WO2024256256A1

WO2024256256A1 - A container containing a transparent laundry fragrance booster composition

Info

Publication number: WO2024256256A1
Application number: PCT/EP2024/065575
Authority: WO
Inventors: Sebastian Emanuel Aputsiaq MJORNSTEDT
Original assignee: Unilever Ip Holdings B.V.; Unilever Global Ip Limited; Conopco, Inc., D/B/A Unilever
Priority date: 2023-06-15
Filing date: 2024-06-06
Publication date: 2024-12-19

Abstract

A container containing a transparent laundry fragrance booster composition, wherein the transparent laundry fragrance booster composition comprises: Perfume; and Ethoxylated triglyceride; and wherein the container comprises 25 to 100 wt.% post-consumer recycled resin.

Description

A CONTAINER CONTAINING A TRANSPARENT LAUNDRY FRAGRANCE BOOSTER COMPOSITION

Field of the Invention

The invention relates to transparent liquid fragrance boosters.

of the Invention

Fragrance boosters are used in the laundry process to deliver fragrance, in addition to any detergent or fabric conditioner being used. Fragrance boosters allow consumers to tailor their fragrance experience during the laundry process. The consumer can select the fragrance and the quantity of product to add. This prevents the tendency to over-dose products such as fabric conditioner in order to increase fragrance delivery. Consumers also desire transparent products since transparency signals to consumers that the product does not contain high levels of chemicals. There is a need for transparent liquid fragrance boosters; however transparent formulations provided in recycled resin bottles have stability issues. of the Invention

It has been found that careful selection of a nonionic surfactant improved the stability of a transparent fragrance booster in a post-consumer recycled resin bottle.

Accordingly in one aspect of the present invention is provided a container containing a transparent laundry fragrance booster composition, wherein the transparent laundry fragrance booster composition comprises: a Perfume; and b Ethoxylated triglyceride; and wherein the container comprises 25 to 100 wt.% post-consumer recycled resin.

Detailed Description of the Invention

These and other aspects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. For the avoidance of doubt, any feature of one aspect of the present invention may be utilised in any other aspect of the invention. The word “comprising” is intended to mean “including” but not necessarily “consisting of” or “composed of.” In other words, the listed steps or options need not be exhaustive. It is noted that the examples given in the description below are intended to clarify the invention and are not intended to limit the invention to those examples per se. Similarly, all percentages are weight/weight percentages unless otherwise indicated. Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description indicating amounts of material or conditions of reaction, physical properties of materials and/or use are to be understood as modified by the word “about”. Numerical ranges expressed in the format "from x to y" are understood to include x and y. When for a specific feature multiple preferred ranges are described in the format "from x to y", it is understood that all ranges combining the different endpoints are also contemplated.

Composition

The compositions described herein are transparent. For the purposes of the present invention, transparency is measured by light transmission. The formulation has a light transmission of 60 to 100%, more preferably 60 to 100%, even more preferably 70 to 100% and most preferably 80 to 90%. The light transmission is measured at 25°C and can suitably be measured using a TurbiscanOLAB ex. Formulation Scientific Instruments with a 880 nm wavelength and a glass vials having a diameter of 25 mm and height of 55mm. A transparent formulation may comprise dyes to colour the formulation, such dyes preferably do not affect the transparency of the formulation.

The composition comprises perfume. The compositions preferably comprise 0.1 to 20 wt.% perfume by weight of the composition, more preferably 0.5 to 10 wt.% perfume by weight of the composition. Many suitable examples of perfumes are provided in the CTFA (Cosmetic, Toiletry and Fragrance Association) 1992 International Buyers Guide, published by CFTA Publications and OPD 1993Chemicals Buyers Directory 80th Annual Edition, published by Schnell Publishing Co.

