Laroflex MP 45 Laroflex MP 45 a copolymer of vinyl chloride and vinyl isobutyl ether. Used as a binder in paints for iron and steel structures, mineral substrates, plastics, shipbuilding and underwater applications, mechanical and automotive engineering, transportation, protection of buildings and in printing inks industry and road marking paints. Compatible with vinyl chloride copolymers, polyacrylates, unsaturated polyester resins, maleate resins, cyclohexanone resins, aldehyde resins, coumarone and hydrocarbon resins. Also compatible with urea resins, alkyd resins modified by oils and fatty acids, natural resins, drying oils, plasticizers, tars and bitumen. Laroflex MP 45 provides hydrolysis resistance. Laroflex MP 45 gradeschlorinated binders, resistant to hydrolysis, for the manufacture of physically drying coatings on iron and steel, nonferrous metals, mineral substrates as well as for printing inksand road marking paints Nature copolymers based on vinyl chloride and vinyl isobutyl ether Range Laroflex MP 15 Laroflex MP 25 Laroflex MP 35 Laroflex MP 45 Laroflex MP 60 Physical form fine white powderStorage Laroflex MP 45 grades can be stored for 2 years if kept away fromheat and moisture.Laroflex MP 45 Product specification MP 15 MP 25 MP 35 MP 45 MP 60 of 12 Laroflex MP 45 grades Application Laroflex MP 45 grades are binders resistant to hydrolysis. They can beused for anti-corrosion coatings, for coatings on galvanized steel,other non-ferrous metals, concrete, fiber cement, for road markingpaints, flame-retardant coatings on non-flammable building materials, printing inks, marine and container paints. They are compatiblewith most alkyd resins, dry oils, polyacrylic resins, liquid epoxy resins, tars and bitumens. Overview Laroflex MP 45 grades offer advantages to both manufacturers andusers of coatings: • broad choice of solvents, particularly budget-priced blends ofaromatic and aliphatic hydrocarbons • good compatibility with other coatings raw materials • good pigment binding capacity even at high solids • unrestricted choice of pigments and extenders • easy application by all common techniques, no cob-webbingeven at high solids • thermal stability allows force drying • good adhesion on iron, steel and many unrelated coatings systems, good intercoat adhesion • good resistance of properly formulated coatings to aqueousalkalis and acids, salt solutions, to stress from water, humiditychanges, low and cyclic temperatures as well as to chalkingand yellowing • long lasting corrosion protection even under extreme outdoorconditions Differences in properties Laroflex MP 45 grades mainly differ in their viscosities and the rheology of their solutions. Viscosity ranges given in the table relate to20 % solutions in toluene at 23 °C (73 °F). The less polar the solvent,the greater the differences in viscosity. The low-viscous solutions of Laroflex MP 45 and Laroflex MP 45are diluted easiest with aliphatic hydrocarbons, their viscositychanges the least during storage and they produce highest gloss. The high-viscous solutions of Laroflex MP 45 tend to gel, particularly in non-polar solvents. Choosing the right solvent Suitable solvents are aromatic hydrocarbons or their blends withesters and glycolether acetates. Aliphatic hydrocarbons and/oralcohols are used as diluents. Ketones, in general, are less suited since they are retained by vinylchloride polymers longer than other solvents with equal volatility,resulting in slower drying coatings. 12 Laroflex MP 45 grades The diluent fraction of the solvent blend mainly depends on the solvency of the true solvent. Depending on the type of solvent andwhen Laroflex MP 45 or Laroflex MP 45 are used, the diluentproportion must be reduced by up to 40 % as compared with Laroflex MP 45. The diluent proportion can be increased if other raw materials inthe formulation are readily compatible with Laroflex MP 45 gradesand soluble in aliphatic hydrocarbons or alcohols. Examples arehard resins such as Laropal K 80, many alkyd resins, higharomatic grades of tar, soft resins and plasticizers present ingreater proportions.Aromatic hydrocarbons or blends of aromatic and aliphatic hydrocarbons are best suitable for coatings that are to be exposed towater very soon after application.High-volatile solvents and/or diluents produce faster drying coatings.Coatings containing a blend of xylene and butanol instead of xylenealone will dry faster. Polymers release esters more easily than ketones and aromatic hydrocarbons of the same volatility. The mostfavorable low-volatile solvent is ethoxypropyl acetate. Note that thesolvent retention also depends on the other constituents of theformulation. Gloss and flow of coatings can be improved by adding high-boilingsolvents, e.g., ethoxypropyl acetate. High proportions of low-volatilediluents, however, may result in precipitating of binder constituents,impairing both gloss and mechanical properties of the coatings. Greater proportions (20–25 %) of high-boiling solvents, e.g., ethoxypropyl acetate or blends of aromatic hydrocarbons with a boilingrange of 150 °C (302 °F) to 190 °C (374 °F) reduceblistering whichmay occur in airless-sprayed coatings, particularly those with a lowpigment content.High proportions of diluent in the solvent blend reduce the risk ofprevious coats pulling up. Clear or almost clear solutions can be obtained in aromatic hydrocarbons such as toluene, xylene or Solvesso1 100 as well as inchlorinated hydrocarbons, anone and tetrahydrofuran. Solutionswith other solvents may be somewhat cloudy but will not adverselyinfluence hardness and homogeneity of the film, provided the solution dries to form a clear film. Viscosity behavior of the solution The viscosity of solutions of Laroflex MP 45 grades not only dependson the concentration, the composition of the solvent blend and itstemperature, but also on the conditions under which they are prepared.registered trademark of Exxon Mobil Corporation of 12 Laroflex MP 45 grades The higher the temperature as well as duration and extent of shearforces, the lower the viscosity of the solution will be after coolingdown to room temperature. After extended storage, the viscositymay increase again, an effect that is more pronounced the less thesolvating power and the affinity between solvents and polymer. Unpigmented concentrated solutions of Laroflex MP 45 grades inxylene may tend to gel – often only months after they have beenprepared and without undergoing a gradual increase in viscosity. Adding ketones and esters reduces the tendency to gel, in particular if the binder concentration is high. By adding 10–20 % of analcohol to the solvent blend, gelling generally can be suppressedcompletely. Likewise, no gelling has been observed yet in formulations containing blends of high-boiling aromatics such asby intensive stirring, heating or by milling with pigments. This rheological behavior is quite pronounced in Laroflex MP 45. Itis scarcely noticed in Laroflex MP 45 and not at all in Laroflex MP 45 and Laroflex MP 45. Typical solvent blends 1. Coatings based on Laroflex MP 45 grades without significant amounts of cobinders:of 12 Laroflex MP 45 grades 2. Coatings based on 1:1 blends of Laroflex MP 45 grades and Plasticizing Laroflex MP 45 grades are internally plasticized. Coatings based on 4 F) or polyester resins in larger proportions of 15–30 %. In formulations based on Laroflex MP 45, the plasticizer propotion should be kept some 10–15 % lower than in those based onthe other Laroflex MP 45 grades. Too much plasticizer will adversely affect the hardness and thermostability of the dried coatings and can promote shrinkage, alligatoring and soiling of outdoor coatings. Coatings that have to withstand chemicals and salt water are formulated with plasticizers resistant to saponification, e.g., chlorinated paraffin waxes. Saponifiable plasticizers (phthalates, adulatesor phosphates) can be used when resistance to chemicals is lessimportant. Plastigen G is the plasticizer of choice for coatings onalkaline substrates (e.g., concrete) and for top coats extraordinarilyresistant to yellowing and chalking. Laroflex MP 45 gradesAcronal 4 F and its mixtures with phthalates are particularly suitable to increaseadhesion to aluminum and its alloys and otherdifficult substrates. The flexibility and adhesion of films based on Laroflex MP 45 grades at low temperatures can be increased by using low-viscosity, high-efficiency plasticizers (Palatinol 911 andPlastomoll DOA). Plasticizers which are insoluble in aliphatic hydrocarbons (Palamoll 646) least impair the resistance of filmsbased on Laroflex MP 45 grades to lubricants and fuel oil.Modification by other coatings raw materialsHard resins Solids content, gloss and adhesion can be increased by adding hard resins.Non-saponifiable hard resins such as Laropal K 80 are recommended for coatings resistant to chemicals and water. For nonpale coatings or when less emphasis is put on resistance to light and weathering, coumarone, indene or hydrocarbon resins can beused. Saponifiable hard resins (e.g., maleate or modified phenolicresins) can be used if good resistance to chemicals is not required.Hard resins which are compatible with Laroflex MP 45 grades (e.g.,Laropal K 80 or Laropal A 81) are often able to overcome anyslight incompatibility on the part of other materials present in theformulation. Laropal K 80 and Laropal A 81 increase the diluenttolerance of coatings based on Laroflex MP 45 grades for aliphatic hydrocarbons.Air-drying bindersAir-drying binders reduce the thermoplasticity of Laroflex MP 45 grades.Combined with a predominant proportion of air-drying binder,Laroflex MP 45 grades improve the coating’s • surface drying and thus its initial hardness, • resistance to chemicals and water, • outdoor performance, particularly in industrial environments. If resistance to chemicals and water is essential, the proportion of Laroflex MP 45 should be at least the same as that of the air-drying binder. The lower acid value and average molecular mass of an alkyd resin, the better its compatibility – which should be checked in each case. The most compatible alkyd resins are those containing about 45– 55 % drying or 25–50 % semidrying oils. Other compatible binders are bodied oils with modified phenolic resins, various urethane/alkyd resins and some epoxy resins modified by oil fatty acids. 12 Laroflex MP 45 grades In many cases, air-drying binders can be made perfectly compatible with Laroflex MP 45 grades by including other compatible components, e.g., Laropal K 80, Laropal A 81 or plasticizers. In combinations of Laroflex MP 45 grades with alkyd resins, theamount of white spirit in the solvent blend can often be increasedwell above the proportion normally used in coatings solely containing Laroflex MP 45 grades (see Typical solvent blends earlier in this chapter). If these “hybrid binder” coatings are to be overcoated, care must betaken to ensure that oxidative drying has progressed so far thatthere is no risk of “pulling up” caused by excessive softening of thefirst coat by the solvent phase of the second coat. The tendency ofpulling up can be reduced by increasing the proportion of Laroflex MP 45 grades. Equally, the solvent can be diluted with more whitespirit. Solvent blends whose proportion of diluents increases gradually and only to a limited extent perform best. An example is a blendconsisting of equal parts of xylene and white spirit. Pigmentation Any conventional anti-corrosion pigment can be used in primersbased on Laroflex MP 45 grades as chemical reactions between thetwo are unlikely. Based on our current experience, the binder – ifstored under normal conditions – does not need to be stabilizedagainst attack by active metal powders such as aluminum bronze. If there are any doubts, small proportions of zinc oxide or epoxycompounds may be added. registered trademark of Resolution Nederland B. V. Laroflex MP 45 grades Higher proportions of flake extenders or pigments in the pigmentblend (e.g., talc, micaceous iron oxide or aluminum bronze) improve the coatings’ adhesion and impermeability to water vapor,they also facilitate airless spraying of thick coats. Pigments and extenders resistant to weathering should be preferredfor topcoats. Some extenders – including a few natural magnesium,aluminum or potassium-aluminum silicates as well as barytes –contain impurities, which may cause yellowing of white topcoats. Asmall amount of zinc white generally prevents such discoloration. Pigments resistant to acids and alkalis must be used for coatingsresistant to chemicals. Effective corrosion protection is achieved with coatings having apigment volume concentration (PVC) of 16–35 %. For coatingsparticularly resistant to chemicals, a lower PVC range of 16–22 %should be preferred. Well-formulated high-build finishes, on theother hand, can be pigmented up to about 35 %. In general, thepigmentation level should be limited to 90 % of the critical PVC. Stabilizers Laroflex MP 45 grades are sufficiently stable to dehydrochlorination. Thus no stabilizers are normally needed. Exceptions are coatingsthat are either exposed to heat or unpigmented or – in some casesof coatings based on transparent pigments – exposed to UV radiation for extended periods. Note that chlorinated binders are less stable if moisture or somechemicals are present. Generally, coatings systems based on Laroflex MP 45 grades shouldnot be exposed to heat above 70–80 °C (158–176 °F) for prolongedperiods.Heat stabilizers should be added for force drying at temperatures ofup to 130 °C (266 °F). Adding 2 % Mark®4 17 M and 3 % Drapex439 (respective to Laroflex MP 45) provides adequate stabilization. Dispersants,antisettling agents,thixotropes Some dispersants or antisettling agents, particularly in higher proportions, may act with chlorinated binders to cause corrosion ofmetal containers and thus reduce the coating’s anticorrosion protection. Trials are recommended. Thixotropes derived from hydrogenated castor oil (e.g., Luvotix5 or Thixatrol6 ST) can be used for high-build coatings. Manufacturer’s instructions on their use should be observed. registered trademark of Crompton Vinyl Additives registered registered trademark of Elementis plc 12 Laroflex MP 45 grades Further, suitable thickeners and antisettling agents consist of anapproximately 10 % gel paste made from Bentone®6 38 or Bentone®639 and Anti-Terra®7 U in aromatic solvents. Processing Production of coatings Laroflex MP 45 grades dissolve very rapidly even without heating. Caking is avoided by immediately and uniformly distributing thepowder: thoroughly stirring, it is slowly added to the diluent (aliphatic hydrocarbons, alcohols). Proportions of Laroflex MP 45 powder and diluent should be approximately equal. Then, solvent(s)and other diluents are added while stirring. Subsequently, plasticizers and combination resins may be added. Solutions of Laroflex MP 45 grades that contain plasticizers and possibly other binder components are used to paste and mill pigments. If alkyd resin cobinders are present in the formulation, thesecan be used to prepare the pigment paste. Application techniques Coatings based on Laroflex MP 45 grades are suitable for all common application techniques such as high-pressure spraying, airlessspraying, hot spraying, brushing, dipping, curtain or roller coatingor paint roller. No cob webbing occurs during the application of coatings basedon Laroflex MP 45 grades even at high solids or if they contain highlyvolatile solvents. Blistering and pore formation during airless spraying can beavoided by keeping the proportion of highly volatile esters (e.g.,ethyl acetate and butyl acetate) in the solvent blend low. The inclusion of high-boiling aromatic hydrocarbons or ethoxypropyl acetatein advantageous. Good results are also obtained with defoamers,especially in paints with low PVC. Solutions of Laroflex MP 45 grades that contain plasticizers and possibly other binder components are used to paste and mill pigments. If alkyd resin cobinders are present in the formulation, thesecan be used to prepare the pigment paste. Application techniques Coatings based on Laroflex MP 45 grades are suitable for all common application techniques such as high-pressure spraying, airlessspraying, hot spraying, brushing, dipping, curtain or roller coatingor paint roller. registered trademark of Byk-Chemie GmbH Laroflex MP 45 grades No cob webbing occurs during the application of coatings based on Laroflex MP 45 grades even at high solids or if they contain highlyvolatile solvents. Blistering and pore formation during airless spraying can beavoided by keeping the proportion of highly volatile esters (e.g.,ethyl acetate and butyl acetate) in the solvent blend low. Theinclusion of high-boiling aromatic hydrocarbons or ethoxypropyl acetatein advantageous. Good results are also obtained with defoamers,especially in paints with low PVC. Drying Coatings based on Laroflex MP 45 grades surface-dry rapidly butrequire some length of time to through-dry since Laroflex MP 45grades, like all polymers, tend to hold back residual solvent. Consequently, a drying time of one or two days should be left betweencoats to prevent pulling up. Coatings to be exposed to water orliquid chemicals must be allowed to through-dry thoroughly. In thiscase, polar solvents should be avoided as any residual solventcould absorb large amounts of water and cause swelling. Drying time can be reduced by choosing suitable solvent blends,reducing the plasticizer proportion, a higher PVC or adding voluminous extenders or diatomite. Excessive quantities of these extenders and inadequate pigment dispersion can easily lead to porouscoatings with greater permeability to water vapor. Fields of application Industrial corrosion protection Combinations of equal proportions of Laroflex MP 45 grades and airdrying binders have proven effective. Two to three coats of thixotropic high-build coatings are needed toobtain the overall thickness of 200–250 µm necessary for effectivecorrosion protection. Depending on the make-up of the system andthe quality of pigments and extenders, the PVC is 30–40 %. Lowerpigmented gloss coats may be used for top coats. Marine coatings, underwater corrosion protection Coatings having to withstand sea or river water can be formulatedwith Laroflex MP 45 grades and non-saponifiable hydrophobic plasticizers. Combinations with tar and/or hydrocarbon resins can also beused, some of the Laroflex MP 45 proportion may be replaced by apolyamine-cured epoxy resin. A PVC of 35–40 % is ideal for highbuild coatings. These adhere extremely well to sandblasted steel,commercial shop primers and other unrelated coating systems. Laroflex MP 45 grades being resistant to alkalis allow formulatingunderwater coatings that give excellent performance in cathodicprotection and on zinc/ethyl silicate primers. Since high-build coatings based on Laroflex MP 45 grades can be sprayed outstandinglywell, only two or three spray coats are needed to achieve perfectcorrosion protection. 11 of 12 Laroflex MP 45 grades Laroflex MP 45 grades can also be used as binders in antifoulingpaints. Hydrophylic cobinders like Lutonal M 40 approx. 70 % inethanol and/or rosin ensure that the antifouling agent is released ata uniform rate. Machinery, automotive and container finishes Suitable coatings can be formulated from Laroflex MP 45 grades androughly equal amounts of air-drying binder. Coatings on galvanized steel and aluminumAir-drying binders should be avoided in primers and top coats onaluminum or, in particular, galvanized steel. Coatings based onsuch binders could flake or peel off after prolonged exposure tomoisture and fluctuating temperature. Addition of special hardresins, talc and/or micaceous iron oxide allow coats with extremelygood adhesion. Coatings for mineral substrates Laroflex MP 45 grades and alkali-resistant plasticizers are used toobtain coatings for mineral substrates. The pigmentation dependson the desired degree of gloss. Architectural finishes with adequate permeability to water vaporshould have a PVC of 50–60 %.Combinations of Laroflex MP 45 grades, polyamine-cured epoxyresins and tar are used for underwater and underground mineralsubstrates. The PVC for swimming pool coatings should be at least 50 % inorder to avoid blisters forming from osmosis, even in high-buildcoats. Since they are resistant to hydrolysis, Laroflex MP 45 grades aresuitable binders for sealing and impregnating primers for stabilizingmineral substrates and reliably ensuring that subsequent coats ofarchitectural finishes adhere well. Depending on the substrate’sactual porosity, the binder concentration in these coatings shouldbe 8–15 %. Road marking paintsRoad marking paints can be formulated from Laroflex MP 45 gradesalone or combined with air-drying binders. Note, however, that airdrying binders will reduce the life of road markings.Flame-retardant coatings Laroflex MP 45 grades are suitable binders for flame-retardant coatings on non-flammable substrates. of 12 Laroflex MP 45 grades Other fields of application: • indoor and outdoor coatings on wood and duroplastics • printing inks • impregnating and coating of paper, cardboard and textiles • effect paints such as wrinkle, hammer and crackle finishes Safety When handling these products, advice and information given in thesafety data sheet must be complied with. Further, protective andworkplace hygiene measures adequate for handling chemicalsmust be observed.NoteThe data contained in this publication are based on our currentknowledge and experience. In view of the many factors that mayaffect processing and application of our product, these data do notrelieve processors from carrying out their own investigations andtests; neither do these data imply any guarantee of certain properties, nor the suitability of the product for a specific purpose. Anydescriptions, drawings, photographs, data, proportions, weights,etc. given herein may change without prior information and do notconstitute the agreed contractual quality of the product. It is theresponsibility of the recipient of our products to ensure that anyproprietary rights and existing laws and legislation are observed. olubility: Laroflex MP 45 is well soluble in aromatic and chlorinated hydrocarbons, ester, ketone, glycol ether acetates, and some glycol ether. Usually Laroflex MP 45 is dissolved in 20% toluene/xylene solvent at normally temperatures. Compatibility: Laroflex MP 45 miscible with or partly miscible with vinyl chloride copolymer, polyacrylic ester, unsaturated polyester resins, aldehyde resins, petroleum resin, natural resins, alkyd resins modified by oil and fatty acids, drying oil, tars, and bitumen, etc. Application: Laroflex MP 45 is well used as basic resins in anticorrosion paint (steel structure, container, marine, underwater structure, machinery and automobile engineering, transport equipment & industrial paint) and it is also well-known in composite inks. Laroflex MP 45 is a binder resistant to hydrolysis. It can be used for anti-corrosion coatings, for coatings on galvanized steel, other non-ferrous metals, concrete, fiber cement, road marking paints, flame-retardant coatings on non-flammable building materials, and marine and container paints. Laroflex MP 45 is recommended for applications such as: •Interior/exterior general industrial metal coating applications •Interior/exterior plastic component applications •Interior/exterior concrete coating applications •Product Description •Laroflex MP 45 has good binding property as a result of its special molecular structure in which ester bond is resistance to hydrolysis and combined chlorine atom is very stable. So Laroflex MP 45 can be used to produce hign quality paints with good water resistance, salt resistance and chemical resistance. •Good adhesion •Laroflex MP 45 contain copolymer of vinyl chloride ester, which ensure the paints good adhesion on various materials. Even on the surface of aluminum or zinc, the paints still have good adhesion. •Good compatibility •Laroflex MP 45 is easily compatible with other resins in paints, and can modify and improve the characteristics of paints, which for mulated by drying oils, tars and bitumen. •Solubility •Laroflex MP 45 is soluble in aromatic and halohydrocarbon, esters, ketones, glycol, ester acetates and some glycol ethers. Aliphatic hydrocarbons and alcohols are diluents and not true solvents for Laroflex MP 45 •Compatibility •Laroflex MP 45 is compatible with vinyl chloride copolymers, unsaturated polyester resins, cyclohexanone resins, aldehyde resins, coumarone resins, hydrocarbon resins, urea resins, alkyd resins modified by oil and fatty acids, natural resins, drying oil, plasticizers, tars, and bitumen. •Fireproof Ability •Laroflex MP 45 contain chlorine atom, which gives the resins fireproof ability. With addition of other flame resistant pigment, filler and fire retardant, they can be used in fire retardant paint for construction and other fields.

SYNONYMS 2-Aminobutanedioic acid; 2-aminosuccinic acid; Asp; L-2-Aminobutanedioic acid; L-Aminosuccinic acid; L-Aspartic acid; (S)-(+)-Aspartic Acid; sparaginic Acid; (S)-Aminobutanedioic acid; L-(+)-Aspartic acid; CAS NO:56-84-8

Dodecyl-N,N-bis(2-hydroxyethyl) Amide; Lauric DEA; Bis(2-hydroxyethyl)lauramide; Diethanolamine lauric acid amide; diethanollauramide; Diethanol lauric acid amide; N,N-diethanollauramide; N,N-diethanollauric acid amide; N,N-bis(hydroxyethyl)lauramide; Lauramide DEA; N,N-bis(2-hidroxietil)dodecanamida; N,N-bis(2-hydroxyéthyl)dodecanamide; cas no: 120-40-1

LAURAMINE OXIDE, LAURAMIDOPROPYLAMINE OXIDE, N-[3-(dimethylamino)propyl]dodecanamide N-oxide; 3-(dodecanoylamino)-N,N-dimethylpropan-1-amine oxide; 3-[dodecanoyl(oxido)amino]-N,N-dimethylpropan-1-amine; N° CAS : 61792-31-2, Nom INCI : LAURAMIDOPROPYLAMINE OXIDE, Nom chimique : N-[3-(Dimethylamino)propyl]dodecanamide N-oxide, N° EINECS/ELINCS : 263-218-7, Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Agent nettoyant : Aide à garder une surface propre Sinergiste de mousse : Améliore la qualité de la mousse produite en augmentant une ou plusieurs des propriétés suivantes: volume, texture et / ou stabilité Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance Hydrotrope : Augmente la solubilité d'une substance qui est peu soluble dans l'eau. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : (3-LAURAMIDOPROPYL)DIMETHYLAMINE OXIDE; 3-LAURAMIDO-N,N-DIMETHYLPROPYLAMINE OXIDE; DODECANAMIDE, N-(3-(DIMETHYLAMINO)PROPYL)-, N-OXIDE; LAUROYLAMINOPROPYLDIMETHYLAMINE OXIDE ; N-(3-(DIMETHYLAMINO)PROPYL)-N-OXYDE DODECANAMIDE. Utilisation et sources d'émission: Fabrication d'imperméabilisants

Lauryldimethylamine oxide, Lauramine oxide; Dodecyldimethylamine oxide; Dimethyldodecylamine-N-oxide, N,N-Dimethyldodecan-1-amine oxide, N° CAS : 1643-20-5, Nom INCI : LAURAMINE OXIDE, Nom chimique : Dodecyldimethylamine oxide. N° EINECS/ELINCS : 216-700-6. Ses fonctions (INCI): Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Agent nettoyant : Aide à garder une surface propre. Sinergiste de mousse : Améliore la qualité de la mousse produite en augmentant une ou plusieurs des propriétés suivantes: volume, texture et / ou stabilité. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Hydrotrope : Augmente la solubilité d'une substance qui est peu soluble dans l'eau.Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques. Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. Noms français : 1-DODECANAMINE, N,N-DIMETHYL-, N-OXIDE; DODECYLAMINE, N,N-DIMETHYL-, N-OXIDE; LAURYLDIMETHYLAMINE N-OXIDE; N,N-DIMETHYL-1-DODECANAMINE N-OXIDE;N,N-DIMETHYL-1-DODECANAMINE-N-OXIDE; N,N-DIMETHYL-1-DODECYLAMINE-N-OXIDE; N,N-DIMETHYL-N-DODECYLAMINE OXIDE; N,N-DIMETHYLDODECYLAMINE OXIDE; N-DODECYLDIMETHYLAMINE OXIDE; N-LAURYL-N,N-DIMETHYLAMINE OXIDE; N-LAURYLDIMETHYLAMINE N-OXIDE; N-OXYDE DE DIMETHYLAURYLAMINE; Oxyde de lauryldiméthylamine Noms anglais : DDNO; DIMETHYLAURYLAMINE OXIDE; DIMETHYLDODECYLAMINE OXIDE; DIMETHYLLAURYLAMINE OXIDE; DODECYL DIMETHYLAMINE OXIDE; DODECYLDIMETHYLAMINE OXIDE; LAURAMINE OXIDE; Lauryldimethylamine oxide. Utilisation et sources d'émission: Fabrication de savons, agent dispersant

LAURAMIDE N° CAS : 1120-16-7 Nom INCI : LAURAMIDE Nom chimique : Lauramide N° EINECS/ELINCS : 214-298-7 Ses fonctions (INCI) Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques

Lauramine oxide; Lauryldimethylamine oxide; Dodecyldimethylamine oxide; Lauryldimethylamine N-oxide; LDAO; Dimethyldodecylamine oxide; 1-Dodecanamine, N,N-dimethyl-, N-oxide; Ammonyx AO; Ammonyx LO; Empigen OB; Aromox DMCD; Conco XA; Dimethylaurylamine oxide; n-Dodecyldimethylamine oxide; Dimethyldodecylamine N-oxide; Dodecyldimethylamine N-oxide; dodecyl(dimethyl)amine oxide; N,N-Dimethyldodecylamine N-oxide; N,N-dimethyldodecan-1-amine oxide; CAS NO:1643-20-5

SYNONYMS n-Dodecylamine; 1-Dodecanamine; Lauramine; 1-Aminododecane; Laurinamine;CAS NO. 124-22-1

LAURETH-1, peg-1 lauryl ether, polyethylene glycol (1) lauryl ether, polyethylene glycol (1) lauryl ether, polyethylene glycol (1) monolauryl ether, polyoxyethylene (1) lauryl ether, polyoxyethylene (1) monolauryl ether, LAURETH-1, N° CAS : 4536-30-5, Nom INCI : LAURETH-1, Nom chimique : 2-(Dodecyloxy)ethanol, N° EINECS/ELINCS : 224-886-5, Classification : Composé éthoxylé, Ses fonctions (INCI): Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile).Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant; 2-(Dodecyloxy)ethanol [ACD/IUPAC Name] 2-(Dodecyloxy)ethanol [German] [ACD/IUPAC Name] 2-(Dodécyloxy)éthanol [French] [ACD/IUPAC Name] 224-886-5 [EINECS] 4536-30-5 [RN] Dodecylglycol Ethanol, 2-(dodecyloxy)- [ACD/Index Name] Ethylene Glycol Monododecyl Ether IAC0DWO8W5 J89TKQ5R54 KK7650000 MFCD00042657 [4536-30-5] 2-(Decyloxy)ethanol [ACD/IUPAC Name] 2-(dodecyloxy)ethan-1-ol 2-decoxyethanol 2-dodecoxyethanol 2-dodecyloxyethan-1-ol 2-Hydroxyethyl lauryl ether 2-lauryloxyethanol 3,6,9,12-Tetraoxadocosan-1-ol [ACD/Index Name] [ACD/IUPAC Name] 4-01-00-02386 [Beilstein] aethoxysklerol Asclera Brij 35 (Laureth-23) CE1 Cimagel Decylglycol Dodecanol, ethoxylate Dodecyl-β-D-maltoside Ethanol, 2-(decyloxy)- [ACD/Index Name] Ethanol,2-(dodecyloxy)- ethylene glycol dodecyl ether Ethylene glycol monodecyl ether Ethylene glycol monolauryl ether Ethylene glycol mono-n-dodecyl ether ethyleneglycol monododecyl ether Ethyleneglycoldodecylether ethyleneglycolmonododecylether Laureth Laureth- 23 laureth-4 Lauryl ethoxylate Lauryl monoethoxylate LMT Nikkol BL O-DODECANYL OCTAETHYLENE GLYCOL Rokanol L Romopal LN Siponic L Slovasol O Slovasol S Thesat Thesit UNII:J89TKQ5R54 UNII-3Y76363WPB UNII-J89TKQ5R54 UNII-P30F471M6B VARITHENA

akypo rox RLM22 britex l 20 2- dodecoxyethanol (peg-2) 2-(2- dodecoxyethoxy)ethanol 2-[2-( dodecyloxy)ethoxy]ethanol peg-2 lauryl ether poly(oxy-1,2-ethanediyl), .alpha.-dodecyl-.omega.-hydroxy- (2 mol EO average molar ratio) polyethylene glycol (2) lauryl ether polyethylene glycol (2) monolauryl ether polyoxyethylene (2) lauryl ether polyoxyethylene (2) monolauryl ether CAS Number: 9002-92-0

ameroxol LE-23 brij 23 brij 35P brij L23 brij L23-25 britex L 230 chemal LA 23 2- dodecoxyethanol (peg-23) emulgen 123P ethosperse LA 23 lipocol L-23 macol LA-23 peg-23 lauryl ether poly(oxy-1,2-ethanediyl), .alpha.-dodecyl-.omega.-hydroxy- (23 mol EO average molar ratio) polyethylene glycol (23) lauryl ether polyethylene glycol (23) monolauryl ether polyoxyethylene (23) lauryl ether polyoxyethylene (23) monolauryl ether simulsol P 23 volpo L 23 CAS Number 9002-92-0

SYNONYMS alpha-Dodecyl-omega-hydroxy-polyoxyethylene;PolyethyleneGlycols, monododecyl ether; Dodecanol ethoxylate; Dodecanol, polyethoxylated; Dodecyl poly(oxyethylene)ether; Ethoxylated lauryl alcohol; Lauromacrogol; Lauryl alcohol, ethoxylated; Lauryl poly(oxyethylene) ether; Lauryl polyethylene glycol ether; CAS NO:9002-92-0

LAURETH-10, peg-10 lauryl ether, polyethylene glycol (10) lauryl ether, polyethylene glycol (10) lauryl ether, polyethylene glycol (10) monolauryl ether, polyoxyethylene (10) lauryl ether, polyoxyethylene (10) monolauryl ether, LAURETH-10, N° CAS : 9002-92-0 / 6540-99-4 / 68002-97-1. Nom INCI : LAURETH-10. N° EINECS/ELINCS : 500-002-6 / - / 500-182-6. Classification : Composé éthoxylé, Tensioactif non ionique. Le Laureth-10 est un tensioactif non ionique très doux. Il est produit par éthoxylation à partir d'alcool laurique. Le chiffre 10 indique le nombre moyen d'unités d'oxyde d'éthylène répétées dans la molécule. Il est souvent utilisé dans les cosmétiques en tant qu'agent émulsifiant (permet aux corps gras de se mélanger facilement à l'eau).Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-10 CARBOXYLIC ACID, N° CAS : 27306-90-7, Nom INCI : LAURETH-10 CARBOXYLIC ACID. Classification : Composé éthoxylé. Ses fonctions (INCI) : Agent nettoyant : Aide à garder une surface propre. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation

LAURETH-12, peg-12 lauryl ether, polyethylene glycol (12) lauryl ether, polyethylene glycol (12) lauryl ether, polyethylene glycol (12) monolauryl ether, polyoxyethylene (12) lauryl ether, polyoxyethylene (12) monolauryl ether, LAURETH-12, N° CAS : 3056-00-6 / 9002-92-0, Nom INCI : LAURETH-12. Nom chimique : 3,6,9,12,15,18,21,24,27,30,33,36-Dodecaoxaoctatetracontan-1-ol. N° EINECS/ELINCS : 221-286-5, Classification : Composé éthoxylé.Ses fonctions (INCI). Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

Laureth-10 Carboxylic Acid is an organic acid.


CAS Number: 27306-90-7
Chem/IUPAC Name: Poly(oxy-1,2-ethanediyl),.alpha.-carboxymethyl-.omega.-dodecyloxy-, (10 mol EO average molar ratio)


Dive into the world of Laureth-10 Carboxylic Acid, a powerful anionic surfactant renowned for its superior detergency and foaming abilities.
This versatile chemical compound, Laureth-10 Carboxylic Acid, is utilized in a range of applications, from personal care products to industrial cleaners, and offers excellent emulsifying and wetting properties.


It's ability to boost foam production and effectively remove dirt and oils makes Laureth-10 Carboxylic Acid a valuable addition to your formulations.
Laureth-10 Carboxylic Acid is a mild co-surfactant and functions as an emulsifier and solubilizer.
Laureth-10 Carboxylic Acid is extremely mild and compatible with other surfactants as well as ideal as co-surfactants and coupling agents.


Laureth-10 Carboxylic Acid has all the qualities that show outstanding pH stability and high tolerance against electrolytes and builders.
Laureth-10 Carboxylic Acid is a crypto-anionic surfactant - Laureth-10 carboxylic acid - (Laureth-10 Carboxylic Acidcombines the properties of the anionic and non-ionic surfactants).


Laureth-10 Carboxylic Acid has good foaming and solubilizing properties being very mild for the skin.
Laureth-10 Carboxylic Acid is a wide range of secondary surfactants with excellent tolerance against hard water.
Laureth-10 Carboxylic Acid is an essential additive for long-lifetime metalworking fluids.
Laureth-10 Carboxylic Acid is characterized by their outstanding hard water and electrolyte tolerance compared to other emulsifiers used in metalworking.


"Laureth-" refers to a PEG-(polyethylene glycol-) ether of lauryl alcohol.
The number behind "laureth-" refers to the average number of molecular units -CH2-CH2-O-.
"Carboxylic acid" refers generally to a carboxylic or carbonic acid.



USES and APPLICATIONS of LAURETH-10 CARBOXYLIC ACID:
Laureth-10 Carboxylic Acid is depending on the carbon chain length and the ethoxylation degree the products show characteristic application properties.
Laureth-10 Carboxylic Acid brings excellent lime soap dispersing properties and adds some anti-corrosion benefits.
Laureth-10 Carboxylic Acid can be used in conveyor belt lubricants.


Laureth-10 Carboxylic Acid has all the qualities that show outstanding pH stability and high tolerance against electrolytes and builders.
Laureth-10 Carboxylic Acid is an extremely mild surfactant with good emulsifying properties and insensitive to water hardness, it substantially improves the skin’s tolerance of cleansers.


Laureth-10 Carboxylic Acid is particularly suitable for high-quality formulations, baby shampoos, and products designed for sensitive skin.
Laureth-10 Carboxylic Acid is used high foaming mild co-surfactant for cosmetic applications.
Laureth-10 Carboxylic Acid is used in Hard water stable.


Laureth-10 Carboxylic Acid is used applicable in hypochlorite solutions.
Laureth-10 Carboxylic Acid is used emulsifying and solubilizing properties
Laureth-10 Carboxylic Acid is mainly used in various shampoos and personal care liquid products, especially for the preparation of baby shampoo, also used as detergents and industrial emulsifiers, dispersing agents, foaming agents and wetting agent.


Laureth-10 Carboxylic Acid combines the properties of the anionic and non-ionic surfactants.
Laureth-10 Carboxylic Acid has good foaming and solubilizing properties with excellent mildness to skin and mucous membranes
Laureth-10 Carboxylic Acid is used as emulsifier or coemulsifier for paste cosmetics.


Laureth-10 Carboxylic Acid is used Mild shampoo, body wash, facial cleanser, hand sanitizer and other personal cleaning and protection products.
Laureth-10 Carboxylic Acid is used mixed into the soap block mild, calcium soap dispersion, foam performance and bath feeling.
Laureth-10 Carboxylic Acid is used for household detergents, industrial cleaning agents and phosphorus free detergents.


Laureth-10 Carboxylic Acid is used in textile industry refining, mercerizing, bleaching, soft, dyeing and other processes.
Laureth-10 Carboxylic Acid is used as an emulsifier and viscosity reducer resistant to high concentration electrolyte, it is used in tertiary oil recovery and oil transportation to provide crude oil recovery.


Laureth-10 Carboxylic Acid is used surfactant for mild personal care products (shampoos, shower gels, foam baths, other low-irritation formulations); surfactant for industrial applications (agrochemicals, textile treatment); detergent for carpet cleaners especially aerosols
Laureth-10 Carboxylic Acid is used Paper industry for waste paper deinking and softening agent formula.


Laureth-10 Carboxylic Acid is used as foaming agent for foam fire extinguishing.
Laureth-10 Carboxylic Acid uses and applications include: Surfactant, emulsifier, dispersant, superfatting agent, foam stabilizer for emulsions, detergents, shampoos, bubble baths


Laureth-10 Carboxylic Acid is used with overall physico-chemical stability, that improves lathering, enhances quat's and hair dyes efficiency providing combined benefits of nonionic and anionic surfactants.
Applications of Laureth-10 Carboxylic Acid: Beauty & Care, Hair Care, Oral Care, Skin Care, Home Care, Auto Care, Carpet & Upholstery, Dish Care, and Laundry & Fabric Care


Other Home Care Applications of Laureth-10 Carboxylic Acid: Surface Care Institutional & Industrial Care, Commercial Laundry, Food Facility Cleaning & Sanitization, Industrial Cleaning, and Institutional & Catering.
Laureth-10 Carboxylic Acid is used Other Institutional & Industrial Care, Vehicle & Machinery, Personal Hygiene, Hand Hygiene, Processing & Packaging, and Food & Beverage Manufacturing.


Hair Care Applications of Laureth-10 Carboxylic Acid: Hair Color, Home Care Applications, Household Cleaners, I&I Cleaning Applications, Automotive Cleaners, and Industrial Cleaners.
Laureth-10 Carboxylic Acid is used as a degreaser component in the leather industry.



