounded with) the balsam of Peru.

It is tapped from the living trunks of Myroxylon balsamum var. balsamum.^[1] The fresh balsam of Tolu is a brownish, sticky, semifluid mass. It gradually becomes a brittle solid, but softens again when it is warm.^[2] The balsam contains a fairly large amount of benzyl and cinnamyl esters of benzoic and cinnamic acid (benzyl benzoate, benzyl cinnamate).^[3]

FEMA 2711-2-3;Methyl irisone;ISORALDEINE 70;Einecs 204-842-1;GAMMA-METHYLIONONE;alpha-,beta-mixture;METHYL IONONE GAMMA;Alpha-n-predominant);alpha-n-predominantly;METHYL IONONE GAMMA USP/EP/BP