It is commonplace for a plurality of perfume components to be present in a free oil perfume composition. In the compositions for use in the present invention it is envisaged that there will be three or more, preferably four or more, more preferably five or more, most preferably six or more. The compositions described herein comprise ethoxylated triglyceride. The compositions preferably comprise 1 to 30 wt.% ethoxylated triglyceride, more preferably 2 to 25 wt.% ethoxylated triglyceride, most preferably 4 to 20 wt.% ethoxylated triglyceride by weight of the composition.

The triglyceride may be any suitable triglyceride. Preferably the triglyceride is fully saturated. Full saturation may be naturally occurring or may be achieved by hydrogenation. Preferably the triglyceride chains comprise alcohol groups. Preferred sources of triglyceride are plant oils and combinations thereof. Preferably the triglycerides are sourced from the following oils: almond, argan, babassu, borage, camelina, canola, castor, chia, cherry, coconut, corn, cotton, coffee, Cuphea Viscosissima , flax (linseed), grape, hemp, hepar, jatropha, jojoba, Lesquerella Fendleri, Moringa Oleifera, macadamia, mango, mustard, neem, olive, palm, palm kernel, perilla, rapeseed, safflower, sesame, shea, stillingia, soybean, sunflower, tonka bean, tung and combinations thereof.

The ethoxylated triglyceride preferably comprises 6 to 100 moles of ethoxylation, more preferably 12 to 80, and even more preferably 20 to 60 moles of ethoxylation. Most preferably the ethoxylated triglyceride comprises about 40 moles of ethoxylation (i.e. 35 to 45 moles of ethoxylation).

Most preferably the ethoxylated triglyceride comprises PEG-40 hydrogenated castor oil.

The ethoxylated triglyceride enhances the transparency of the formulations. Preferably the ratio of perfume to ethoxylated triglyceride is 1 :1 to 1:15, more preferably 1 :2 to 1 :10.

The compositions described herein preferably comprise beads having a diameter of 50 pm to 2000 pm. The compositions comprise 0.001 to 10 wt.% beads by weight of the composition, preferably 0.005 to 5 wt.% beads and more preferably 0.01 to 2 wt.% beads by weight of the composition.

The beads may be made of any suitable material. The beads preferably comprise a structure formed from inorganic material, plant based solids or waxes, polymeric material or a combination thereof.

Inorganic materials include materials such as such clays (e.g. bentonite), silicates (e.g. sodium or potassium silicates), carbonates (e.g. calcium carbonate), or materials comprising calcium, phosphorus, potassium, sodium, chloride, magnesium, iron or zinc. Preferably inorganic materials are selected from clays, silicates, carbonates and combinations thereof.

Plant based solids are taken from the hard materials found in plants, for example the stones or pits in fruit or the shells of nuts. Plant based solids are preferably selected from olive pit, almond shell, peach stones, pistachio shell, avocado shell, apricot stone, argan shell, walnut shell, jojoba seeds, oats, bamboo, loofah, poppy seeds, strawberry seeds, raspberry seeds, blackberry seeds and combinations thereof. The plant solids may be ground to a suitable particle size. Plant based waxes such as beads formed from hydrogenated plant oils e.g. hydrogenated jojoba oil or hydrogenated castor oil, examples of suitable beads formed from plant based waxes are available from Vantage.

Polymeric materials include any polymers which can form beads having a diameter of 50 pm to 2000 pm. Preferably the polymer is a polysaccharide. The polysaccharide is preferably selected from cellulose (including microcrystalline cellulose, carboxymethyl cellulose and other cellulose ethers, hydroxyethyl and hydroxypropyl cellulose), guar, agar, carrageenan, alginates, pectins, hemicellulose, alginate, locust bean gum, starch, gelatin, xanthan gum and combinations thereof. More preferably the polysaccharide comprises cellulose (including microcrystalline cellulose, carboxymethyl cellulose and other cellulose ethers, hydroxyethyl and hydroxypropyl cellulose) and combinations thereof. Preferably the beads comprise 10 to 100 wt.% polysaccharide by weight of the bead, more preferably 15 to 95 wt.% polysaccharide by weight of the bead most preferably 25 to 90 wt.% polysaccharide by weight of the beads.