FUNCTIONS OF LAURETH-10 CARBOXYLIC ACID:
*Cleansing :
Laureth-10 Carboxylic Acid helps to keep a clean surface
*Surfactant :
Laureth-10 Carboxylic Acid reduces the surface tension of cosmetics and contributes to the even distribution of the product when it is used



FUNCTIONS OF LAURETH-10 CARBOXYLIC ACID:
*Surfactant,
*Surfactant (Anionic),
*Solubilizer,
*Foaming Agent,
*Foam Booster,
*Cosurfactant,
*Cleansing Agent



INDUSTRIES OF LAURETH-10 CARBOXYLIC ACID:
*Oral Care
*Trends
*Hair Care
*Skin Care



PROPERTIES OF LAURETH-10 CARBOXYLIC ACID:
*Co-Surfactant
*Emulsifier
*Solubilizer
*Mild



FUNCTIONS OF LAURETH-10 CARBOXYLIC ACID IN COSMETIC PRODUCTS:
*CLEANSING
Cleans skin, hair or teeth
*SURFACTANT - CLEANSING
Surface-active agent to clean skin, hair and / or teeth



WHAT DOES LAURETH-10 CARBOXYLIC ACID DO IN A FORMULATION?
*Cleansing
*Surfactant



PERFORMANCE OF LAURETH-10 CARBOXYLIC ACID:
1, Laureth-10 Carboxylic Acid has good decontamination, emulsification, dispersibility and dispersion of calcium soap.
2, Laureth-10 Carboxylic Acid has good foaming power and foam stability.
3, Laureth-10 Carboxylic Acid has resistance to acid and alkali, hard water and oxidants, reducing agents.
4, Laureth-10 Carboxylic Acid has good compatibility, no interference with the performance of the cation.
5, Laureth-10 Carboxylic Acid has solubilization performance, suitable for preparation of functional transparent products.
6. Laureth-10 Carboxylic Acid is easy to biodegrade.



CHARACTERISTICS OF LAURETH-10 CARBOXYLIC ACID:
1. Good foaming performance and detergency;
2. Strong resistance to hard water, high solubility in water;
3. Mildness, good compatibility with other surfactants;
4. Be stable under acid, alkali, high temperature, low irritation to the skin and clothes



FAMILIES OF LAURETH-10 CARBOXYLIC ACID:
*Cleaning Aids
*Emulsifiers & Demulsifiers



FUNCTIONAL ADDITIVES OF LAURETH-10 CARBOXYLIC ACID:
*Foam Control Agents,
*Other Functional Additives,
*Performance Additives



FUNCTIONALS OF LAURETH-10 CARBOXYLIC ACID:
*Emulsifiers, Solubilizers & Dispersants
*Soaps & Surfactants
*Anionic Surfactants,
*Blends & Other Surfactants
*Surfactants & Cleansers
*Anionic Surfactants



CLEANING INGREDIENTS FUNCTIONS OF LAURETH-10 CARBOXYLIC ACID:
*Cleansing Agent,
*Co Emulsifier,
*Cosurfactant,
*Emulsifier,
*Foam Booster,
*Foaming Agent,
*Solubilizer,
*Surfactant,
*Surfactant (Anionic)



FEATURES AND BENEFITS OF LAURETH-10 CARBOXYLIC ACID:
*Mild



MARKETS OF LAURETH-10 CARBOXYLIC ACID:
*Food & Nutrition,
*HI&I Care,
*Personal Care



FIRST AID MEASURES of LAURETH-10 CARBOXYLIC ACID:
-General advice:
Consult a physician.
-If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
-In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
-In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes.
Consult a physician.
-If swallowed:
Rinse mouth with water.
Consult a physician.



ACCIDENTAL RELEASE MEASURES of LAURETH-10 CARBOXYLIC ACID:
-Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.



FIRE FIGHTING MEASURES of LAURETH-10 CARBOXYLIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURETH-10 CARBOXYLIC ACID:
-Control parameters:
*Occupational Exposure limit values: no data available
*Biological limit values: no data available
-Appropriate engineering controls:
Wash hands before breaks and at the end of workday.
-Individual protection measures, such as personal protective equipment (PPE):
*Eye/face protection:
Safety glasses.
*Skin protection:
Handle with gloves.



HANDLING and STORAGE of LAURETH-10 CARBOXYLIC ACID:
-Conditions for safe storage, including any incompatibilities:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of LAURETH-10 CARBOXYLIC ACID:
-Reactivity: no data available
-Chemical stability:
Stable under recommended storage conditions.



SYNONYMS:
LAURETH-10 CARBOXYLIC ACID
LAURETH-10 CARBOXYLIC ACID [INCI]
PEG-10 LAURYL ETHER CARBOXYLIC ACID
POLYOXYETHYLENE (10) LAURYL ETHER CARBOXYLIC ACID
POLYOXYETHYLENE (9) CARBOXYMETHYL DODECYL ETHER

DESCRIPTION:
LAURETH-11 Carboxylic Acid is a crypto-anionic surfactant - laureth-11 carboxylic acid - (it combines the properties of the anionic and non-ionic surfactants).
LAURETH-11 Carboxylic Acid has good foaming and solubilizing properties with excellent mildness to skin and mucous membranes


CAS Number, 27306-90-7
Chem/IUPAC Name:, Poly(oxy-1,2-ethanediyl)



SYNONYMS OF LAURETH-11 CARBOXYLIC ACID:
Laureth-11 carboxylic acid,AKYPO RLM 100,CK7N38KKFK,CORUM 3611EMPICOL CBJ,PEG-11 LAURYL ETHER CARBOXYLIC ACID,POLYETHYLENE GLYCOL (11) LAURYL ETHER CARBOXYLIC ACID,POLYOXYETHYLENE (11) LAURYL ETHER CARBOXYLIC ACID, alpha.-carboxymethyl-.omega.-dodecyloxy-, (10 mol EO average molar ratio) Laureth-11 Carboxylic Acid, PEG-11 Lauryl Ether Carboxylic Acid, Polyethylene Glycol (11) Lauryl Ether Carboxylic Acid, Polyoxyethylene (11) Lauryl Ether Carboxylic Acid, GLYCOLIC ACID ETHOXYLATE LAURYL ETHER, M N CA. 690; GLYCOLIC ACID ETHOXYLATE LAURYL ETHER, M N CA. 360; GLYCOLIC ACID ETHOXYLATE LAURYL ETHER, M N CA. 460; Glycolic acid ethoxylate lauryl ether average Mn ~360; Glycolic acid ethoxylate lauryl ether average Mn ~690; Glycolic acid ethoxylate lauryl ether average Mn ~460;GLYCOLIC ACID ETHOXYLATE LAURYL ETHER;Laureth-11 carboxylic acid;Glycolic acid ethoxylate lauryl ether; PEG-11 lauryl ether carboxylic acid; POE (11) lauryl ether carboxylic acid


CHEMICAL AND PHYSICAL PROPERTIES OF LAURETH-11 CARBOXYLIC ACID:
Molecular Weight
288.42 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
XLogP3-AA
5.1
Computed by XLogP3 3.0 (PubChem release 2021.10.14)
Hydrogen Bond Donor Count
1
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Hydrogen Bond Acceptor Count
4
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Rotatable Bond Count
16
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Exact Mass
288.23005950 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
Monoisotopic Mass
288.23005950 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
Topological Polar Surface Area
55.8Ų
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Heavy Atom Count
20
Computed by PubChem
Formal Charge
0
Computed by PubChem
Complexity
207
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Isotope Atom Count
0
Computed by PubChem
Defined Atom Stereocenter Count
0
Computed by PubChem
Undefined Atom Stereocenter Count
0
Computed by PubChem
Defined Bond Stereocenter Count
0
Computed by PubChem
Undefined Bond Stereocenter Count
0
Computed by PubChem
Covalently-Bonded Unit Count
1
Computed by PubChem
Compound Is Canonicalized
Yes





SAFETY INFORMATION ABOUT LAURETH-11 CARBOXYLIC ACID:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product

LAURETH-15, peg-15 lauryl ether, polyethylene glycol (15) lauryl ether, polyethylene glycol (15) lauryl ether, polyethylene glycol (15) monolauryl ether, polyoxyethylene (15) lauryl ether, polyoxyethylene (15) monolauryl ether, LAURETH-15, N° CAS : 9002-92-0, Nom INCI : LAURETH-15. Classification : Composé éthoxylé : Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-16, LAURETH-16, peg-16 lauryl ether, polyethylene glycol (16) lauryl ether, polyethylene glycol (16) lauryl ether, polyethylene glycol (16) monolauryl ether, polyoxyethylene (16) lauryl ether, polyoxyethylene (16) monolauryl ether, LAURETH-16, N° CAS : 9002-92-0. Nom INCI : LAURETH-16. Classification : Composé éthoxylé. Ses fonctions (INCI) : Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

Numéro CAS : 3055-93-4, Noms français :((DODECYLOXY)-2 ETHOXY)-2 ETHANOL, (DODECYLOXY-2 ETHOXY)-2 ETHANOL, Noms anglais : ETHANOL, 2-(2-(DODECYLOXY)ETHOXY)-, LAURYL ALCOHOL MONO(OXYETHYLENE) ETHANOL, laureth-2, synonyme : Laurylalcohol-2-polyglycolether (Nom chimique), Inci : laureth-2, Cas : 68439-50-9, EC : 500-213-3 synonyme : Laurylalcohol-3-polyglycolether (Nom chimique), Inci : laureth-3, Cas : 68439-50-9, EC : 500-213-3 synonyme : Laurylalcohol-4-polyglycolether (Nom chimique), Inci : laureth-4, Cas : 68439-50-9, EC : 500-213-3 ; 2-(2-(Dodecyloxy)ethoxy)ethanol; 2-[2-(dodecyloxy)ethoxy]ethanol; 2-[[]2-(dodecyloxy)ethoxy]ethanol; Bis(oxyethylene) dodecyl ether; Diethylene glycol dodecyl ether; Diethylene glycol monododecyl ether; Diethyleneglycol lauryl ether; Diethyleneglycol monolauryl ether ; Dodecyl diethylene glycol; Ethanol, 2-(2-(dodecyloxy)ethoxy)-; LA 2; LA 2 (alcohol); Laureth-2; Lauryl alcohol mono(oxyethylene) ethanol. : 2-(2-dodecoxyethoxy)ethanol; 2-[2-(dodecyloxy)ethoxy]ethan-1-ol; 2-¢2-(DODECYLOXY)ETHOXY!ETHANOL; Fettalkoholethoxylat C12 2EO

LAURETH-2, peg-2 lauryl ether, polyethylene glycol (2) lauryl ether, polyethylene glycol (2) lauryl ether, polyethylene glycol (2) monolauryl ether, polyoxyethylene (2) lauryl ether, polyoxyethylene (2) monolauryl ether, LAURETH-2, Laureth-2 (éthoxylé), N° CAS : 3055-93-4 / 9002-92-0 / 68439-50-9, Nom INCI : LAURETH-2, Nom chimique : 2-[2-(Dodecyloxy)ethoxy]ethanol, N° EINECS/ELINCS : 221-279-7 / 500-002-6 / 500-213-3. Classification : Composé éthoxylé. Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

Nom INCI : LAURETH-2 PHOSPHATE Nom chimique : 2-[2-(Dodecyloxy)ethoxy]ethanol phosphate Classification : Composé éthoxylé Ses fonctions (INCI) Agent nettoyant : Aide à garder une surface propre

LAURETH-20, peg-20 lauryl ether, polyethylene glycol (20) lauryl ether, polyethylene glycol (20) lauryl ether, polyethylene glycol (20) monolauryl ether, polyoxyethylene (20) lauryl ether, polyoxyethylene (20) monolauryl ether, LAURETH-20, N° CAS : 9002-92-0, Nom INCI : LAURETH-20, Classification : Composé éthoxylé. Ses fonctions (INCI). Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-21, peg-21 lauryl ether, polyethylene glycol (21) lauryl ether, polyethylene glycol (21) lauryl ether, polyethylene glycol (21) monolauryl ether, polyoxyethylene (21) lauryl ether, polyoxyethylene (21) monolauryl ether, LAURETH-21. N° CAS : 9002-92-0. Nom INCI : LAURETH-21. Classification : Composé éthoxylé Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre.Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-23, peg-23 lauryl ether, polyethylene glycol (23) lauryl ether, polyethylene glycol (23) lauryl ether, polyethylene glycol (23) monolauryl ether, polyoxyethylene (23) lauryl ether, polyoxyethylene (23) monolauryl ether, N° CAS : 9002-92-0. Origine(s) : Végétale, Synthétique. Nom INCI : LAURETH-23. Le Laureth-23 est un tensioactif non ionique préparé à partir d'alcool laurylique et de 23 moles d'oxyde d'éthylène. Il est utilisé en cosmétique comme tensioactif et émulsifiant : HLB (16.9). Il permet de créer des émulsions de type huile dans eau.Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

C12 Alcohol, predominately linear 23 EO; Tricosaethylene glycol mono-N-dodecyl ether; Polyoxyethylene (23) lauryl ether cas no: 9002-92-0

LAURETH-25, LAURETH-25, LAURETH-25, peg-25 lauryl ether, polyethylene glycol (25) lauryl ether, polyethylene glycol (25) lauryl ether, polyethylene glycol (25) monolauryl ether, polyoxyethylene (25) lauryl ether, polyoxyethylene (25) monolauryl ether, N° CAS : 9002-92-0, Nom INCI : LAURETH-25. Classification : Composé éthoxylé. Ses fonctions (INCI) : Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-30, LAURETH-30, LAURETH-30, peg-30 lauryl ether, polyethylene glycol (30) lauryl ether, polyethylene glycol (30) lauryl ether, polyethylene glycol (30) monolauryl ether, polyoxyethylene (30) lauryl ether, polyoxyethylene (30) monolauryl ether, LAURETH-30, N° CAS : 9002-92-0. Nom INCI : LAURETH-30 Classification : Composé éthoxylé.Ses fonctions (INCI) : Agent nettoyant : Aide à garder une surface propre. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-4, peg-4 lauryl ether, polyethylene glycol (4) lauryl ether, polyethylene glycol (4) lauryl ether, polyethylene glycol (4) monolauryl ether, polyoxyethylene (4) lauryl ether, polyoxyethylene (4) monolauryl ether, LAURETH-4, N° CAS : 5274-68-0 / 9002-92-0 / 68439-50-9, Nom INCI : LAURETH-4, N° EINECS/ELINCS : 226-097-1 / 500-002-6 / 500-213-3, Classification : Composé éthoxylé,Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

Synonyms: 8/5000 Emulsifier earth-sized - 3;C12-14 alcohol polyether;Penetrant JFC;AEO-3、4、5、7、9、15、20;Alcohols, C12-14, ethoxylated;FATTYALCOHOL(C12-C14)POLYGLYCOL(3OEO)ETHER;POLYALKOXYLATEDALIPHATICALCOHOL;Alcohol-(C12-C14), ethoxylated CAS: 68439-50-9

LAURETH-50, peg-50 lauryl ether, polyethylene glycol (50) lauryl ether, polyethylene glycol (50) lauryl ether, polyethylene glycol (50) monolauryl ether, polyoxyethylene (50) lauryl ether, polyoxyethylene (50) monolauryl ether, LAURETH-50, Classification : Composé éthoxylé. Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-6, N° CAS : 3055-96-7 / 68439-50-9, Nom INCI : LAURETH-6, peg-6 lauryl ether, polyethylene glycol (6) lauryl ether, polyethylene glycol (6) lauryl ether, polyethylene glycol (6) monolauryl ether, polyoxyethylene (6) lauryl ether, polyoxyethylene (6) monolauryl ether. Nom chimique : 3,6,9,12,15,18-Hexaoxatriacontan-1-ol, N° EINECS/ELINCS : 221-282-3 / 500-213-3, Classification : Composé éthoxylé. Ses fonctions (INCI). Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURETH-7, N° CAS : 3055-96-7 / 68439-50-9, Nom INCI : LAURETH-7, peg-7 lauryl ether, polyethylene glycol (7) lauryl ether, polyethylene glycol (7) lauryl ether, polyethylene glycol (7) monolauryl ether, polyoxyethylene (7) lauryl ether, polyoxyethylene (7) monolauryl ether, LAURETH-7, N° CAS : 3055-97-8 / 68439-50-9 / 9002-92-0. Nom INCI : LAURETH-7. Nom chimique : 3,6,9,12,15,18,21-Heptaoxatritriacontanol. N° EINECS/ELINCS : 221-283-9 / 500-213-3 / 500-002-6. Classification : Composé éthoxylé. Ses fonctions (INCI) : Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL) ; ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE ;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

Laureth-6 Carboxylic Acid is an organic acid.


CAS Number: 27306-90-7
Chem/IUPAC Name: Poly(oxy-1,2-ethanediyl),.alpha.-carboxymethyl-.omega.-dodecyloxy-, (5 mol EO average molar ratio)
Chemical family: Polyoxyethylene alkylether carboxylic acid
INCI Name: Laureth-6 Carboxylic Acid
Molecular Formula: C24H48O8


Laureth-6 Carboxylic Acid is an essential additive for long-lifetime metalworking fluids.
Laureth-6 Carboxylic Acid is characterized by their outstanding hard water and electrolyte tolerance compared to other emulsifiers used in metalworking.
Dive into the world of Laureth-6 Carboxylic Acid , a powerful anionic surfactant renowned for its superior detergency and foaming abilities.


This versatile chemical compound, Laureth-6 Carboxylic Acid, is utilized in a range of applications, from personal care products to industrial cleaners, and offers excellent emulsifying and wetting properties.
It's ability to boost foam production and effectively remove dirt and oils makes Laureth-6 Carboxylic Acid a valuable addition to your formulations.


Laureth-6 Carboxylic Acid is a wide range of secondary surfactants with excellent tolerance against hard water.
Laureth-6 Carboxylic Acid is a crypto-anionic surfactant - laureth-6 carboxylic acid - (Laureth-6 Carboxylic Acidcombines the properties of the anionic and non-ionic surfactants).


Laureth-6 Carboxylic Acid has good foaming and solubilizing properties being very mild for the skin.
Laureth-6 Carboxylic Acid is a mild co-surfactant and functions as an emulsifier and solubilizer.
Laureth-6 Carboxylic Acid is extremely mild and compatible with other surfactants as well as ideal as co-surfactants and coupling agents.
Laureth-6 Carboxylic Acid has all the qualities that show outstanding pH stability and high tolerance against electrolytes and builders.


"Laureth-" refers to a PEG-(polyethylene glycol-) ether of lauryl alcohol.
The number behind "laureth-" refers to the average number of molecular units -CH2-CH2-O-.
"Carboxylic acid" refers generally to a carboxylic or carbonic acid.



USES and APPLICATIONS of LAURETH-6 CARBOXYLIC ACID:
Laureth-6 Carboxylic Acid is used high foaming mild co-surfactant for cosmetic applications.
Laureth-6 Carboxylic Acid is used Paper industry for waste paper deinking and softening agent formula.
Laureth-6 Carboxylic Acid is used as a degreaser component in the leather industry.


Laureth-6 Carboxylic Acid is used as foaming agent for foam fire extinguishing.
Laureth-6 Carboxylic Acid is depending on the carbon chain length and the ethoxylation degree the products show characteristic application properties.
Laureth-6 Carboxylic Acid brings excellent lime soap dispersing properties and adds some anti-corrosion benefits.


Laureth-6 Carboxylic Acid has all the qualities that show outstanding pH stability and high tolerance against electrolytes and builders.
Laureth-6 Carboxylic Acid is an extremely mild surfactant with good emulsifying properties and insensitive to water hardness, it substantially improves the skin’s tolerance of cleansers.


Laureth-6 Carboxylic Acid is used surfactant for mild personal care products (shampoos, shower gels, foam baths, other low-irritation formulations); surfactant for industrial applications (agrochemicals, textile treatment); detergent for carpet cleaners especially aerosols.
Applications of Laureth-6 Carboxylic Acid: Beauty & Care, Hair Care, Oral Care, Skin Care, Home Care, Auto Care, Carpet & Upholstery, Dish Care, and Laundry & Fabric Care.


Laureth-6 Carboxylic Acid is used in Hard water stable.
Laureth-6 Carboxylic Acid is used applicable in hypochlorite solutions.
Laureth-6 Carboxylic Acid is used emulsifying and solubilizing properties.


Other Home Care Applications of Laureth-6 Carboxylic Acid
Surface Care Institutional & Industrial Care, Commercial Laundry, Food Facility Cleaning & Sanitization, Industrial Cleaning, and Institutional & Catering.
Laureth-6 Carboxylic Acid is mainly used in various shampoos and personal care liquid products, especially for the preparation of baby shampoo, also used as detergents and industrial emulsifiers, dispersing agents, foaming agents and wetting agent.


Laureth-6 Carboxylic Acid combines the properties of the anionic and non-ionic surfactants.
Laureth-6 Carboxylic Acid has good foaming and solubilizing properties with excellent mildness to skin and mucous membranes
Laureth-6 Carboxylic Acid is used as emulsifier or coemulsifier for paste cosmetics.


Laureth-6 Carboxylic Acid is used Other Institutional & Industrial Care, Vehicle & Machinery, Personal Hygiene, Hand Hygiene, Processing & Packaging, and Food & Beverage Manufacturing.
Hair Care Applications of Laureth-6 Carboxylic Acid: Hair Color, Home Care Applications, Household Cleaners, I&I Cleaning Applications, Automotive Cleaners, and Industrial Cleaners.


Laureth-6 Carboxylic Acid uses and applications include: Surfactant, emulsifier, dispersant, superfatting agent, foam stabilizer for emulsions, detergents, shampoos, bubble baths.
Laureth-6 Carboxylic Acid is used with overall physico-chemical stability, that improves lathering, enhances quat's and hair dyes efficiency providing combined benefits of nonionic and anionic surfactants.


Laureth-6 Carboxylic Acid is used Mild shampoo, body wash, facial cleanser, hand sanitizer and other personal cleaning and protection products.
Laureth-6 Carboxylic Acid is used mixed into the soap block mild, calcium soap dispersion, foam performance and bath feeling.
Laureth-6 Carboxylic Acid is used for household detergents, industrial cleaning agents and phosphorus free detergents.


Laureth-6 Carboxylic Acid is used in textile industry refining, mercerizing, bleaching, soft, dyeing and other processes.
Laureth-6 Carboxylic Acid is used as an emulsifier and viscosity reducer resistant to high concentration electrolyte, it is used in tertiary oil recovery and oil transportation to provide crude oil recovery.


Laureth-6 Carboxylic Acid is particularly suitable for high-quality formulations, baby shampoos, and products designed for sensitive skin.
Laureth-6 Carboxylic Acid can be used in conveyor belt lubricants.



FUNCTIONS OF LAURETH-6 CARBOXYLIC ACID:
*Surfactant,
*Surfactant (Anionic),
*Solubilizer,
*Foaming Agent,
*Foam Booster,
*Cosurfactant,
*Cleansing Agent



INDUSTRIES OF LAURETH-6 CARBOXYLIC ACID:
*Oral Care
*Trends
*Hair Care
*Skin Care



PROPERTIES OF LAURETH-6 CARBOXYLIC ACID:
*Co-Surfactant
*Emulsifier
*Solubilizer
*Mild



FUNCTIONS OF LAURETH-6 CARBOXYLIC ACID IN COSMETIC PRODUCTS:
*CLEANSING
Cleans skin, hair or teeth
*SURFACTANT - CLEANSING
Surface-active agent to clean skin, hair and / or teeth



WHAT DOES LAURETH-6 CARBOXYLIC ACID DO IN A FORMULATION?
*Cleansing
*Surfactant



FUNCTIONS OF LAURETH-6 CARBOXYLIC ACID:
*Cleansing :
Laureth-6 Carboxylic Acid helps to keep a clean surface
*Surfactant :
Laureth-6 Carboxylic Acid reduces the surface tension of cosmetics and contributes to the even distribution of the product when it is used



PERFORMANCE OF LAURETH-6 CARBOXYLIC ACID:
1, Laureth-6 Carboxylic Acid has good decontamination, emulsification, dispersibility and dispersion of calcium soap.
2, Laureth-6 Carboxylic Acid has good foaming power and foam stability.
3, Laureth-6 Carboxylic Acid has resistance to acid and alkali, hard water and oxidants, reducing agents.
4, Laureth-6 Carboxylic Acid has good compatibility, no interference with the performance of the cation.
5, Laureth-6 Carboxylic Acid has solubilization performance, suitable for preparation of functional transparent products.
6. Laureth-6 Carboxylic Acid is easy to biodegrade.



CHARACTERISTICS OF LAURETH-6 CARBOXYLIC ACID:
1. Good foaming performance and detergency;
2. Strong resistance to hard water, high solubility in water;
3. Mildness, good compatibility with other surfactants;
4. Be stable under acid, alkali, high temperature, low irritation to the skin and clothes



FAMILIES OF LAURETH-6 CARBOXYLIC ACID:
*Cleaning Aids
*Emulsifiers & Demulsifiers



FUNCTIONAL ADDITIVES OF LAURETH-6 CARBOXYLIC ACID:
*Foam Control Agents,
*Other Functional Additives,
*Performance Additives



FUNCTIONALS OF LAURETH-6 CARBOXYLIC ACID:
*Emulsifiers, Solubilizers & Dispersants
*Soaps & Surfactants
*Anionic Surfactants,
*Blends & Other Surfactants
*Surfactants & Cleansers
*Anionic Surfactants



CLEANING INGREDIENTS FUNCTIONS OF LAURETH-6 CARBOXYLIC ACID:
*Cleansing Agent,
*Co Emulsifier,
*Cosurfactant,
*Emulsifier,
*Foam Booster,
*Foaming Agent,
*Solubilizer,
*Surfactant,
*Surfactant (Anionic)



FEATURES AND BENEFITS OF LAURETH-6 CARBOXYLIC ACID:
*Mild



MARKETS OF LAURETH-6 CARBOXYLIC ACID:
*Food & Nutrition,
*HI&I Care,
*Personal Care



PHYSICAL and CHEMICAL PROPERTIES of LAURETH-6 CARBOXYLIC ACID:
Boiling point: 552.2±45.0 °C(Predicted)
Density: 1.015±0.06 g/cm3(Predicted)
pka: 3.39±0.10(Predicted)
FDA UNII: 1LS4J5883P
Molecular Weight: 464.6g/mol
Molecular Formula: C24H48O8
Compound Is Canonicalized: True
XLogP3-AA: 4.5
Exact Mass: 464.33491849
Monoisotopic Mass: 464.33491849
Complexity: 368
Rotatable Bond Count: 28
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 8
Topological Polar Surface Area: 92.7
Heavy Atom Count: 32
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Isotope Atom Count: 0
Covalently-Bonded Unit Count: 1



FIRST AID MEASURES of LAURETH-6 CARBOXYLIC ACID:
-General advice:
Consult a physician.
-If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
-In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
-In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes.
Consult a physician.
-If swallowed:
Rinse mouth with water.
Consult a physician.



ACCIDENTAL RELEASE MEASURES of LAURETH-6 CARBOXYLIC ACID:
-Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.



FIRE FIGHTING MEASURES of LAURETH-6 CARBOXYLIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURETH-6 CARBOXYLIC ACID:
-Control parameters:
*Occupational Exposure limit values: no data available
*Biological limit values: no data available
-Appropriate engineering controls:
Wash hands before breaks and at the end of workday.
-Individual protection measures, such as personal protective equipment (PPE):
*Eye/face protection:
Safety glasses.
*Skin protection:
Handle with gloves.



HANDLING and STORAGE of LAURETH-6 CARBOXYLIC ACID:
-Conditions for safe storage, including any incompatibilities:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of LAURETH-6 CARBOXYLIC ACID:
-Reactivity: no data available
-Chemical stability:
Stable under recommended storage conditions.



SYNONYMS:
3,6,9,12,15,18-Hexaoxatriacontanoic acid
AKYPO RLM 45 CA
LAURETH-6 CARBOXYLIC ACID
LAURETH-6 CARBOXYLIC ACID [INCI]
PEG-6 LAURYL ETHER CARBOXYLIC ACID
POLYOXYETHYLENE (6) LAURYL ETHER CARBOXYLIC ACID
Laureth-6 carboxylic acid
PEG-6 lauryl ether carboxylic acid
PEG 300 lauryl ether carboxylic acid
POE (6) lauryl ether carboxylic acid

LAURETH-7 CITRATE, N° CAS : 161756-30-5, Nom INCI : LAURETH-7 CITRATE. Classification : Composé éthoxylé. Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation

LAURETH-7 CARBOXYLIC ACID = 2-(2-DODECOXYETHOXY)ACETIC ACID = LAURYL POLYGLYCOL ETHER CARBOXYLIC ACID


CAS Number: 27306-90-7 / 33939-64-9
EC Number: 608-079-9
Molecular Formula: C16H32O4


Laureth-7 carboxylic acid is a sodium salt of the carboxylic acid derived from laureth-7.
Laureth-7 carboxylic acid is a crypto-anionic surfactant.
Laureth-7 carboxylic acid combines the properties of the anionic and non-ionic surfactants.
Laureth-7 carboxylic acid is a non-ionic surfactant based on C12-C16 lauryl alcohol.


Laureth-7 carboxylic acid belongs to the group of fatty alcohol ethoxylates with the INCI name: C12-16 Laureth-7.
Laureth-7 carboxylic acid is well soluble in water.
The HLB value for Laureth-7 carboxylic acid is approximate 13, and the solidification point is 10°C.
Laureth-7 carboxylic acid is easily biodegradable in the natural environment.


Laureth-7 carboxylic acid shows high chemical activity in acidic and neutral baths and diluted alkalies.
Laureth-7 carboxylic acid is a non-ionic surfactant from the group of fatty alcohol ethoxylates, very good solubility in water.
Laureth-7 carboxylic acid is biodegradable product.
Laureth-7 carboxylic acid has been identified in human blood.


Technically Laureth-7 carboxylic acid is part of the human exposome.
Laureth-7 carboxylic acid is also excellent in mixtures with anionic and cationic surfactants.
Carboxylic acids are compounds containing a carboxylic acid group with the formula -C(=O)OH.
Based on a literature review very few articles have been published on Laureth-7 carboxylic acid.


Laureth-7 carboxylic acid combines the properties of the anionic and non-ionic surfactants.
Laureth-7 carboxylic acid is an extremely mild surfactant with good emulsifying properties and insensitive to water hardness, Laureth-7 carboxylic acid substantially improves the skin’s tolerance of cleansers.
Laureth-7 carboxylic acid is classified as cleansing, foaming and surfactant.


In formulations containing alkyl sulphates and alkyl aryl sulfonates, Laureth-7 carboxylic acid shows a synergistic cleaning effect.
Laureth-7 carboxylic acid belongs to the class of organic compounds known as carboxylic acids.
Laureth-7 carboxylic acid has good foaming and solubilizing properties with excellent mildness to skin and mucous membranes.
Laureth-7 carboxylic acid comes in a highly concentrated form.


The content of the active ingredient in the product exceeds 99%.
Laureth-7 carboxylic acid has the additional advantage of being highly compatible with non-ionic excipients.
Laureth-7 carboxylic acid is an AKYPO RLM product.
The Akypo products offer a wide range of secondary surfactants with excellent tolerance against hard water.


Depending on the carbon chain length and the ethoxylation degree the products show characteristic application properties.
Akypo LF grades, with a chain length from C4 to C8, are low foaming surfactants with high dispersing and hydrotropic abilities.
Akypo RLM products have a C12-C14 alkyl chain and their degree of ethoxylation ranges from 2.5 to 10 EO.


They offer good foaming at different pHs.
Similar to the Akypo soft grades they are mild co-surfactants and function as emulsifiers and solubilizers.
Finally the Akypo ro products bring excellent lime soap dispersing properties and add some anti-corrosion benefits.
They can be used in conveyor belt lubricants.



USES and APPLICATIONS of LAURETH-7 CARBOXYLIC ACID:
Laureth-7 carboxylic acid is Mild rapid foam-booster with improved foam behaviour for Personal Care products and for all kind of cleaners including Car Care, Dishwashing, Household, Industrial and Instituional.
Laureth-7 carboxylic acid is an intermediate for resins, plasticizers, and rubber chemicals.
Laureth-7 carboxylic acid is also an ingredient that removes excess dyes from the bath in the final stage of textiles.


It's very good fabric wetting properties (especially of cotton), Laureth-7 carboxylic acid is suitable as an ingredient in bleaching compositions for raw knitwear and cotton fabrics.
Laureth-7 carboxylic acid is used Sensitive skin products, Toothpaste, Mouthwash, Household cleaners, Laundry care, LDLD liquid detergents, and Surface care.


Laureth-7 carboxylic acid is particularly suitable for high-quality formulations, baby shampoos, and products designed for sensitive skin.
Laureth-7 carboxylic acid provides cleansing function as well as emulsifying in a hair and skin care systems.
Laureth-7 carboxylic acid is used Face and body care cosmetics (scrubs, moisturisers, anti-acne creams, anti-wrinkle creams, eye creams, hand creams, body lotions, sunscreen creams), Face and body cleansers (face wash gels, body wash and gels, liquid soaps, bubble baths).


Laureth-7 carboxylic acid is also used as a lubricant in the textile industry, as a humectant and softening agent for hides, as an alkalizing agent and surfactant in pharmaceuticals, as an absorbent for acid gases, and in organic syntheses.
Laureth-7 carboxylic acid is perfectly suited for the textile and clothing industry.
The uses of Laureth-7 carboxylic acid are in rinse-off products, and are in hair coloring formulations.


Laureth-7 carboxylic acid is used in fibre pretreatment processes as a component of mixtures dedicated to removing greasy oil stains (mineral oils) from fabrics and knitwear.
Laureth-7 carboxylic acid is highly compatible with other non-ionic surfactants, as well as anionic and cationic surfactants.
Laureth-7 carboxylic acid is suitable for use in environments of reducing and oxidising agents and in hard and cold water.


Laureth-7 carboxylic acid is used Bathroom cleaners, Industrial cleaners, Institutional cleaners, Hotel cleaners, Restaurant cleaners, Catering facility cleaners, Food facility cleaners, Beverage facility cleaners, CIP cleaners, OPC cleaners, and Surfactant
Laureth-7 carboxylic acid is used Efficient cleaning, High foaming mild co-surfactant for cosmetic applications, Applicable in hypochlorite solution, and Emulsifying and solubilizing properties


Laureth-7 carboxylic acid is used in the production of cosmetic products such as skincare and cleansing cosmetics and hair care cosmetics, and primarily in hair coloring products.
Laureth-7 carboxylic acid is used Foaming co-surfactant, enhances quat's and dyes efficiency; with solubilizing properties and very mild for the skin, and Foaming surfactant with excellent physico-chemical stability.


Laureth-7 carboxylic acid has a wide range of functions in formulations – wetting agent, washing agent, emulsifying and dispersing agent.
Laureth-7 carboxylic acid is used Hair color protection, Skin cleansing, Shower gel, Shower cream, Shower oil, Liquid hand soap, Foaming bath products, Baby and child skin cleansing, Sensitive skin products, Toothpaste, Skin Care, Creams and lotions, Face care, Body care, Hand care, Face cleanser, Eye makeup remover, Hair care, Shampoo, Hair colorants, and Hair color protection


Laureth-7 carboxylic acid is effective in acidic and neutral environments and in dilute alkalies.
Laureth-7 carboxylic acid functions in cosmetics as pH adjusters.
Laureth-7 carboxylic acid acts as both anionic surfactant and co-surfactant.
Laureth-7 carboxylic acid functions as a hair fixative.


Laureth carboxylic acids function as surfactants.
Laureth-7 carboxylic acid is used Skin cleansing, Shower gel, Shower cream, Shower oil, Liquid hand soap, Foaming bath products, Baby and child skin cleansing, Solubilizer, Skin care, Face cleanser, Eye makeup remover, Hair care, Shampoo, and Hair colorants.
Laureth-7 carboxylic acid is used in non-coloring hair preparations and rinse-off formulations, and in leave-on formulations.


Owing to Laureth-7 carboxylic acid's wetting, emulsifying and dispersing properties as well as very good detergency properties, Laureth-7 carboxylic acid is used as a basic surfactant in the production of detergents (powders and liquids), household and professional cleaning products and hand cleaning formulations.
Laureth-7 carboxylic acid is used in the manufacture of emulsifiers and dispersing agents for textile specialties, agricultural chemicals, waxes, mineral and vegetable oils, paraffin, polishes, cutting oils, petroleum demulsifiers, and cement additives.


Laureth-7 carboxylic acid is also a raw material often used in the manufacture of colour cosmetics, sunscreen products, shaving products and aftershave cosmetics.
Laureth-7 carboxylic acid is used Formulations for removing oil stains from knitted and woven fabrics, Additive to bleach baths in the textile industry, and Additive to washing baths after dyeing fabrics and knitwear.
Laureth-7 carboxylic acid used Colour cosmetics (make-up primers, fluids, eye shadows, concealers, bronzers), Shaving and aftershave cosmetics, and Household detergents (liquid and powdered detergents, surface cleaning agents, wash-up liquids, handwash products).


-Hair care products uses of Laureth-7 carboxylic acid: hair washing, care and styling products (shampoos, conditioners, serum, gels, styling foams)
-Cosmetic Uses of Laureth-7 carboxylic acid:
*cleansing agents
*surfactants



ALTERNATIVE PARENTS of LAURETH-7 CARBOXYLIC ACID:
*Monocarboxylic acids and derivatives
*Dialkyl ethers
*Primary alcohols
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS of LAURETH-7 CARBOXYLIC ACID:
*Monocarboxylic acid or derivatives
*Ether
*Dialkyl ether
*Carboxylic acid
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Primary alcohol
*Organooxygen compound
*Carbonyl group
*Alcohol
*Aliphatic acyclic compound



BENEFITS of LAURETH-7 CARBOXYLIC ACID:
*Personal Care
*Hair Cleansing
*Multifunctional
*Nature-derived
*Preservative-free
*Anionic surfactant
*Cleansing agent
*Foaming agent
*Emulsifier
*Stabilizer
*Disperser
*Ultra mild
*Lamellar structure
*Hydrotropic
*Hard water stable
*Organic acid
*Acid stable
*Alkaline stable
*Electrolyte stable
*Oxidizing agent stable
*Improves color uptake
*Great hair color retention
*Environmental label free
*Vegetable origin
*Readily biodegradable
*A broad spectrum of applications
*Excellent emulsifying, dispersing, wetting, washing and cleaning properties
*High resistance to acidic environments and diluted alkalis,
*High efficiency in hard water
*Very good compatibility with non-ionic, anionic and cationic surfactants
*High concentration of the active ingredient – 99% biodegradable product.



FUNCTIONS of LAURETH-7 CARBOXYLIC ACID:
*Cleansing :
Helps to keep a clean surface
*Emulsifying :
Promotes the formation of intimate mixtures between immiscible liquids by modifying the interfacial tension (water and oil).
*Foaming :
Capturing small air bubbles or other gases in a small volume of liquid by changing the surface tension of the liquid.
*Surfactant :
Reduces the surface tension of cosmetics and contributes to the even distribution of the product when Laureth-7 carboxylic acid is used.
*Dispersant
*Stabilizer



PRODUCT FAMILIES of LAURETH-7 CARBOXYLIC ACID:
-Cleaning Ingredients — Cleaning Aids:
*Emulsifiers & Demulsifiers
-Cleaning Ingredients — Functional Additives:
*Foam Control Agents
*Other Functional Additives
-Cosmetic Ingredients — Functionals:
*Emulsifiers
*Solubilizers & Dispersants
*Other Functional Additives
-Cleaning Ingredients — Soaps & Surfactants:
*Anionic Surfactants
-Cosmetic Ingredients — Surfactants & Cleansers:
*Anionic Surfactants



PROPERTIES of LAURETH-7 CARBOXYLIC ACID:
*Chemical stability
*Solubilizer & Emulsifier
*Foam booster
*Foaming
*Surfactant (Anionic)
*Cosurfactant
*Cleansing Agent
*Emulsifier



PHYSICAL and CHEMICAL PROPERTIES of LAURETH-7 CARBOXYLIC ACID:
Molecular Weight: 288.42
XLogP3-AA: 5.1
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 16
Exact Mass: 288.23005950
Monoisotopic Mass: 288.23005950
Topological Polar Surface Area: 55.8 Ų
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 207
Isotope Atom Count: 0

Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Average Mass: 288.428 g/mol
Monoisotopic Mass: 288.23006 g/mol
XLogP3-AA: 5.1
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 16

Exact Mass: 288.23005950
Monoisotopic Mass: 288.23005950
Topological Polar Surface Area: 55.8 Ų
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 207
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Physical state: no data available

Colour: no data available
Odour: no data available
Melting point/ freezing point: no data available
Boiling point or initial boiling point and boiling range: 410.4oC at 760mmHg
Flammability: no data available
Lower and upper explosion limit / flammability limit: no data available
Flash point: 138.1oC
Auto-ignition temperature: no data available
Decomposition temperature: no data available
pH: no data available
Kinematic viscosity: no data available
Solubility: no data available
Partition coefficient n-octanol/water (log value): no data available
Vapour pressure: 6.94E-08mmHg at 25°C
Density and/or relative density: 0.961g/cm3
Relative vapour density: no data available
Particle characteristics: no data available



FIRST AID MEASURES of LAURETH-7 CARBOXYLIC ACID:
-General advice:
Consult a physician.
-If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
-In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
-In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes.
Consult a physician.
-If swallowed:
Rinse mouth with water.
Consult a physician.



ACCIDENTAL RELEASE MEASURES of LAURETH-7 CARBOXYLIC ACID:
-Personal precautions, protective equipment and emergency procedures:
Use personal protective equipment.
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.



FIRE FIGHTING MEASURES of LAURETH-7 CARBOXYLIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURETH-7 CARBOXYLIC ACID:
-Control parameters:
*Occupational Exposure limit values: no data available
*Biological limit values: no data available
-Appropriate engineering controls:
Wash hands before breaks and at the end of workday.
-Individual protection measures, such as personal protective equipment (PPE):
*Eye/face protection:
Safety glasses.
*Skin protection:
Handle with gloves.



HANDLING and STORAGE of LAURETH-7 CARBOXYLIC ACID:
-Conditions for safe storage, including any incompatibilities:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of LAURETH-7 CARBOXYLIC ACID:
-Reactivity: no data available
-Chemical stability:
Stable under recommended storage conditions.



SYNONYMS:
Laureth-7 carboxylic acid
2-(2-dodecoxyethoxy)acetic acid
33939-64-9
27306-90-7
Sodium laureth-6 carboxylate
Sodium laureth-13 carboxylate
3,6-dioxaoctadecanoic acid
SCHEMBL7649590
DTXSID70181754
Poly(oxy-1,2-ethanediyl), .alpha.-(carboxymethyl)-.omega.-(dodecyloxy)-, sodium salt
2-(2-dodecoxyethoxy)acetic acid
Sodium laureth-6 carboxylate
Sodium laureth-13 carboxylate
3,6-dioxaoctadecanoic acid
[2-(Dodecyloxy)ethoxy]acetic acid
2-(2-dodecoxyethoxy)acetic acid (peg-7)
peg-10 lauryl ether carboxylic acid
poly(oxy-1,2-ethanediyl), .alpha.-carboxymethyl-.omega.-dodecyloxy-, (7 mol EO average molar ratio)
polyethylene glycol (7) lauryl ether carboxylic acid
polyoxyethylene (7) lauryl ether carboxylic acid
3,6,9,12,15-pentaoxaheptacosanoic acid
AEC4-Na
sodium 3,6,9,12,15-heptacosanoate
3,6,9,12,15-pentaoxaheptacosanoic acid
AEC4-Na
sodium 3,6,9,12,15-heptacosanoate

Poly(oxy-1,2-ethanediyl), .alpha.-hydro-.omega.-dodecyloxy-, dihydrogen citrate cas no: 161756-30-5

LAURETH-9, peg-9 lauryl ether, polyethylene glycol (9) lauryl ether, polyethylene glycol (9) lauryl ether, polyethylene glycol (9) monolauryl ether, polyoxyethylene (9) lauryl ether, polyoxyethylene (9) monolauryl ether, LAURETH-9, N° CAS : 3055-99-0 / 9002-92-0 / 68439-50-9, Nom INCI : LAURETH-9. Nom chimique : 3,6,9,12,15,18,21,24,27-Nonaoxanonatriacontan-1-ol. N° EINECS/ELINCS : 221-284-4 / 500-002-6 / 500-213-3. Classification : Composé éthoxylé. Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Noms français : ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXY-1,2-ETHANEDIYL); ALPHA-DODECYL-OMEGA-HYDROXYPOLY(OXYETHYLENE); DODECYL POLY(OXYETHYLENE) ETHER; ETHER DE MONODODECYL POLY(OXY-1,2 ETHANE); POLY(ETHYLENE OXIDE) DODECYL ETHER; POLY(OXY-1,2-ETHANEDIYL), ALPHA-DODECYL-OMEGA-HYDROXY-; POLY(OXYETHYLENE) DODECYL ETHER; POLY(OXYETHYLENE) MONODODECYL ETHER; POLYETHYLENE GLYCOL DODECYL ETHER; POLYETHYLENE GLYCOL MONODODECYL ETHER; Éther de lauryl poly(oxyéthylène). Noms anglais : ALPHA-DODECYL-OMEGA-HYDROXY-POLYOXYETHYLENE; DODECYL ALCOHOL, ETHOXYLATED; DODECYL POLY(OXYETHYLENE)ETHER; Ethoxylated lauryl alcohol;HYDROXYPOLYETHOXYDODECANE;LAURYL POLY(OXYETHYLENE) ETHER; LAURYL POLYETHYLENE GLYCOL ETHER; OXYETHYLENATED DODECYL ALCOHOL; Poly(oxyethylene) lauryl ether;POLY(OXYETHYLENE) MONOLAURYL ETHER;POLYETHOXYLATED DODECANOL; POLYETHYLENE GLYCOL LAURYL ALCOHOL ETHER; POLYETHYLENE GLYCOL LAURYL ETHER;POLYOXYETHYLENE DODECYL ALCOHOL ETHER; POLYOXYETHYLENE LAURIC ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL; POLYOXYETHYLENE LAURYL ALCOHOL ETHER;POLYOXYETHYLENE LAURYL ETHER. Utilisation et sources d'émission: Agent dispersant

LAURIC ACID; n-Dodecanoic acid; Dodecylic acid; Dodecoic acid; Laurostearic acid; Vulvic acid; 1-Undecanecarboxylic acid; Duodecylic acid; cas no: 143-07-7

Lauric acid is a naturally occurring fatty acid common in coconut oil.
Lauric Acid, also known as dodecanoate, belongs to the class of organic compounds known as medium-chain fatty acids.
Lauric acid is a middle chain-free fatty acid with strong bactericidal properties.


CAS Number: 143-07-7
EC Number: 205-582-1
MDL number: MFCD00002736
Chemical formula: C12H24O2
Linear Formula: CH3(CH2)10COOH


Lauric acid is one of several fatty acids found in coconut oil, babassu butter and other natural fats.
Lauric Acid’s a medium chain triglyceride (MCT) also naturally present in skin’s oil.
This fatty acid, Lauric Acid, plays an important role in reinforcing skin’s innate defenses by strengthening its microbiome.


As a raw material, lauric acid can appear as a colorless solid or as a slightly glossy white or yellow crystalline solid or powder.
Lauric acid is a fatty acid, esters of which occur in natural substances such as coconut milk and palm kernel oil.
Lauric acid has a role as a plant metabolite, an antibacterial agent and an algal metabolite.


Lauric acid's formula C12H24O2 responds to saturated monocarboxylic acid and corresponds to a straight chain carboxylic acid with 12 carbon atoms.
Lauric acid is a straight-chain saturated fatty acid and a medium-chain fatty acid.
Lauric acid is a conjugate acid of a dodecanoate.


Lauric acid increases total serum lipoproteins more than many other fatty acids, but mostly high-density lipoprotein (HDL).
Lauric acid belongs to the class of organic compounds known as medium-chain fatty acids.
Lauric Acid may be animal- or plant-derived.


Lauric acid is obtained from fractionation of a lauric-type oil.
Lauric Acid obtained has a melting point above 43 º C. Lauric Acid is solid at room temperature, opaque white and with a characteristic odour.
Lauric acid and myristic acid are saturated fatty acids.


Both are white solids that are very slightly soluble in water.
Lauric acid esters (principally triglycerides) are found only in vegetable fats, primarily from coconut milk and oil, laurel oil, and palm kernel oil.
In contrast, myristic acid triglycerides occur in plants and animals, notably in nutmeg butter, coconut oil, and mammalian milk.


People also use Lauric Acid as medicine.
People use lauric acid for viral infections such as the flu, common cold, genital herpes, and many other conditions, but there is no good scientific evidence to support any use.


Lauric Acid, also known as dodecanoate, belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
Lauric Acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


Lauric acid is a middle chain-free fatty acid with strong bactericidal properties.
Lauric acid derives from a hydride of a dodecane.
Lauric acid is also called dodecanoic acid.


Lauric acid is a medium-chain saturated fatty acid.
Lauric acid is a precursor to dilauroyl peroxide, a common initiator of polymerizations.
Lauric acid is found in many vegetable fats and in coconut and palm kernel oils.


Lauric acid belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
Lauric acid is one of those active parts.


Lauric Acid’s a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.
Lauric acid, myristic acid, and palmitic acid all increased LDL and HDL cholesterol concentrations as compared with carbohydrates.
Lauric acid, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.


Lauric acid is a saturated fat.
Lauric acid belongs to the group of saturated fatty acids since there is no double bond in the aliphatic chain, so its shorthand notation is 12:0.
Lauric acid is found in many vegetable fats, particularly in coconut and palm kernel oils.


Lauric Acid is properly known as dodecanoic acid, is a saturated fatty acid commonly found in coconut and palm oils, as well as in milk.
Lauric acid, CAS 143-07-7, chemical formula C12H24O2, is produced as a white crystalline powder, has a slight odor of bay oil, and is soluble in water, alcohols, phenyls, haloalkanes, and acetates.


Lauric Acid, the chemical name of which is dodecanoic acid, is a medium chain fatty acid that is found in coconut oil.
Lauric Acid is a bright white, powdery solid with a faint odor of bay oil or soap.
Lauric acid is a major component of coconut oil and palm kernel oil.


Lauric acid is a saturated fatty acid, which is found in animal and plant fats and oils, and is a major component of coconut oil and palm kernel oil.
Otherwise, Lauric Acid is relatively uncommon.
Lauric Acid is also found in human breast milk (6.2% of total fat), cow's milk (2.9%), and goat's milk (3.1%).


Lauric acid, a saturated medium-chain fatty acid with a 12-carbon backbone, is naturally found in various plant and animal fats and oils, which is a major component of palm kernel oil and coconut oil.
Lauric acid esters (principally triglycerides) are found only in vegetable fats, primarily from coconut milk and oil, laurel oil, and palm kernel oil.


The salts and esters of Lauric Acid are known as laurates.
Lauric Acid, as a component of triglycerides, comprises about half of the fatty-acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil).


Lauric acid and myristic acid are saturated fatty acids.
Lauric acid is a member of the sub-group called medium chain fatty acids or MCFA, namely fatty acids containing from 6 to 12 carbon atoms.
Their formal names are dodecanoic acid and tetradecanoic acid, respectively.


Both are white solids that are very slightly soluble in water.
Like many other fatty acids, Lauric Acid is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.
Lauric Acid is used mainly for the production of soaps and cosmetics.


For these purposes, Lauric Acid is reacted with sodium hydroxide to give sodium laurate, which is a soap.
Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
These precursors give mixtures of sodium laurate and other soaps.


Lauric acid is a precursor to dilauroyl peroxide, a common initiator of polymerizations.
Lauric acid is one of those active parts.
Lauric acid’s a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.


Lauric acid is the major fatty acid present in vegetable oils such as coconut oil in and palm kernel oil.
Lauric acid is a straight-chain, twelve-carbon medium-chain saturated fatty acid with strong bactericidal properties; the main fatty acid in coconut oil and palm kernel oil.


In nature Lauric acid is accompanied by other saturated fatty acids as caprylic acid, capric, myristic, palmitic and stearic.
Lauric acid is non-toxic, safe to handle, inexpensive, and has a long shelf life.
Lauric acid has multiple uses in cosmetics, including as an emulsifier and texture-enhancing ingredient.


Lauric acid, systematically dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.
A 12 carbon length fatty acid that can be found naturally in coconut milk, coconut oil, laurel oil, and palm kernel oil.
Lauric acid's also in breast milk.


Lauric acid, C12H24O2, also known as dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain.
Lauric acid is a bright white, powdery solid with a faint odor of bay oil or soap.
Lauric acid is also called dodecanoic acid.


The salts and esters of lauric acid are known as laurates.
Like many other fatty acids, lauric acid is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.
Lauric acid is mostly derived from the hydrolysis of coconut oil or palm kernel oil, and its subsequent distillation (approx. 50% wealth).


Lauric acidacts as a surfactant.
Lauric acidis a main renewable ingredient for production of soaps.
Lauric acidacts as a surfactant.


Lauric acidis fatty acid derived from renewable vegetable oils.
Lauric acidcontains C12 (>99%) fatty acid.
Lauric acidis readily biodegradable and is GMO-free.


Lauric acidis bovine spongiform encephalopathy/ transmissible spongiform encephalopathy-free.
Lauric acidis a main renewable ingredient for production of soaps.
Lauric acidis a biodegradable, GMO-free and fatty oil derived from renewable vegetable oil by KLK Oleo works as a surfactant, emollient and cleansing agent.
Lauric acidis Halal and Kosher certified.



USES and APPLICATIONS of LAURIC ACID:
Lauric Acid is a versatile oleochemical with applications in everything from plastics to personal care.
Lauric acid is used mainly for the production of soaps and cosmetics.
For these purposes, lauric acid is reacted with sodium hydroxide to give sodium laurate, which is a soap.


Lauric acid is typically used in under 10% concentration in cosmetic formulas but has been deemed safe in higher concentrations (up to 25%).
Lauric Acid is also used for preventing the transmission of HIV from mothers to children.
Lauric acid is widely used in cosmetics, latex and gloves.


Lauric acid is used in the medicine industry.
Lauric Acid's natural bay leaf-like scent can be used in high amounts to add fragrance to products, but it’s more often used as a base for cleansing agents, and, increasingly, for its skin-soothing actions.


Lauric acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Some studies have shown Lauric Acid can also have antimicrobial activity.


Lauric acid is an emulsifying agent, also used as a cleaning agent or as a surfactant.
Lauric acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Research continues to investigate lauric acid’s benefits as an adjunct to anti-acne treatments.


Lauric acid is a medium-chain saturated fatty acid.
Lauric Acid is found in many vegetable fats and in coconut and palm kernel oils.
Lauric acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.


Lauric acid is used for treating viral infections including influenza (the flu); swine flu; avian flu; the common cold; fever blisters, cold sores, and genital herpes caused by herpes simplex virus (HSV); genital warts caused by human papillomavirus (HPV); and HIV/AIDS.
Lauric acid is also used for preventing the transmission of HIV from mothers to children.
Lauric acid is a solid at room temperature but melts easily in boiling water, so liquid lauric acid can be treated with various solutes and used to determine their molecular masses.


Palmera A 9912's applications include toiletries, transparent soaps and other cosmetic care products.
Lauric acidis used in production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines and fatty amines.


Lauric acidis suitable for soaps, toiletries, transparent soaps, and other cosmetic care products.
In addition, Lauric acidis used in the production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines, and fatty amines.


Lauric acidis used Pharma and healthcare, Lubricants, Paints and coatings, Industrial chemistry, Personal hygiene, and home care.
Lauric acidis mainly used as a raw material for the production of alkyd resins, wetting agents, detergents, insecticides, surfactants, food additives and cosmetics.


Lauric acidis often used as a lubricant and has multiple functions such as lubricant and vulcanizing agent.
However, due to its corrosive effect on metals, Lauric acidis generally not used in plastic products such as wires and cables.
Lauric acidis most widely used in the surfactant industry and can also be used in the perfume industry and pharmaceutical industry.


Lauric acidis used as a surface treatment agent for the preparation of bonding.
Lauric acidis also used in the manufacture of alkyd resins, chemical fiber oils, insecticides, synthetic fragrances, plastic stabilizers, anti-corrosion additives for gasoline and lubricating oils.


Lauric acidis widely used in the manufacture of various types of surfactants, such as cationic laurylamine, trilaurylamine, lauryl dimethylamine, lauryl trimethylammonium salt, etc.; anionic types include sodium lauryl sulfate and lauric acid sulfuric acid Ester salts, triethanol ammonium lauryl sulfate, etc.; zwitterionic types include lauryl betaine, imidazoline laurate, etc.; non-ionic surfactants include poly-L-alcohol monolaurate, polyoxyethylene laurate , glyceryl laurate polyoxyethylene ether, lauric acid diethanolamide, etc.


In addition, Lauric acidis also used as a food additive and in the manufacture of cosmetics.
Lauric acidis the raw material for producing soap, detergent, cosmetic surfactant, and chemical fiber oil.


-Uses & Applications of Lauric Acid:
*Plastics: Intermediate
*Food and Beverage: Raw Material for Emulsifiers
*Surfactants and Esters: Anionic and Nonionic Surfactants
*Textiles: Lubricant & Process Agent
*Personal Care: Emulsifier for Facial Creams and Lotions
*Soaps and Detergents: A Base in the Production of Liquid and Transparent Soaps


-Cosmetic Uses:
*cleansing agents
*surfactants
*surfactant - emulsifying



LAURIC ACID AT A GLANCE:
*Natural component of skin’s oil
*Plays a role in reinforcing skin’s innate defenses by strengthening its microbiome
*Functions as a cleansing agent/emulsifier in cosmetic formulas
*Studies have shown lauric acid offers antimicrobial activity
*Can be sourced from coconut oil, babassu butter and other natural fats



WHAT DOES LAURIC ACID DO IN A FORMULATION?
*Cleansing
*Emulsifying
*Surfactant



PROPERTIES OF LAURIC ACID:
Lauric acidenhances the antimicrobial protective properties of the skin, has an antibacterial effect, negatively affects a variety of pathogenic microorganisms, bacteria, yeast, fungi and viruses.



ALTERNATIVE PARENTS OF LAURIC ACID:
*Straight chain fatty acids
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



RELATED COMPOUNDS OF LAURIC ACID:
*Undecanoic acid
*Tridecanoic acid
*Dodecanol
*Dodecanal
*Sodium lauryl sulfate



SUBSTITUENTS OF LAURIC ACID:
*Medium-chain fatty acid
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



LAURIC ACID FOR PSORIASIS:
Bloggers and natural health websites often recommend coconut oil as a treatment for dry skin and conditions such as psoriasis.
Again, because lauric acid is only part of what makes up coconut oil, it’s difficult to say if the fatty acid alone or a combination of coconut oil components is responsible for these benefits.



LAURIC ACID FOR ACNE:
Because lauric acid has antibacterial properties, it’s been found to effectively combat acne.
The bacteria Propionibacterium acnes are found naturally on the skin.
When they overgrow, they lead to the development of acne.
The results of a 2009 study found that lauric acid could reduce inflammation and the number of bacteria present.

Lauric acid worked even better than benzoyl peroxide, a common acne treatment.
A 2016 study also reconfirmed the acne-fighting properties of lauric acid.
This doesn’t mean you should put coconut oil on your acne.
The researchers used pure lauric acid and suggested that it could be developed into an antibiotic therapy for acne in the future.



HOW TO USE LAURIC ACID:
To reap the topical benefits of lauric acid and coconut oil, apply it directly to your skin.
While this isn’t recommended for people with acne, the risks are minimal when it comes to addressing issues such as skin hydration and psoriasis.
Coconut oil can be used in cooking as well.
Its sweet, nutty flavor makes Lauric Acid the perfect addition to desserts, including double chocolate paleo brownies and paleo banana bread.
You can also use Lauric Acid to sauté vegetables or to add flavor to mashed sweet potatoes or a Caribbean curry soup.



IN VARIOUS PLANTS, LAURIC ACID:
The palm tree Attalea speciosa, a species popularly known in Brazil as babassu – 50% in babassu oil
Attalea cohune, the cohune palm (also rain tree, American oil palm, corozo palm or manaca palm) – 46.5% in cohune oil
Astrocaryum murumuru (Arecaceae) a palm native to the Amazon – 47.5% in "murumuru butter"
Coconut oil 49%

Pycnanthus kombo (African nutmeg)
Virola surinamensis (wild nutmeg) 7.8–11.5%
Peach palm seed 10.4%
Betel nut 9%

Date palm seed 0.56–5.4%
Macadamia nut 0.072–1.1%
Plum 0.35–0.38%
Watermelon seed 0.33%
Viburnum opulus 0.24-0.33%

Citrullus lanatus (egusi melon)
Pumpkin flower 205 ppm, pumpkin seed 472 ppm
In Insects
Black soldier fly Hermetia illucens 30–50 mg/100 mg fat.



WHERE TO FIND LAURIC ACID:
Lauric acid is a powerful substance that’s sometimes extracted from the coconut for use in developing monolaurin.
Monolaurin is an antimicrobial agent that’s able to fight pathogens such as bacteria, viruses, and yeasts.



NUTRITIONAL AND MEDICAL ASPECTS OF LAURIC ACID:
Although 95% of medium-chain triglycerides are absorbed through the portal vein, only 25–30% of lauric acid is absorbed through it.
Lauric acid increases total serum lipoproteins more than many other fatty acids, but mostly high-density lipoprotein (HDL).
As a result, lauric acid has been characterized as having "a more favorable effect on total HDL than any other fatty acid [examined], either saturated or unsaturated".

In general, a lower total/HDL serum lipoprotein ratio correlates with a decrease in atherosclerotic incidence.
Nonetheless, an extensive meta-analysis on foods affecting the total LDL/serum lipoprotein ratio found in 2003 that the net effects of lauric acid on coronary artery disease outcomes remained uncertain.
A 2016 review of coconut oil (which is nearly half lauric acid) was similarly inconclusive about the effects on cardiovascular disease incidence



PHYSICAL and CHEMICAL PROPERTIES of LAURIC ACID:
Chemical formula: C12H24O2
Molar mass: 200.322 g·mol−1
Appearance: White powder
Odor: Slight odor of bay oil
Density: 1.007 g/cm3 (24 °C)
0.8744 g/cm3 (41.5 °C)
0.8679 g/cm3 (50 °C)
Melting point: 43.8 °C (110.8 °F; 316.9 K)
Boiling point: 297.9 °C (568.2 °F; 571.0 K)
282.5 °C (540.5 °F; 555.6 K) at 512 mmHg
225.1 °C (437.2 °F; 498.2 K) at 100 mmHg
Solubility in water: 37 mg/L (0 °C)
55 mg/L (20 °C), 63 mg/L (30 °C)
72 mg/L (45 °C), 83 mg/L (100 °C)

Solubility: Soluble in alcohols, diethyl ether, phenyls, haloalkanes, acetates
Solubility in methanol: 12.7 g/100 g (0 °C)
120 g/100 g (20 °C), 2250 g/100 g (40 °C)
Solubility in acetone: 8.95 g/100 g (0 °C)
60.5 g/100 g (20 °C), 1590 g/100 g (40 °C)
Solubility in ethyl acetate: 9.4 g/100 g (0 °C)
52 g/100 g (20°C), 1250 g/100 g (40°C)
Solubility in toluene: 15.3 g/100 g (0 °C)
97 g/100 g (20°C), 1410 g/100 g (40°C)
log P: 4.6
Vapor pressure: 2.13·10−6 kPa (25 °C)
0.42 kPa (150 °C), 6.67 kPa (210 °C)
Acidity (pKa): 5.3 (20 °C)
Thermal conductivity: 0.442 W/m·K (solid)
0.1921 W/m·K (72.5 °C)
0.1748 W/m·K (106 °C)
Refractive index (nD): 1.423 (70 °C), 1.4183 (82 °C)

Viscosity: 6.88 cP (50 °C), 5.37 cP (60 °C)
Structure
Crystal structure: Monoclinic (α-form)
Triclinic, aP228 (γ-form)
Space group: P21/a, No. 14 (α-form)
P1, No. 2 (γ-form)
Point group: 2/m (α-form), 1 (γ-form)
Lattice constant:
a = 9.524 Å, b = 4.965 Å, c = 35.39 Å (α-form)
α = 90°, β = 129.22°, γ = 90°
Thermochemistry
Heat capacity (C): 404.28 J/mol·K
Std enthalpy of formation (ΔfH⦵298): −775.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 7377 kJ/mol, 7425.8 kJ/mol (292 K)
CAS number: 143-07-7
EC number: 205-582-1
Hill Formula: C₁₂H₂₄O₂

Chemical formula: CH₃(CH₂)₁₀COOH
Molar Mass: 200.32 g/mol
HS Code: 2915 90 30
Water Solubility: 0.01 g/L
logP: 5.13
logP: 4.48
logS: -4.3
pKa (Strongest Acidic): 4.95
Physiological Charge: -1
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 1
Polar Surface Area: 37.3 Ų
Rotatable Bond Count: 10
Refractivity: 58.68 m³·mol⁻¹
Polarizability: 25.85 ų
Number of Rings: 0
Bioavailability: 1
Rule of Five: Yes
Ghose Filter: Yes
Veber's Rule: Yes
MDDR-like Rule: Yes

Boiling point: 299 °C (1013 hPa)
Density: 0.883 g/cm3 (50 °C)
Explosion limit: 0.6 %(V)
Flash point: 176 °C
Ignition temperature: 250 °C
Melting Point: 43 - 45 °C
Vapor pressure: Bulk density: 490 kg/m3
Solubility: 4.81 mg/l
Physical state: solid
Color: white, to, light yellow
Odor: weak characteristic odour
Melting point/freezing point:
Melting point: 43 - 45 °C
Initial boiling point and boiling range: 299 °C at 1.013 hPa
Flammability (solid, gas): The product is not flammable.
Upper/lower flammability or explosive limits:

Lower explosion limit: 0,6 %(V)
Flash point: 176 °C - closed cup
Autoignition temperature: > 250 °C
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 7 mPa.s at 50 °C
Water solubility: 0,058 g/l at 20 °C
Partition coefficient: n-octanol/water:
log Pow: 4,6 - (Lit.), Potential bioaccumulation
Vapor pressure 0,15 hPa at 100 °C < 0,1 hPa at 25 °C - (Lit.)
Density: 0,883 g/cm3 at 50 °C
Relative density No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available

Oxidizing properties: none
Other safety information:
Bulk density: ca.490 kg/m3
Surface tension: 26,6 mN/m at 70 °C
Dissociation constant: 5,3 at 20 °C
Relative vapor density: 6,91
Molecular Weight: 278.43
Molecular Formula: C18H30O2
Boiling Point: 230-232ºC1 mm Hg(lit.)
Melting Point: -11ºC(lit.)
Flash Point: >230 °F
Purity: 95%
Density: 0.914 g/mL at 25 °C(lit.)
Storage: 2-8ºC
Assay: 0.99
Refractive Index: n20/D 1.480(lit.)

Appearance: white to pale yellow waxy crystalline solid (est)
Assay: 95.00 to 100.00 sum of isomers
Water Content: <0.20%
Food Chemicals Codex Listed: Yes
Melting Point: 45.00 to 48.00 °C. @ 760.00 mm Hg
Boiling Point: 225.00 °C. @ 100.00 mm Hg
Boiling Point: 252.00 to 287.00 °C. @ 760.00 mm Hg
Congealing Point: 26.00 to 44.00 °C.
Saponification Value: 253.00 to 287.00
Unsaponifiable Matter: <0.30%
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Vapor Density: 6.91 ( Air = 1 )
Flash Point: 329.00 °F. TCC ( 165.00 °C. )
logP (o/w): 4.600
Soluble in: alcohol, chloroform, ether
water, 12.76 mg/L @ 25 °C (est)
water, 4.81 mg/L @ 25 °C (exp)



FIRST AID MEASURES of LAURIC ACID:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of LAURIC ACID:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LAURIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LAURIC ACID:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of LAURIC ACID:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .



SYNONYMS:
Dodecanoic acid
n-Dodecanoic acid
Dodecylic acid
Dodecoic acid
Laurostearic acid
Vulvic acid
1-Undecanecarboxylic acid
Duodecylic acid, C12:0 (Lipid numbers)
Dodecanoic acid, ABL, Lauric acid
C18:3 (ALL CIS-9,12,15) ACID
CIS,CIS,CIS-9,12,15-OCTADECATRIENOIC ACID
DELTA 9 CIS 12 CIS 15 CIS OCTADECATRIENOIC ACID
9,12,15-OCTADECATRIENIC ACID
9,12,15-OCTADECATRIENOIC ACID
ALFA-LINOLENIC ACID
ALL CIS-9,12,15-OCTADECATRIENOIC ACID
ALPHA-LINOLENIC AC
1-Undecanecarboxylate
1-Undecanecarboxylic acid
ABL
Acide Laurique
C12 fatty acid
C12:0
Coconut oil fatty acids
DAO
Dodecanoate
dodecanoic acid
dodecoate
Dodecoic acid
Dodecylate
dodecylcarboxylate
Dodecylic acid
duodecyclate
Duodecyclic acid
duodecylate
Duodecylic acid
LAP
LAU
Laurate
Lauric acid
Laurinsaeure
Laurostearate
Laurostearic acid
MYR
n-Dodecanoate
n-Dodecanoic acid
Sorbitan laurate
Sorbitan monolaurate (NF)
undecane-1-carboxylate
Undecane-1-carboxylic acid
Vulvate
Vulvic acid
CH3-[CH2]10-COOH
Dodecylcarboxylic acid
Laate
Laic acid
Aliphat no. 4
Edenor C 1298-100
Emery 651
Hystrene 9512
Kortacid 1299
Lunac L 70
Lunac L 98
Neo-fat 12
Neo-fat 12-43
Nissan naa 122
Philacid 1200
Prifac 2920
Univol u 314
1-Dodecanoic acid
FA(12:0)

cas no 143-07-7 ABL; Dodecanoic acid; Lauric acid; n-Dodecanoic acid; Dodecylic acid; Dodecoic acid; Laurostearic acid; Vulvic acid; 1-Undecanecarboxylic acid; Duodecylic acid;

SYNONYMS n-Dodecanoic acid; Dodecylic acid; Dodecoic acid; Laurostearic acid; Vulvic acid; 1-Undecanecarboxylic acid; Duodecylic acid; CAS NO. 143-07-7

Lauric Acid (Dodecanedioic acid) is an earlier developed industrial product in long-chain dicarboxylic acid.
Lauric Acid (Dodecanedioic acid) is a white solid with a slight odor of bay oil.


CAS Number: 143-07-7
EC Number: 205-582-1
MDL number: MFCD00002736
Linear Formula: CH3(CH2)10COOH
Chemical formula: C12H24O2


Dodecanoic acid, n-Dodecanoic acid, Dodecylic acid, Dodecoic acid, Laurostearic acid, Vulvic acid, 1-Undecanecarboxylic acid, Duodecylic acid, C12:0 (Lipid numbers), Dodecanoic acid, ABL, Lauric acid, C18:3 (ALL CIS-9,12,15) ACID, CIS,CIS,CIS-9,12,15-OCTADECATRIENOIC ACID, DELTA 9 CIS 12 CIS 15 CIS OCTADECATRIENOIC ACID, 9,12,15-OCTADECATRIENIC ACID, 9,12,15-OCTADECATRIENOIC ACID, ALFA-LINOLENIC ACID, ALL CIS-9,12,15-OCTADECATRIENOIC ACID, ALPHA-LINOLENIC AC, 1-Undecanecarboxylate, 1-Undecanecarboxylic acid, ABL, Acide Laurique, C12 fatty acid, C12:0, Coconut oil fatty acids, DAO, Dodecanoate, dodecanoic acid, dodecoate, Dodecoic acid, Dodecylate, dodecylcarboxylate, Dodecylic acid, duodecyclate, Duodecyclic acid, duodecylate, Duodecylic acid, LAP, LAU, Laurate, Lauric acid, Laurinsaeure, Laurostearate, Laurostearic acid, MYR, n-Dodecanoate, n-Dodecanoic acid, Sorbitan laurate, Sorbitan monolaurate (NF), undecane-1-carboxylate, Undecane-1-carboxylic acid, Vulvate, Vulvic acid, CH3-[CH2]10-COOH, Dodecylcarboxylic acid, Laate, Laic acid, Aliphat no. 4, Edenor C 1298-100, Emery 651, Hystrene 9512, Kortacid 1299, Lunac L 70, Lunac L 98, Neo-fat 12, Neo-fat 12-43, Nissan naa 122, Philacid 1200, Prifac 2920, Univol u 314, 1-Dodecanoic acid, FA(12:0), lauric acid, DODECANOIC ACID, 143-07-7, n-Dodecanoic acid, Dodecylic acid, Vulvic acid, Laurostearic acid, Dodecoic acid, Duodecylic acid, 1-Undecanecarboxylic acid, Aliphat No. 4, Ninol AA62 Extra, Wecoline 1295, Hydrofol acid 1255, Hydrofol acid 1295, Dodecanoate, Duodecyclic acid, Hystrene 9512, Univol U-314, Lauric acid, pure, Dodecylcarboxylate, Lauric acid (natural), Laurinsaeure, Undecane-1-carboxylic acid, ABL, NSC-5026, FEMA No. 2614, laurate, C-1297, Philacid 1200, CCRIS 669, C12:0, Emery 651, Lunac L 70, CHEBI:30805, HSDB 6814,
EINECS 205-582-1, UNII-1160N9NU9U, BRN 1099477, n-Dodecanoate, Kortacid 1299, Dodecanoic Acid Anion, DTXSID5021590, Prifrac 2920, AI3-00112, Lunac L 98, Univol U 314, Prifac 2920, 1160N9NU9U, MFCD00002736, DAO, DTXCID801590, CH3-[CH2]10-COOH, NSC5026, EC 205-582-1, dodecylate, laurostearate,
vulvate, 4-02-00-01082 (Beilstein Handbook Reference), DODECANOIC ACID (LAURIC ACID) 1-undecanecarboxylate, LAURIC ACID (USP-RS), LAURIC ACID [USP-RS],
CH3-(CH2)10-COOH, 8000-62-2, CAS-143-07-7, SMR001253907, laurinsaure, dodecanic acid, Nuvail, lauric-acid, Acide Laurique, n-Dodecanoicacid, 3uil, Lauric acid (NF), DODECANOICACID, fatty acid 12:0, Lauric Acid, Reagent, Nissan NAA 122, Emery 650, Dodecanoic acid, 98%, Dodecanoic acid, 99%, Guaranteed Reagent,99%, Dodecanoic (Lauric) acid, LAURIC ACID [MI], bmse000509, LAURIC ACID [FCC], LAURIC ACID [FHFI], LAURIC ACID [INCI], SCHEMBL5895, NCIOpen2_009480, MLS002177807, MLS002415737, WLN: QV11, Dodecanoic acid (lauric acid), LAURIC ACID [WHO-DD], Dodecanoic acid, >=99.5%, Edenor C 1298-100, DODECANOIC ACID [HSDB], CHEMBL108766, GTPL5534, NAA 122, NAA 312, HMS2268C14, HMS3649N06, HY-Y0366, STR08039, Dodecanoic acid, analytical standard, Lauric acid, >=98%, FCC, FG, Tox21_202149, Tox21_303010, BDBM50180948, LMFA01010012, s4726, AKOS000277433, CCG-266587, DB03017, FA 12:0, HYDROFOL ACID 1255 OR 1295, NCGC00090919-01, NCGC00090919-02, NCGC00090919-03, NCGC00256486-01, NCGC00259698-01, AC-16451, BP-27913, Dodecanoic acid, >=99% (GC/titration), LAU,
Dodecanoic acid, purum, >=96.0% (GC), Lauric acid, natural, >=98%, FCC, FG, CS-0015078, FT-0625572, FT-0695772, L0011, NS00008441, EN300-19951, C02679,
D10714, A808010, LAURIC ACID (CONSTITUENT OF SAW PALMETTO), Q422627, SR-01000838338, J-007739, SR-01000838338-3, F0001-0507, LAURIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC], Z104476194, 76C2A2EB-E8BA-40A6-8032-40A98625ED7B, Lauric acid, European Pharmacopoeia (EP) Reference Standard, Lauric acid, United States Pharmacopeia (USP) Reference Standard, Lauric Acid, Pharmaceutical Secondary Standard; Certified Reference Material, 203714-07-2, 7632-48-6, InChI=1/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14), 1,10-Decanedicarboxylic acid, 1,10-Dicarboxydecane, 1,12-Dodecanedioic acid, Decamethylenedicarboxylic acid, 1,10-Decanedicarboxylate, 1,12-Dodecanedioate, Decamethylenedicarboxylate, Dodecanedioate, Corfree m 2, N-Dodecane-a,W-dioate, N-Dodecane-a,W-dioic acid, N-Dodecanedioate, N-Dodecanedioic acid, SL-AH, Dodecandioic acid, Dodecanedioic acid, sodium salt, DDDA, dodecanedioate,
1.10-Decanedic, Dodecanedioic acid, Twelve alkyl acid, Dodecanedioic acid, RARECHEM AL BO 0308, 1,10-dicarboxydecane, Dodecandioic acid (DDA), 1,10-decandicarboxylicacid, 1,10-Decanedicarboxylic acid, DODECANEDIOIC ACID FOR SYNTHESIS, DODECANE, DDA, DDDA, DODECANEDIOIC, Twelve alkyl acid, 1,12-DODECANEDIOIC ACID, SL-AH, α,ω-DC12, NSC 400242, Corfree M 2, Dodecanedioic acid, 1,10-Decanedicarboxylic acid, 1,12-Dodecanedioic acid, Decamethylenedicarboxylic acid, 1,10-Dicarboxydecane, n-Dodecanedioic acid, SL-AH, Corfree M 2, n-Dodecane-α,ω-dioic acid, NSC 400242, LCA 141, 142610-44-4, 91485-80-2,



Lauric Acid (Dodecanedioic acid) is a metabolite found in or produced by Escherichia coli.
Lauric Acid (Dodecanedioic acid) is a white solid with a slight odor of bay oil.
Lauric Acid (Dodecanedioic acid) is a straight-chain, twelve-carbon medium-chain saturated fatty acid with strong bactericidal properties; the main fatty acid in coconut oil and palm kernel oil.


Lauric Acid (Dodecanedioic acid) has a role as a plant metabolite, an antibacterial agent and an algal metabolite.
Lauric Acid (Dodecanedioic acid) is a straight-chain saturated fatty acid and a medium-chain fatty acid.
Lauric Acid (Dodecanedioic acid) is a conjugate acid of a dodecanoate. It derives from a hydride of a dodecane.


Lauric Acid (Dodecanedioic acid) is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Lauric Acid (Dodecanedioic acid) is an alpha,omega-dicarboxylic acid that is dodecane in which the methyl groups have been oxidised to the corresponding carboxylic acids.


Lauric Acid (Dodecanedioic acid) is a white solid with a slight odor of bay oil.
Lauric Acid (Dodecanedioic acid) is a white crystalline powder.
Lauric Acid (Dodecanedioic acid) is induced mutation of dodecanedioic acid producing Candida tropicalis.


Lauric Acid (Dodecanedioic acid) is a chemical compound with the molecular formula C12H22O2.
This white crystalline substance, Lauric Acid (Dodecanedioic acid), is soluble in water and alcohols.
Lauric Acid (Dodecanedioic acid) has been shown to inhibit the enzyme activities of ethylene diamine oxidase, malonic acid oxidase, and insulin-stimulated glucose.


Lauric Acid (Dodecanedioic acid) also has been associated with increased uptake of glucose by adipocytes.
Lauric Acid (Dodecanedioic acid) is a fatty acid that contains a hydroxyl group, which can be converted to trifluoroacetic acid in a reaction solution.
Lauric Acid (Dodecanedioic acid) has chemical structures that are similar to those of p-hydroxybenzoic acid (p-OHBA), but it does not have the same enzyme inhibiting properties.


Lauric Acid (Dodecanedioic acid) is a pure C12 dibasic acid that is mainly used in antiseptics, painting materials, top-grade coatings, corrosion inhibitors, surfactants and engineering plastics.
Lauric Acid (Dodecanedioic acid) is available in a white, flaky form and has a long shelf life of approximately 3 years, depending on the storage methods.


Lauric Acid (Dodecanedioic acid) is a dicarboxylic acid which is water soluble and involves in a metabolic pathway intermediate to those of lipids and carbohydrates.
Lauric Acid (Dodecanedioic acid) is a natural product found in Staphisagria macrosperma, Cleome amblyocarpa, and other organisms with data available.