The beads may further comprise sugar, sugar alcohol or combinations thereof in addition to the inorganic material, plant based solids or waxes, or polymeric material. Suitable sugars or sugar alcohols include lactose, sucrose, dextrose, mannitol, xylitol, sorbitol, isomalt, lactitol, erythritol and combinations thereof. The beads preferably comprise 5 to 80 wt.% sugar, sugar alcohol or combinations thereof by weight of the beads, more preferably 10 to 70 wt.%, most preferably 15 to 60 wt.% sugar, sugar alcohol or combinations thereof.

The beads may preferably comprise optical enhancers, preferably pearliser, pigments, dyes and combinations thereof. The optical enhancers should be non-substantive to fabrics and are present to enhancer the aesthetics of the beads. These are particularly preferred for mineral or polymeric beads. The beads may consist essentially of inorganic material, plant based solids or waxes, or a polymeric material optionally with minor quantities of optical enhancers further present. Alternatively, the beads may consist essentially of inorganic material, plant based solids or waxes, or a polymeric material in combination with sugar and/or sugar alcohol, optionally with minor quantities of optical enhancers further present.

Alternatively, when the beads are mineral or polymeric based beads, they may comprise benefit agents, preferred benefit agents are selected from: perfumes, perfume microcapsules, oils, silicone, plant extracts, fabric care ingredients, vitamins, enzymes, shading dyes, antibacterial agents, malodor reduction or prevention agents, fabric softening agents, insect replants, shading or hueing dyes, fabric dyes, soil-release agents, sunscreens, and combinations thereof. Preferably the beads comprise hydrophobic benefit agents, such as perfumes. When present, the beads preferably comprise 0.01 to 50 wt.% benefit agent by weight of the beads, more preferably 1 to 40 wt.% benefit agent, even more preferably 4 to 30 wt.% benefit agent and most preferably 6 to 25 wt.% benefit agent by weight of the beads.

The beads may be prepared by mixing all the raw components together, preferably in a powder form. Water and/or another aqueous component is then added to the powders, and mixed to form a bulk that is further granulated. The wet granulates are dried to reduce the water content. The bulk may be dried using conventional drying procedure such as air drying, spray drying, belt drying, freeze drying, drum drying or flash drying.

Examples of commercially available polysaccharide beads are Unispheres® ex. Givaudan.

The compositions described herein preferably comprise a network forming polymer. A network forming polymer is a cross-linked polymer. The polymer may be cross-linked prior to addition to the composition or may form cross-linking in the formulation or may be cross-linked prior to addition to the composition and further cross linking occurs in the formulation. Preferably the polymer is cross-linked before addition to the composition, further cross-linking may occur in the composition.

The compositions described herein preferably comprise 0.05 to 5 wt.% network forming polymer by weight of the composition, more preferably 0.01 to 2 wt.% network forming polymer by weight of the composition. The network forming polymer may be synthetic, natural or a modified natural polymer (for example, micro fibrillated cellulose, which may be derived from a bacterial, fungal, or plant origin, including from wood).

The network forming polymer may carry a cationic or anionic charge, or may be neutral. Preferably the network forming polymer is anionic or neutral, most preferably anionic.