Lauric Acid (Dodecanedioic acid) is a saturated medium-chain fatty acid with a 12-carbon backbone.
Lauric Acid (Dodecanedioic acid) is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil.
Lauric Acid (Dodecanedioic acid) is the main fatty acid in coconut oil and in palm kernel oil, and is believed to have antimicrobial properties.


Lauric Acid (Dodecanedioic acid) is a white, powdery solid with a faint odor of bay oil.
Lauric Acid (Dodecanedioic acid) is a metabolite found in or produced by Saccharomyces cerevisiae.
Lauric Acid (Dodecanedioic acid) is a kind of important chemical products having broad use in industries, it is the material needed to produce Polyamide, Nylon and other engineering plastics.


Lauric Acid (Dodecanedioic acid) can also serve as plasticizer for polyvinyl chloride, cellulose acetate and nitrocellulose.
Besides, DDDA act as an important ingredient for refined lubricant and low-temperature greases.
Lauric Acid (Dodecanedioic acid) is an aliphatic dicarboxylic acid containing 12 carbon atoms.


More formally Lauric Acid (Dodecanedioic acid) is an alpha,omega-dicarboxylic acid with both the first and last carbons of the aliphatic chain having carboxylic acids.
Lauric Acid (Dodecanedioic acid) is water soluble.


Lauric Acid (Dodecanedioic acid) can be produced in yeast and fungi through the oxidation of dodecane via fungal peroxygenases.
Lauric Acid (Dodecanedioic acid) belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.


Lauric Acid (Dodecanedioic acid) is a dicarboxylic acid which is a water-soluble substance with a metabolic pathway intermediate to those of lipids and carbohydrates.
Lauric Acid (Dodecanedioic acid) is an alpha,omega-dicarboxylic acid that is dodecane in which the methyl groups have been oxidised to the corresponding carboxylic acids.


Lauric Acid (Dodecanedioic acid) has a role as an EC 1.1.1.1 (alcohol dehydrogenase) inhibitor and a human metabolite.
Lauric Acid (Dodecanedioic acid) is a highly pure C12 dibasic acid that is available in white flake form, mainly used in antiseptics, top-grade coatings, painting materials, corrosion inhibitor, surfactant, and engineering plastics such as nylon 612.


Lauric Acid (Dodecanedioic acid) is an alpha,omega-dicarboxylic acid and a lipid.
Lauric Acid (Dodecanedioic acid) is a conjugate acid of a dodecanedioate(2-).
Lauric Acid (Dodecanedioic acid) derives from a hydride of a dodecane.



USES and APPLICATIONS of LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is used as an intermediate for plasticizers, lubricants and adhesives.
Lauric Acid (Dodecanedioic acid) is also used in antiseptics, top-grade coatings, painting materials, corrosion inhibitor and surfactant.
Lauric Acid (Dodecanedioic acid) finds application in engineering plastics such as nylon 612.


Lauric Acid (Dodecanedioic acid) is used as an intermediate for plasticizers, lubricants and adhesives.
Lauric Acid (Dodecanedioic acid) is also used in antiseptics, top-grade coatings, painting materials, corrosion inhibitor and surfactant.
Lauric Acid (Dodecanedioic acid) finds application in engineering plastics such as nylon 612.


Lauric Acid (Dodecanedioic acid) is mainly used in the synthesis of polymer materials, spices, drugs, etc.
Among them, as a polycondensation monomer and diamine condensation reaction to synthesize long carbon chain nylon (also known as polyamide resin) engineering plastics, is one of the most important applications.


Lauric Acid (Dodecanedioic acid) is used condensed with hexamethylenediamine to produce engineering plastic nylon 6-12, diesters of alcohols such as butanol
Lauric Acid (Dodecanedioic acid) can be used as plasticizers for polyvinyl chloride, nitrocellulose and cellulose acetate, and diesters synthesized with octanol are also used as advanced lubricating oils for jet engines and gas turbines, or low temperature grease base oil.


Twelve double acid can also be used as a modifier of saturated polyester, metal precipitation agent and perfume, special polyurethane raw materials.
Lauric Acid (Dodecanedioic acid) is used in the synthesis of polyamide, long carbon chain nylon, high-grade lubricating oil, etc., is the main raw material of nylon 1212, nylon 612 and nylon 1012


Lauric Acid (Dodecanedioic acid) is used in the synthesis of nylon 612, model resin, modified saturated polyester, powder coating, plasticizer, lubricating oil, metal precipitant, etc.
Lauric Acid (Dodecanedioic acid) is used in cosmetic compositions.


Lauric Acid (Dodecanedioic acid) is used as intermediate for plasticizers, lubricants, adhesives, polyesters, and others.
Lauric Acid (Dodecanedioic acid) is a highly pure C12 dibasic acid that is available in white flake form, mainly used in antiseptics, top-grade coatings, painting materials, corrosion inhibitor, surfactant, and engineering plastics such as nylon 612.


Lauric Acid (Dodecanedioic acid) is used in cosmetic composition
Lauric Acid (Dodecanedioic acid) is used for synthetic nylon 612, model resin, modified saturated polyester, powder coating, plasticizer, lubricating oil, metal precipitant, etc


Lauric Acid (Dodecanedioic acid) is used in the production of nylon (nylon - 6,12), polyamides, coatings, adhesives, greases, polyesters, dyestuffs, detergents, flame retardants, and fragrances.
Lauric Acid (Dodecanedioic acid) is now produced by fermentation of long-chain alkanes with a specific strain of Candida tropicalis.


Lauric Acid (Dodecanedioic acid)'s monounsaturated analogue (traumatic acid) is described below.
Lauric Acid (Dodecanedioic acid) is used as an intermediate for plasticizers, lubricants and adhesives.
Lauric Acid (Dodecanedioic acid) is also used in antiseptics, top-grade coatings, painting materials, corrosion inhibitor and surfactant.


Lauric Acid (Dodecanedioic acid) finds application in engineering plastics such as nylon 612.
Lauric Acid (Dodecanedioic acid) is a solid at room temperature but melts easily in boiling water, so liquid lauric acid can be treated with various solutes and used to determine their molecular masses.
Lauric Acid (Dodecanedioic acid), although slightly irritating to mucous membranes, has a very low toxicity and so is used in many soaps and shampoos.



ALTERNATIVE PARENTS OF LAURIC ACID (DODECANEDIOIC ACID):
*Straight chain fatty acids
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



RELATED COMPOUNDS OF LAURIC ACID (DODECANEDIOIC ACID):
*Undecanoic acid
*Tridecanoic acid
*Dodecanol
*Dodecanal
*Sodium lauryl sulfate



SUBSTITUENTS OF LAURIC ACID (DODECANEDIOIC ACID):
*Medium-chain fatty acid
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



PRODUCTION METHOD OF LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is industrially possible to trimerize butadiene to give cyclododecatriene, which is then hydrogenated to cyclododecane, then, dodecanone is oxidized by nitric acid to give Lauric Acid (Dodecanedioic acid).

Lauric Acid (Dodecanedioic acid) is also possible to react with hydrogen peroxide in methanol from cyclohexane to form alkoxy cyclohexyl peroxide, and then ring-opening and dimerization to form dodecanedioic acid methyl ester.

After saponification, twelve double acid can be obtained.
In laboratory preparation, dodecanol was used as raw material to get Lauric Acid (Dodecanedioic acid) by nitric acid oxidation.



FEATURES & APPLICATIONS OF LAURIC ACID (DODECANEDIOIC ACID):
*High purity with fine quality
*Excellent thermal stability
*Material for Polyamide, Nylon、Polyester、Polyurethane and plasticizer
*Act as modifier for saturated polyester,
*Ingredient for metal precipitator
*Metal machine oil and lubricant



PHYSICAL AND CHEMICAL PROPERTIES OF LAURIC ACID (DODECANEDIOIC ACID):
*White powder or flaky crystals.
*Melting point 128.7-129 ℃, boiling point 254 ℃(2.0kPa),245 ℃(1.33kPa), molar heat of combustion 6.740MJ/mol.
*Small solubility in water, good thermal stability.



PREPARATION OF LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is prepared from cyc1ododecene (obtained from butadiene) by methods which are entirely analogous to those used to prepare adipic acid from benzene.
The cyclododecene is reduced to cyclododecane, which is oxidized firstly to a mixture of cyc1ododecanol and cyclododecanone and then to dodecanedioic acid.
Lauric Acid (Dodecanedioic acid) is a colourless crystalline solid, m.p. 129°C.



PURIFICATION METHODS OF LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is crystallise the dioic acid from water, 75% or 95% EtOH (solubility is 10%), or glacial acetic acid



SOLUBILITY OF LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is soluble in water, ethanol, hot methanol, hot toluene and hot acetic acid.



NOTES, LAURIC ACID (DODECANEDIOIC ACID):
Lauric Acid (Dodecanedioic acid) is incompatible with strong oxidizing agents and reducing agents.



REFINING METHOD OF LAURIC ACID (DODECANEDIOIC ACID):
add 1000 L90wt to 400kg of ordinary Lauric Acid (Dodecanedioic acid) and 3kg of coconut shell activated carbon.
In% edible alcohol, the slurry is adjusted in a 2m3 glass-lined decolorizing kettle, heated to 65 ℃, filtered by 30m2 box-type Dark Flow Plate and Frame, and the filtrate is filtered through a precision filter to a crystallization tank, cooled to 25 ℃, centrifuge, centrifuge the material into the brush clean glass lining low-temperature wash tank, add 200 L95wt.%, 15 ℃ alcohol, stirring evenly, two centrifugation, centrifugal material into the double cone vacuum dryer drying, temperature control at 45 ℃ ± 1 ℃, vacuum degree -0.085 ~-0.10MPa, dry to a moisture content of less than 0.1wt.
After completion of drying, 328kg of purified acid was obtained.

Determination of mono-acid content of product by gas chromatography. 99.17wt.%, neutralization titration determination of total acid content 99.5wt.%, the ester content was not detected, the mother liquor and the drying and recovery of alcohol during the distillation of the distillation kettle feed liquid with 30% liquid alkali control at pH 12, the distillation of alcohol 1180L, alcohol content of 92wt.%.

Mixed acid was produced by distillation of high boiling mixture with alcohol, and 63.5 of mixed acid was obtained, with total acid content of 98.5wt.%, Lauric Acid (Dodecanedioic acid) content (GC) of 90.26wt.% and water content of 0.35wt.%.



PHYSICAL and CHEMICAL PROPERTIES of LAURIC ACID (DODECANEDIOIC ACID):
Exact Mass：230.30
EC Number：211-746-3
UNII：978YU42Q6I
NSC Number：400242
DSSTox ID：DTXSID3027297
HScode：2917190090
PSA：74.60000
XLogP3：3.2
Density：1.15
Melting Point：130-132 °C
Boiling Point：205-210 °C @ Press: 1 Torr
Flash Point：220ºC
Refractive Index：1.475
Water Solubility：< 0.1 g/L (20 ºC)

Storage Conditions：-20ºC
Vapor Pressure：21 mm Hg ( 222 °C)
Molecular Formula:C12H22O4
Molecular Weight:230.30
Synonyms: dodecanedioic acid
IUPAC Name: dodecanedioic acid
Canonical SMILES: C(CCCCCC(=O)O)CCCCC(=O)O
InChI: InChI=1S/C12H22O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h1-10H2,(H,13,14)(H,15,16)
InChI Key: TVIDDXQYHWJXFK-UHFFFAOYSA-N
Boiling Point: 245 ℃ / 10 mmHg
Melting Point: 127-129 ℃
Flash Point: 220 ℃ (C.C)
Purity: 99 %
Density: 1.15 g/cm3

Solubility: Sol in hot toluene, Alc, Hot acetic acid; slightly sol in hot water
Appearance: White to almost white powder to crystal
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 128.00 °C. @ 760.00 mm Hg
Boiling Point: 393.98 °C. @ 760.00 mm Hg (est)
Flash Point: 422.00 °F. TCC ( 216.60 °C. ) (est)
logP (o/w): 2.920 (est)
Soluble in: water, 40 mg/L @ 20 °C (exp)
water, 146.4 mg/L @ 25 °C (est)
Water Solubility: 0.29 g/L
logP: 2.86
logP: 3.16
logS: -2.9
pKa (Strongest Acidic): 4.65

Physiological Charge: -2
Hydrogen Acceptor Count: 4
Hydrogen Donor Count: 2
Polar Surface Area: 74.6 Ų
Rotatable Bond Count: 11
Refractivity: 60.34 m³·mol⁻¹
Polarizability: 26.85 ų
Number of Rings: 0
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: Yes
Veber's Rule: No
MDDR-like Rule: No
Boiling point: 299 °C (1013 hPa)
Density: 0.883 g/cm3 (50 °C)
Explosion limit: 0.6 %(V)
Flash point: 176 °C

Ignition temperature: 250 °C
Melting Point: 43 - 45 °C
Vapor pressure: Bulk density: 490 kg/m3
Solubility: 4.81 mg/l
Physical state: solid
Color: white, to, light yellow
Odor: weak characteristic odour
Melting point/freezing point:
Melting point: 43 - 45 °C
Initial boiling point and boiling range: 299 °C at 1.013 hPa
Flammability (solid, gas): The product is not flammable.
Upper/lower flammability or explosive limits:
Lower explosion limit: 0,6 %(V)
Flash point: 176 °C - closed cup

Autoignition temperature: > 250 °C
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 7 mPa.s at 50 °C
Water solubility: 0,058 g/l at 20 °C
Partition coefficient: n-octanol/water:
log Pow: 4,6 - (Lit.), Potential bioaccumulation
Vapor pressure 0,15 hPa at 100 °C < 0,1 hPa at 25 °C - (Lit.)
Density: 0,883 g/cm3 at 50 °C
Relative density No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none

Other safety information:
Bulk density: ca.490 kg/m3
Surface tension: 26,6 mN/m at 70 °C
Dissociation constant: 5,3 at 20 °C
Relative vapor density: 6,91
Molecular Weight: 278.43
Molecular Formula: C18H30O2
Boiling Point: 230-232ºC1 mm Hg(lit.)
Melting Point: -11ºC(lit.)
Flash Point: >230 °F
Purity: 95%
Density: 0.914 g/mL at 25 °C(lit.)
Storage: 2-8ºC
Assay: 0.99
Refractive Index: n20/D 1.480(lit.)
Chemical formula: C12H24O2

Molar mass: 200.322 g·mol−1
Appearance: White powder
Odor: Slight odor of bay oil
Density: 1.007 g/cm3 (24 °C)
0.8744 g/cm3 (41.5 °C)
0.8679 g/cm3 (50 °C)
Melting point: 43.8 °C (110.8 °F; 316.9 K)
Boiling point: 297.9 °C (568.2 °F; 571.0 K)
282.5 °C (540.5 °F; 555.6 K) at 512 mmHg
225.1 °C (437.2 °F; 498.2 K) at 100 mmHg
Solubility in water: 37 mg/L (0 °C)
55 mg/L (20 °C), 63 mg/L (30 °C)
72 mg/L (45 °C), 83 mg/L (100 °C)
Solubility: Soluble in alcohols, diethyl ether, phenyls, haloalkanes, acetates

Solubility in methanol: 12.7 g/100 g (0 °C)
120 g/100 g (20 °C), 2250 g/100 g (40 °C)
Solubility in acetone: 8.95 g/100 g (0 °C)
60.5 g/100 g (20 °C), 1590 g/100 g (40 °C)
Solubility in ethyl acetate: 9.4 g/100 g (0 °C)
52 g/100 g (20°C), 1250 g/100 g (40°C)
Solubility in toluene: 15.3 g/100 g (0 °C)
97 g/100 g (20°C), 1410 g/100 g (40°C)
log P: 4.6
Vapor pressure: 2.13·10−6 kPa (25 °C)
0.42 kPa (150 °C), 6.67 kPa (210 °C)
Acidity (pKa): 5.3 (20 °C)
Thermal conductivity: 0.442 W/m·K (solid)
0.1921 W/m·K (72.5 °C)
0.1748 W/m·K (106 °C)

Refractive index (nD): 1.423 (70 °C), 1.4183 (82 °C)
Viscosity: 6.88 cP (50 °C), 5.37 cP (60 °C)
Structure
Crystal structure: Monoclinic (α-form)
Triclinic, aP228 (γ-form)
Space group: P21/a, No. 14 (α-form)
P1, No. 2 (γ-form)
Point group: 2/m (α-form), 1 (γ-form)
Lattice constant:
a = 9.524 Å, b = 4.965 Å, c = 35.39 Å (α-form)
α = 90°, β = 129.22°, γ = 90°
Thermochemistry
Heat capacity (C): 404.28 J/mol·K
Std enthalpy of formation (ΔfH⦵298): −775.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 7377 kJ/mol, 7425.8 kJ/mol (292 K)

CAS number: 143-07-7
EC number: 205-582-1
Hill Formula: C₁₂H₂₄O₂
Chemical formula: CH₃(CH₂)₁₀COOH
Molar Mass: 200.32 g/mol
HS Code: 2915 90 30
Water Solubility: 0.01 g/L
logP: 5.13
logP: 4.48
logS: -4.3
pKa (Strongest Acidic): 4.95
Physiological Charge: -1
Hydrogen Acceptor Count: 2
Hydrogen Donor Count: 1
Polar Surface Area: 37.3 Ų

Rotatable Bond Count: 10
Refractivity: 58.68 m³·mol⁻¹
Polarizability: 25.85 ų
Number of Rings: 0
Bioavailability: 1
Rule of Five: Yes
Ghose Filter: Yes
Veber's Rule: Yes
MDDR-like Rule: Yes
Appearance: white to pale yellow waxy crystalline solid (est)
Assay: 95.00 to 100.00 sum of isomers
Water Content: <0.20%
Food Chemicals Codex Listed: Yes
Melting Point: 45.00 to 48.00 °C. @ 760.00 mm Hg
Boiling Point: 225.00 °C. @ 100.00 mm Hg
Boiling Point: 252.00 to 287.00 °C. @ 760.00 mm Hg
Congealing Point: 26.00 to 44.00 °C.

Saponification Value: 253.00 to 287.00
Unsaponifiable Matter: <0.30%
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Vapor Density: 6.91 ( Air = 1 )
Flash Point: 329.00 °F. TCC ( 165.00 °C. )
logP (o/w): 4.600
Soluble in: alcohol, chloroform, ether
water, 12.76 mg/L @ 25 °C (est)
water, 4.81 mg/L @ 25 °C (exp)
Chemical Formula: C12H22O4
Average Molecular Weight: 230.3007
Monoisotopic Molecular Weight: 230.151809192
IUPAC Name: dodecanedioic acid

Traditional Name: dodecanedioic acid
CAS Registry Number: 693-23-2
SMILES: OC(=O)CCCCCCCCCCC(O)=O
InChI Identifier: InChI=1S/C12H22O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h1-10H2,(H,13,14)(H,15,16)
InChI Key: TVIDDXQYHWJXFK-UHFFFAOYSA-N
CAS Index Name: Dodecanedioic acid
Molecular formula: C12H22O4
Molecular weight: 230.3
Lipid number: C12:0
Smiles: O=C(O)CCCCCCCCCCC(=O)O
Isomeric Smiles: C(CC(O)=O)CCCCCCCCC(O)=O
InChI: InChI=1S/C12H22O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h1-10H2,(H,13,14)(H,15,16)
InChIKey: InChIKey=TVIDDXQYHWJXFK-UHFFFAOYSA-N
Molecular Weight： 230.30100



FIRST AID MEASURES of LAURIC ACID (DODECANEDIOIC ACID):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of LAURIC ACID (DODECANEDIOIC ACID):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LAURIC ACID (DODECANEDIOIC ACID):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURIC ACID (DODECANEDIOIC ACID):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LAURIC ACID (DODECANEDIOIC ACID):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
*Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of LAURIC ACID (DODECANEDIOIC ACID):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .

Lauric Acid, also known as Dodecanoic Acid, is a saturated fatty acid, specifically a medium-chain fatty acid.
Lauric Acid (Dodecanoic acid) is characterized by its 12-carbon atom chain and the presence of a carboxylic acid functional group (-COOH).
Lauric Acid (Dodecanoic acid) is considered a saturated fatty acid due to its lack of double bonds between carbon atoms, rendering it solid at room temperature.

CAS Number: 143-07-7
EC Number: 205-582-1



APPLICATIONS


Lauric Acid (Dodecanoic acid) finds extensive use in the production of soaps and cleansers due to its cleansing properties.
Lauric Acid (Dodecanoic acid) serves as an essential ingredient in various skincare products like lotions and creams.
As a key component of coconut oil, Lauric Acid (Dodecanoic acid) is widely used in food products, contributing to their texture and stability.

Lauric Acid (Dodecanoic acid) is crucial in the manufacturing of margarine for its solidifying effect at room temperature.
Its presence in confectionery products aids in emulsification and texture enhancement.
In the pharmaceutical industry, it's used as an excipient in drug formulations.
Lauric Acid's antimicrobial properties make it valuable in oral care products like mouthwashes and toothpaste.

Lauric Acid (Dodecanoic acid) is employed in the production of detergents and surfactants for its cleansing abilities.
In cosmetics, Lauric Acid (Dodecanoic acid) contributes to the formulation of lipsticks and makeup products.

Lauric Acid (Dodecanoic acid) is utilized in the creation of hair care products like shampoos and conditioners.
Its stability makes it a useful additive in the production of lubricants and industrial fluids.

As an essential fatty acid in human breast milk, Lauric Acid (Dodecanoic acid) contributes to infant nutrition.
Lauric Acid (Dodecanoic acid)'s antimicrobial qualities aid in wound care and medical ointments.
Lauric Acid (Dodecanoic acid) plays a role in the creation of candle wax for its solidifying properties.

Lauric Acid (Dodecanoic acid) is present in some traditional medicine and alternative therapies.
In pet care products, it's used in the creation of grooming and fur care items.
The stability of Lauric Acid contributes to the production of emulsions and stabilizers in various formulations.

Lauric Acid (Dodecanoic acid) is utilized in the production of certain insect repellents due to its properties.
Lauric Acid (Dodecanoic acid) is an essential ingredient in the formulation of certain dietary supplements.
Its presence in palm kernel oil adds to the stability and texture of the product.
Lauric Acid (Dodecanoic acid) is involved in the creation of perfumes and scented oils.
In the textile industry, it aids in the production of certain fabric treatments and finishes.

Lauric Acid (Dodecanoic acid)'s use in industrial coatings contributes to their stability and texture.
Lauric Acid (Dodecanoic acid) is a significant component in the formulation of certain industrial adhesives.
The applications of Lauric Acid (Dodecanoic acid) are diverse, spanning across personal care, food, industrial, and medicinal uses due to its stability, antimicrobial properties, and role in product formulation.

Lauric Acid (Dodecanoic acid) is a vital component in the creation of biofuels and biodiesel due to its potential as a renewable energy source.
Lauric Acid (Dodecanoic acid) is used in the production of synthetic rubber for its stabilizing and curing effects.
In the creation of candles, it contributes to their firmness and burn stability.

Lauric Acid (Dodecanoic acid) plays a role in the synthesis of herbicides and certain agricultural chemicals.
In the leather industry, it's used in tanning and leather treatments for its softening effects.

Lauric Acid (Dodecanoic acid) is present in some herbal remedies and holistic therapies.
Lauric Acid (Dodecanoic acid) is an essential ingredient in the production of some traditional medicines and ointments.

In the creation of antifungal treatments, it aids in the stability and efficacy of the product.
Lauric Acid (Dodecanoic acid) contributes to the formulation of antiperspirants and deodorants due to its odor-masking properties.
Lauric Acid (Dodecanoic acid) is used in the production of certain antiviral and antibacterial pharmaceuticals.

Lauric Acid (Dodecanoic acid) aids in the creation of wax coatings for fruits and vegetables to extend their shelf life.
In the manufacture of certain animal feed additives, it contributes to their nutritional content.
Lauric Acid (Dodecanoic acid) is employed in the production of essential oils and aromatherapy blends.

Lauric Acid (Dodecanoic acid)'s stability contributes to the production of stable and long-lasting paints and coatings.
Lauric Acid (Dodecanoic acid) plays a role in the production of certain dietary supplements for its potential health benefits.

In the creation of adhesives and glues, it contributes to their bonding properties.
Lauric Acid (Dodecanoic acid) is utilized in the formulation of rust preventatives and metal polishes.
In the creation of hair serums and styling products, it aids in texture and hold.

Lauric Acid (Dodecanoic acid) is involved in the synthesis of certain antiseptic and disinfectant solutions.
Lauric Acid (Dodecanoic acid) is used in the formulation of pet grooming and fur care products.
In the production of waterproofing agents, it aids in their water-repelling properties.

Lauric Acid (Dodecanoic acid) is employed in the creation of biodegradable detergents and cleaners.
Lauric Acid (Dodecanoic acid) contributes to the formulation of insecticides and pest control products.

Lauric Acid (Dodecanoic acid) plays a role in the production of stable and odor-masking body powders.
The applications of Lauric Acid highlight its significance across multiple industries, contributing to stability, preservation, and functional properties in various products.

Lauric Acid (Dodecanoic acid) is a key component in the creation of solid surfactants for household and industrial cleaning products.
In the creation of facial cleansers and exfoliating scrubs, it aids in skin purification.
Lauric Acid (Dodecanoic acid) is utilized in the formulation of wound healing creams due to its antimicrobial properties.

In the production of personal lubricants, it contributes to their texture and glide.
Lauric Acid (Dodecanoic acid) is involved in the creation of certain antacid medications for their buffering effect.
Lauric Acid (Dodecanoic acid) aids in the production of biodegradable soaps and detergents for environmentally friendly cleaning solutions.
Lauric Acid is used in the creation of stable and long-lasting crayons and markers.

Lauric Acid (Dodecanoic acid) is involved in the synthesis of certain paints and coatings for their adherence and longevity.
In the creation of wood preservatives, it aids in protecting against rot and decay.
Lauric Acid (Dodecanoic acid) contributes to the stability and texture of certain cosmetic foundations and concealers.
Lauric Acid (Dodecanoic acid) is utilized in the formulation of stable and long-lasting body lotions and moisturizers.

Lauric Acid (Dodecanoic acid) is an essential component in the production of lip balms and chapsticks for their hydrating effect.
Lauric Acid (Dodecanoic acid) aids in the synthesis of stable and long-lasting printing inks and pigments.

In the creation of aromatherapy massage oils, it acts as a carrier oil and fragrance enhancer.
Lauric Acid (Dodecanoic acid) contributes to the stability of certain pet shampoos and grooming products.
Lauric Acid (Dodecanoic acid) aids in the production of stable and long-lasting air fresheners and room sprays.

Lauric Acid (Dodecanoic acid) is used in the creation of certain anti-itch and anti-inflammatory skin treatments.
Lauric Acid (Dodecanoic acid) is involved in the formulation of certain sunscreen lotions and creams for skin protection.
Lauric Acid (Dodecanoic acid) is utilized in the creation of stable and long-lasting industrial and household polishes.

In the production of shoe creams and leather treatments, it aids in conditioning and preserving leather.
Lauric Acid (Dodecanoic acid) contributes to the formulation of certain therapeutic massage creams and ointments.
Lauric Acid (Dodecanoic acid) is used in the creation of stable and long-lasting eye makeup products.

Lauric Acid (Dodecanoic acid) plays a role in the synthesis of certain dental care products for their cleansing properties.
In the production of massage candles, Lauric Acid (Dodecanoic acid) aids in their fragrance and melting properties.
The diverse applications of Lauric Acid highlight its value across multiple industries, contributing to stability, texture, and functionality in various products.



DESCRIPTION


Lauric Acid, also known as Dodecanoic Acid, is a saturated fatty acid, specifically a medium-chain fatty acid.
Lauric Acid (Dodecanoic acid) is characterized by its 12-carbon atom chain and the presence of a carboxylic acid functional group (-COOH).

Lauric Acid (Dodecanoic acid) is considered a saturated fatty acid due to its lack of double bonds between carbon atoms, rendering it solid at room temperature.
Lauric Acid, also recognized as Dodecanoic Acid, is a saturated fatty acid with a 12-carbon chain.
Its chemical formula is C12H24O2, belonging to the carboxylic acid group.
At room temperature, it appears as a white, solid substance.

Lauric Acid (Dodecanoic acid) possesses a distinctive faint odor, often likened to the aroma of coconuts.
Lauric Acid (Dodecanoic acid) is insoluble in water but exhibits solubility in various organic solvents.
Known for its cleansing properties, iLauric Acid (Dodecanoic acid) is a common ingredient in soaps and shampoos.

Lauric Acid (Dodecanoic acid) produces a rich lather, making it valuable in personal care and cleansing products.
The melting point of Lauric Acid (Dodecanoic acid) is approximately 44-46°C.
Industrially, Lauric Acid (Dodecanoic acid) is used in the production of detergents and surfactants due to its cleansing capabilities.
Lauric Acid (Dodecanoic acid) is a key component in coconut oil, where it's abundantly present.

Lauric Acid (Dodecanoic acid) is found in palm kernel oil and is an essential fatty acid in human breast milk.
As a saturated fatty acid, Lauric Acid (Dodecanoic acid) lacks double bonds between carbon atoms.
Its fatty acid composition contributes to its stability and shelf life in products.

Lauric Acid (Dodecanoic acid) has various derivatives used in pharmaceutical and industrial applications.
In the food industry, it's utilized in confectionery and baked goods for its emulsifying properties.

Its presence contributes to the texture and stability of certain food products.
Lauric Acid (Dodecanoic acid)'s antimicrobial properties add to its value in personal care products.

Lauric Acid (Dodecanoic acid) is an essential constituent in many skincare formulations and cosmetics.
When used in margarine, it contributes to the solidification of the product at room temperature.

Lauric Acid (Dodecanoic acid) is used in the production of various lubricants and industrial fluids.
As a medium-chain fatty acid, it's relatively easier to digest compared to longer-chain fatty acids.

Lauric Acid (Dodecanoic acid) is a significant component in traditional medicine and alternative therapies.
Its potential health benefits have drawn attention in research and studies.

Lauric Acid (Dodecanoic acid)'s prevalence in nature and its versatile applications make it a widely utilized fatty acid.
Its stability, cleansing attributes, and presence in natural sources contribute to its significance across multiple industries.



PROPERTIES


Chemical Properties:

Chemical Formula: C12H24O2.
Molar Mass: Approximately 200.32 g/mol.
Functional Group: Contains a carboxylic acid (-COOH) group at one end of its carbon chain.
Saturated Fatty Acid: Lacks double bonds between carbon atoms, leading to a solid state at room temperature.
Insolubility in Water: Poor solubility in water but dissolves in most organic solvents.


Physical Properties:

Appearance: White, waxy solid or powder.
Melting Point: Approximately 44-46°C.
Boiling Point: Around 225-228°C.
Odor: Faint and characteristic coconut-like aroma.
Solubility: Soluble in most organic solvents like ethanol, ether, and chloroform.



FIRST AID


Skin Contact:

If skin irritation occurs, remove contaminated clothing and rinse the affected area with soap and water.
Seek medical attention if redness, irritation, or any signs of an allergic reaction persist.


Eye Contact:

If Lauric Acid comes into contact with the eyes, flush the eyes with water for at least 15 minutes, ensuring the eyelids are held open.
Seek medical attention if eye irritation persists.


Inhalation:

In case of accidental inhalation causing respiratory discomfort, move to a well-ventilated area for fresh air.
Seek medical attention if breathing difficulties or respiratory irritation continues.


Ingestion:

If Lauric Acid is ingested accidentally, rinse the mouth with water and drink plenty of water.
It's important to seek medical advice, especially if significant quantities have been ingested or if any adverse reactions occur.



HANDLING AND STORAGE


Handling:

Personal Protection:
When handling, wear appropriate personal protective equipment (PPE) like gloves and safety goggles to avoid direct skin or eye contact.

Ventilation:
Work in a well-ventilated area to minimize inhalation of vapors or dust.

Avoidance of Direct Contact:
In case of skin contact, wash the affected skin area thoroughly with soap and water.

Avoid Inhalation:
Use respiratory protection if working with the compound in an enclosed or poorly ventilated area.

Labeling:
Ensure proper labeling of containers to prevent any confusion, and keep safety data sheets (SDS) accessible.


Storage:

Controlled Environment: Store in a cool, dry area away from direct sunlight to maintain stability and quality.

Temperature: Avoid exposure to extreme temperatures, which may alter the composition and properties of the compound.

Container Sealing:
Use tightly sealed containers to prevent moisture absorption and maintain product integrity.

Segregation:
Store away from incompatible substances to prevent reactions or contamination.

Compliance:
Adhere to local regulations and guidelines for the storage of chemical substances.



SYNONYMS


Dodecoic acid
Dodecyl carboxylic acid
Laurostearic acid
1-Undecanecarboxylic acid
Dodecenoic acid
Dodecylic acid
Duodecyclic acid
C12 fatty acid
Laurostearin
N-Dodecanoic acid
Lauroic acid
Lauroleic acid
C12:0 fatty acid
Doecoic acid
N-Lauroylsarcosine
Lauroglycolic acid
C12 acid
N-Lauroyl-L-tyrosine
Lauroylglycine
Dodecanedioic acid
Duodecanedioic acid
N-Lauroylsarcosinate
Laurostearine
N-Lauroyl-L-phenylalanine
Lauroyltyrosine

lauric acid; n-Dodecanoic acid; Dodecylic acid; Dodecoic acid; Laurostearic acid; Vulvic acid; 1-Undecanecarboxylic acid; Duodecylic acid; cas no:143-07-7

LAURIC ACID 99% is fatty acid derived from renewable vegetable oils.
LAURIC ACID 99% generally consists of a straight chain of an even number of carbon atoms, with hydrogen atoms along the chain’s length and at one end of the chain and a carboxyl group at the other end.
LAURIC ACID 99% is an essential component of lipids in plants, animals, and microorganisms.

CAS Number: 143-07-7
EC Number: 205-582-1
Molecular Formula: C12H24O2

LAURIC ACID 99% acts as a surfactant.
LAURIC ACID 99% is fatty acid derived from renewable vegetable oils.

LAURIC ACID 99% contains C12 (>99%) fatty acid.
LAURIC ACID 99% is readily biodegradable and is GMO-free.

LAURIC ACID 99% is bovine spongiform encephalopathy/ transmissible spongiform encephalopathy-free.
LAURIC ACID 99% is a main renewable ingredient for production of soaps.

LAURIC ACID 99% applications include toiletries, transparent soaps and other cosmetic care products.
LAURIC ACID 99% is used in production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines and fatty amines.

LAURIC ACID 99% is approved by ECOCERT Greenlife in accordance with COSMOS standards.
LAURIC ACID 99% is HALAL and KOSHER certified.

LAURIC ACID 99% is an essential component of lipids in plants, animals, and microorganisms.
LAURIC ACID 99% generally consists of a straight chain of an even number of carbon atoms, with hydrogen atoms along the chain’s length and at one end of the chain and a carboxyl group at the other end.

As such, LAURIC ACID 99% is mainly used in soap, detergent, candles, crayons, personal care, and home care products.
Other applications include LAURIC ACID 99% function as emulsifiers, texturizing agents, wetting agents, anti-foam agents, or stabilizing agents.

In soapmaking, LAURIC ACID 99% is considered an essential building block since the bar of soap that we all see and feel in our hands isn’t just a single soap but a combination of different soaps.
LAURIC ACID 99% that make up our soap molecules include four saturated fatty acids (myristic, lauric, palmitic, and stearic) and four unsaturated fatty acids (ricinoleic, oleic, linoleic, and linolenic).

LAURIC ACID 99% is a biodegradable, GMO-free and fatty oil derived from renewable vegetable oil works as a surfactant, emollient and cleansing agent.
LAURIC ACID 99% is suitable for soaps, toiletries, transparent soaps, and other cosmetic care products.

In addition, to use in the production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines, and fatty amines.
LAURIC ACID 99% is Halal and Kosher certified.

PALMERA Distilled and Fractionated Fatty Acids are produced in accordance with the required demands and quality standards such as GMP and HACCP – making them suitable for food, pharmaceutical and personal care applications.
PALMERA fatty acids such as dimer acids, monomer acids, isostearic acids & more can be used as-is, or as a derivative.
Fatty Acids may be found in plastics, rubber, textiles, lubricants, metal-working, crayons, candles, biocides, paints, inks and etc.

LAURIC ACID 99% is produced by splitting fats and oils to give fatty acid and glycerine.

There is a wide range of applications for fatty acids including:
Plastics and rubber
Pharmaceuticals
Soaps and detergents
Crayons and candles
Cosmetics
Food additives
Varnishes and paints
Synthetic lubricants and cutting oils

Applications of LAURIC ACID 99%:
LAURIC ACID 99% is sed in production of various esters, fatty alcohols, fatty acid isethionates, metallic soaps, fatty acid sarcosinates, imidazolines, fatty amines, oxazolines for paint binder, surfactants in cosmetics, liquid and transparent soaps.
LAURIC ACID 99% is used in agricultural chemicals, food etc.

Beauty Applications:
Decorative Cosmetics, Fragrances, Hair Care, Skin Care, Toiletries

Other Applications:
Pharma and healthcare
Lubricants
Paints and coatings
Industrial chemistry
Personal hygiene
home care

Functions of LAURIC ACID 99%:

Beauty Functionalities:
Emulsifier, Surfactant/ Cleansing Agent

LAURIC ACID 99% material function:
LAURIC ACID 99% is mainly used as a raw material for the production of alkyd resins, wetting agents, detergents, insecticides, surfactants, food additives and cosmetics.
LAURIC ACID 99% is often used as a lubricant and has multiple functions such as lubricant and vulcanizing agent.

However, due to LAURIC ACID 99% corrosive effect on metals, LAURIC ACID 99% is generally not used in plastic products such as wires and cables.
LAURIC ACID 99% is most widely used in the surfactant industry and can also be used in the perfume industry and pharmaceutical industry.

LAURIC ACID 99% is used as a surface treatment agent for the preparation of bonding.
LAURIC ACID 99% is also used in the manufacture of alkyd resins, chemical fiber oils, insecticides, synthetic fragrances, plastic stabilizers, anti-corrosion additives for gasoline and lubricating oils.

LAURIC ACID 99% is widely used in the manufacture of various types of surfactants, such as cationic laurylamine, trilaurylamine, lauryl dimethylamine, lauryl trimethylammonium salt, etc.

LAURIC ACID 99% is anionic types include sodium lauryl sulfate and lauric acid sulfuric acid Ester salts, triethanol ammonium lauryl sulfate, etc.
LAURIC ACID 99% is zwitterionic types include lauryl betaine, imidazoline laurate, etc.

LAURIC ACID 99% is non-ionic surfactants include poly-L-alcohol monolaurate, polyoxyethylene laurate, glyceryl laurate polyoxyethylene ether, lauric acid diethanolamide, etc.
In addition, LAURIC ACID 99% is also used as a food additive and in the manufacture of cosmetics.

LAURIC ACID 99% is the raw material for producing soap, detergent, cosmetic surfactant and chemical fiber oil.

Properties of LAURIC ACID 99%:
LAURIC ACID 99% enhances the antimicrobial protective properties of the skin, has an antibacterial effect, negatively affects a variety of pathogenic microorganisms, bacteria, yeast, fungi and viruses.

Storage of LAURIC ACID 99%:
LAURIC ACID 99% should be stored in a cool, ventilated and dry place , away from heat and fire, moisture-proof and sun-proof.

Identifiers of LAURIC ACID 99%:
INCI Names: LAURIC ACID
Chemical Composition: Lauric acid 99%
CAS Number: 143-07-7
EINECS/ELINCS No:: 205-582-1
Product Status: COMMERCIAL

Classification: Lauric acid
CAS No.: A9912
Other Names: PALMERA
Place of Origin: Malaysia
Grade Standard: Agriculture Grade, Food Grade, Industrial Grade, Medicine Grade, Reagent Grade
Purity: 99%
Product name: Lauric acid
Application: industry, pharmaceutical
Material: surfactant, detergent, cosmetic
Melt point: 43.2 °C
Boiling point: 298.9 °C
Sample: Samples Supplied
Brand: PALMERA

Product Name: 12 Acid / LAURIC ACID 99%
INCI Chinese name: lauric acid
English name: Lauric acid
Brand: Malaysia KLK
Appearance state: white granular

Properties of LAURIC ACID 99%:
Acid Value: 278 – 282
Saponification Value: 279 – 283
Iodine Value: 0.3 max.
Titre: 42 – 44°C
APHA: 40 max
Unsaponifiable matter: % 0.5 max

Specification of LAURIC ACID 99%:
Product Name: Lauric Acid
Application: Wetting agents, Detergents, Surfactants, Food Additives and Cosmetics Raw
Purity: 99%
Feature: White Bead - White Flake
Molecular formula: C12H24O2
Classification: Fatty Acid
Packaging: 25 kg bag , Bulk
MOQ: 1kg-50000kg - Sample Available
Payment: T/T, L/C, D/P, D/A

Other PALMERA products:
PALMERA A2290: Erucic Acid / 112-86-7
PALMERA A2294
PALMERA A1813: Oleic Acid / 112-80-1
PALMERA A1818: Oleic Acid / 112-80-1
PALMERA A5020
PALMERA A5608
PALMERA A7012
PALMERA A8522: Behenic Acid / 112-85-6
PALMERA A8922
PALMERA A9906
PALMERA A9908: Caprylic Acid / 124-07-2
PALMERA A9910: Capric Acid / 334-48-5
PALMERA A9912
PALMERA A9914: Myristic Acid / 544-63-8
PALMERA A9816: Palmitic Acid / 57-11-4
PALMERA A9818: Stearic Acid / 57-11-4
PALMERA B10522
PALMERA B1220: Topped Palm Kernel Fatty Acid / 67701-05-7
PALMERA B1210: Distilled Coconut Fatty Acid / 67701-05-7
PALMERA B1210E: Distilled Coconut Fatty Acid / 67701-05-7
PALMERA B1212E: Distilled Coconut Fatty Acid / 67701-05-7
PALMERA B1217
PALMERA B1640
PALMERA B1800
PALMERA B1802: Tripple Pressed Stearic Acid / 67701-03-5
PALMERA B1802CG: Stearic Acid / 67701-03-5
PALMERA B1899
PALMERA DM
PALMERA IS

Synonyms of LAURIC ACID 99%:
Caprylic – Capric Acid C8 – C10 Blend, PALMERA A5608
Distilled Coconut Fatty Acid, PALMERA B1210
Distilled Palm Kernel Fatty Acid, PALMERA B1217
Distilled Palm Kernel Fatty Acid, PALMERA B1220
Distilled Palm Stearine Fatty Acid, PALMERA B1640
Lauric Acid 98, PALMERA A9812
Lauric Acid 99, PALMERA A9912
Myristic Acid 99, PALMERA A9914
Oleic Acid PALMERA A1813
PALMERA A9908 Caprylic Acid 99
Palmitic Acid 80, PALMERA A8016
Palmitic Acid 92, PALMERA A9216
Palmitic Acid 95, PALMERA A9516
Palmitic Acid 98, PALMERA A9816
Rubber Grade Stearic Acid, PALMERA B1810
Stearic Acid PALMERA A5518
Stearic Acid PALMERA A6518
Stearic Acid PALMERA A7018
Stearic Acid, PALMERA A9218
Stearic Acid, PALMERA B1800
Stearic Acid, PALMERA B1801
Stearic Acid, PALMERA B1802
PALMERA A9912 Lauric Acid
Bergazid C12-99
Cremer Lauric Acid
CremerAC C12/99
Chemceed Lauric Acid
Prifrac 2920 (D)
Prifrac 2922
BAFRORII T40
Lauric acid, food grade
Linatural MBS-2
Linatural MBS-3
Lincoserve WF-1
Lincoserve WF-2
Stearic Acid
Ryoto Sugar Ester LWA-1570
KORTACID 1299
Parchem Lauric Acid
Protameen Chemicals - Lauric Acid
GCA (Glutamate Cystine Arginine)
Miracare MAP-2K14

cas no 111-82-0 dodecanoic acid, methyl ester; Methyl dodecanoate; Methyl laurate; NSC 5027; Methyl dodecanoate; Methyl dodecylate;

Inci : Lauric acid, Cas : 143-07-7, EC : 205-582-1, Synonyme de Acide dodécanoïque,Acide dodécanoïque, Acide laurique, Dodecanoic acid, LAURIC ACID, LAUROSTEARIC ACID. Acid lauric (ro), Acide laurique (fr), Acido laurico (it), Aċidu lawriku (mt), Ido láurico (pt), Kwas laurynowy (pl), Kyselina dodekánová (sk), Lauric acid (no), Lauriinhape (et), Lauriinihappo (fi), Laurinezuur (nl), Laurinsav (hu), Laurinska kiselina (hr), Laurinsyra (sv), Laurinsyre (da), Laurinsäure (de), Laurová kyselina (cs), Laurīnskābe (lv), Lavrinska kislina (sl), Uro rūgštis (lt), Ácido láurico (es), Λαυρικό οξύ (el), Додеканова киселина (bg), laurik asit, laurik asid, lorik asit, lorik asid, 1-Dodecansäure, docecanoic acid

SODIUM LAUROYL LACTYLATE N° CAS : 13557-75-0 - Lauroyl lactylate de sodium Nom INCI : SODIUM LAUROYL LACTYLATE Nom chimique : Sodium 2-(1-carboxylatoethoxy)-1-methyl-2-oxoethyl laurate N° EINECS/ELINCS : 236-942-6 Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile)

Sıvı ürünlerde köpük özelliklerini arttırıcı, düşük irritasyonlu yüzey aktif

Laurostearic Acid is a versatile oleochemical with applications in everything from plastics to personal care.
Laurostearic Acid is a saturated fatty acid with a chain of 12 carbon atoms, hence it has many properties.
Laurostearic Acid and monolaurin have significantly significant antimicrobial activity against gram-positive bacteria and a number of fungi and viruses.

CAS number: 143-07-7
EC number: 205-582-1
Molecular formula: C12H24O2
Molar mass: 200.322 g·mol−1

Synonyms: Emery651, Laurostearic Acid(C12:0), Lauric acid 98%, yeuguisuan, Laurosteaic acid, Lauric acid 98-101 % (acidimetric), lauric acid, pure, LAURIC ACID, 99.5+%, LAURIC ACID, STANDARD FOR GC, LAURIC ACID 98+% FCC, LAURIC ACID 98+% NATURAL FCC, LauricAcid99%Min., LauricAcidPureC12H24O2, Lauric Acid-methyl-D3, lauricacid,dodecanoicacid, n-Dodecanoic, LAURICACID,REAGENT, LAURIC ACID(SG), LAURIC ACID FCC, LAURIC ACID, NATURAL & KOSHER, LAURIC ACID, NATURAL & KOSHER (POWDER), Dodecanoic acid, typically 99%, N-DODECANOIC ACID, RARECHEM AL BO 0156, acidelaurique, Aliphat no. 4, AliphatNo.4, C-1297, Dodecanoic (Lauric) acid, dodecanoic acid (lauric acid), Dodecansαure, Dodecylic acid, dodecylicacid, Duodecyclic acid, Duodecylic acid, duodecylicacid, Emery 650, 1-Dodecanoic acid, LAURINSAEURE, Lauric acid,99.8+%, Lauric acid,95%, Lauric acid,99%, Dodecanoic acid, typically 99.5%, NSC 5026, Palmac 99-12, Trichloroacetic acid lauryl ester, Hendecane-1-carboxylic acid, Lauric acid≥ 98% (GC), AKOS 222-45, C12, C12:0 ACID, CARBOXYLIC ACID C12, LAUROSTEARIC ACID, LAURIC ACID, FEMA 2614, DODECOIC ACID, DODECANOIC ACID, 1-Undecanecarboxylic acid

Laurostearic Acid is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids, is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic Acid are known as laureates.

Laurostearic Acid is a naturally occurring compound found in a variety of animal and vegetable fats and oils, particularly coconut oil and palm kernel oil.
Laurostearic Acid is carried to the whole body by lymphatic portal systems.

Laurostearic Acid or systematically, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids, is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic Acid are known as laureates a fatty acid, CH3(CH2)10COOH, occurring in coconut, palm and laurel oil
Mostly used in making cosmetics and soaps Laurostearic Acid, fatty crystalline acid that is mostly found in coconut and laurel oil (used to make soaps, cosmetic products, etc.) a crystalline fatty acid occurring as glycerides in natural fats and oils (especially coconut oil and palm-kernel oil)

Laurostearic Acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.
Laurostearic Acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Laurostearic Acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.
Laurostearic Acid is a potentially toxic compound.

Laurostearic Acid, C12H24O2, also known as dodecanoic acid, is a saturated fatty acid with a 12-carbon atom chain.
The powdery, white crystalline acid has a slight odor of oil of bay and occurs naturally in various plant and animal fats and oils.

Laurostearic Acid is a major component of coconut oil and palm kernel oil.
Laurostearic Acid is used as an intermediate and surface active agent in industry and in the manufacture of personal care products in the consumer market.

Laurostearic Acid is a saturated medium-chain fatty acid with a 12-carbon backbone.
Laurostearic Acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil.

Laurostearic Acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Laurostearic Acid is a solid at room temperature but melts easily in boiling water, so liquid Laurostearic Acid can be treated with various solutes and used to determine their molecular masses.

Glycerides of Laurostearic Acid are produced by an esterification reaction between Laurostearic Acid and glycerol creating a covalent bond between these two molecules.
They show to possess strong antibacterial properties, especially against Gram-positive pathogenic bacteria.
Laurostearic Acid glycerides interfere with the cell membrane and disturbs vital cell processes of the bacteria.

Laurostearic Acid, also known as dodecanoate or Laurostearic Acid, belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Laurostearic Acid is used for treating viral infections including influenza (the flu); swine flu; avian flu; the common cold; fever blisters, cold sores, and genital herpes caused by herpes simplex virus (HSV); genital warts caused by human papillomavirus (HPV); and HIV/AIDS.
Laurostearic Acid is also used for preventing the transmission of HIV from mothers to children.

Laurostearic Acid is the most abundant fatty acid present in coconut oil.
Laurostearic Acid is also one of the main flavor constituents of Chinese rice wine and sweet cream butter.
Laurostearic Acid is commonly used in lubricants and also in edible-coating formulations.

Laurostearic Acid’s a powerful substance that is sometimes extracted from the coconut for use in developing monolaurin.
Monolaurin is an antimicrobial agent that is able to fight bacteria, viruses, yeasts, and other pathogens.
Because you can’t ingest Laurostearic Acid alone (it’s irritating and not found alone in nature), you’re most likely to get Laurostearic Acid in the form of coconut oil or from fresh coconuts.

Though coconut oil is being studied at a breakneck pace, much of the research doesn’t pinpoint what in the oil is responsible for Laurostearic Acid reported benefits.
Because coconut oil contains much more than just Laurostearic Acid, Laurostearic Acid would be a stretch to credit Laurostearic Acid with all of the coconut oil benefits.

Still, a 2015 analysis suggests that many of the benefits tied to coconut oil are directly linked to Laurostearic Acid.
Among the benefits, they suggest Laurostearic Acid could aid weight loss and even protect against Alzheimer’s disease.

Laurostearic Acids effects on blood cholesterol levels still need to be clarified.
This research suggests that the benefits of Laurostearic Acid are due to how the body uses Laurostearic Acid.

The majority of Laurostearic Acid is sent directly to the liver, where Laurostearic Acid converted to energy rather than stored as fat.
When compared with other saturated fats, Laurostearic Acid contributes the least to fat storage.

To reap the topical benefits of Laurostearic Acid and coconut oil, apply Laurostearic Acid directly to your skin.
While this isn’t recommended for people with acne, the risks are minimal when Laurostearic Acid comes to addressing issues such as skin hydration and psoriasis.

Laurostearic Acid is a saturated fat.
Laurostearic Acid is found in many vegetable fats, particularly in coconut and palm kernel oils.
People use Laurostearic Acid as medicine.

Laurostearic Acid or systematically, is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids, is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic Acid are known as laurates.

Laurostearic Acid is a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.

Laurostearic Acid ( systematically: dodecanoic acid ), the saturated fatty acid with a 12-carbon atom chain, thus falling into the medium chain fatty acids, is a white, powdery solid with a faint odor of bay oil or soap.

Laurostearic Acid is found in many vegetable fats, particularly in coconut and palm kernel oils.
People use Laurostearic Acid as medicine.

Other uses for Laurostearic Acid include treatment of bronchitis, gonorrhea, yeast infections, chlamydia, intestinal infections caused by a parasite called Giardia lamblia, and ringworm.
In foods, Laurostearic Acid is used as a vegetable shortening.
In manufacturing, Laurostearic Acid is used to make soap and shampoo.

Laurostearic Acid and myristic acid are saturated fatty acids.
Their formal names are Laurostearic Acid and tetradecanoic acid, respectively.
Both are white solids that are very slightly soluble in water.

Laurostearic Acid esters (principally triglycerides) are found only in vegetable fats, primarily from coconut milk and oil, laurel oil, and palm kernel oil.
In contrast, myristic acid triglycerides occur in plants and animals, notably in nutmeg butter, coconut oil, and mammalian milk.

Fatty acids have a bad name because they are strongly associated with high serum cholesterol levels in humans.
Lauric and myristic acids are among the worst offenders; therefore, many governmental and health organizations advise that coconut oil and milk, among other high–saturated fat substances, should be excluded from the diet.

Glycerides of Laurostearic Acid are gaining more interest in the fight against viral diseases.
Their molecular structure makes them able to attack fat-enveloped viruses by destroying their fat-envelope.

Several in vitro trials reveal that the antiviral effects of Laurostearic Acid glycerides are outperforming glycerides of other MCFAs.
Globally, glycerides of Laurostearic Acid are applied to suppress the negative impact of Infectious Bronchitis (IB), Newcastle Disease (ND), Avian Influenza (AI), Marek’s disease (MD) and others.

As a result of the multiple actions of Laurostearic Acid glycerides, FRA C12 is a successful tool in antibiotic free diets.
One will notice a reduction in curative antibiotic usage as well as improved animal health and performance with the use of glycerides of Laurostearic Acid.

Laurostearic Acid is a white coat that is slightly soluble in water.
Laurostearic Acid esters (mainly triglycerides) are only found in vegetable oils, particularly coconut milk and oil, bay oil, and palm kernel oil.
In contrast, myristic acid triglycerides occur in plants and animals, particularly nutmeg oil, coconut oil, and mammalian milk.

Fatty acids have a bad name because they are strongly associated with high serum cholesterol levels in humans.
Lauric and myristic acids are among the worst offenders;

Laurostearic Acid is a saturated fatty acid with a chain of 12 carbon atoms, hence a Laurostearic Acid has many properties.
Laurostearic Acid is a dark colored oil solid, a dark colored oil solid and a dark oil.
Laurostearic Acid and monolaurin have significantly significant antimicrobial activity against gram positive bacteria and a number of fungi and viruses.
Today, there are many commercial products that use Laurostearic Acid and monolaurin as antimicrobial agents.

Because of the significant differences in Laurostearic Acid properties compared to longer chain fatty acids, they are typically divided into medium chain fatty acids covering C6 - C12 and long chain fatty acids covering C14 and longer.
Coconut oil is all the rage in natural beauty and wellness regimens.

Numerous blogs and natural health websites have come out as a miracle product and have been able to do anything to relieve chapped skin.
However, when you break down coconut oil into Laurostearic Acid active parts, things start to look less miraculous and more like science.
Laurostearic Acid is one of those active parts.

Laurostearic Acid is a versatile oleochemical with applications in everything from plastics to personal care.
Found in numerous plants including the palm tree and cohune palm, as well as in coconut oil, palm seeds, betel nuts and macadamia nuts, Laurostearic Acid is classified as a saturated fat featuring a 12-carbon atom chain.

There are some researchers who believe that Laurostearic Acid may be safer than trans-fats when used in food preparation.
Laurostearic Acid is a white, powdery solid that exhibits a slight odor reminiscent of bay oil or soap.

As with most fatty acids, Laurostearic Acid is non-toxic, making Laurostearic Acid safe for use in a wide range of applications.
Additionally, Laurostearic Acid is relatively inexpensive, making Laurostearic Acid a popular ingredient in manufacturing processes where cost is a key consideration.

Laurostearic Acid is a saturated fatty acid.
Laurostearic Acids official name is dodecanoic acid.

Laurostearic Acid is a medium-length long-chain fatty acid or lipid that makes up about half of the fatty acids in coconut oil.
Laurostearic Acid is often used in lab research of melting point depression Used, inexpensive, non-toxic and safe to use.
Laurostearic Acid is a solid at room temperature but dissolves easily in boiling water, so liquid Laurostearic Acid can be processed with a variety of solutes and used to determine their molecular mass.

Laurostearic Acid is a fatty acid obtained from coconut oil and other veg- etable fats.
Laurostearic Acid is practically insoluble in water but is soluble in alco- hol, chloroform, and ether.
Laurostearic Acid functions as a lubricant, binder, and defoaming agent.

Laurostearic Acid is a carboxylic acid.
Carboxylic acids donate hydrogen ions if a base is present to accept them.

They react in this way with all bases, both organic (for example, the amines) and inorganic.
Their reactions with bases, called "neutralizations'', are accompanied by the evolution of substantial amounts of heat.
Neutralization between an acid and a base produces water plus a salt.

Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt.
Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry.
Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Laurostearic Acid to corrode or dissolve iron, steel, and aluminum parts and containers.

Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide.
The reaction is slower for dry, solid carboxylic acids.

Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide.
Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides.
Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionite (SO2), to generate flammable and/or toxic gases and heat.

Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat.
Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents.
These reactions generate heat.

Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Laurostearic Acid can react with oxidizing materials.

Some surfactants of the derivatives of Laurostearic Acid and dodecanol are also antiseptics, such as dodecyl dimethyl benzyl ammonium chloride (geramine), dodecyl dimethyl benzyl ammonium bromide (bromo-geramine) and dodecyl dimethyl (2-phenoxyethyl) ammonium bromide (domiphen bromide).
The dodecyldimethyllammonium-2,4,5-trichlorophenolate in these derivatives can be used as citrus preservative.
Laurostearic Acid also has many applications in plastic additives, food additives, spices and pharmaceutical industries.

Laurostearic Acid (C-12) is very common in nature.
Which is a type of monoglyceride when Laurostearic Acid enters the body converted to monolaurin.
Monolaurin; antiviral, antimicrobial, antiprotozoal and antifungal Laurostearic Acid is a substance that stands out with Laurostearic Acid features.

Laurostearic Acid is a saturated fatty acid with a chain of 12 carbon atoms, hence Laurostearic Acid has many properties of medium chain fatty acids, Laurostearic Acid is a dark fatty solid and a dark fatty solid and a dark oil.
Salts and esters of Laurostearic Acid are known as laureates.
Laurostearic Acids chemical formula is CH3 (CH2) 1 (/ 0) COOH.

Production methods of Laurostearic Acid:

Industrial production methods of Laurostearic Acid can be grouped into two categories:
1) Derived from the saponification or high temperature and pressure decomposition of natural vegetable oils and fats;

2) Separated from the synthetic fatty acid.
Japan mainly uses coconut oil and palm kernel oil as the raw materials for the preparation of Laurostearic Acid.

The natural vegetable oils used to produce Laurostearic Acid include coconut oil, litsea cubeba kernel oil, palm kernel oil and mountain pepper seed oil.
Other plants oil, such as palm kernel oil, tea tree seed oil and camphor tree seed oil, can also service industry to produce Laurostearic Acid.
The residual C12 distillate from the extraction of Laurostearic Acid, containing a large number of dodecenoic acid, can be hydrogenated at atmospheric pressure, without catalyst, to convert into Laurostearic Acid with a yield of more than 86%.

Laurostearic Acid derived from the separation and purification of coconut oil and other vegetable oil.

Laurostearic Acid naturally exists in coconut oil, litsea cubeba kernel oil, palm kernel oil and pepper kernel oil in the form of glyceride.
Laurostearic Acid can be derived from the hydrolysis of natural oils and fats in industry.
The coconut oil, water and catalyst are added into the autoclave and hydrolyzed to glycerol and fatty acid at 250 ℃ under the pressure of 5MPa.

The content of Laurostearic Acid is 45%~80%, and can be further distilled to obtain Laurostearic Acid.
Laurostearic Acid is a fatty carboxylic acid isolated from vegetable and animal fats or oils.

For example, coconut oil and palm kernel oil both contain high proportions of Laurostearic Acid.
Isolation from natural fats and oils involves hydrolysis, separation of the fatty acids, hydrogenation to convert unsaturated fatty acids to saturated acids, and finally distillation of the specific fatty acid of interest.

Occurrence of Laurostearic Acid:
Laurostearic Acid, a component of triglycerides, makes up about half the fatty acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil), otherwise, Laurostearic Acid is relatively rare.
Laurostearic Acid is also found in breast milk (6.2% of total fat), cow's milk (2.9%) and goat's milk (3.1%).

Laurostearic Acid is one of these active parts.
Laurostearic Acid is a medium-length long-chain fatty acid or lipid that makes up about half of the fatty acids in coconut oil.

Laurostearic Acid is a potent substance sometimes extracted from coconut for use in developing monolaurin.
Monolaurin, bacteria, Laurostearic Acid is an antimicrobial agent that can fight pathogens such as viruses and yeasts.
You cannot digest Laurostearic Acid alone, as Laurostearic Acid is irritating and does not occur alone in nature.

You are most likely to get Laurostearic Acid in the form of coconut oil or fresh coconut.
While coconut oil is being studied at breakthrough speed, most of the research does not pinpoint exactly what is responsible for the oil's reported benefits.
Since coconut oil contains a lot more than Laurostearic Acid, Laurostearic Acid would be too long to credit Laurostearic Acid with all the benefits of coconut oil.

Still, a 2015 analysis suggested that most of the benefits linked to coconut oil were directly attributed to Laurostearic Acid.
They suggest that Laurostearic Acid may aid weight loss and protect against Alzheimer's disease, among other benefits.
The effects on blood cholesterol levels still need to be cl.

Laurostearic Acid, as a component of triglycerides, comprises about half of the fatty-acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil), Otherwise, Laurostearic Acid is relatively uncommon.
Laurostearic Acid is also found in human breast milk (6.2% of total fat), cow's milk (2.9%), and goat's milk (3.1%).

Like many other fatty acids, Laurostearic Acid is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.
Laurostearic Acid is used mainly for the production of soaps and cosmetics.

For these purposes, Laurostearic Acid is reacted with sodium hydroxide to give sodium laurate, which is a soap.
Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
These precursors give mixtures of sodium laurate and other soaps.

Applications of Laurostearic Acid:
Laurostearic Acid is mainly used in the manufacturing of soaps and other cosmetics.
In scientific laboratories, Laurostearic Acid is often used to investigate the molar mass of unknown substances via freezing-point depression.
In industry, Laurostearic Acid is used as an intermediate and as a surface active agent.

The consumer market uses Laurostearic Acid in the cleaning, furnishing, and production of personal care products.
In medicine, Laurostearic Acid is known to increase total serum cholesterol more than many of the other fatty acids.
Laurostearic Acid uses include acid chlorides, amphoteric surfactant intermediate, anti ageing creams & lotions, antiperspirants, bar soap, betaines, body wash, cosmetics, deodorants, emollient, emulsifier, exfoliant scrub, facial cleaner, foundations, glycerol esters, hair care, hair colorants, imidazolines, lip balm, liquid hand soap, lubricant, moisturizing cream formulations, organic peroxides, sarcosinates, shaving cream, shower gels, skin care products, etc.

Treatment for intestinal infections and ringworm caused by the parasite.
Laurostearic Acid in foods is used as a vegetable abbreviation.

In manufacturing, Laurostearic Acid is used to make soap and shampoo.
Laurostearic Acid is not known how Laurostearic Acid works as a medicine.
Some research suggests that Laurostearic Acid may be a safer oil than trans fats in food preparations.

Pharmaceutical Applications of Laurostearic Acid:
Laurostearic Acid has also been examined for use as an enhancer for topical penetration and transdermal absorption, rectal absorption, buccal delivery, and intestinal absorption.
Laurostearic Acid is also useful for stabilizing oil-in-water emulsions.
Laurostearic Acid has also been evaluated for use in aerosol formulations.

Uses of Laurostearic Acid:
Laurostearic Acid Used for the preparation of alkyd resins, as well as wetting agents, detergents and pesticides
Laurostearic Acid is used for peeling vegetables and fruits with a maximum amount of 3.0g/kg.

Laurostearic Acid is used as defoamer; GB 2760-86 provides for the spices allowed to use; used for the preparation of other food grade additives.
Laurostearic Acid is widely used in the surfactant industry and can be, according to the classification of surfactants, divided into cationic, anionic, non-ionic and amphoteric type.

Some surfactants of the derivatives of Laurostearic Acid and dodecanol are also antiseptics, such as dodecyl dimethyl benzyl ammonium chloride (geramine), dodecyl dimethyl benzyl ammonium bromide (bromo-geramine) and dodecyl dimethyl (2-phenoxyethyl) ammonium bromide (domiphen bromide).
The dodecyldimethyllammonium-2,4,5-trichlorophenolate in these derivatives can be used as citrus preservative.
Laurostearic Acid also has many applications in plastic additives, food additives, spices and pharmaceutical industries.

Consumer Uses of Laurostearic Acid:
Laurostearic Acid is used in the following products: washing & cleaning products, coating products, fillers, putties, plasters, modelling clay, finger paints, polishes and waxes, air care products and plant protection products.
Other release to the environment of Laurostearic Acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Cleaning and furnishing care products,
Cleaning compound,
Floor coverings,
Industrial organic chemicals used in commercial and consumer products,
Lubricants and greases,
Personal care products.

Industry Uses of Laurostearic Acid:
Laurostearic Acid is used in the following products: washing & cleaning products, leather treatment products, polymers, textile treatment products and dyes, pH regulators and water treatment products and lubricants and greases.
Laurostearic Acid is used in the following areas: formulation of mixtures and/or re-packaging and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.

Laurostearic Acid is used for the manufacture of: textile, leather or fur.
Release to the environment of Laurostearic Acid can occur from industrial use: in processing aids at industrial sites, in the production of articles, as processing aid and as processing aid.

Commercial and industrial products,
Dyes,
Intermediates.

Widespread uses of Laurostearic Acid by professional workers:
Laurostearic Acid is used in the following products: washing & cleaning products, polishes and waxes, adhesives and sealants, cosmetics and personal care products and laboratory chemicals.
Laurostearic Acid is used in the following areas: formulation of mixtures and/or re-packaging and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.

Laurostearic Acid is used for the manufacture of: textile, leather or fur.
Release to the environment of Laurostearic Acid can occur from industrial use: formulation of mixtures and in processing aids at industrial sites.
Other release to the environment of Laurostearic Acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Biocidal Uses of Laurostearic Acid:
Laurostearic Acid is approved for use as a biocide in the EEA and/or Switzerland, for: repelling or attracting pests.

Laurostearic Acid For Acne Uses:
Because Laurostearic Acid has antibacterial properties, Laurostearic Acid been found to effectively combat acne.
The bacteria Propionibacterium acnes are found naturally on the skin.
When they overgrow, they lead to the development of acne.

The results of a 2009 study found that Laurostearic Acid could reduce inflammation and the number of bacteria present.
Laurostearic Acid worked even better than benzoyl peroxide, a common acne treatment.
A 2016 study also reconfirmed the acne-fighting properties of Laurostearic Acid.

This doesn’t mean you should put coconut oil on your acne.
The researchers used pure Laurostearic Acid and suggested that Laurostearic Acid could be developed into an antibiotic therapy for acne in the future.

Laboratory uses of Laurostearic Acid:
In the laboratory, Laurostearic Acid may be used to investigate the molar mass of an unknown substance via the freezing-point depression.
The choice of Laurostearic Acid is convenient because the melting point of the pure compound is relatively high (43.8°C).

Laurostearic Acid cryoscopic constant is 3.9°C·kg/mol.
By melting Laurostearic Acid with the unknown substance, allowing Laurostearic Acid to cool, and recording the temperature at which the mixture freezes, the molar mass of the unknown compound may be determined.

Intermediates of Liquid Crystals:
Given Laurostearic Acids foaming properties, the derivatives of Laurostearic Acid (h-dodecanoic acid) are widely used as a base in the manufacture of soaps, detergents, and lauryl alcohol.
Laurostearic Acid is a common constituent of vegetable fats, especially coconut oil and laurel oil.

Laurostearic Acid may have a synergistic effect in a formula to help fight against mircoorganisms.
Laurostearic Acid is a mild irritant but not a sensitizer, and some sources cite Laurostearic Acid as comedogenic.

Laurostearic Acid is a fatty acid obtained from coconut oil and other veg- etable fats.
Laurostearic Acid is practically insoluble in water but is soluble in alco- hol, chloroform, and ether.
Laurostearic Acid functions as a lubricant, binder, and defoaming agent.

Other Uses of Laurostearic Acid:

In Plastics of Laurostearic Acid:
In plastics manufacturing applications, Laurostearic Acid serves as an intermediate, which is substance formed during the middle stages of a chemical reaction between the reactants and the finished product.

In Food and Beverage of Laurostearic Acid:
One of the more common uses of Laurostearic Acid is as raw material for emulsifiers in various food and beverage additives, particularly in the manufacturing of vegetable shortening.
Laurostearic Acids nontoxicity also makes Laurostearic Acid safe for use in food production.

In Surfactants and Esters of Laurostearic Acid:
When used as anionic and nonionic surfactants, Laurostearic Acid has the ability to reduce surface tension between liquids and solids.

In Textiles of Laurostearic Acid:
Laurostearic Acid works well as a lubricant & process agent in textile manufacturing applications, as Laurostearic Acid has the ability to help water mix with oil.

In Personal Care of Laurostearic Acid:
One of the more common Laurostearic Acid uses is as an emulsifier for facial creams and lotions, as Laurostearic Acid possesses a strong ability to cleanse skin and hair.
Laurostearic Acid is also easy to wash away after use.
You can find Laurostearic Acid in many personal care products such as shampoos, body washes and shower gels.

In Soaps and Detergents of Laurostearic Acid:
When used as a base in the production of liquid and transparent soaps, Laurostearic Acid can control the level of lathering, add conditioning properties and enhance overall cleaning ability.

In Medical of Laurostearic Acid:
Laurostearic Acid can be found in a variety of medicines used for treating viral infections, certain forms of influenza, fever blisters, cold sores, bronchitis, yeast infections, gonorrhea, genital herpes and many others.
However, there is insufficient evidence to determine Laurostearic Acid overall effectiveness in treating these conditions.
Preliminary research also indicates that Laurostearic Acid may aid in the treatment of acne as well.

Laurostearic Acid, or dodecanoic acid, is the main acid in coconut oil and in palm kernel oil, and is believed to have antimicrobial properties.
The detected values of half maximal effective concentration (EC(50)) of Laurostearic Acid on P. acnes, S. aureus, and S. epidermidis growth indicate that P. acnes is the most sensitive to Laurostearic Acid among these bacteria.

In addition, Laurostearic Acid did not induce cytotoxicity to human sebocytes.
This data highlight the potential of using Laurostearic Acid as an alternative treatment for antibiotic therapy of acne vulgaris.
Laurostearic Acid is used in the manufacture of soaps, detergents, cosmetics, and lauryl alcohol.

In Cleansing of Laurostearic Acid:
Helps to keep a clean surface

In Emulsifying of Laurostearic Acid:
Promotes the formation of intimate mixtures between immiscible liquids by modifying the interfacial tension (water and oil)

In Surfactant of Laurostearic Acid:
Reduces the surface tension of cosmetics and contributes to the even distribution of the product when Laurostearic Acid is used

Diet With Laurostearic Acid:
Laurostearic Acid can be taken as a supplement, but Laurostearic Acid is most commonly consumed as part of coconut oil or palm kernel oil.
Laurostearic Acid is considered to be safe based on the amounts generally found in food.

However, because they are still pure oil, limit your intake of MCTs to stay within the recommended 5 to 7 teaspoons of oil per day as set out by the U.S. Department of Agriculture.
You can use coconut and palm kernel oil for stir-fries because both oils withstand high heat.
They can also be used in baking, adding a natural richness to your food.

Manufacture of Laurostearic Acid:
Release to the environment of Laurostearic Acid can occur from industrial use: manufacturing of Laurostearic Acid.

Industry Processing Sectors of Laurostearic Acid:
All other basic organic chemical manufacturing,
All other chemical product and preparation manufacturing,
Petroleum lubricating oil and grease manufacturing,
Plastic material and resin manufacturing,
Soap, cleaning compound, and toilet preparation manufacturing,
Synthetic dye and pigment manufacturing,
Textiles, apparel, and leather manufacturing.

Chemical properties of Laurostearic Acid:
Laurostearic Acid is colorless needle-like crystals.
Laurostearic Acid is soluble in methanol, slightly soluble in acetone and petroleum ether.

Like many other fatty acids, Laurostearic Acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle.
Laurostearic Acid is mainly used for the production of soaps and cosmetics.
For these purposes, Laurostearic Acid is neutralized with sodium hydroxide to give sodium laurate, which is a soap.

Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
These precursors give mixtures of sodium laurate and other soaps.
Laurostearic Acid occurs as a white crystalline powder with a slight odor of bay oil.

Laurostearic Acid is a white solid with a faint odour of bay oil
Laurostearic Acid has a fatty odor.
Laurostearic Acid is a common constituent of most diets; large doses may produce gastrointestinal upset

Potential medicinal properties of Laurostearic Acid:
Laurostearic Acid increases total serum cholesterol more than many other fatty acids, but mostly high-density lipoprotein (HDL) (the "good" blood cholesterol).
As a result, Laurostearic Acid has been characterized as having "a more favorable effect on total HDL cholesterol than any other fatty acid, either saturated or unsaturated".

In general, a lower total/HDL serum cholesterol ratio correlates with a decrease in atherosclerotic risk.
Nonetheless, an extensive meta-analysis on foods affecting the total LDL/serum cholesterol ratio found in 2003 that the net effects of Laurostearic Acid on coronary artery disease outcomes remained uncertain.
A 2016 review of coconut oil (which is nearly half Laurostearic Acid) was similarly inconclusive about the effects on cardiovascular disease risk.

Formulation or re-packing of Laurostearic Acid:
Laurostearic Acid is used in the following products: polymers, pH regulators and water treatment products, leather treatment products, coating products, fillers, putties, plasters, modelling clay, finger paints, inks and toners, cosmetics and personal care products, lubricants and greases and textile treatment products and dyes.
Release to the environment of Laurostearic Acid can occur from industrial use: formulation of mixtures and formulation in materials.

Storage of Laurostearic Acid:
Laurostearic Acid is stable at normal temperatures and should be stored in a cool, dry place.
Avoid sources of ignition and contact with incompatible materials.

Release Of Laurostearic Acid Into The Environment:
Release to the environment of Laurostearic Acid can occur from industrial use: industrial abrasion processing with high release rate (e.g. sanding operations or paint stripping by shot-blasting) and industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).
Other release to the environment of Laurostearic Acid is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).

Laurostearic Acid can be found in complex articles, with no release intended: vehicles and machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines).
Laurostearic Acid can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture) and paper used for packaging (excluding food packaging).

Identifiers of Laurostearic Acid:
CAS Number: 143-07-7
CHEBI:30805
ChEMBL: ChEMBL108766
ChemSpider: 3756
ECHA InfoCard: 100.005.075
EC Number: 205-582-1
IUPHAR/BPS: 5534
KEGG: C02679
PubChem CID: 3893
UNII: 1160N9NU9U
CompTox Dashboard (EPA): DTXSID5021590

Properties of Laurostearic Acid:
Chemical formula: C12H24O2
Molar mass: 200.322 g·mol−1
Appearance: White powder
Odor: Slight odor of bay oil
Density:
1.007 g/cm3 (24 °C)
0.8744 g/cm3 (41.5 °C)
0.8679 g/cm3 (50 °C)
Melting point: 43.8 °C (110.8 °F; 316.9 K)
Boiling point:
297.9 °C (568.2 °F; 571.0 K)
282.5 °C (540.5 °F; 555.6 K) at 512 mmHg
225.1 °C (437.2 °F; 498.2 K) at 100 mmHg
Solubility in water:
37 mg/L (0 °C)
55 mg/L (20 °C)
63 mg/L (30 °C)
72 mg/L (45 °C)
83 mg/L (100 °C)
Solubility: Soluble in alcohols, diethyl ether, phenyls, haloalkanes, acetates
Solubility in methanol:
12.7 g/100 g (0 °C)
120 g/100 g (20 °C)
2250 g/100 g (40 °C)
Solubility in acetone:
8.95 g/100 g (0 °C)
60.5 g/100 g (20 °C)
1590 g/100 g (40 °C)
Solubility in ethyl acetate:
9.4 g/100 g (0 °C)
52 g/100 g (20°C)
1250 g/100 g (40°C)
Solubility in toluene:
15.3 g/100 g (0 °C)
97 g/100 g (20°C)
1410 g/100 g (40°C)
log P 4.6
Vapor pressure:
2.13·10−6 kPa (25 °C)
0.42 kPa (150 °C)
6.67 kPa (210 °C)
Acidity (pKa):5.3 (20 °C)
Thermal conductivity:
0.442 W/m·K (solid)
0.1921 W/m·K (72.5 °C)
0.1748 W/m·K (106 °C)
Refractive index (nD):
1.423 (70 °C)
1.4183 (82 °C)
Viscosity:
6.88 cP (50 °C)
5.37 cP (60 °C)

Names of Laurostearic Acid:

Regulatory process names of Laurostearic Acid:
Dodecanoic acid
Lauric acid
Lauric Acid
Lauric acid
lauric acid

Translated names of Laurostearic Acid:
Acid lauric (ro)
Acide laurique (fr)
Acido laurico (it)
Aċidu lawriku (mt)
Ido láurico (pt)
Kwas laurynowy (pl)
Kyselina dodekánová (sk)
Lauric acid (no)
Lauriinhape (et)
Lauriinihappo (fi)
Laurinezuur (nl)
Laurinsav (hu)
Laurinska kiselina (hr)
Laurinsyra (sv)
Laurinsyre (da)
Laurinsäure (de)
Laurová kyselina (cs)
Laurīnskābe (lv)
Lavrinska kislina (sl)
Uro rūgštis (lt)
Ácido láurico (es)
Λαυρικό οξύ (el)
Додеканова киселина (bg)

CAS names of Laurostearic Acid:
Dodecanoic acid

IUPAC names of Laurostearic Acid:
1-Dodecansäure
docecanoic acid
DODECANOIC ACID
Laurostearic Acid
Dodecanoic acid
dodecanoic acid
Lauric Acid
Lauric acid
lauric acid
Lauric Acid
Lauric acid
lauric acid
Laurinic acid
Laurinsäure
n-Dodecanoic acid

Trade names of Laurostearic Acid:
DODECANOIC ACID
KORTACID 1299/ 1298/ 1295
Lauric Acid
MASCID 1298
MASCID 1299
PALMAC 98-12
PALMAC 99-12
Palmata 1299
PALMERA
RADIACID 0653
SINAR - FA1299
Tefacid Lauric 98
UNIOLEO FA 1299

Other identifiers of Laurostearic Acid:
143-07-7
203714-07-2
203714-07-2
7632-48-6
7632-48-6
8000-62-2
8000-62-2
8045-27-0
8045-27-0

Laurostearic acid is a white, powdery solid with a faint odor of bay oil or soap.
Laurostearic acid, Reagent, also known as N-Dodecanoic acid, is a medium chain fatty acid that has a vague smell of soap and is a powder.
Laurostearic acid is a saturated fatty acid with the structural formula CH3(CH2)10COOH .