Synthetic network forming polymers may comprise polycarboxylates, polyacrylates, hydrophobically modified ethoxylated urethanes, hydrophobically modified non-ionic polyols, acrylic polymers, polyamino acids, polyuronic acids, polyvinyl sulfonic acids, polyalkene dicarboxylic acids and mixtures thereof. Polycarboxylate polymers may comprise a polyacrylate, polymethacrylate or mixtures thereof. Polyacrylates may for example comprise a copolymer of unsaturated mono- or di-carbonic acid and C1-C30 alkyl ester of the (meth)acrylic acid. The term acrylic polymer is understood to mean homopolymers or copolymers that comprise at least acrylic acid or methacrylic acid as a monomer. Polyuronic acids include homopolymers or copolymers of these sugar acids. The term polyvinyl sulfonic acids includes homopolymers or copolymers that comprise vinyl sulfonic acid as a monomer. In the context of this invention, the term polyalkene dicarboxylic acids includes for example homopolymers or copolymers with maleic acid or fumaric acid as a monomer. Suitable polymers are sold under the trade names Acusol ex. Dow and Carbopol Aqua 30 or Carbopol aqua CC. ex. Lubrizol.

Natural network forming polymers are preferably polysaccharides. Suitable polysaccharides are selected form: pectin, alginate, arabinogalactan (gum Arabic), carrageenan, gellan gum, locust bean gum xanthan gum, guar gum and mixtures thereof. Modified natural polymers are preferably modified polysaccharides. Suitable modified polysaccharides may comprise hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose and mixtures thereof.

Preferably the network forming polymer is selected from polyacrylates, polysaccharides, polysaccharide derivatives, or combinations thereof. Preferably the network forming polymer is anionic. Preferably the network forming polymer comprises hydrophobic modification.

Particularly preferred polyacrylates include HASE polymers selected from crosslinked copolymers that are prepared by the polymerization of a monomer mixture comprising (i) from 5 to 85 percent, more preferably from 25 to 70 percent, and most preferably from 35 to 65 percent (by weight based on the total weight of the monomer mixture) of nonionic monomers; (ii) from 5 to 85 percent, more preferably from 25 to 70 percent, and most preferably from 35 to 65 percent (by weight based on the total weight of the monomer mixture) of anionic or anionisable monomers; (iii) from 0.5 to 35 percent, more preferably from 1 to 25 percent (by weight based on the total weight of the monomer mixture) of hydrophobic monomers having an ethylenically unsaturated section (for addition polymerization with the other monomers in the mixture) and a hydrophobic section, and (iv) optionally, from 0.001 to 5 percent, preferably from 0.01 to 0.1 percent (by weight based on the total weight of the monomer mixture) of polyethylenically unsaturated copolymerizable monomers effective for crosslinking.

The nonionic monomers (i) are suitably selected from Ci-Cs alkyl and C2-C8 hydroxyalkyl esters of acrylic and methacrylic acid. Preferred are ethyl acrylate, methyl acrylate, and butyl acrylate.

The anionic or anionisable monomers (ii) are suitably selected from acrylic acid, methacrylic acid, crotonic acid, 2-acrylamido-2-methyl-1 -propanesulfonic acid, sodium vinyl sulfonate, itaconic acid, fumaric acid, maleic acid, monomethyl itaconate, monomethyl fumarate, monobutyl fumarate, and maleic anhydride. Preferred are acrylic acid and methacrylic acid. In one suitable type of hydrophobic monomer (iii), the hydrophobic section is constituted by a homopolymeric, random copolymeric or block copolymeric chain formed from repeating units selected from C1-C22 alkyl acrylates, C1-C22 alkyl methacrylates, methacrylic acid, acrylic acid or combinations thereof. Examples of such units include methyl methacrylate, ethyl methacrylate, butyl methacrylate, ethylhexyl methacrylate, stearylmethacrylate and mixtures thereof. One of the units at an end of the chain will remain available as an ethylenically unsaturated section for addition polymerisation with the other monomers in the mixture. Hydrophobic monomers of this type are usually referred to as"macromonomers" and may be prepared by catalytic chain transfer (OCT) procedures utilizing catalysts effective to achieve OCT such as the cobalt porphyrins and the cobaloximes. Macromonomers may advantageously have a number average molecular weight (Mn as determined by liquid permeation chromatography) ranging from about 200 to about 50,000, preferably from about 400 to about 10,000, and optimally from about 500 to about 3,000. Preferred examples of macromonomers include poly(methylmethacrylate)/poly(methacrylic acid), poly(methylmethacrylate), poly(butyl methacrylate), poly(ethylhexylmethacrylate) and combinations thereof. Another suitable type of hydrophobic monomer (iii) includes a polyoxyalkylene section between the ethylenically unsaturated section and the hydrophobic section. Hydrophobic monomers of this type are sometimes referred to as "surfmers" and may typically be prepared by the acid catalyzed condensation of commercially available nonionic polyoxyalkylene surfactant alcohols with acrylic, methacrylic, crotonic, maleic, fumaric, itaconic or aconitic acid. Preferred examples of surfmers include C8-C30 alkylated polyethoxylated (meth) acrylates (i.e. methacrylates and/or acrylates) in which the polyethoxylated portion comprises about 5 to about 100, preferably about 10 to about 80, and more preferably about 15 to about 60 ethylene oxide (EO) units, such as CI8H37(EO)2O (meth)acrylate and C12H25(EO)23 methacrylate.