CAS Number: 143-07-7
EC Number: 205-582-1
MDL Number: MFCD00004440
Molecular formula: C10H18O4 / HOOC(CH2)8COOH



SYNONYMS:
Dodecanoic acid, n-Dodecanoic acid, Dodecylic acid, Dodecoic acid, Laurostearic acid, Vulvic acid, 1-Undecanecarboxylic acid, Duodecylic acid, C12:0 (Lipid numbers), Laurostearic acid, Laurates, NSC 5026, Vulvic acid, 1-Dodecanoic acid, Dodecanoates, Lauric acid, Dodecylic acid, 1-Undecanecarboxylic acid, FA12:0, n-Dodecanoic acid, lauric acid, n-dodecanoic acid, dodecylic acid, vulvic acid, laurostearic acid, dodecoic acid, duodecylic acid, 1-undecanecarboxylic acid, aliphat no. 4, neo-fat 12, Decanedioic acid, 1,8-Octanedicarboxylic acid, Decane-1,10-dioic acid, sebacic acid, DECANEDIOIC ACID, 111-20-6, 1,8-Octanedicarboxylic acid, 1,10-Decanedioic acid, Sebacic acids, Sebacinsaure, Decanedicarboxylic acid, n-Decanedioic acid, Acide sebacique, Sebacinsaeure, USAF HC-1, Ipomic acid, Seracic acid, Decanedioic acid, homopolymer, NSC 19492, UNII-97AN39ICTC, 1,8-dicarboxyoctane, 26776-29-4, NSC19492, 97AN39ICTC, octane-1,8-dicarboxylic acid, CHEBI:41865, NSC-19492, DSSTox_CID_6867, DSSTox_RID_78231, DSSTox_GSID_26867, SebacicAcid, CAS-111-20-6, CCRIS 2290, EINECS 203-845-5, BRN 1210591, n-Decanedioate, Iponic acid, AI3-09127, disodium-sebacate, 4-oxodecanedioate, MFCD00004440, 1,10-Decanedioate, Sebacic acid, 94%, Sebacic acid, 99%, Dicarboxylic acid C10, 1i8j, 1l6s, 1l6y, 1,8-Octanedicarboxylate, WLN: QV8VQ, SEBACIC ACID, EC 203-845-5, SCHEMBL3977, NCIOpen2_008624, SEBACIC ACID, 4-02-00-02078, SEBACIC ACID, CHEMBL1232164, DTXSID7026867, Sebacic acid, >=95.0% (GC), ZINC1531045, Tox21_201778, Tox21_303263, BBL011473, LMFA01170006, s5732, STL146585, AKOS000120056, CCG-266598, CS-W015503, DB07645, GS-6713, HY-W014787, NCGC00164361-01, NCGC00164361-02, NCGC00164361-03, NCGC00257150-01, NCGC00259327-01, BP-27864, NCI60_001628, DB-121158, FT-0696757, C08277, A894762, C10-120, C10-140, C10-180, C10-220, C10-260, C10-298, Q413454, Q-201703, Z1259273339, 301CFA7E-7155-4D51-BD2F-EB921428B436, 1,8-Octanedicarboxylic acid, Decanedioic acid, Octane-1,8-dicarboxylic acid, 1,10-Decanedioic Acid, 1,8-Octanedicarboxylic Acid, NSC 19492, NSC 97405, n-Decanedioic Acid, 1,10-Decanedioate, 1,10-Decanedioic acid, 1,8-Dicarboxyoctane, 1,8-Octanedicarboxylate, 1,8-Octanedicarboxylic acid, 4,7-Dioxosebacic acid, 4,7-dioxosebacic acid, 4-Oxodecanedioate, 4-oxodecanedioate, 4-Oxodecanedioic acid, 1,10-Decanedioic acid, 1,8-Dicarboxyoctane, Decanedioic acid, Sebacinsaeure, 1,10-Decanedioate, Decanedioate, Sebacate, 1,8-Octanedicarboxylate, 1,8-Octanedicarboxylic acid, 4,7-Dioxosebacic acid, 4-Oxodecanedioate, 4-Oxodecanedioic acid, Acide sebacique, Decanedicarboxylic acid, Dicarboxylic acid C10, Ipomic acid, N-Decanedioate, N-Decanedioic acid, Sebacic acids, Sebacinsaure, Seracic acid, Sebacic acid, aluminum salt, Sebacic acid, monocadmium salt, Sebacic acid, sodium salt, DECANEDIOIC ACID, sebacic, USAF hc-1, acidesebacique, SEBACIC ACID pure, n-Decanedioic acid, 1,10-Decanedioic acid, Decanedicarboxylic acid, sebacate (decanedioate), 1,8-OCTANEDICARBOXYLIC ACID, 1,10-Decanedioate, 1,10-Decanedioic acid, 1,8-Octanedicarboxylate, 1,8-Octanedicarboxylic acid, 4,7-Dioxosebacic acid, 4-Oxodecanedioate, 4-Oxodecanedioic acid, Acide sebacique, Decanedicarboxylic acid, Decanedioate, 1,8-Octanedicarboxylic acid, 1,10-Decanedioic acid, n-Decanedioic acid, 4-Oxodecanedioate, 1,8-Dicarboxyoctane, Octane-1,8-dicarboxylic acid, Sebacic acid, Ipomic acid, Seracic acid, lauric acid, DODECANOIC ACID, 143-07-7, n-Dodecanoic acid, Dodecylic acid, Laurostearic acid, Vulvic acid, Dodecoic acid, Duodecylic acid, 1-Undecanecarboxylic acid, Aliphat No. 4, Ninol AA62 Extra, Wecoline 1295, Hydrofol acid 1255, Hydrofol acid 1295, Duodecyclic acid, Hystrene 9512, Univol U-314, Lauric acid, pure, Dodecylcarboxylate, Lauric acid (natural), Laurinsaeure, Undecane-1-carboxylic acid, ABL, NSC-5026, FEMA No. 2614, laurate, C-1297, Philacid 1200, CCRIS 669, C12:0, Emery 651, Lunac L 70, CHEBI:30805, HSDB 6814, EINECS 205-582-1, UNII-1160N9NU9U, BRN 1099477, n-Dodecanoate, Kortacid 1299, Dodecanoic Acid Anion, DTXSID5021590, Prifrac 2920, AI3-00112, Lunac L 98, Univol U 314, Prifac 2920, 1160N9NU9U, MFCD00002736, DAO, DTXCID801590, CH3-[CH2]10-COOH, NSC5026, EC 205-582-1, dodecylate, laurostearate, vulvate, 4-02-00-01082 (Beilstein Handbook Reference), DODECANOIC ACID (LAURIC ACID), 1-undecanecarboxylate, LAURIC ACID (USP-RS), LAURIC ACID [USP-RS], CH3-(CH2)10-COOH, 8000-62-2, CAS-143-07-7, SMR001253907, laurinsaure, dodecanic acid, Nuvail, lauric-acid, Acide Laurique, 3uil, Lauric acid (NF), DODECANOICACID, fatty acid 12:0, Lauric Acid, Reagent, Nissan NAA 122, Emery 650, Dodecanoic acid, 98%, Dodecanoic acid, 99%, Guaranteed Reagent,99%, Dodecanoic (Lauric) acid, LAURIC ACID [MI], bmse000509, LAURIC ACID [FCC], LAURIC ACID [FHFI], SCHEMBL5895, NCIOpen2_009480, MLS002177807, MLS002415737, WLN: QV11, Dodecanoic acid (lauric acid), LAURIC ACID [WHO-DD], Dodecanoic acid, >=99.5%, Edenor C 1298-100, DODECANOIC ACID [HSDB], CHEMBL108766, GTPL5534, NAA 122, NAA 312, HMS2268C14, HMS3649N06, HY-Y0366, STR08039, Dodecanoic acid, analytical standard, Lauric acid, >=98%, FCC, FG, Tox21_202149, Tox21_303010, BDBM50180948, LMFA01010012, s4726, STL281860, AKOS000277433, CCG-266587, DB03017, FA 12:0, HYDROFOL ACID 1255 OR 1295, NCGC00090919-01, NCGC00090919-02, NCGC00090919-03, NCGC00256486-01, NCGC00259698-01, AC-16451, BP-27913, DA-64879, Dodecanoic acid, >=99% (GC/titration), LAU, Dodecanoic acid, purum, >=96.0% (GC), Lauric acid, natural, >=98%, FCC, FG, CS-0015078, L0011, NS00008441, EN300-19951, C02679, D10714, A808010, LAURIC ACID (CONSTITUENT OF SAW PALMETTO), Q422627, SR-01000838338, J-007739, SR-01000838338-3, BRD-K67375056-001-07-9, F0001-0507, LAURIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC], Z104476194, 76C2A2EB-E8BA-40A6-8032-40A98625ED7B, Lauric acid, European Pharmacopoeia (EP) Reference Standard, Lauric acid, United States Pharmacopeia (USP) Reference Standard, Lauric Acid, Pharmaceutical Secondary Standard; Certified Reference Material, 203714-07-2, 7632-48-6, InChI=1/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14, 1-Undecanecarboxylate, 1-Undecanecarboxylic acid, ABL, Acide Laurique, C12 fatty acid, C12:0, Coconut oil fatty acids, DAO, Dodecanoate, dodecanoic acid, dodecoate, Dodecoic acid, Dodecylate, dodecylcarboxylate, Dodecylic acid, duodecyclate, Duodecyclic acid, duodecylate, Duodecylic acid, LAP, LAU, Laurate, Lauric acid, Laurinsaeure, Laurostearate, Laurostearic acid, MYR, n-Dodecanoate, n-Dodecanoic acid, Sorbitan laurate, Sorbitan monolaurate (NF), undecane-1-carboxylate, Undecane-1-carboxylic acid, Vulvate, Vulvic acid, CH3-[CH2]10-COOH, Dodecylcarboxylic acid, Laate, Laic acid, Aliphat no. 4, Edenor C 1298-100, Emery 651, Hystrene 9512, Kortacid 1299, Lunac L 70, Lunac L 98, Neo-fat 12, Neo-fat 12-43, Nissan naa 122, Philacid 1200, Prifac 2920, Univol u 314, 1-Dodecanoic acid, FA(12:0), 1-Undecanecarboxylic acid, ABL, Aliphat no. 4, C12 fatty acid, Coconut oil fatty acids, Dodecanoate, Dodecanoic (lauric) acid, Dodecanoic acid (lauric acid), Dodecoic acid, Dodecylcarboxylate, Dodecylic acid, Duodecyclic acid, Duodecylic acid, Emery 650, Lauric acid, Lauric acid, pure, Laurinsaeure, Laurostearic acid, Lunac L 70, n-Dodecanoic Acid, N-Dodecanoate, Neo-fat 12, Ninol aa62 extra, Undecane-1-carboxylic acid, Univol U 314, Univol U-314, Vulvic acid, AI3-00112, BRN 1099477, C-1297, CCRIS 669, EINECS 205-582-1, FEMA NO. 2614, HSDB 6814, HYDROFOL ACID 1255, HYDROFOL ACID 1295, HYSTRENE 9512, NEO-FAT 12-43, PHILACID 1200, PRIFRAC 2920, WECOLINE 1295, 1-Undecanecarboxylic acid, ABL, AC-16451, AC1L1GY2, AC1Q5W8C, AKOS000277433, Aliphat No. 4, CH3-[CH2]10-COOH, Coconut oil fatty acids, DAO, DODECANOIC ACID, DODECANOIC ACID (LAURIC ACID), Dodecanoate, Dodecanoic (Lauric) acid, Dodecanoic acid (lauric acid), Dodecanoic acid(Lauric acid), Dodecoic acid, Dodecylcarboxylate, Dodecylic acid, Duodecyclic acid, Duodecylic acid, Emery 650, Hydrofol acid 1255, Hydrofol acid 1295, Hystrene 9512, I04-1205, L-ALFA-LYSOPHOSPHATIDYLCHOLINE, LAUROYL, L0011, LAP, LAU, Lauric acid, pure, Laurinsaeure, Laurostearic acid, Lunac L 70, Neo-fat 12, Neo-fat 12-43, Ninol AA62 Extra, Philacid 1200, Prifrac 2920, SMR001253907, ST023796, Undecane-1-carboxylic acid, Univol U-314, Vulvic acid, Wecoline 1295, [2-((1-OXODODECANOXY-(2-HYDROXY-3-PROPANYL))-PHOSPHONATE-OXY)-ETHYL]-TRIMETHYLAMMONIUM, n-Dodecanoate, n-Dodecanoic acid, nchembio.364-comp10, Dodecanoic acid, n-Dodecanoic acid, Neo-fat 12, Aliphat no. 4, Abl, Dodecylic acid, Lauric acid, Laurostearic acid, Neo-fat 12-43, Ninol aa62 extra, Univol u-314, Vulvic acid, 1-Undecanecarboxylic acid, Duodecylic acid, C-1297, Coconut oil fatty acids, Hydrofol acid 1255, Hydrofol acid 1295, Wecoline 1295, Dodecoic acid, Hystrene 9512, Lunac L 70, Duodecyclic acid, Emery 650, n-Dodecanoate, Philacid 1200, Prifrac 2920, Undecane-1-carboxylic acid, C-1297, dodecanoic acid, dodecoic acid, duodecylic acid, ndodecanoic acid, Hydrofol acid 1255, Hydrofol acid 1295, Hystrene 9512, laurostearic acid, Neo-fat 12, Neo-fat 12-43, Ninol AA62 Extra, 1-undecanecarboxylic acid, vulvic acid, Wecoline 1295, Dodecoic acid, Duodecyclic acid, Edenor C 1298-100, Emery 650, Hydrofol acid 1295, Hystrene 9512, Kortacid 1299, Laurostearate, Lunac L 70, Lunac L 98, Neo-fat 12, Ninol AA62 extra, Nissan naa 122, Philacid 1200, Prifac 2920, Prifrac 2920, Univol U 314, Vulvate, Vulvic acid, Wecoline 1295, 1-Undecanecarboxylate, 1-Undecanecarboxylic acid, Dodecylate, Dodecylcarboxylate, Dodecylic acid, Duodecylic acid, Laurostearic acid, n-Dodecanoic acid, Undecane-1-carboxylic acid, LAP, LAU, DAO, lauric acid, n-dodecanoic acid, dodecylic acid, vulvic acid, laurostearic acid, dodecoic acid, duodecylic acid, 1-undecanecarboxylic acid, aliphat no. 4, neo-fat 12, 143-07-7, 205-582-1, 1-UNDECANECARBOXYLIC ACID, DODECANOIC ACID, DODECANOIC ACID [HSDB], DODECOIC ACID, FEMA NO. 2614, LAURATE, LAURIC ACID (CONSTITUENT OF SAW PALMETTO) [DSC], LAURIC ACID [FCC], LAURIC ACID [FHFI], LAURIC ACID [MI], LAURIC ACID [USP-RS], LAURIC ACID [WHO-DD], LAUROSTEARIC ACID, N-DODECANOIC ACID, NSC-5026, Dodecanoic acid, Lauric acid, Laurostearic acid, 1-Undecanecarboxylic acid, ABL, Aliphat No. 4, Univol U 314, Dodecylic acid, Vulvic acid, Neo-Fat 12-43, n-Dodecanoic acid, Neo-Fat 12, Lunac L 70, Emery 651, Prifac 2920, Nissan NAA 122, Lunac L 98, Hystrene 9512, NAA 312, Kortacid 1299, Philacid 1200, Edenor C 1298-100, NSC 5026, NAA 122, Prifac 2922, Edenor C 12, Prifrac 2920, ContraZeck, 1-Dodecanoic acid, Imex C 1299, Palmac 98-12, Edenor 12/98-100, Palmera B 1231, Edenor C 12-98-100, Lasacid FC 12, Laurates, Dodecanoates, Palmae 99-12, D 97385, Edenor C12-99, Coconut Hard 34, Coconut Hard 42, Radiacid 0624, NS 6, 7632-48-6, 8000-62-2, 8045-27-0, 203714-07-2, 55621-34-6, DODECANOIC ACID, C12, Emery651, Vulvic acid, FEMA 2614, lauric acid, pure, N-DODECANOIC ACID, LAUROSTEARIC ACID, Lauric acid 98-101 % (acidimetric), Fatty acid methyl ester sulfonate (MES), Dodecanoic D23 Acid, Dodecanoic Acid-d23,1-Dodecanoic Acid-d23, 1-Undecanecarboxylic Acid-d23, ABL-d23, Aliphat No. 4-d23, ContraZeck-d23, Dodecylic Acid-d23, Edenor C 12-d23,Edenor C 1298-100-d23, Emery 651-d23, Hystrene 9512-d23, Imex C 1299-d23, Kortacid 1299-d23, Laurostearic Acid-d23, Lunac L 70-d23, Lunac L 98-d23, NAA 122-d23, NAA 312-d23, NSC 5026-d23, Neo-Fat 12-d23, Neo-Fat 12-43-d23, Nissan NAA 122-d23, Philacid 1200-d23, Prifac 2920-d23, Prifac 2922-d23, Prifrac 2920-d23, Univol U 314-d23, Vulvic Acid-d23, n-Dodecanoic Acid-d23, Dodecanoate, Coconut Oil Fatty Acids, Laurostearic Acid, N-Dodecanoic Acid, C12 Fatty Acid, Duodecyclic Acid, Vulvic Acid, Dodecanoic Acid (Lauric Acid), Duodecylic Acid, N-Dodecanoate, Dodecanoic (Lauric) Acid, Laurinsaeure, Lauric Acid, Pure, Lauric Acid (Natural), Dodecylcarboxylate, Abl, Dao, Lap, Lau, Myr



Laurostearic acid is a saturated fatty acid with the structural formula CH3(CH2)10COOH .
Laurostearic acid is the main acid in coconut oil and in palm kernel oil, and is believed to have antimicrobial properties.
Laurostearic acid is also found in human milk(5.8% of total fat), cows milk(2.2%), and goat milk(4.5%).


Laurostearic acid is a white, powdery solid with a faint odor of bay oil or soap.
Laurostearic acid, Reagent, also known as Laurostearic acid, is a medium chain fatty acid that has a vague smell of soap and is a powder.
Laurostearic acid is found naturally in human breast milk as well as cow's and goat's milk.


Laurostearic acid's reagent grade means this is the highest quality commercially available for this chemical and that the American Chemical Society has not officially set any specifications for this material.
Laurostearic acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.


Laurostearic acid is a solid at room temperature but melts easily in boiling water, so liquid Laurostearic acid can be treated with various solutes and used to determine their molecular masses.
Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.


Laurostearic acid is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic acid are known as laurates.
Laurostearic acid is a saturated fatty acid with a terminal carboxylic acid.


The terminal carboxylic acid, Laurostearic acid, can react with primary amine groups in the presence of activators such as HATU.
Laurostearic acid is a carbon 13 labeled form of a saturated fatty acid found in coconut milk, coconut oil, laurel oil, and palm kernel oil, as well as in human breast milk and other animal milks.


Laurostearic acid is a proton pump inhibitor potentially for the treatment of helicobacter pylori infections.
In vitro experiments have suggested that some fatty acids including Laurostearic acid could be a useful component in a treatment for acne, but no clinical trials have yet been conducted to evaluate this potential benefit in humans.


Laurostearic acid increases total serum cholesterol more than many other fatty acids.
But most of the increase is attributable to an increase in high-density lipoprotein (HDL) (the "good" blood cholesterol).
As a result, Laurostearic acid has been characterized as having "a more favorable effect on total HDL cholesterol than any other fatty acid, either saturated or unsaturated.


Laurostearic acid, identified by CAS number 143-07-7, is a saturated medium-chain fatty acid with a 12-carbon atom backbone, prominently known for its role in the manufacturing of soaps, detergents, and cosmetics.
As a fundamental component, Laurostearic acid is celebrated for its surfactant properties, which enable the production of a rich lather in cleansing products.


In research, Laurostearic acid is extensively used to study lipid behavior in various systems due to its amphiphilic nature, which allows it to assemble into micelles and other nanostructures in aqueous solutions.
These studies are crucial for advancing the fields of material science and nanotechnology, particularly in the development of delivery systems and the enhancement of product formulations.


Additionally, Laurostearic acid is employed in food science research where it serves as a model to understand the digestion and metabolism of medium-chain fatty acids.
Laurostearic acid's antimicrobial properties are also examined in terms of how they can be leveraged in non-medical applications, such as in food preservation and safety, where reducing microbial growth is essential.


Moreover, Laurostearic acid′s role in industrial applications extends to its use as a raw material in the synthesis of various chemical derivatives, including esters used in flavorings and fragrances, showcasing its versatility and importance in both scientific research and industrial applications.
Laurostearic acid is a saturated medium-chain fatty acid with a 12-carbon backbone.


Laurostearic acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil.
Laurostearic acid, C12H24O2, also known as Laurostearic acid, is a saturated fatty acid with a 12-carbon atom chain.
The powdery, white crystalline acid, Laurostearic acid, has a slight odor of oil of bay and occurs naturally in various plant and animal fats and oils.


Laurostearic acid is found in many vegetable fats and in coconut and palm kernel oils.
Laurostearic acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.


Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.
Laurostearic acid is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic acid are known as laurates.


Laurostearic acid is a precursor to dilauroyl peroxide, a common initiator of polymerizations.
Laurostearic acid belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.


Laurostearic acid, also known as dodecanoate or lauric acid, belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
Laurostearic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


Laurostearic acid is the main fatty acid in coconut oil and in palm kernel oil, and is believed to have antimicrobial properties.
Laurostearic acid is a white, powdery solid with a faint odour of bay oil.
Laurostearic acid, although slightly irritating to mucous membranes, has a very low toxicity and so is used in many soaps and shampoos.


Laurostearic acid is a fatty acid that has been shown to inhibit the growth of bacteria.
Laurostearic acid inhibits bacterial growth by binding to the active site of the enzyme dihydrolipoamide acetyltransferase, which catalyzes the conversion of dihydrolipoamide and acetyl-CoA to succinyl-CoA and acetoacetyl-CoA.


Laurostearic acid also binds to dinucleotide phosphate, which is involved in regulation of phase transition temperature and biological samples.
Laurostearic acid has also been shown to act as an active inhibitor of fatty acid synthase, an enzyme that catalyzes the synthesis of fatty acids from acetyl-coenzyme A (acetyl-CoA).


This process is essential for bacterial growth.
Laurostearic acid has synergistic effects with other antibiotics such as ampicillin, erythromycin, and tetracycline.
Laurostearic acid is a saturated medium-chain fatty acid with a 12-carbon backbone.


Laurostearic acid is a major component of coconut oil and palm kernel oil.
Laurostearic acid, CAS 143-07-7, chemical formula C12H24O2, is produced as a white crystalline powder, has a slight odor of bay oil, and is soluble in water, alcohols, phenyls, haloalkanes, and acetates.


Laurostearic acid is non-toxic, safe to handle, inexpensive, and has a long shelf life.
Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain, thus falling into the medium chain fatty acids.
Laurostearic acid is a white, powdery solid with a faint odor of bay oil or soap.


Laurostearic acid belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
Laurostearic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


Laurostearic acid is a potentially toxic compound.
Laurostearic acid has the chemical formula C12H24O2.
Laurostearic acid appears as a white crystalline solid with a characteristic odor like oil of bay.


Laurostearic acid is insoluble in Water and soluble in Ether, Chloroform, and Alcohol.
Laurostearic acid is found naturally in some plant and animal fats and is a key component of coconut oil.
Laurostearic acid is synthetically prepared by the fractional distillation of other acids of mixed coconut.


Laurostearic acid is a white solid with a slight odor of bay oil.
Laurostearic acid is a straight-chain, twelve-carbon medium-chain saturated fatty acid with strong bactericidal properties; the main fatty acid in coconut oil and palm kernel oil.


Laurostearic acid has a role as a plant metabolite, an antibacterial agent and an algal metabolite.
Laurostearic acid is a straight-chain saturated fatty acid and a medium-chain fatty acid.
Laurostearic acid is a conjugate acid of a dodecanoate.


Laurostearic acid derives from a hydride of a dodecane.
Laurostearic acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Laurostearic acid is a solid at room temperature but melts easily in boiling water, so liquid lauric acid can be treated with various solutes and used to determine their molecular masses.


Laurostearic acid is a metabolite found in or produced by Escherichia coli.
Laurostearic acid is a natural product found in Ipomoea leptophylla, Arisaema tortuosum, and other organisms with data available.
Laurostearic acid is a saturated medium-chain fatty acid with a 12-carbon backbone.


Laurostearic acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil.
Laurostearic acid is the main fatty acid in coconut oil and in palm kernel oil, and is believed to have antimicrobial properties.
Laurostearic acid is a white, powdery solid with a faint odor of bay oil.


Laurostearic acid, although slightly irritating to mucous membranes, has a very low toxicity and so is used in many soaps and shampoos.
Laurostearic acid is a metabolite found in or produced by Saccharomyces cerevisiae.
Laurostearic acid is a medium-chain saturated fatty acid.


Laurostearic acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil.
Laurostearic acid is a medium-length long-chain fatty acid, or lipid, that makes up about half of the fatty acids within coconut oil.
Laurostearic acid’s a powerful substance that is sometimes extracted from the coconut for use in developing monolaurin.


Monolaurin is an antimicrobial agent that is able to fight bacteria, viruses, yeasts, and other pathogens.
Because you can’t ingest Laurostearic acid alone (it’s irritating and not found alone in nature), you’re most likely to get it in the form of coconut oil or from fresh coconuts.


Though coconut oil is being studied at a breakneck pace, much of the research doesn’t pinpoint what in the oil is responsible for its reported benefits.
Because coconut oil contains much more than just Laurostearic acid, it would be a stretch to credit it with all of the coconut oil benefits.
Still, a 2015 analysis suggests that many of the benefits tied to coconut oil are directly linked to Laurostearic acid.


Among the benefits, they suggest Laurostearic acid could aid weight loss and even protect against Alzheimer’s disease.
Its effects on blood cholesterol levels still need to be clarified.
This research suggests that the benefits of Laurostearic acid are due to how the body uses it.


The majority of Laurostearic acid is sent directly to the liver, where it’s converted to energy rather than stored as fat.
When compared with other saturated fats, Laurostearic acid contributes the least to fat storage.
Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain, thus having many properties of medium-chain fatty acids.


Laurostearic acid is a bright white, powdery solid with a faint odor of bay oil or soap.
The salts and esters of Laurostearic acid are known as laurates.
Like many other fatty acids, Laurostearic acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle.


Laurostearic acid is mainly used for the production of soaps and cosmetics.
For these purposes, Laurostearic acid is neutralized with sodium hydroxide to give sodium laurate, which is a soap.
Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.


These precursors give mixtures of sodium laurate and other soaps. Laurostearic acid occurs as a white crystalline powder
Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain used in industrial cleaners, lubricants, soaps, surfactants, agricultural additives, coatings, food additives, textile additives.


Laurostearic acid, the saturated fatty acid with a 12-carbon atom chain, thus falling into the medium chain fatty acids, is a white, powdery solid with a faint odor of bay oil or soap.
Laurostearic acid, as a component of triglycerides, comprises about half of the fatty acid content in coconut oil, laurel oil, and in palm kernel oil.


Otherwise Laurostearic acid is relatively uncommon.
Laurostearic acid increases total serum cholesterol the most of any fatty acid.
But most of the increase is attributable to an increase in high-density lipoprotein (HDL) (the "good" blood cholesterol).


As a result, Laurostearic acid has been characterized as having "a more favorable effect on total:HDL cholesterol than any other fatty acid, either saturated or unsaturated."
In general, a lower total/HDL serum cholesterol ratio correlates with a decrease in atherosclerotic risk.


For these purposes, Laurostearic acid is neutralized with sodium hydroxide to give sodium laurate, which is a soap.
Laurostearic acid is a saturated fatty acid with a 12-carbon atom chain, thus falling into the medium chain fatty acids.
Laurostearic acid is a white crystalline carboxylic acid with a faint odor of bay oil or soap.


Laurostearic acid has been found at high levels in coconut oil.
Laurostearic acid induces the activation of NF-κB and the expression of COX-2, inducible nitric oxide synthase (iNOS), and IL-1α in RAW 264.7 cells when used at a concentration of 25 μM.


Laurostearic acid is a straight-chain, twelve-carbon medium-chain saturated fatty acid with strong bactericidal properties; the main fatty acid in coconut oil and palm kernel oil.
Laurostearic acid has a role as a plant metabolite, an antibacterial agent and an algal metabolite.


Laurostearic acid is a straight-chain saturated fatty acid and a medium-chain fatty acid.
Laurostearic acid is a conjugate acid of a dodecanoate.
Laurostearic acid derives from a hydride of a dodecane.


Laurostearic acid is a white crystalline carboxylic acid.
Laurostearic acid is used as a plasticizer and for making detergents and soaps.
Laurostearic acid's glycerides occur naturally in coconut and palm oils.


Laurostearic acid is a white solid with a slight odor of bay oil.
Laurostearic acid belongs to the class of organic compounds known as medium-chain fatty acids.
These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.


Laurostearic acid is a white, powdery solid with a faint odour of mild fatty coconut bay oil or soap.
Laurostearic acid is the main fatty acid in coconut oil (49%) and in palm kernel oil (47-50%), and is found in lesser amounts in wild nutmeg, human breast milk, cow’s milk, goat milk, watermelon seeds, plum and macadamia nut.


Laurostearic acid, although slightly irritating to mucous membranes, has an extremely low toxicity, is inexpensive, has antimicrobial properties and so is used in many soaps and shampoos.
Laurostearic acid is a weakly acidic compound.


Laurostearic acid is reacted with sodium hydroxide to generate sodium laurate, which is soap.
Laurostearic acid has been characterized as having "a more favorable effect on total HDL cholesterol than any other fatty acid either saturated or unsaturated"



USES and APPLICATIONS of LAUROSTEARIC ACID:
Laurostearic acid is used in the preparation of cosmetics, soaps, alkyd resins and wetting agents.
Laurostearic acid is also used to measure the molar mass of an unknown substance through freezing point depression.
Laurostearic acid is also used as a food additive and an active component in a treatment for acne.


Laurostearic acid is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Laurostearic acid is approved for use as a biocide in the EEA and/or Switzerland, for: repelling or attracting pests.


People also use Laurostearic acid as medicine.
People use Laurostearic acid for viral infections such as the flu, common cold, genital herpes, and many other conditions, but there is no good scientific evidence to support any use.


Laurostearic acid is used in the following products: washing & cleaning products, coating products, fillers, putties, plasters, modelling clay, finger paints, polishes and waxes, air care products and plant protection products.
Other release to the environment of Laurostearic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Release to the environment of Laurostearic acid can occur from industrial use: industrial abrasion processing with high release rate (e.g. sanding operations or paint stripping by shot-blasting) and industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).


Other release to the environment of Laurostearic acid is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints).


Laurostearic acid can be found in complex articles, with no release intended: vehicles and machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines).
Laurostearic acid is also used as a food additive and an active component in a treatment for acne.


Laurostearic acid can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture) and paper used for packaging (excluding food packaging).


In addition to this, Laurostearic acid is a substrate for acylation of certain proteins based on the murine studies.
Laurostearic acid is used in the preparation of cosmetics, soaps, alkyd resins and wetting agents.
Laurostearic acid is also used to measure the molar mass of an unknown substance through freezing point depression.


The consumer market uses Laurostearic acid in the cleaning, furnishing, and production of personal care products.
In medicine, Laurostearic acid is known to increase total serum cholesterol more than many of the other fatty acids.
Laurostearic acid is mainly used in the manufacture and production of soaps and other cosmetics as well as scientific laboratory uses.


Laurostearic acid is used as an intermediate and surface active agent in industry and in the manufacture of personal care products in the consumer market.
Laurostearic acid is used in the preparation of cosmetics, soaps, alkyd resins and wetting agents.
Laurostearic acid is also used to measure the molar mass of an unknown substance through freezing point depression.


Laurostearic acid is also used as a food additive and an active component in a treatment for acne.
In addition to this, Laurostearic acid is a substrate for acylation of certain proteins based on the murine studies.
Laurostearic acid is used in the preparation of cosmetics, soaps, alkyd resins and wetting agents.


Laurostearic acid is also used to measure the molar mass of an unknown substance through freezing point depression.
Laurostearic acid is also used as a food additive and an active component in a treatment for acne.
In addition to this, Laurostearic acid is a substrate for acylation of certain proteins based on the murine studies.


Laurostearic acid is used in the preparation of cosmetics, soaps, alkyd resins and wetting agents.
Laurostearic acid is also used to measure the molar mass of an unknown substance through freezing point depression.
Laurostearic acid is also used as a food additive and an active component in a treatment for acne.


In addition to this, Laurostearic acid is a substrate for acylation of certain proteins based on the murine studies.
Laurostearic acid is generally used to produce cosmetic products but is also used in the laboratory to obtain the molar mass of substances.
Laurostearic acid, although slightly irritating to mucous membranes, has a very low toxicity and so is used in many soaps and shampoos.


Sodium lauryl sulfate is the most common Laurostearic acid derived compound used for this purpose.
Because Laurostearic acid has a non-polar hydrocarbon tail and a polar carboxylic acid head, it can interact with polar solvents (the most important being water) as well as fats, allowing water to dissolve fats.


This accounts for the abilities of shampoos to remove grease from hair.
Another use is to raise metabolism, believed to derive from Laurostearic acid's activation of 20% of thyroidal hormones, otherwise which lay dormant.
This is supposed from Laurostearic acid's release of enzymes in the intestinal tract which activate the thyroid.


This could account the metabolism-raising properties of coconut oil.
Because Laurostearic acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle, it is often used in laboratory investigations of melting-point depression.


In addition to this, Laurostearic acid is a substrate for acylation of certain proteins based on the murine studies.
Laurostearic acid is used in the following products: washing & cleaning products, polishes and waxes, adhesives and sealants, cosmetics and personal care products and laboratory chemicals.


Laurostearic acid is used in the following areas: formulation of mixtures and/or re-packaging and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.
Laurostearic acid is used for the manufacture of: textile, leather or fur.


Release to the environment of Laurostearic acid can occur from industrial use: formulation of mixtures and in processing aids at industrial sites.
Other release to the environment of Laurostearic acid is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Laurostearic acid is used in the following products: polymers, pH regulators and water treatment products, leather treatment products, coating products, fillers, putties, plasters, modelling clay, finger paints, inks and toners, cosmetics and personal care products, lubricants and greases and textile treatment products and dyes.


Release to the environment of Laurostearic acid can occur from industrial use: formulation of mixtures and formulation in materials.
Laurostearic acid is used in the following products: washing & cleaning products, leather treatment products, polymers, textile treatment products and dyes, pH regulators and water treatment products and lubricants and greases.


Laurostearic acid is used in the following areas: formulation of mixtures and/or re-packaging and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.
Laurostearic acid is used for the manufacture of: textile, leather or fur.


Release to the environment of Laurostearic acid can occur from industrial use: in processing aids at industrial sites, in the production of articles, as processing aid and as processing aid.
Release to the environment of Laurostearic acid can occur from industrial use: manufacturing of the substance.


Laurostearic acid is an inexpensive, non-toxic and safe to handle compound often used in laboratory investigations of melting-point depression.
Laurostearic acid is a solid at room temperature but melts easily in boiling water, so liquid lauric acid can be treated with various solutes and used to determine their molecular masses.


In the laboratory, Laurostearic acid may be used to investigate the molar mass of an unknown substance via the freezing-point depression.
The choice of Laurostearic acid is convenient because the melting point of the pure compound is relatively high (43.8°C).
Its cryoscopic constant is 3.9°C•kg/mol.


By melting Laurostearic acid with the unknown substance, allowing it to cool, and recording the temperature at which the mixture freezes, the molar mass of the unknown compound may be determined.
In industry, Laurostearic acid is used as an intermediate and as a surface active agent.


Industrial applications of Laurostearic acid and its derivatives include the fatty acid as a component of alkyd resins, wetting agents, a rubber accelerator and softener, detergents, and insecticides.
The consumer market uses Laurostearic acid in the cleaning, furnishing, and production of personal care products.


In medicine, Laurostearic acid is known to increase total serum cholesterol more than many of the other fatty acids.
Common Uses and Applications of Laurostearic acid: Additive, Acidifiers, Chemical intermediate, Lubricant, Synthesis of substances, Industries, Chemical Production, Personal Care, and Laboratories.


Laurostearic acid is mainly used in the manufacturing of soaps and other cosmetics.
In scientific laboratories, Laurostearic acid is often used to investigate the molar mass of unknown substances via freezing-point depression.
In industry, Laurostearic acid is used as an intermediate and as a surface active agent.


Laurostearic acid is a solid at room temperature but melts easily in boiling water, so liquid it can be treated with various solutes and used to determine their molecular masses.
Laurostearic acid is widely used in cosmetics and food products.


In pharmaceutical applications Laurostearic acid has also been examined for use as an enhancer for topical penetration and transdermal absorption, rectal absorption, buccal delivery, and intestinal absorption.
Laurostearic acid is also useful for stabilizing oil-in-water emulsions.


Laurostearic acid has also been evaluated for use in aerosol formulations.
Laurostearic acid is used in the production of personal care products via the salt sodium laurate.
Laurostearic acid is also studied in metabolic and foodomics research for its potential impact on cardiovascular disease.


Laurostearic acid has been used as a reagent to synthesize MnFe2O4 magnetic nanoparticles by seed mediated growth method.
Laurostearic acid can undergo esterification with 2-ethylhexanol in the presence of sulfated zirconia catalyst to form 2-ethylhexanoldodecanoate, a biodiesel.
Like many other fatty acids, Laurostearic acid is inexpensive, has a long shelf-life, is nontoxic, and is safe to handle.


Laurostearic acid is used mainly for the production of soaps and cosmetics.
For these purposes, Laurostearic acid is reacted with sodium hydroxide to give sodium laurate, which is a soap.
Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.


These precursors give mixtures of sodium laurate and other soaps.
Laurostearic acid is used for the preparation of alkyd resins, as well as wetting agents, detergents and pesticides
Laurostearic acid is used for peeling vegetables and fruits with a maximum amount of 3.0g/kg.


Laurostearic acid is used as defoamer; GB 2760-86 provides for the spices allowed to use; used for the preparation of other food grade additives.
Laurostearic acid is widely used in the surfactant industry and can be, according to the classification of surfactants, divided into cationic, anionic, non-ionic and amphoteric type.


The surfactants types of Laurostearic acid are listed in the attached table of this item.
Some surfactants of the derivatives of Laurostearic acid and dodecanol are also antiseptics, such as dodecyl dimethyl benzyl ammonium chloride (geramine), dodecyl dimethyl benzyl ammonium bromide (bromo-geramine) and dodecyl dimethyl (2-phenoxyethyl) ammonium bromide (domiphen bromide).


The dodecyldimethyllammonium-2,4,5-trichlorophenolate in these derivatives can be used as citrus preservative.
Laurostearic acid is a fatty acid obtained from coconut oil and other veg- etable fats.
Laurostearic acid is practically insoluble in water but is soluble in alcohol, chloroform, and ether.


Laurostearic acid functions as a lubricant, binder, and defoaming agent.
Laurostearic acid is used intermediates of Liquid Crystals
Laurostearic acid is also used as a food additive and an active component in a treatment for acne.


Laurostearic acid also has many applications in plastic additives, food additives, spices and pharmaceutical industries.
Given its foaming properties, the derivatives of lauric acid (h-Laurostearic acid) are widely used as a base in the manufacture of soaps, detergents, and lauryl alcohol.


Laurostearic acid is a common constituent of vegetable fats, especially coconut oil and laurel oil.
Laurostearic acid may have a synergistic effect in a formula to help fight against mircoorganisms.
Laurostearic acid is a mild irritant but not a sensitizer, and some sources cite it as comedogenic.


-Uses of Laurostearic acid in Perfume:
Laurostearic acid is used in Butter flavors and in certain Citrus flavor types, mainly in Lemon.
The concentration of Laurostearic acid used may vasy from 2 to 40 ppm, calculated upon the finished consumer product.


-Pharmaceutical Applications of Laurostearic acid:
pharmaceutical applications it has also been examined for use as an enhancer for topical penetration and transdermal absorption, rectal absorption, buccal delivery,(14) and intestinal absorption.
Laurostearic acid is also useful for stabilizing oil-in-water emulsions.
Laurostearic acid has also been evaluated for use in aerosol formulations.



ALTERNATIVE PARENTS OF LAUROSTEARIC ACID:
*Dicarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS OF LAUROSTEARIC ACID:
*Medium-chain fatty acid
*Dicarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



COMPOUND TYPE OF LAUROSTEARIC ACID:
*Animal Toxin
*Cosmetic Toxin
*Food Toxin
*Industrial/Workplace Toxin
*Metabolite
*Natural Compound
*Organic Compound
*Plasticizer



CHEMICAL PROPERTIES OF LAUROSTEARIC ACID:
Laurostearic acid is a colorless needle-like crystals.
Laurostearic acid is soluble in methanol, slightly soluble in acetone and petroleum ether.



STABILITY AND STORAGE CONDITIONS OF LAUROSTEARIC ACID:
Laurostearic acid is stable at normal temperatures and should be stored in a cool, dry place.



SOURCE AND PREPARATION OF LAUROSTEARIC ACID:
Laurostearic acid is a fatty carboxylic acid isolated from vegetable and animal fats or oils.
For example, coconut oil and palm kernel oil both contain high proportions of Laurostearic acid.
Isolation from natural fats and oils involves hydrolysis, separation of the fatty acids, hydrogenation to convert unsaturated fatty acids to saturated acids, and finally distillation of the specific fatty acid of interest.



OCCURRENCE OF LAUROSTEARIC ACID:
Laurostearic acid, as a component of triglycerides, comprises about half of the fatty acid content in coconut oil, laurel oil, and in palm kernel oil (not to be confused with palm oil).
Otherwise Laurostearic acid is relatively uncommon.
Laurostearic acid is also found in human breast milk ( 6.2 % of total fat), cow's milk (2.9%), and goat's milk (3.1 %).



SAFETY OF LAUROSTEARIC ACID:
Laurostearic acid is widely used in cosmetic preparations, in the manufacture of food-grade additives, and in pharmaceutical formulations.
General exposure to Laurostearic acid occurs through the consumption of food and through dermal contact with cosmetics, soaps, and detergent products.

Occupational exposure may cause local irritation of eyes, nose, throat, and respiratory tract, although Laurostearic acid is considered safe and nonirritating for use in cosmetics.
No toxicological effects were observed when Laurostearic acid was administered to rats at 35% of the diet for 2 years.



MEDIUM-CHAIN TRIGLYCERIDES OF LAUROSTEARIC ACID:
Medium-chain triglycerides, or fatty acids, such as Laurostearic acid, are characterized by a specific chemical structure that allows your body to absorb them whole.

This makes them more easily digestible--your body processes them as it would carbohydrates, and they are used as a source of direct energy.
Compared to long-chain triglycerides, the type in other saturated fats, MCTs have fewer calories per serving, roughly 8.3 calories per gram rather than the standard 9 calories per gram, according to an article in "Nutrition Review."



NUTRITIONAL AND MEDICAL ASPECTS OF LAUROSTEARIC ACID:
Although 95% of medium-chain triglycerides are absorbed through the portal vein, only 25–30% of Laurostearic acid is absorbed through it.
Laurostearic acid induces apoptosis in cancer and promotes the proliferation of normal cells by maintaining cellular redox homeostasis.
Laurostearic acid increases total serum lipoproteins more than many other fatty acids, but mostly high-density lipoprotein (HDL).

As a result, Laurostearic acid has been characterized as having "a more favorable effect on total HDL than any other fatty acid [examined], either saturated or unsaturated".
In general, a lower total/HDL serum lipoprotein ratio correlates with a decrease in atherosclerotic incidence.

Nonetheless, an extensive meta-analysis on foods affecting the total LDL/serum lipoprotein ratio found in 2003 that the net effects of Laurostearic acid on coronary artery disease outcomes remained uncertain.
A 2016 review of coconut oil (which is nearly half Laurostearic acid) was similarly inconclusive about the effects on cardiovascular disease incidence.



INCLUDING LAUROSTEARIC ACID IN YOUR DIET:
Laurostearic acid can be taken as a supplement, but it is most commonly consumed as part of coconut oil or palm kernel oil.
Laurostearic acid is considered to be safe based on the amounts generally found in food.

According to NYU Langone Medical Center, coconut and palm kernel oil contain up to 15 percent MCTs, along with a number of other fats.
However, because they are still pure oil, limit your intake of MCTs to stay within the recommended 5 to 7 teaspoons of oil per day as set out by the U.S. Department of Agriculture.

You can use coconut and palm kernel oil for stir-fries because both oils withstand high heat.
They can also be used in baking, adding a natural richness to your food.



PHYSICAL PROPERTIES OF LAUROSTEARIC ACID:
Laurostearic acid occurs as a white crystalline powder with a slight odor of bay oil or a fatty odor.
Laurostearic acid is a common constituent of most diets; large doses may produce gastrointestinal upset.



CHEMICAL PROPERTIES OF LAUROSTEARIC ACID:
Like many other fatty acids, Laurostearic acid is inexpensive, has a long shelf-life, and is non-toxic and safe to handle.
Laurostearic acid is mainly used for the production of soaps and cosmetics.

For these purposes, Laurostearic acid is neutralized with sodium hydroxide to give sodium laurate, which is a soap.
Most commonly, sodium laurate is obtained by saponification of various oils, such as coconut oil.
These precursors give mixtures of sodium laurate and other soaps.



PRODUCTION METHODS OF LAUROSTEARIC ACID:
1. Industrial production methods can be grouped into two categories:
* derived from the saponification or high temperature and pressure decomposition of natural vegetable oils and fats;
* separated from the synthetic fatty acid.

Japan mainly uses coconut oil and palm kernel oil as the raw materials for the preparation of Laurostearic acid.
The natural vegetable oils used to produce Laurostearic acid include coconut oil, litsea cubeba kernel oil, palm kernel oil and mountain pepper seed oil.

Other plants oil, such as palm kernel oil, tea tree seed oil and camphor tree seed oil, can also service industry to produce Laurostearic acid.
The residual C12 distillate from the extraction of Laurostearic acid, containing a large number of dodecenoic acid, can be hydrogenated at atmospheric pressure, without catalyst, to convert into Laurostearic acid with a yield of more than 86%.

2. Derived from the separation and purification of coconut oil and other vegetable oil.

3. Laurostearic acid naturally exists in coconut oil, litsea cubeba kernel oil, palm kernel oil and pepper kernel oil in the form of glyceride.
Laurostearic acid can be derived from the hydrolysis of natural oils and fats in industry.
The coconut oil, water and catalyst are added into the autoclave and hydrolyzed to glycerol and fatty acid at 250 ℃ under the pressure of 5MPa.
The content of Laurostearic acid is 45%~80%, and can be further distilled to obtain Laurostearic acid.



AIR AND WATER REACTIONS OF LAUROSTEARIC ACID:
Laurostearic acid is insoluble in water.



AROMA THRESHOLD VALUES OF LAUROSTEARIC ACID:
Aroma threshold values
Aroma characteristics at 1.0%: fatty, creamy, cheeselike, candle waxy with egglike richness



TASTE THRESHOLD VALUES OF LAUROSTEARIC ACID:
Taste characteristics at 5 ppm: waxy,fatty and oily, tallowlike, creamy and dairylike with a coating mouthfeel



REACTIVITY PROFILE OF LAUROSTEARIC ACID:
Laurostearic acid is a carboxylic acid.
Carboxylic acids donate hydrogen ions if a base is present to accept them.
They react in this way with all bases, both organic (for example, the amines) and inorganic.

Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat.
Neutralization between an acid and a base produces water plus a salt.
Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt.

Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry.
Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Laurostearic acid to corrode or dissolve iron, steel, and aluminum parts and containers.

Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide.
The reaction is slower for dry, solid carboxylic acids.
Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide.



PRODUCTION METHODS OF LAUROSTEARIC ACID:
Laurostearic acid is a fatty carboxylic acid isolated from vegetable and animal fats or oils.
For example, coconut oil and palm kernel oil both contain high proportions of Laurostearic acid.
Isolation from natural fats and oils involves hydrolysis, separation of the fatty acids, hydrogenation to convert unsaturated fatty acids to saturated acids, and finally distillation of the specific fatty acid of interest.



SOLUBILITY OF LAUROSTEARIC ACID:
Laurostearic acid is soluble in water, benzene, acetone, alcohol, petroleum ether, dimethyl sulfoxide and dimethyl formamide.
Laurostearic acid is slightly soluble in chloroform.



NOTES OF LAUROSTEARIC ACID:
Laurostearic acid is incompatible with bases, oxidizing agents and reducing agents.



WHERE TO FIND LAUROSTEARIC ACID:
Laurostearic acid is a powerful substance that’s sometimes extracted from the coconut for use in developing monolaurin.
Monolaurin is an antimicrobial agent that’s able to fight pathogens such as bacteria, viruses, and yeasts.



OCCURRENCE OF LAUROSTEARIC ACID:
Laurostearic acid, as a component of triglycerides, comprises about half of the fatty-acid content in coconut milk, coconut oil, laurel oil, and palm kernel oil (not to be confused with palm oil).

Otherwise, Laurostearic acid is relatively uncommon.
Laurostearic acid is also found in human breast milk (6.2% of total fat), cow's milk (2.9%), and goat's milk (3.1%).

In various plants:
*The palm tree Attalea speciosa, a species popularly known in Brazil as babassu – 50% in babassu oil
*Attalea cohune, the cohune palm (also rain tree, American oil palm, corozo palm or manaca palm) – 46.5% in cohune oil
*Astrocaryum murumuru (Arecaceae) a palm native to the Amazon – 47.5% in "murumuru butter"
*Coconut oil 49%
*Pycnanthus kombo (African nutmeg)
*Virola surinamensis (wild nutmeg) 7.8–11.5%
*Peach palm seed 10.4%
*Betel nut 9%
*Date palm seed 0.56–5.4%
*Macadamia nut 0.072–1.1%
*Plum 0.35–0.38%
*Watermelon seed 0.33%
*Viburnum opulus 0.24-0.33%
*Citrullus lanatus (egusi melon)
*Pumpkin flower 205 ppm, pumpkin seed 472 ppm
*Insect
*Black soldier fly Hermetia illucens 30–50 mg/100 mg fat.



PHYSICAL and CHEMICAL PROPERTIES of LAUROSTEARIC ACID:
Chemical formula: C10H18O4
Molar mass: 202.250 g•mol−1
Density: 1.209 g/cm3
Melting point: 131 to 134.5 °C (267.8 to 274.1 °F; 404.1 to 407.6 K)
Boiling point: 294.4 °C (561.9 °F; 567.5 K) at 100 mmHg
Solubility in water: 0.25 g/L
Acidity (pKa): 4.720, 5.450
Molecular Weight: 202.25
XLogP3: 2.1
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4

Rotatable Bond Count: 9
Exact Mass: 202.12050905
Monoisotopic Mass: 202.12050905
Topological Polar Surface Area: 74.6 Ų
Heavy Atom Count: 14
Formal Charge: 0
Complexity: 157
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Physical state: powder
Color: white
Odor: No data available
Melting point/freezing point:
Melting point/range: 133 - 137 °C - lit.
Initial boiling point and boiling range: 294,5 °C at 133 hPa - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available

Flash point: Not applicable
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 0,224 g/l at 20 °C - OECD Test Guideline 105
Partition coefficient:
n-octanol/water: log Pow: 1,5 at 23 °C
Vapor pressure: 1 hPa at 183 °C
Density: 1,210 g/cm3 at 20 °C

Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information: No data available
Water Solubility: 0.91 g/L
logP: 1.93
logP: 2.27
logS: -2.4
pKa (Strongest Acidic): 4.72

Physiological Charge: -2
Hydrogen Acceptor Count: 4
Hydrogen Donor Count: 2
Polar Surface Area: 74.6 Ų
Rotatable Bond Count: 9
Refractivity: 51.14 m³•mol⁻¹
Polarizability: 22.61 ų
Number of Rings: 0
Bioavailability: Yes
Rule of Five: Yes
Ghose Filter: Yes
Veber's Rule: No
MDDR-like Rule: No

Melting point: 133-137 °C (lit.)
Boiling point: 294.5 °C/100 mmHg (lit.)
Density: 1.21
vapor pressure: 1 mm Hg ( 183 °C)
refractive index: 1.422
Flash point: 220 °C
storage temp.: Store below +30°C.
solubility: ethanol: 100 mg/mL
form: Powder or Granules
pka: 4.59, 5.59(at 25℃)
color: White to off-white
Water Solubility: 1 g/L (20 ºC)
Merck: 14,8415

BRN: 1210591
Stability: Stable.
LogP: 1.5 at 23℃
Appearance: white granular powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 130.80 °C. @ 760.00 mm Hg
Boiling Point: 364.00 to 365.00 °C. @ 760.00 mm Hg
Boiling Point: 235.00 to 234.00 °C. @ 10.00 mm Hg
Flash Point: 389.00 °F. TCC ( 198.30 °C. ) (est)
logP (o/w): 1.706 (est)
Soluble in: water, 1000 mg/L @ 20 °C (exp)
water, 1420 mg/L @ 25 °C (est)

Chemical formula: C12H24O2
Molar mass: 200.322 g•mol−1
Appearance: White powder
Odor: Slight odor of bay oil
Density: 1.007 g/cm³ (24 °C),
0.8744 g/cm³ (41.5 °C),
0.8679 g/cm³ (50 °C)
Melting point: 43.8 °C (110.8 °F; 316.9 K)
Boiling point: 297.9 °C (568.2 °F; 571.0 K),
282.5 °C (540.5 °F; 555.6 K) at 512 mmHg,
225.1 °C (437.2 °F; 498.2 K) at 100 mmHg
Solubility in water: 37 mg/L (0 °C), 55 mg/L (20 °C),
63 mg/L (30 °C), 72 mg/L (45 °C), 83 mg/L (100 °C)

Solubility: Soluble in alcohols, diethyl ether,
phenyls, haloalkanes, acetates
Solubility in methanol: 12.7 g/100 g (0 °C),
120 g/100 g (20 °C), 2250 g/100 g (40 °C)
Solubility in acetone: 8.95 g/100 g (0 °C),
60.5 g/100 g (20 °C), 1590 g/100 g (40 °C)
Solubility in ethyl acetate: 9.4 g/100 g (0 °C),
52 g/100 g (20°C), 1250 g/100 g (40°C)
Solubility in toluene: 15.3 g/100 g (0 °C),
97 g/100 g (20°C), 1410 g/100 g (40°C)
log P: 4.6

Vapor pressure: 2.13•10−6 kPa (25 °C),
0.42 kPa (150 °C),
6.67 kPa (210 °C)
Acidity (pKa): 5.3 (20 °C)
Thermal conductivity: 0.442 W/m•K (solid),
0.1921 W/m•K (72.5 °C),
0.1748 W/m•K (106 °C)
Refractive index (nD): 1.423 (70 °C),
1.4183 (82 °C)
Viscosity: 6.88 cP (50 °C), 5.37 cP (60 °C)
Structure:
Crystal structure: Monoclinic (α-form),
Triclinic, aP228 (γ-form)

Space group: P21/a, No. 14 (α-form), P1, No. 2 (γ-form)
Point group: 2/m (α-form)[8], 1 (γ-form)[9]
Lattice constant: a = 9.524 Å, b = 4.965 Å,
c = 35.39 Å (α-form),
α = 90°, β = 129.22°, γ = 90°
Thermochemistry:
Heat capacity (C): 404.28 J/mol•K
Std enthalpy of formation (ΔfH⦵298): −775.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298): 7377 kJ/mol,
7425.8 kJ/mol (292 K)
Molecular Weight: 200.32 g/mol
XLogP3: 4.2
Hydrogen Bond Donor Count: 1

Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 10
Exact Mass: 200.177630004 g/mol
Monoisotopic Mass: 200.177630004 g/mol
Topological Polar Surface Area: 37.3Ų
Heavy Atom Count: 14
Formal Charge: 0
Complexity: 132
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
IUPAC Name: dodecanoic acid
Traditional IUPAC Name: lauric acid
Formula: C12H24O2
InChI: InChI=1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
InChI Key: POULHZVOKOAJMA-UHFFFAOYSA-N
Molecular weight: 200.3178
Exact mass: 200.177630012
SMILES: CCCCCCCCCCCC(O)=O

Chemical Formula: C12H24O2
Average Molecular Weight: 200.3178
Monoisotopic Molecular Weight: 200.177630012
IUPAC Name: dodecanoic acid
Traditional Name: lauric acid
CAS Registry Number: 143-07-7
SMILES: CCCCCCCCCCCC(O)=O
InChI Identifier: InChI=1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
InChI Key: POULHZVOKOAJMA-UHFFFAOYSA-N
Synonyms: n-Dodecanoic acid
IUPAC Name: Dodecanoic acid
Canonical SMILES: CCCCCCCCCCCC(=O)O
InChI: POULHZVOKOAJMA-UHFFFAOYSA-N

InChI Key: InChI=1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
Boiling Point: 225 °C 100mmHg(lit.)
Melting Point: 44-46 °C(lit.)
Flash Point: 156ºC
Density: 0.883g/ml
Appearance: Clear liquid
Storage: Room temperature
CNo.Chain: C12:0
Compound Derivative: Acid
EC Number: 205-582-1
Fatty Acid: Dodecanoic (Lauric)
Hazard Codes: Xi

Hazard Statements: Xi
HS Code: 2916399090
LogP: 3.99190
MDL Number: MFCD00002736
Physical State: Solid
PSA: 37.3
Refractive Index: 1.4304
Safety Description: 37/39-26-39-36
Stability: Stable.
Incompatible with bases, oxidizing agents, reducing agents.
Storage Conditions: Store in a tightly closed container.
Store in a cool, dry, well-ventilated area away from incompatible substances.

Supplemental Hazard Statements: H401-H318-H319
Symbol: GHS05, GHS07
Vapor Pressure: 1 mm Hg ( 121 °C)
Formula: C12H24O2
InChI: InChI=1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
InChIKey: POULHZVOKOAJMA-UHFFFAOYSA-N
Molecular Weight: 200.322 g/mol
SMILES: OC(CCCCCCCCCCC)=O
SPLASH: splash10-0706-9000000000-b974e08e305014657f85
Source of Spectrum: HE-1982-0-0
CB Number: CB0357278
Molecular Formula: C12H24O2
Lewis structure
Molecular Weight: 200.32

MDL Number: MFCD00002736
MOL File: 143-07-7.mol
Melting point: 44-46 °C (lit.)
Boiling point: 225 °C/100 mmHg (lit.)
Density: 0.883 g/mL at 25 °C (lit.)
Vapor pressure: 1 mm Hg (121 °C)
Refractive index: 1.4304
FEMA: 2614 | LAURIC ACID
Flash point: >230 °F
Storage temp.: 2-8°C
Solubility: 4.81 mg/L
Form: Crystalline Powder of Flakes
pKa: 4.92 (H2O, t =25.0) (Uncertain)
Specific Gravity: 0.883
Color: White

Odor: at 100.00 % mild fatty coconut bay oil
Odor Type: fatty
Explosive limit: 0.6% (V)
Water Solubility: insoluble
λmax: 207 nm (MeOH) (lit.)
JECFA Number: 111
Merck: 14,5384
BRN: 1099477
Stability: Stable.
Incompatible with bases, oxidizing agents, reducing agents.
InChIKey: POULHZVOKOAJMA-UHFFFAOYSA-N
LogP: 5

Dissociation constant: 5.3 at 20°C
Substances Added to Food (formerly EAFUS): LAURIC ACID
CAS DataBase Reference: 143-07-7 (CAS DataBase Reference)
EWG's Food Scores: 1
FDA UNII: 1160N9NU9U
NIST Chemistry Reference: Dodecanoic acid (143-07-7)
EPA Substance Registry System: Lauric acid (143-07-7)
Molecular Weight: 200.32
Exact Mass: 200.32
BRN: 1099477
EC Number: 205-582-1
HS Code: 29159010

Characteristics
PSA: 37.3
XLogP3: 4.2
Appearance: White Crystalline Powder of Flakes
Density: 0.883 g/cm³ @ Temp: 20 °C
Melting Point: 44.2 °C
Boiling Point: 298.9 °C
Flash Point: >230 °F
Refractive Index: 1.4304
Water Solubility: H2O: insoluble
Storage Conditions: Store below +30°C
Vapor Pressure: 1 mm Hg (121 °C)
Toxicity: LD50 i.v. in mice: 131 ±5.7 mg/kg (Or, Wretlind)
Explosive limit: 0.6% (V)
Odor: Characteristic, like oil of bay
pKa: 5.3 (at 20 °C)



FIRST AID MEASURES of LAUROSTEARIC ACID:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of LAUROSTEARIC ACID:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.



FIRE FIGHTING MEASURES of LAUROSTEARIC ACID:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAUROSTEARIC ACID:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LAUROSTEARIC ACID:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry



STABILITY and REACTIVITY of LAUROSTEARIC ACID:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Conditions to avoid:
no information available

N-lauroyl-L-arginine; (2S)-5-(diaminomethylideneamino)-2-(dodecanoylamino)pentanoic acid; N-lauroyl-laevo-arginine CAS NO:42492-22-8

L-glutamic acid, N-(1-oxododecyl)-; (2S)-2-(dodecanoylamino)pentanedioic acid; N-lauroyl-L-glutamic acid CAS NO:3397-65-7

N-Dodecanoylsarcosine, SODIUM N-LAUROYLSARCOSINATE; N-Dodecanoyl-N-methylglycine, LAUROYL SARCOSINE, N° CAS : 97-78-9. Nom INCI : LAUROYL SARCOSINE, N° EINECS/ELINCS : 202-608-3. Ses fonctions (INCI), Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Agent nettoyant : Aide à garder une surface propre. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. SELSODIQUE DE LAUROYLE ET DE SARCOSINATE - Synonyme de LAUROYL SARCOSINE; Numéro CAS : 137-16-6 ; Noms français :GLYCINE, N-METHYL-N-(1-OXODODECYL)-, SODIUM SALT; Lauroylsarcosinate de sodium; N-lauroylsarcosinate de sodium. Noms anglais : SODIUM N-LAUROYLSARCOSINATE. Utilisation et sources d'émission :Agent antiseptique

1-Dodecanol; Dodecyl alcohol, Lauryl alcohol; 1-DODECANOL; 1-DODECYLALCOHOL; ALCOHOL C12; ALCOHOL C-12 LAURIC; DODECAN-1-OL; DODECANOL; DODECYL ALCOHOL; FEMA 2617; LAURYL ALCOHOL; N-DODECYL ALCOHOL CAS NO:112-53-8

Lauryl / myristyl glucoside is a Colorless to pale yellow transparent aqueous solution or paste.
Lauryl / myristyl glucoside is a yellowish slightly cloudy viscous liquid.
Lauryl / myristyl glucoside is biodegradable.


CAS Number: 110615-47-9
EC Number: 600-975-8
Molecular Formula: C18H36O6



Lauryl / Myristyl Glucoside, C18H36O6, Dodecyl D-glucoside, D-Glucopyranoside, Dodecyl, Lauryl D-glucopyranoside, Glucopon 600 UP, Unipon 600U, Lauryl/ Myristyl Glucoside Unpreserved, Dodecyl glucoside, Dodecyl –D-glucopyranoside



Lauryl / myristyl glucoside is a Colorless to pale yellow transparent aqueous solution or paste.
Lauryl / myristyl glucoside is mild in performance, less irritating to the human body, has a softening effect on the skin, no irritation to the eyes, and has good ecological compatibility.


Lauryl / myristyl glucoside is widely used in personal care and household washing: shampoo, hand soap, facial cleanser, body wash And other cosmetics and transparent soaps, laundry detergents, detergents and other daily chemical detergents and other fields, especially in the field of pregnancy and baby cosmetics has been recognized by consumers.


Lauryl / myristyl glucoside’s non-rinsing and non-staining characteristics make it especially suitable for use in dishwashing detergents, hard surface cleaning and other fields.
During the storage process of Lauryl / myristyl glucoside at low temperature, a small amount of solids precipitated or the appearance was turbid due to the influence of single glycosides and high pH value.


This turbidity had no negative impact on the performance of the product.
With the increase of temperature and pH value, Lauryl / myristyl glucoside was adjusted to 7- 9 The cloudiness will disappear.
Lauryl / myristyl glucoside can also be specially processed into products with pH: 7-10.0 according to the needs of customers.


Lauryl / myristyl glucoside is a cleaning agent, an Amine Oxide surfactant, that can also be found in a variety of products including shampoos and dishwashing detergents.
Lauryl / myristyl glucoside removes dirt and deposits by surrounding dirt particles to loosen them from the surface they’re attached to, so they can be rinsed away.


Lauryl / myristyl glucoside is a Colorless to pale yellow transparent aqueous solution or paste.
Lauryl / myristyl glucoside is a yellowish slightly cloudy viscous liquid.
Lauryl / myristyl glucoside is a product obtained by the condensation of myristyl alcohol with aglucose polymer.


Lauryl / myristyl glucoside is a multi-carbon type APG with 12 to 14 carbons in the alkyl glycoside series, with higher foam, which is relatively lower than that of APG0814 and APG0810.
Lauryl / myristyl glucoside is a non-ionic surfactant made from renewable plant raw materials.


Lauryl / myristyl glucoside is an alkyl polyglucoside (APG).
Lauryl / myristyl glucoside is a low foam non-ionic surfactant made from natrual fatty alcohl and glucose which are drived from plant sources.
Lauryl / myristyl glucoside is a liquid with a pale yellow appearance.


Lauryl / myristyl glucoside exhibits very good wetting, dispersing, and surface tension reduction properties for increased soil removal and emulsification.
Lauryl / myristyl glucoside also offers excellent caustic stability, builder compatibility, detergency and hydrotropic properties which combine to offer the formulator greater flexibility and better cost performance.


Lauryl / myristyl glucoside is very mild, low in toxicity, and readily biodegradable due to their natural chemistry.
Lauryl / myristyl glucoside is a plant-based surfactant that is commonly used in personal care products such as shampoos, body washes, and household cleaning products.


Lauryl / myristyl glucoside is derived from corn, coconuts, and other plant materials.
Lauryl / myristyl glucoside is produced by reacting glucoside from corn starch with the fatty alcohol decanol, which is derived from coconut.
Lauryl / myristyl glucoside is a thick yellow substance that is derived from palm kernel oil, corn sugar or coconut.


Lauryl / myristyl glucoside is an alkyl glucoside.
Lauryl / myristyl glucoside is a class of ingredients that are made by mixing alcohols and a sugar like glucose.
Generally, Lauryl / myristyl glucoside is derived from naturally-occurring ingredients but can also be made synthetically.


Synthetic production of Lauryl / myristyl glucoside minimizes the pressure on natural resources and reducing environmental issues with harvesting, processing, and transportation.
Due to the ability of Lauryl / myristyl glucoside to be made from naturally-occurring ingredients, it is considered to be an eco-friendly or sustainable ingredient.


Lauryl / myristyl glucoside is a non-ionic surfactant and member of the alkyl glucoside family (e.g. coco glucoside, decyl glucoside) which are substances formed by mixing alcohols and sugar and/or glucose.
Lauryl / myristyl glucoside is usually sustainably sourced from palm kernel oil, corn sugar, or coconut.


Lauryl / myristyl glucoside improves the cleansing process without stripping necessary moisture.
Lauryl / myristyl glucoside is a sugar derived surfactant for the laundry and manual Dish applications.
Raw materials for the surfactant are fatty alcohols from coconut or palm kernel oil and glucose of corn.


Lauryl / myristyl glucoside foams synergistically with other surfactants, are effective emulsifiers, contribute to dye transfer inhibition and are mild to the skin.
As a result of the alkaline pH adjustment Lauryl / myristyl glucoside is sufficiently protected against microbiological contamination.


Lauryl / myristyl glucoside is a plant-based surfactant that usually appears as a clear liquid with a mild sweet fatty aroma, and is found in many cleaning products, soaps and cleansers.
We use Lauryl / myristyl glucoside in some of our personal care and cleaning products for its gentle but effective cleansing properties, and general compatibility with sensitive skin.


Lauryl / myristyl glucoside is derived from lauryl alcohol (from coconut or palm) and glucose (from corn or potato).
Lauryl / myristyl glucoside's what's known as a ‘non-ionic surfactant’, which means the molecules have no charge and help deliver non-streak cleaning.
Lauryl / myristyl glucoside also contributes to lather, wetting and suspension of soils in products like shampoo, body wash, bubble bath, laundry products, facial cleansers and toothpastes.


Regarding its safety profile, a group of Alkyl Glucosides, including Lauryl / myristyl glucoside, were assessed by the Cosmetic Ingredient Review (CIR) Expert Panel in 2013.
They reviewed their safety for dermal exposure in cosmetics and concluded they are “safe in the present practices of use and concentration when formulated to be nonirritating.”


EWG notes studies showing allergic contact dermatitis to decyl and Lauryl / myristyl glucoside exists in a small percentage of the population, and appropriate care should be taken for those with sensitivities.
Lauryl / myristyl glucoside adds high foaming capacity to your foaming product, if you want more foam in your product add Lauryl / myristyl glucoside.


Lauryl / myristyl glucoside is an non-ionic surfactant that can be used as a foaming agent, conditioner or emulsifier.
We recommend adding 5% Lauryl / myristyl glucoside to your glucoside based surfactant formulation to boost foam.
Lauryl / myristyl glucoside aids the viscosity build up of your final product.
Lauryl / myristyl glucoside increases the foaming ability



USES and APPLICATIONS of LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside is a multi-carbon type APG with 12 to 14 carbons in the alkyl glycoside series, with higher foam, which is relatively lower than that of APG0814 and APG0810.
Lauryl / myristyl glucoside is a non-ionic surfactant made from renewable plant raw materials.


Lauryl / myristyl glucoside is mainly used as a surfactant.
Surfactants help to break down the surface tension between two liquids allowing for a deeper clean.
This is why Lauryl / myristyl glucoside is used in products such as cleansers, shampoos, body washes, hand soap and eco-friendly household cleaning products.


Lauryl / myristyl glucoside is an ingredient used in skincare and cosmetic formulations to improve the cleansing abilities of cleansers, body washes and soaps.
Lauryl / myristyl glucoside is used as a surfactant that helps to lift dirt and oils from the skin, allowing them to be washed away.
This is why you will often find Lauryl / myristyl glucoside in cleansing products such as washes and cleansers.


Cosmetics: Lauryl / myristyl glucoside is often used as a cleansing agent and surfactant in cosmetics, including makeup primer, eye makeup remover, BB creams, and eye cream.
Instead of sulfates, Puracy uses Lauryl / myristyl glucoside as a surfactant and cleanser in many of our foaming products.


Lauryl / myristyl glucoside is used Household Detergents, Hard Surface Cleaning, Clean In Place (CIP), and Scouring Agents - Textiles.
Dental Care: As a surfactant, Lauryl / myristyl glucoside has foaming qualities that make it an effective ingredient in toothpaste and tooth whitening products.


Lauryl / myristyl glucoside has the best foaming capacity of the glucosides and good dermatological compatibility.
Therefore Lauryl / myristyl glucoside is suitable for use as a base surfactant or a co-surfactant in cosmetic surfactant cleansing preparations.
Lauryl / myristyl glucoside is also used in a variety of other applications such as cleaning products, textile processing, and industrial applications.


Lauryl / myristyl glucoside is a non-ionic surfactant, which means that it does not have a charge and does not interact with other ions in solution.
This property makes Lauryl / myristyl glucoside a good choice for use in products that are meant to be pH balanced and gentle on the skin.


-Skincare and Body Care uses of Lauryl / myristyl glucoside:
As a surfactant and cleansing agent, Lauryl / myristyl glucoside breaks surface tension so dirt and oil are lifted and washed away more easily.
This is a great reason that you can find Lauryl / myristyl glucoside in shampoo, face washes, bubble bath, body wash, and other personal care products.



BENEFITS INCLUDE OF LAURYL / MYRISTYL GLUCOSIDE:
• Derived from natural feedstocks (from renewable resources)
• Rapidly biodegradable (under aerobic and anaerobic conditions)
• Offer excellent detergency, wetting and surface active properties
• Solubility in highly built caustic soda / electrolyte formulations
• Hydrotropic properties / will aid the solubility of less soluble ingredients (in strong acid or alkaline conditions)
• Compatibility with other surfactants – synergistic effects can be found
• Produces rich stable foam
• Improvement in dissolving surfactants and adjuvants



PROPERTIES OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside is a new type of non-ionic surfactant alkyl glycoside (APG), which has the characteristics of common non-ionic and anionic surfactants.
Lauryl / myristyl glucoside is the APG with the best foaming power and the best detergency.
Lauryl / myristyl glucoside is especially suitable for washing



FUNCTION OF LAURYL / MYRISTYL GLUCOSIDE:
*Surfactant – cleaning agent



CHARACTERISTICS OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside creates an excellent and stable foam.
Lauryl / myristyl glucoside is useful in hair care products where it aids hair cleaning abilities without stripping the hair.
Lauryl / myristyl glucoside can be used alongside other glucosides to enhance the foam and skin conditioning properties.

Lauryl / myristyl glucoside is very effective when used in ionic formulations to add foam depth and emulsifying properties.
Lauryl / myristyl glucoside is very useful for Bath Foams, Shower Gel and Shampoo where you wish to increase the foaming ability of the product without a decrease in the natural formulation.



FUNCTION OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside is a sugar derived surfactant for the laundry and manual dish applications.
Raw materials for the Lauryl / myristyl glucoside surfactant are fatty alcohols from coconut or palm kernel oil and glucose of corn.

Lauryl / myristyl glucoside foams synergistically with other surfactants, are effective emulsifiers, contribute to dye transfer inhibition and are mild to the skin.
As a result of the alkaline pH adjustment Lauryl / myristyl glucoside is sufficiently protected against microbiological contamination.



STORAGE OF LAURYL / MYRISTYL GLUCOSIDE:
Store Lauryl / myristyl glucoside in sealed original container.
Protect Lauryl / myristyl glucoside from frost.


HOW LAURYL / MYRISTYL GLUCOSIDE IS MADE:
Commercial production of lauryl glucoside generally starts by mixing palm, corn, or coconut alcohol with either sugar, glucose, or a glucose polymer under acidic conditions.


LAURYL / MYRISTYL GLUCOSIDE, THE GOOD:
Lauryl / myristyl glucoside helps to improve the cleansing abilities of products.
Acting as a surfactant Lauryl / myristyl glucoside helps to lift dirt and oil, allowing them to be washed more easily from the skin.


LAURYL / MYRISTYL GLUCOSIDE, THE NOT SO GOOD:
Like any ingredient, Lauryl / myristyl glucoside can cause allergies for some people.
Lauryl / myristyl glucoside is generally considered to be non-irritating, however can cause irritation in some skin types.


WHO IS LAURYL / MYRISTYL GLUCOSIDE FOR?
All skin types except those that have an identified allergy to Lauryl / myristyl glucoside.


SYNERGETIC INGREDIENTS OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside works well with most ingredients.


KEEP LAURYL / MYRISTYL GLUCOSIDE AN EYE ON:
Nothing to keep an eye on here.



IS LAURYL / MYRISTYL GLUCOSIDE GENTLER THAN DECYL GLUCOSIDE OR COCO-GLUCOSIDE?
Lauryl / myristyl glucoside is part of a group of ingredients called the alkyl glucosides.
This group includes decyl glucoside and coco-glucoside.

These three ingredients are the most commonly used alkyl glucosides in skincare, cosmetics and household cleaning products, however, they do vary slightly in mildness.

Decyl glucoside and coco-glucoside are considered to be the mildest of the alkyl glucosides.
Lauryl / myristyl glucoside is slightly more irritating than decyl glucoside and coco-glucoside but isn’t considered to be as irritating as caprylyl/ capryl glucoside which is another alkyl glucoside used in the same way.



EXTRACTION OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside is an organic compound derived from lauric and myristylic alcohols (fatty alcohols present in coconut and palm oils) and ricinoleic acid (a fatty acid found in castor oil).



BENEFITS OF LAURYL / MYRISTYL GLUCOSIDE:
Lauryl / myristyl glucoside has conditioning properties and is used in hair care to provide moisture, and leave a soft feel that facilitates styling.



HOW TO USE LAURYL / MYRISTYL GLUCOSIDE:
Blend with other surfactants to produce a foaming product with skin cleansing abilities.
Lauryl / myristyl glucoside works excellently blended with Cocamidopropyl betaine.



PROPERTIES OF LAURYL / MYRISTYL GLUCOSIDE:
*Exceptional cleaning performance
*Excellent wetting properties,
*Safe for all surfaces,
*Compatibility with a variety of surfactants,
*Synergies with common anionic surfactants,
*Good detergency,
*Excellent gloss retention,
*Extremely mild to surfaces and skin,
*No plastic stress cracking,
*Hydrotrope properties,
*Dispersant properties,
*Enhanced distribution of polymers



IS LAURYL / MYRISTYL GLUCOSIDE SAFE?
Lauryl / myristyl glucoside is generally considered to be safe for use in personal care products.
Lauryl / myristyl glucoside has a low potential for irritation and is less likely to cause allergic reactions compared to some other surfactants.
However, Lauryl / myristyl glucoside is derived from corn, which is a common allergen, so it is important to carefully read ingredient lists and patch test new products before use, especially if you have a history of allergies or sensitivities.



PHYSICAL and CHEMICAL PROPERTIES of LAURYL / MYRISTYL GLUCOSIDE:
CAS: 110615-47-9
MF: C18H36O6
MW: 348.47484
EINECS: 600-975-8
Origin: Vegetable/Synthetic
Shelf life: 1 year from mfg. date
Freight Classification: NMFC48580 S3 CL55
Kosher Status: Not Kosher
Flash Point: > 200.12 øF (> 93.40 øC)
Melting Point: 32 øC
API: NO
Allergen: NO
Hazmat: YES
Molecular Weight: 348.48 g/mol

Specific Gravity @ 25°C 1.06 - 1.09 @ 25 °C (77 °F) Reference Material: (water = 1)
Color Light yellow
Odor Characteristic
pH 11.5 - 12.5 @ 20 - 25 °C (68 - 77 °F)
Boiling Point > 250 °C (> 482 °F)
Flash Point > 100 °C (212 °F)
Vapor Pressure < 0.075 mmHg @ 20 °C (68 °F)
Auto-ignition Temperature > 300 °C (> 572 °F)
Viscosity, Dynamic 2,500 - 16,000 mPa.s @ 23 - 40 °C (73 - 104 °F)
Applications Non-Ionic Surfactant
Chemical Form Liquid



FIRST AID MEASURES of LAURYL / MYRISTYL GLUCOSIDE:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person. Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of LAURYL / MYRISTYL GLUCOSIDE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of LAURYL / MYRISTYL GLUCOSIDE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURYL / MYRISTYL GLUCOSIDE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LAURYL / MYRISTYL GLUCOSIDE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.



STABILITY and REACTIVITY of LAURYL / MYRISTYL GLUCOSIDE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

Lauryl alcohol is a fatty alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group.
Lauryl alcohol is a white low melting crystalline solid that has a melting point of 24°C.
The air odor threshold for Lauryl alcohol (isomer not specified) is reported to be 7.1 ppb.

CAS: 112-53-8
MF: C12H26O
MW: 186.33
EINECS: 203-982-0

Reported found in the oil of Mexican lime and in the oil from flowers of Furcraea gigantean.
Also reported found in apple, banana, sour cherry, citrus peel oils, melon, pineapple, potato, thymus, cheeses, butter, milk powder, chicken and beef fat, cooked pork, beer, whiskies, white wine, peanuts, beans, mushrooms, mango, coriander seed and leaf, rice, Bourbon vanilla, endive, crab, clam, Cape gooseberry, pawpaw and maté.