The crosslinking comonomers (iv) are suitably selected from diallylphthalate, divinylbenzene, allyl methacrylate, trimethylol propane triacrylate, ethylene glycol diacrylate or dimethacrylate; 1 ,6-hexanediol diacrylate or dimethacrylate; and diallyl benzene.

Particularly preferred polysaccharides include cellulose and xanthan gum. Particularly preferred polysaccharide derivatives include hydroxyethyl cellulose, hydrophobically modified hydroxyethyl cellulose, carboxymethyl cellulose and mixtures thereof.

The network forming polymer preferably has a weight average molecular weight (Mw) of about 30,000 g/mol to about 10,000,000 g/mol, for example about 30,000 to about 500,000 g/mol, more typically 50,000 g/mol to 500,000 g/mol. Molecular weight can be determined by physical properties such as intrinsic viscosity or by spectrophotometric analysis such as light scattering.

The composition may comprise a single species of network forming polymer or may comprise a mixture of different polymers to provide optimal performance.

The compositions described herein preferably comprise alcohol ethoxylate. The compositions preferably comprise 1 to 30 wt.% alcohol ethoxylate, more preferably 2 to 25 wt.% alcohol ethoxylate, most preferably 4 to 20 wt.% alcohol ethoxylate.

Alcohol ethoxylates have a formula:

RO(CH₂CH₂O)XH

R represents the fatty alcohol chain. Preferably R is saturated. Preferably R = Cs to C₂4 fatty alcohol, more preferably R = C to C₂₂ fatty alcohol, even more preferably R = Ci₂ to C₂o fatty alcohol and most preferably R = Ci6 to Cis fatty alcohol. In other words, preferably the alcohol ethoxylate comprises a Cs to C24 fatty alcohol, more preferably a C10 to C22 fatty alcohol and most preferably a R = C16 to C18 fatty alcohol. x represents the degree of ethoxylation. Preferably x is 5 to 100, more preferably 10 to 80, even more preferably 12 to 60 and most preferably 15 to 40. In other words, preferably the alcohol ethoxylate comprises 5 to 100 ethoxylate groups, more preferably 12 to 60 ethoxylate groups and most preferably 15 to 40 ethoxylate groups.

Most preferably the alcohol ethoxylate comprises R = C16 to C18 fatty alcohol and x = 25. Suitable commercially available materials are available under the trade name Lutensol AT25 ex. BASF.

The alcohol ethoxylate prevents residues in the rinse drawer when the composition is used in conjunction with a fabric conditioner.

Preferably the compositions described herein comprise both ethoxylated triglyceride and alcohol ethoxylate. The ratio of ethoxylated triglyceride to alcohol ethoxylate is preferably 1 :2 to 2:1 , more preferably 2:3 to 3:2.

The compositions described herein preferably have a pH of 4 to 9. The composition may comprise pH adjusters to reach the desired pH. A suitable acid pH adjuster in hydrochloric acid. A suitable base pH adjuster is triethanolamine.

The compositions described herein preferably comprise benefit agents. Benefit agents are known to the person skilled in the art to deliver benefits to fabric. Such ingredient include: perfumes, perfume carriers, antibacterial agents, malodor reduction or prevention agents, fabric softening agents, insect replants, shading or hueing dyes, fabric dyes, hydrotropes, antiredeposition agents, soil-release agents, anti-wrinkle agents, anti-oxidants, sunscreens, antistatic agents, sequestrants and ironing aids.

The compositions described herein may preferably further comprise preservatives. Suitable preservatives include isothiazolinones, organic acids, alcohols or combinations thereof. Specifically the preservative may preferably be selected from: benzisothiazolinone (BIT), Methylisothiazolinone (MIT), lactic acid, citric acid, sodium benzoate, sodium citrate, itaconic acid, potassium sorbate, anisic acid, phenoxyethanol, propanediol and combinations thereof.

Some preservatives may require the presence of pH adjusters to maintain the optimal pH.

The compositions described herein may preferably further comprise dyes for colouring the compositions. Such dyes are intended to colour the composition, but not be substantive to fabrics. Such dyes are available under the Liquitint trade name ex. Milliken.

The compositions described herein may preferably comprise a sequestrant. It is understood that the sequestrant prevents yellowing of the compositions. This is particularly important for transparent formulations. Examples of suitable sequestrants are available under the trade names Dequest 2010 or 2066.

The compositions described herein are fragrance booster compositions. They are intended to provide additional perfume to the laundry process, not to provide cleaning or conditioning. Accordingly, the compositions preferably comprise 0 to 7 wt.% cationic surfactant, anionic surfactant or mixtures thereof, by weight of the composition. More preferably the compositions comprise 0 to 4 wt.% cationic surfactant, anionic surfactant or mixtures thereof, by weight of the composition, even more preferably 0 to 2 wt.% and most preferably 0 to 1 wt.% cationic surfactant, anionic surfactant or mixtures thereof, by weight of the composition.

The compositions of the present invention preferably comprise water. Preferably the compositions comprise more than 50 wt.% water by weight of the composition, more preferably at least 60 wt.% water by weight of the composition. A suitable upper limit is preferably 98 wt.% of the composition.

The compositions described herein may be produced by any suitable method. Preferably when perfume and ethoxylated triglyceride are both present, these ingredients are pre-mixed prior to addition to the main mix. Preferably the water for the main mix is heated to 30-70°C prior to the addition of any further ingredients, more preferably 40-60°C.

The compositions described herein may be used in any stage of the laundry process to deliver benefit agents into the laundry process. Preferably the compositions are used in the rinse stage. The compositions may be used in conjunction with a fabric conditioner or may be used on their own. Preferably the composition is used with a fabric conditioner. In one aspect of the present invention is provided a method wherein the compositions described herein are added in the rinse stage of the laundry process. Preferably the compositions are added to the rinse stage of the laundry process in addition to a fabric conditioner. In one aspect of the present invention is provided a use of the compositions described herein to provide fragrance in the rinse stage of the laundry process.

Packaging

The composition described herein is packaged or contained in a container wherein the container comprises 25% to 100 wt.% post-consumer recycled resin by weight of the container.

In the context of the present invention, the reference to “post-consumer recycled resin (PCR)” typically means plastic that has been collected via established consumer recycling streams, sorted, washed and reprocessed into pellets.

PCR is preferably made from the mechanical recycling of plastic, typically packaging plastic and is described in Mechanical Recycling of Packaging Plastics: A Review, Z. O. G. Schyns,; M. P. Shaver Macromol. Rapid. Common. 2021, 42, 2000415.

Types of post-consumer recycled resin include: recycled high-density polyethylene (HDPE), recycled polypropylene (PP), recycled low density polyethylene (LDPE), recycled medium density polyethylene and recycled polyethylene terephthalate (PET).

Preferably the post-consumer recycled resin is selected from recycled polyethylene terephthalate (PET), recycled polypropylene (PP) or combinations thereof. More preferably the post-consumer recycled resin is transparent and most preferably the post-consumer recycled resin is transparent PET. Transparency of the post-consumer recycled resin is measured by the ‘haze’ of the material. Haze is measured as the percentage of incident light scattered by more than 2.5° through the plastic specimen. Haze is measured as a percentage, and a lower value indicates a higher level of clarity. Haze can be measured using ASTM D1003. The haze % of the post-consumer recycled resin is 0 to 15%, more preferably 0 to 10 %, even more preferably 0 to 5% and most preferably 0 to 2.5%.

The container is preferably a bottle, with a lid. Preferably the container is blow molded. Blow molding involves the formation of a parison or preform which is placed and clamped into the mould. Air is passed into the parison/preform to expand the parison/preform such that it expands to fill the space in the mould. Once the plastic has hardened sufficiently, the mould is de-coupled and the molded article is removed.

Preferably the container comprises 30% to 100% PCR, more preferably 50 to 100% and even more preferably 75 to 100% PCR and most preferably 95 to 100% PCR.

The container may be formed from a multi-layer material. The material may comprise multiple layers (more than one) of the same post-consumer recycled resin or may comprise multiple layers (more than 1) of different post-consumer recycled resins or may comprise a mixture of at least one post-consumer recycled resin layer and at least one virgin resin layer. When a virgin layer of resin is used, it is preferred that this material is not in contact with the compositions, i.e. that a post-consumer recycled resin layer is the inner most layer of the bottle, in direct contact with the composition.

Examples

Table 1: Example compositions

Cellulose beads¹ - Unispheres® ex. Givaudan

Ethoxylated triglyceride² - PEG 40 hydrogenated castor oil

Alcohol ethoxylate³ - Lutensol AT25 ex. BASF

Network forming polymer⁴ - Acusol millennium ex. Dow

The compositions can be prepared by premixing the perfume and ethoxylated triglycerides. Then heating the water to 50°C, and adding the preservatives, alcohol ethoxylate, premix, polymer and pH adjuster. Checking the pH and adjusting to reach a pH of 7.6. Finally cooling the mixture to room temperature.

Claims

1. A container containing a transparent laundry fragrance booster composition, wherein the transparent laundry fragrance booster composition comprises: a Perfume; and b Ethoxylated triglyceride; and wherein the container comprises 25 to 100 wt.% post-consumer recycled resin by weight of the container; wherein the transparent laundry fragrance booster composition has a light transmission of 60 to 100%.

2. A container containing a transparent laundry fragrance booster composition according to claim 1, wherein the composition comprises 1 to 30 wt.% ethoxylated triglyceride by weight of the composition.

3. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the triglyceride is fully saturated.

4. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the triglyceride comprises 6 to 100 moles of ethoxylation.

5. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the ethoxylated triglyceride comprises PEG-40 hydrogenated castor oil.

6. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the composition comprises 0.1 to 20 wt.% perfume by weight of the composition.

7. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the composition further comprises beads having a diameter of 50 pm to 2000 pm.

8. A container containing a transparent laundry fragrance booster composition according to claim 7, wherein the beads comprise a structure formed from inorganic material, plant based solids or waxes, polymeric material or a combination thereof.

9. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the composition comprises a network forming polymer.

10. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the composition comprises alcohol ethoxylate.

11. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the post-consumer recycled resin comprises recycled polyethylene terephthalate (PET), recycled polypropylene (PP) or combinations thereof.

12. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the post-consumer recycled resin is transparent, wherein the haze % of the post-consumer recycled resin is 0 to 15% as measured using ASTM D1003.

13. A container containing a transparent laundry fragrance booster composition according to any preceding claim, wherein the post-consumer recycled resin is transparent recycled polyethylene terephthalate (PET).