Lauryl alcohol, is an organic compound produced industrially from palm kernel oil or coconut oil.
Lauryl alcohol is a fatty alcohol.
Sulfate esters of lauryl alcohol, especially sodium lauryl sulfate, are very widely used as surfactants.
Lauryl alcohol, ammonium lauryl sulfate, and sodium laureth sulfate are all used in shampoos.
Lauryl alcohol is tasteless and colorless with a floral odor.

A fatty alcohol that is dodecane in which a hydrogen from one of the methyl groups is replaced by a hydroxy group.
Lauryl alcohol is registered for use in apple and pear orchards as a Lepidopteran pheromone/sex attractant, used to disrupt the mating behaviour of certain moths whose larvae destroy crops.

Ethoxylated alcohol formulas such as Lauryl Alcohol are classified as surfactants, which means they reduce surface tension in a liquid, or between a liquid and a solid.
As with all types of ethoxylated alcohol, Lauryl Alcohol Ethoxylate is a nonionic compound — Lauryl alcohol has no electrical charge on the hydrophilic end and generally takes the form of a thick liquid that is often sticky to the touch.
The ethoxylation process also tends to increase the water solubility of the material.
Products that typically contain Lauryl Alcohol Ethoxylate include cosmetics, laundry detergents, surface cleaners and personal care products, to name a few.

Lauryl alcohol Chemical Properties
Melting point: 22-26 °C(lit.)
Boiling point: 260-262 °C(lit.)
Density: 0.833 g/mL at 25 °C(lit.)
Vapor density: 7.4 (vs air)
Vapor pressure: 0.1 mm Hg ( 20 °C)
Refractive index: n20/D 1.442(lit.)
FEMA: 2617 | LAURYL ALCOHOL
Fp: >230 °F
Storage temp.: Store below +30°C.
Solubility water: slightly soluble1g/L at 23°C
Form: Liquid
pka: 15.20±0.10(Predicted)
Color: APHA: ≤10
Odor: Typical fatty alcohol odor; sweet.
Odor Type: waxy
Explosive limit: 4%
Water Solubility: insoluble
Merck: 14,3405
JECFA Number: 109
BRN: 1738860
InChIKey: LQZZUXJYWNFBMV-UHFFFAOYSA-N
LogP: 5.4 at 23℃
CAS DataBase Reference: 112-53-8(CAS DataBase Reference)
NIST Chemistry Reference: Lauryl alcohol (112-53-8)
EPA Substance Registry System: Lauryl alcohol (112-53-8)

Lauryl alcohol has a characteristic fatty odor; unpleasant at high concentrations, but delicate and floral on dilution.
Lauryl alcohol is a saturated 12-carbon fatty alcohol obtained from coconut oil fatty acids.
Lauryl alcohol has a fatty, waxy flavor and is used in detergents, lubricating oils, and pharmaceuticals.

Uses
Lauryl alcohol is used as a cosmetic, textile auxiliaries, synthetic oil, emulsifiers and flotation agent of raw materials, a detergent raw material, a foaming agent of the toothpaste.
Lauryl alcohol is used in chemical formulations for a variety of purposes, including as an emulsion stabilizer, a skin-conditioning emollient, and a viscosity-increasing agent.
Lauryl alcohol is used primarily as a chemical intermediate in surfactants containing fatty alcohol sulfates and ethoxylates.
Lauryl alcohol is also used as a thickener, emollient and foam control agent in soaps and personal care products, among other applications.

Lauryl alcohol is used vastly in the cosmetic industry in preparation of emulsion.
When Lauryl alcohol is used in emulsion it can stabilize emulsion by getting incorporated into water and oil phase.
Lauryl alcohol is fatty in nature, so when it is used on the skin, it also provides fat and moisture to the dried skin.
Lauryl alcohol forms a layer on the skin which does not allow moisture to evaporate.
So, when applied on the dried skin Lauryl alcohol gets a boost of moisture as well.
Lauryl alcohol can also be used as a viscosity increasing agent.
Lauryl alcohol is used in skincare, haircare, and body care product.

Preparation
Commercially Lauryl alcohol may be prepared by hydrogenation of lauric acid; normally employed as a replacement for the corresponding aldehyde.

Production Methods
Lauryl alcohol is produced commercially by the oxo process and from ethylene by the Ziegler process, which involves oxidation of trialkylaluminum compounds.
Lauryl alcohol can also be produced by sodium reduction or high-pressure hydrogenation of esters of naturally occurring lauric acid.

In 1993, the European demand of dodecanol was around 60 thousand tons per year (Tt/a).
Lauryl alcohol can be obtained from palm kernel or coconut oil fatty acids and methyl esters by hydrogenation.
Lauryl alcohol may also be produced synthetically via the Ziegler process.
A classic laboratory method involves Bouveault-Blanc reduction of ethyl laurate.

Lauryl alcohol is used to make surfactants, lubricating oils, pharmaceuticals, in the formation of monolithic polymers and as a flavor enhancing food additive.
In cosmetics, Lauryl alcohol is used as an emollient.
Lauryl alcohol is also the precursor to dodecanal, an important fragrance, and 1-bromododecane, an alkylating agent for improving the lipophilicity of organic molecules.

Reactivity Profile
Lauryl alcohol is an alcohol.
Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents.
They react with oxoacids and carboxylic acids to form esters plus water.
Oxidizing agents convert them to aldehydes or ketones.
Alcohols exhibit both weak acid and weak base behavior.
They may initiate the polymerization of isocyanates and epoxides.

Carcinogenicity
Lauryl alcohol showed weak tumor-promoting activity when applied three times a week for 60 weeks to the skin of mice that had previously received an initiating dose of dimethylbenz[a]anthracene.
Papillomas developed in 2 of 30 mice after 39 and 49 weeks of treatment.

Synonyms
1-DODECANOL
Dodecan-1-ol
Dodecyl alcohol
Dodecanol
Lauryl alcohol
112-53-8
n-Dodecyl alcohol
Undecyl carbinol
Dodecylalcohol
Lauric alcohol
Laurinic alcohol
1-Dodecyl alcohol
Pisol
n-Dodecan-1-ol
Duodecyl alcohol
1-Hydroxydodecane
Siponol L5
Karukoru 20
Lauroyl alcohol
Siponol 25
Lorol 5
Lorol 7
n-Dodecanol
Lauryl 24
Alcohol C-12
Alfol 12
Lorol 11
Sipol L12
Dytol J-68
Siponol L2
Cachalot L-50
Cachalot L-90
Dodecyl alcoho
n-Lauryl alcohol
C12 alcohol
Hainol 12SS
Hydroxydodecane
Conol 20P
Conol 20PP
Lorol
EPAL 12
Adol 10
Adol 12
Dodecanol-1
n-Lauryl alcohol, primary
Nacol 12-96
Alcohol C12
FEMA No. 2617
NAA 42
CO-1214
Lipocol L
CO-1214N
CO-1214S
MFCD00004753
S 1298
MA-1214
Lorol C12
Co-1214S1-dodecanol
27342-88-7
DTXSID5026918
CHEBI:28878
178A96NLP2
NSC-3724
68551-07-5
DTXCID906918
Adol 11
Lorol C 12
FEMA Number 2617
Dytol J-68 (VAN)
Lorol C 12/98
1DO
CAS-112-53-8
CCRIS 662
Dodecanol, 1-
HSDB 1075
NSC 3724
EINECS 203-982-0
BRN 1738860
laurylalcohol
Lorol special
UNII-178A96NLP2
AI3-00309
EINECS 271-359-0
Philcohol 1200
LAUREX NC
LAUREX L1
1-DODECANOL [MI]
1-Dodecanol, 98.0%
EC 203-982-0
SCHEMBL6844
1-DODECANOL [HSDB]
LAURYL ALCOHOL [FCC]
4-01-00-01844 (Beilstein Handbook Reference)
CHEMBL24722
LAURYL ALCOHOL [FHFI]
LAURYL ALCOHOL [INCI]
C12H25OH
WLN: Q12
Lauryl alcohol, >=98%, FG
NACOL 12-99 ALCOHOL
LAURYL ALCOHOL [USP-RS]
1-dodecanol (ACD/Name 4.0)
1-Dodecanol, analytical standard
ALFOL 1216 CO ALCOHOL
NSC3724
12 OH
1-Dodecanol, reagent grade, 98%
BCP29203
CS-D1360
HY-Y0289
Tox21_202124
Tox21_300120
LMFA05000001
STL301829
CACHALOT L-90 LAURYL ALCOHOL
Co 12Co-1214Co-1214N
AKOS009031450
DB06894
1-Dodecanol, ACS reagent, >=98.0%
NCGC00164341-01
NCGC00164341-02
NCGC00164341-03
NCGC00253987-01
NCGC00259673-01
BP-31213
CS-16955
1-Dodecanol 100 microg/mL in Acetonitrile
DB-003637
1-Dodecanol, SAJ special grade, >=97.0%
1-Dodecanol, Selectophore(TM), >=98.0%
1-dodecanol; dodecyl alcohol; lauryl alcohol
D0978
FT-0607710
FT-0693265
1-Dodecanol, Vetec(TM) reagent grade, 98%
EN300-20043
C02277
Q161617
Q-200121
Dodecan-1-ol;Dodecyl alcohol;Lauryl alcohol;Dodecanol
Z104476554
Lauryl alcohol, United States Pharmacopeia (USP) Reference Standard

LAURYL ALCOHOL 70%; 1-Dodecanol, Alcohol C12, Dodecyl alcohol, Lauryl alcohol CAS Number 112-53-8

LAURALDEHYDE, N° CAS : 112-54-9, Nom INCI : LAURALDEHYDE, Nom chimique : Lauryl aldehyde, N° EINECS/ELINCS : 203-983-6. Ses fonctions (INCI) : Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit

LAURYL ALCOHOL ETHOXYLATE (3 EO) = ALCOHOLS, c12-16, ETHOXYLATED


CAS Number: 68439-50-9
EC Number: 500-213-3
Molecular Formula: C30H62O10
Chemical name: Alcohols C12-14 Ethoxylated


Lauryl Alcohol Ethoxylate (3 EO) is biodegradable nonionic surfactants composed of ethylene oxide adduct of Lauryl Alcohol.
Lauryl Alcohol Ethoxylate (3 EO) vary in physical appearance, from clear or slightly hazy, colorless liquids to white solids, depending upon the level of ethoxylation.
In general, with increase in the ethylene oxide chain attached to the Lauryl Alcohol hydrophobe increases the HLB value (water solubility), pour point, cloud point, density, viscosity, and flash point of the ethoxylate.


Lauryl Alcohol Ethoxylate (3 EO) is non-ionic surfactant.
Lauryl Alcohol Ethoxylate (3 EO) generally takes the form of a thick liquid.
Lauryl Alcohol Ethoxylate (3 EO) is a liquid surfactant.
Lauryl Alcohol Ethoxylate (3 EO) has a hydroxyl value of 171-180 mg KOH/g.


Function of Lauryl Alcohol Ethoxylate (3 EO): Oil soluble dispersant, degreaser.
Lauryl Alcohol Ethoxylate (3 EO) is a liquid surfactant.
Lauryl Alcohol Ethoxylate (3 EO) has a hydroxyl value of 171-180 mg KOH/g.
Ethoxylated alcohol formulas such as Lauryl Alcohol are classified as surfactants, which means they reduce surface tension in a liquid, or between a liquid and a solid.



USES and APPLICATIONS of LAURYL ALCOHOL ETHOXYLATE (3 EO):
Lauryl Alcohol Ethoxylate (3 EO) is used Wetting agent, cleansing agent, and low foaminess.
Lauryl Alcohol Ethoxylate (3 EO) is used in Emulsifiers & Wetting Agents, Industrial and institutional cleaners, Agricultural chemicals, Textile and leather processing, and Metalworking systems
Lauryl Alcohol Ethoxylate (3 EO) can also be used in ether sulfates and ether carboxylates, Cosmetics as well as other industrial and agricultural applications.
Lauryl Alcohol Ethoxylate (3 EO) is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


The ethoxylation process also tends to increase the water solubility of Lauryl Alcohol Ethoxylate (3 EO).
Products that typically contain Lauryl Alcohol Ethoxylate (3 EO) include cosmetics, laundry detergents, surface cleaners and personal care products, to name a few.
Use Lauryl Alcohol Ethoxylate (3 EO) as a wetting agent to reduce the surface tension in liquids, and as an emulsifier in paints and coatings to promote dispersion.
Lauryl Alcohol Ethoxylate (3 EO) is used as a raw material for the manufacture of sodium lauryl ether sulphate (SLES) for shampoos and detergents.
Lauryl Alcohol Ethoxylate (3 EO) is used Coatings, Personal Care, Crop Solutions, Home Care and I&I, Industrial Applications, and Oil & Gas


Lauryl Alcohol Ethoxylate (3 EO) is mainly used in cleaning agents, detergents, home care and emulsifier production.
Lauryl Alcohol Ethoxylate (3 EO) is used as an emulsifiers in pesticides formulation and surfactant in production.
Lauryl Alcohol Ethoxylate (3 EO) is used as a foaming agent in shampoos and bath gels, and as a wetting agent in detergents, laundry pre-spotters and hard surface cleaners.
The natural source and biodegradable nature of Lauryl Alcohol Ethoxylate (3 EO) prompt their use in shampoo and liquid detergent formulations for personal care segments.
Lauryl Alcohol Ethoxylate (3 EO) is used in personal care and cosmetics as emulsifiers in creams, cleansing agents in shampoos and liquid detergents, solubilizers for fragrances.


Lauryl Alcohol Ethoxylate (3 EO) is a foaming agent in personal care products such as shampoos and bath gels as it reduces the surface tension in liquid.
The effective wetting property of Lauryl Alcohol Ethoxylate (3 EO) finds use in household cleaning products including detergents, laundry pre-spotters and hard surface cleaners.
While in industrial settings like textile and leather processing the wetting property effectively helps, reduce surface tension.
Lauryl Alcohol Ethoxylate (3 EO) is used as a foaming agent in shampoos and bath gels, and as a wetting agent in detergents, laundry pre-spotters and hard surface cleaners.


Lauryl Alcohol Ethoxylate (3 EO) is used in the following products: washing & cleaning products, plant protection products, fertilisers, air care products, lubricants and greases, polishes and waxes and coating products.
Personal Care uses of Lauryl Alcohol Ethoxylate (3 EO): Lauryl Alcohol Ethoxylate (3 EO) works extremely well as a foaming agent in personal care products such as shampoos and bath gels.
Textiles: Use Lauryl Alcohol Ethoxylate (3 EO) as a wetting agent in textile and leather processing applications to reduce surface tension.


Lauryl Alcohol Ethoxylate (3 EO) is used Wetting Agent and Emulsifier in Paints and Coatings.
Personal Care uses of Lauryl Alcohol Ethoxylate (3 EO): Foaming Agent in Shampoos and Bath Gels
Soaps and Detergents uses of Lauryl Alcohol Ethoxylate (3 EO): Wetting Agent in Detergents, Laundry Pre-spotters and Hard Surface Cleaners
Surfactants and Esters uses of Lauryl Alcohol Ethoxylate (3 EO): Surfactant Intermediate, Sulfonated to Make SLES (Sodium Lauryl Ether Sulfate)


Textiles uses of Lauryl Alcohol Ethoxylate (3 EO): Wetting Agent in Textile and Leather Processing
Soaps and Detergents: Lauryl Alcohol serves as a reliable wetting agent in a wide range of industrial and household cleaning products including detergents, laundry pre-spotters and hard surface cleaners.
Other release to the environment of Lauryl Alcohol Ethoxylate (3 EO) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


-Key applications of Lauryl Alcohol Ethoxylate (3 EO)
*Leather processing
*Cleaning products
*Agricultural
*Cosmetic products
*Paint and Coatings
*Rubber



PHYSICAL and CHEMICAL PROPERTIES of LAURYL ALCOHOL ETHOXYLATE (3 EO):
Appearance: Liquid
Appearance (at 25°C): Clear to slightly hazy liquid
Color (at 40°C) APHA: 30 Max
Moisture (% wt.): 0.1 Max
Hydroxyl Value (mg KOH/g): 165 - 174
pH (1% solution): 5 - 7
Product Form: Liquid
Boiling point: 267℃[at 101 325 Pa]
Density: 0.89[at 20℃]
vapor pressure: 1.47Pa at 38℃
Water Solubility: 1.3mg/L at 20℃
LogP: 5.24 at 25℃
Physical state solid; 20 °C; 1,013 hPa
Form liquid
Colour white

Odour slight, characteristic
Odour Threshold no data available
pH 5 - 7; 10 g/l; 20 °C
Drop point ca. 35 °C; 1,013 hPa
Boiling point/boiling range > 250 °C; 1,013 hPa
Flash point > 125 °C; 1,013 hPa
Evaporation rate not determined
Flammability (solid, gas) not applicable (liquid)
Lower explosion limit no data available
Upper explosion limit not determined
Vapour pressure < 0.0015 hPa; 20 °C
< 0.015 hPa; 20 °C
Relative vapour density not determined
Density ca.1.060 g/cm3; 50 °C; 1,013 hPa
Relative density not applicable
Bulk density no data available

Solubility in other solvents Medium: Alcohol; 20 °C; soluble
Medium: Acetone; 20 °C; soluble
Medium: Hydrocarbons; 20 °C; negligible
Water solubility 20 °C; 1,013 hPa; soluble
Partition coefficient: noctanol/water
not applicable
Justification: surface-active substance
Ignition temperature
Autoignition temperature no data available
not applicable
Viscosity, dynamic > 50 mPas; 50 °C
Explosive properties Not explosive
Oxidizing properties not expected based on structure and functional groups
Other data
None known.



FIRST AID MEASURES of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Description of first aid measures
*General advice:
If you feel unwell, seek medical advice (show the label where possible).
Consult a physician.

*In case of skin contact:
Wash off immediately with plenty of water.
Consult a physician if necessary.
*In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Call a physician immediately.

-Most important symptoms and effects, both acute and delayed:
Symptoms: No information available.
Risks: No information available.

-Indication of any immediate medical attention and special treatment needed:
Treatment: No information available.




ACCIDENTAL RELEASE MEASURES of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Personal precautions, protective equipment and emergency procedures:
*Personal precautions:
Use personal protective equipment.
-Environmental precautions:
Do not flush into surface water or sanitary sewer system.
-Methods and materials for containment and cleaning up:
*Methods for cleaning up:
Use mechanical handling equipment.
The material taken up must be disposed of in accordance with regulations.




FIRE FIGHTING MEASURES of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Extinguishing media:
*Suitable extinguishing media: Water spray, Dry powder, Foam, Carbon dioxide (CO2)



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Exposure controls:
--PERSONAL PROTECTIVE EQUIPMENT
*Respiratory protection:
No personal respiratory protective equipment normally required.
*Hand protection:
gloves suitable for permanent contact:
Material: butyl-rubber
Break through time: >= 480 min
Material thickness: >= 0.7 mm
gloves suitable for splash protection:
Material: Nitrile rubber/nitrile latex
Break through time: >= 30 min
Material thickness: >= 0.4 mm
*Eye protection:
Use tightly fitting safety goggles, and Safety glasses with side-shields
*Skin and body protection:
Protective suit
**Hygiene measures:
General industrial hygiene practice.
Handle in accordance with good industrial hygiene and safety practice.
Keep away from food, drink and animal feedingstuffs.
When using, do not eat, drink or smoke.
*Protective measures:
Wear suitable gloves and eye/face protection.





HANDLING and STORAGE of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Precautions for safe handling:
*Advice on safe handling:
Wear personal protective equipment.
-Conditions for safe storage, including any incompatibilities:
*Requirements for storage areas and containers:
Keep tightly closed in a dry and cool place.
*Other data: Stable at normal ambient temperature and pressure.
-Specific end uses:
Specific use(s): This information is not available.





STABILITY and REACTIVITY of LAURYL ALCOHOL ETHOXYLATE (3 EO):
-Chemical stability:
Note: No decomposition if stored and applied as directed.
-Possibility of hazardous reactions:
Hazardous reactions:
None known.
-Hazardous decomposition products:
No decomposition if stored normally.



SYNONYMS:
lauryl alcoholethoxylate , 1-dodecanol, ethoxilated
Alcohols, C12-14, ethoxylated
Dehydol LS 2
Syntanol ES 3
Penetrant JFC
Synperonic L 7
Syntanol ALM 8
Tergitol 24L50
Tergitol 24L92;
Surfonic L 24-2
Surfonic L 24-9
Surfonic L 24-2
Surfonic L 24-22
Surfonic L 24-3
Surfonic L 24-7
Surfonic L 24-9
Synperonic L 11
Synperonic L 7
Syntanol ALM 10
Syntanol ALM 8
Syntanol ES 3
Tergitol 24L50
Tergitol 24L60N
Tergitol 24L75N
Tergitol 24L92
Tergitol 24L98N

LAURYL AMINE OXIDE; N,N-dimethyldodecylamine-N-oxide; Lauramine oxide; Dimethyldodecylamine oxide; dimethyldodecylamine-N-oxide; DDNO; N,N-dimethyldodecylamine oxide; dodecycldimethylamine oxide; N-dodecyldimethylamine oxide; Lauryldimethylamine N-oxide; cas no: 1643-20-5

CAS NUMBER: 308062-28-4

Lauryl amine oxide, also known as dodecyldimethylamine oxide (DDAO), is an amine oxide based zwitterionic surfactant, with a C12 (dodecyl) alkyl tail.
Lauryl amine oxide is one of the most frequently-used surfactants of this type.
Like other amine oxide based surfactants Lauryl amine oxide is antimicrobial, being effective against common bacteria such as S. aureus and E. coli, however it is also non-denaturing and may be used to solubilize proteins.
Lauryl amine oxide has a role as a plant metabolite and a detergent.

Lauryl amine oxide derives from a hydride of a dodecane.
Lauryl Amine Oxide (LAO) is a standard liquid surfactant.
Lauryl amine oxide appears as a clear yellow liquid.

USES of Lauryl Amine Oxide:
-Washes and Cleaners
-Body Washes
-Conditioners
-Alkaline and Acid Cleaners
-Bleach Cleaners
-Body Washes
-Bubble Bath
-Car and Truck Wash Soaps
-Conditioners
-Dishwash Detergents
-Facial Cleansers
-Foam Booster
-Green Products
-Industrial cleaners
-Roof and House washes

APPLICATIONS of Lauryl Amine Oxide:
-Fabric care
-Hard surface care
-Home & industrial care intermediates
-Industrial cleaners
-Institutional cleaners
-Soap/detergents
-Cationic surfactants used as disinfectants, fungicides, germicide and other uses Amphoteric surfactants and Amine oxides used as antistatic agent, textile scouring agent,
-ingredient for low irritation shampoo, liquid detergent, foam boosters
-As fabric softeners and other speciality chemicals
-Dispersants, lubricants, water treatment agents

Lauryl amine oxide was nonmutagenic in the Ames assay, but was mutagenic after nitrosation.
Lauryl amine oxide at 0.1% in drinking water was not carcinogenic in rats, but at 0.1% with 0.2% sodium nitrate did increase the incidence of liver neoplasms.
Lauryl amine oxide is an excellent, versatile highly efficent surfactant for cleaning, contributing good foam and solubilizing properties to all kinds of cleaners, shampoos, bath and body products, and even detergents and cleaners for hard surfaces and even formulations for washing fine fabrics.

Lauryl amine oxide is a clear, pale-yellow, amine oxide liquid derived from coconut.
Coconuts grow on the cocos nucifera, or coconut palm tree.
Coconut palms grow around the world in lowland tropical and subtropical areas where annual precipitation is low.
Widely cultivated, healthy coconut palms produce 50 nuts per year, and the tree can be used to produce everything from food and drink to fibers, building materials, and natural ingredients.
Lauryl amine oxide (LDAO), also known as dodecyldimethylamine oxide (DDAO), is an amine oxide based zwitterionic surfactant, with a C12 (dodecyl) alkyl tail.

Lauryl amine oxide is one of the most frequently-used surfactants of this type.
Like other amine oxide based surfactants Lauryl amine oxide is antimicrobial, being effective against common bacteria such as S. aureus and E. coli, however Lauryl amine oxide is also non-denaturing and may be used to solubilize proteins.
At high concentrations, LDAO forms liquid crystalline phases.

Despite having only one polar atom that is able to interact with water the oxygen atom (the quaternary nitrogen atom is hidden from intermolecular interactions), DDAO is a strongly hydrophilic surfactant: Lauryl amine oxide forms normal micelles and normal liquid crystalline phases.
High hydrophilicity of this surfactant can be explained by the fact that Lauryl amine oxide forms very strong hydrogen bonds with water: the energy of DDAO – water hydrogen bond is about 50 kJ/mol.
Dodecyldimethylamine N-oxide is a tertiary amine oxide resulting from the formal oxidation of the amino group of dodecyldimethylamine.

Lauryl amine oxide is used as a viscosity modifier and foam enhancer for shampoos and shower gels.
Lauryl amine oxide is also applied as a foam enhancer and detergent in hard surface cleaners, sanitizing products, dishwashing liquids, and car wash systems.
In addition, this product is suitable as a water-based nonionic surfactant compatible with anionic and cationic systems.
A 30% aqueous solution of lauryl dimethylamine oxide which is based on a tertiary amine derived from natural alcohols.

Lauryl amine oxide is a strongly hydrophilic surfactant and is a colourless, viscous and foamy water based surfactant with a mild odour.
When mixed with acids, LAO can behave as a cationic surfactant but in neutral or alkaline conditions, it acts as a non-ionic surfactant.
When blended with anionic surfactants, LAO is an excellent foam booster.
Lauryl amine oxide is commonly used in washing up liquids, shampoos, bubble baths, thickened bleach cleaners, vehicle cleaners and a wide range of other cleaners.

Compatible with bleach and hypochlorite.
Lauryl amine oxide is often added to them to produce foaming, allowing hypochlorite solutions to cling to surfaces and increase contact time.
Lauryl amine oxide also allows bleach stable fragrances to be added to hypochlorite to help reduce the odours associated with bleach.
In cosmetics and personal-care products, Lauramine and Stearamine Oxides are amine oxides that are used mostly in hair-care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents and wetting agents.

Lauramine and Steramine Oxides are used mainly in hair-care products such as shampoos, hair rinses, tonics and hair-grooming aids.
Lauryl amine oxide is a clear, pale-yellow, amine oxide liquid derived from coconut.
Coconuts grow on the cocos nucifera, or coconut palm tree.
Coconut palms grow around the world in lowland tropical and subtropical areas where annual precipitation is low.
Widely cultivated, healthy coconut palms produce 50 nuts per year, and the tree can be used to produce everything from food to building materials to natural ingredients.

Lauryl amine oxide is a surfactant, meaning it breaks surface tension in liquids, allowing things to become clean.
Lauryl amine oxide is also a foam builder, stabilizer, viscosity enhancer, emollient, and conditioner.
Lauryl amine oxide can be found in personal care products such as shampoo, facial cleansers, body wash, sunscreen, and a variety of other products.

Lauryl amine oxide oxide is a cleaning agent, or "surfactant," that can also be found in a variety of products including shampoos and dishwashing detergents.
We use Lauryl amine oxide in our products to remove dirt and deposits by surrounding dirt particles to loosen them from the surface they're attached to, so they can be rinsed away.

Lauryl Myristyl Amine Oxide surfactant exhibits good tolerance to electrolytes which permits improved performance of formulations containing this surfactant in hard water.
Foaming properties are stable within a wide pH range of 5-12.
Lauryl Amine Oxide is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions.

Lauryl Amine Oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
An estimated BCF of 0.7 was calculated for Lauryl Amine Oxide(SRC), using a water solubility of 190,000 mg/L and a regression-derived equation.

According to a classification scheme, this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Koc of Lauryl Amine Oxide is estimated as 5.5(SRC), using a water solubility of 190,000 mg/L and a regression-derived equation.
According to a classification scheme, this estimated Koc value suggests that Lauryl Amine Oxide is expected to have very high mobility in soil.

The Henry's Law constant for Lauryl Amine Oxide is estimated as 6.6X10-11 atm-cu m/mole(SRC) using a fragment constant estimation method.
This Henry's Law constant indicates that Lauryl Amine Oxide is expected to be essentially nonvolatile from water surfaces(2).
Lauryl Amine Oxide's Henry's Law constant indicates that volatilization from moist soil surfaces is not likely to occur(SRC).
Lauryl Amine Oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method(3).
NIOSH (NOES Survey 1981-1983) has statistically estimated that 91,001 workers

(38,251 of these were female) were potentially exposed to Lauryl Amine Oxide in the US. Occupational exposure may occur through dermal contact with this compound at workplaces where Lauryl Amine Oxide is produced or used.
The general population may be exposed to Lauryl Amine Oxide via dermal contact with this compound and consumer products containing Lauryl Amine oxide(SRC).
Lauryl Amine Oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
Lauryl Amine Oxide, present at 100 mg/L, was 100% removed in 4 weeks as measured by liquid chromatography-mass spectrometry, using an activated sludge inoculum at 30 mg/L in the Japanese MITI test.

An inherent biodegradability test using an activated sludge inoculum at 100 mg/L and Lauryl Amine Oxide at 30 mg/L showed the compound to reach 88% of its theoretical total organic carbon in 4 weeks.
The rate constant for the vapor-phase reaction of Lauryl Amine Oxide with photochemically-produced hydroxyl radicals has been estimated as 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method.
This corresponds to an atmospheric half-life of about 14.1 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm.
The general population may be exposed to Lauryl Amine Oxide via dermal contact with this compound in consumer products containing

Lauryl Amine Oxide.Lauryl Amine Oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in its release to the environment through various waste streams(SRC).
Based on a classification scheme, an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L and a regression-derived equation, indicates that Lauryl Amine Oxide is expected to have very high mobility in soil(SRC).

Volatilization of Lauryl Amine Oxide from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method.
Lauryl Amine Oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm

Hg(SRC), determined from a fragment constant method.
In aqueous biodegradation screening tests, Lauryl Amine Oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil is an important fate process(SRC).
Based on a classification scheme, an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L and a regression-derived equation, indicates that Lauryl Amine Oxide is not expected to adsorb to suspended solids and sediment(SRC).

Volatilization from water surfaces is not expected based upon an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), developed using a fragment constant estimation method.
According to a classification scheme, an estimated BCF of 0.7(SRC), from its water solubility and a regression-derived equation, suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Lauryl amine oxide and Stearamine Oxide enhance the appearance and feel of hair by increasing hair body and volume, suppleness or sheen.
These ingrediets may improve the texture of hair that has been damaged physically or by chemical treatment.
Lauramine and Steramine Oxides also increase foaming capacity and prevents the buildup of static electricity in hair-care product formulations.

Lauryl amine oxide is usually classified as a non-ionic surfactant, as Lauryl amine oxide does not have any formal charges, and thus is compatible with anionic and cationic systems.
These products are often used as replacement of alkanolamides (CDE) due to their mildness and improved conditioning properties.
Technically speaking, amine oxides are the result of the oxidation of tertiary amines.

In other words, you have a tertiary amine and you oxidize Lauryl amine oxide, usually with hydrogen peroxide, and you obtain the amine oxide.
However, sometimes Lauryl amine oxide is also classified as cationic, as under pH below 3 it is protonated ,and the nitrogen receives a formal positive charge.
And some users also classify it as an amphoteric surfactant due to the strong ,dipolar moment between the oxygen and the nitrogen, almost as if there was a positive charge on the nitrogen and a negative charge on the oxygen.
But formally speaking under neutral or alkaline conditions it does not present any formal charges, and therefore is a non-ionic
This amine oxide presents many interesting properties, such as providing a good viscosity response thus allowing efficient thickening of surfactant solutions (the strong dipolar moment helps to structure the surfactant phase), because of its foam boosting and stabilizing it is very efficient even in low pH solutions making it interesting in industrial cleaners as well , with an good resistance to oxidation and excellent skin compatibility

USES:
Personal Care: Viscosity Modifier and Foam Enhancer for Shampoos and Shower GelsSoaps and Detergents: Foam Enhancer and Detergent in Hard Surface Cleaners, Sanitizing Products, Dishwashing Liquids and Car Wash SystemsSurfactants and Esters: Water Based Nonionic Surfactant Compatible with Anionic and Cationic Systems
Lauryl Amine Oxide (LAO) is a standard liquid surfactant.
Lauryl amine oxide appears as a clear yellow liquid.

This product is used as a viscosity modifier and foam enhancer for shampoos and shower gels.
Lauryl amine oxide is also applied as a foam enhancer and detergent in hard surface cleaners, sanitizing products, dishwashing liquids, and car wash systems.
In addition, Lauryl amine oxide is suitable as a water-based nonionic surfactant compatible with anionic and cationic systems.
(1-Dodecyl-14C)Lauryl amine oxide (10 mg with 100 uCi of 14C) was applied to the skin of two humans to study cutaneous absorption and metabolism of Lauryl amine oxide.

Ninety-two percent of the applied radioactivity was recovered from the skin of the test subjects 8 hr after dosing, and 0.1 and 0.23% of the radioactivity was recovered from the excretion products of the test subjects.
The stratum corneum contained <0.2% of the applied dose.
Oral administration of a solution containing 50 mg (1-dodecyl-14C)Lauryl amine oxide (100 uCi of 14C) to two humans resulted in excretion patterns of radioactivity similar to that of the other species studied.

Fifty percent and 37% of the radioactivity was found in the urine within 24 hr of dosing, and expired 14C02 contained between 18 and 22% of the radioactivity administered.
Four Sprague-Dawley rats were given intraperitoneal injections of 22 mg (methyl-14C)Lauryl amine oxide kg (specific activity 1.3 mCi/g).
Sixty-seven percent of the total radioactivity was eliminated in the urine, 8% was expired as I4CO2, and 6% was eliminated in the feces within 24 hr.

The distribution of radioactivity was essentially the same as that seen in rats given oral doses of Lauryl amine oxide.
The conclusion was that " microbial metabolism by gastrointestinal flora does not play a major role in the absorption and excretion of and absorption of the compound.
Over 72 hr, 14.2% of the total radioactivity was found in the urine, 2.5% in the CO2, and 1.8% in the feces.
Radioactivity was detected in the liver, kidneys, testes, blood, and expired CO2.

Characterization of metabolites of Lauryl amine oxide resulted in the positive identification of only one metabolite, N-dimethyl-4-aminobutyric acid N-oxide.
Several pathways exist for metabolism of Lauryl amine oxide: omega,beta-oxidation of alkyl chains (the most common pathway for surfactant metabolism), hydroxylation of alkyl chains, and reduction of the amine oxide group.

Lauryl amine oxide and stearamine oxide are aliphatic tertiary amine oxides that are used in cosmetics as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents.
Acute Exposure/ The ocular irritation potential of formulations containing 0.3% active Lauryl amine oxide was evaluated by instilling 10 uL into the conjunctival sac of New Zealand White rabbits.

The eyes of some rabbits were rinsed with distilled water.
Irritation was scored according to the method of Draize (maximum possible score:). Slight irritation of the conjunctivae was observed in all unrinsed eyes and in two of three rinsed eyes at the 24-hr grading period.
The maximum average score was 2.0 for the animals with unrinsed eyes, and 1.3 for those whose eyes were rinsed.
All eyes were clear after 48 hr.
Acute Exposure/ Liquid droplet aerosol /formulation containing 0.3% active Lauryl amine oxide/ at concentrations of 0.2, 1.0, and 5.2 mg/L were tested on three groups of four male Swiss-Webster mice.

Only the heads of the mice were exposed to the aerosol.
The average respiratory rate was monitored using plethysmography 5 min before, 10 min during, and 10 min after each exposure, and the percentage change in respiratory rate was calculated.
A decrease in respiratory rate was considered a response to upper airway irritation.
A transient decrease was observed in the respiratory rate of the 1.0 mg/L exposed group, but this was not considered significant because no signs of irritation were seen at greater exposure concentrations.

The groups treated with 1.0 mg/L and 5.2 mg/L had a 6% decrease in their average respiratory rates.
However, these decreases were not attributed to upper airway irritation because the respiratory rates were even lower during the postexposure recovery period.
No decrease in respiratory rate was observed in the 0.2 mg/L exposed mice.
Acute Exposure/ The acute inhalation toxicity of a liquid droplet aerosol formulation containing 0.3% active Lauryl amine oxide was evaluated.
Five female and five male albino Sprague-Dawley-derived rats were exposed for 4 hr to this aerosol at a concentration of 5.3 mg/L.

The Equivalent Aerodynamic Diameter of the aerosol was 3.6 um with a geometric standard deviation of 1.91.
The animals were observed during the exposure and two times daily for 14 days, and body weights were recorded before exposure and on days 1, 3, 7, and 14 postexposure.
At necropsy, the major organs in the abdominal and thoracic cavities were weighed and observed.
No deaths occurred during the study and all the rats appeared normal.

A slight drop in body weight was observed in the males on day 1, but weight was gained normally for the remainder of the study.
The weight gain in the females was normal.
The organ weights were all within the anticipated normal control ranges for both sexes.
No exposure-related pharmacotoxic signs were evident in any of the organs.
The 4-hr LD50 for this aerosol was greater than 5.3 mg/L nominal.

Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in its release to the environment through various waste streams.
If released to air, an estimated vapor pressure of 6.2X10-8 mm Hg at 25 °C indicates Lauryl amine oxide will exist in both the vapor and particulate phases in the atmosphere.
Vapor-phase Lauryl amine oxide will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14.1 hours.

Particulate-phase Lauryl amine oxide will be removed from the atmosphere by wet or dry deposition.
Luryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight.
If released to soil, Lauryl amine oxide is expected to have very high mobility based upon an estimated.
Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole.

In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil and water is an important fate process.
If released into water, Lauryl amine oxide is not expected to adsorb to suspended solids and sediment based upon the estimated Koc.
Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant.

An estimated BCF of 0.7 suggests the potential for bioconcentration in aquatic organisms is low.
Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions.
Occupational exposure to Lauryl amine oxide may occur through dermal contact with this compound at workplaces where it is produced or used. The general population may be exposed to Lauryl amine oxide via dermal contact with this compound in consumer products containing Lauryl amine oxide.

Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in its release to the environment through various waste streams(SRC).
Based on a classification scheme, an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L and a regression-derived equation, indicates that Lauryl amine oxide is expected to have very high mobility in soil(SRC).
Volatilization of Lauryl amine oxide from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated

Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method.
Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method. In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil is an important fate process(SRC).

According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere, Lauryl amine oxide, which has an estimated vapor pressure of 6.2X10-8 mm Hg at 25 °C(SRC), determined from a fragment constant method, will exist in both the vapor and particulate phases in the ambient atmosphere.
Vapor-phase Lauryl amine oxide is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 14.1 hours(SRC), calculated from its rate constant of 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method Particulate-phase Lauryl amine oxide may be removed from the air by wet or dry deposition(SRC).

Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
Lauryl amine oxide, present at 100 mg/L, was 100% removed in 4 weeks as measured by liquid chromatography-mass spectrometry, using an activated sludge inoculum at 30 mg/L in the Japanese MITI test.

An inherent biodegradability test using an activated sludge inoculum at 100 mg/L and Lauryl amine oxide at 30 mg/L showed the compound to reach 88% of its theoretical total organic carbon in 4 weeks.
The rate constant for the vapor-phase reaction of Lauryl amine oxide with photochemically-produced hydroxyl radicals has been estimated as 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1).
This corresponds to an atmospheric half-life of about 14.1 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm.

Lauryl amine oxide is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions.
Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).

An estimated BCF of 0.7 was calculated for Lauryl amine oxide(SRC), using a water solubility of 190,000 mg/L and a regression-derived equation.
According to a classification scheme, this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Koc of Lauryl amine oxide is estimated as 5.5(SRC), using a water solubility of 190,000 mg/L and a regression-derived equation.
According to a classification scheme, this estimated Koc value suggests that Lauryl amine oxide is expected to have very high mobility in soil.

The Henry's Law constant for Lauryl amine oxide is estimated as 6.6X10-11 atm-cu m/mole(SRC) using a fragment constant estimation method.
This Henry's Law constant indicates that Lauryl amine oxide is expected to be essentially nonvolatile from water surfaces.
Lauryl amine oxide's Henry's Law constant indicates that volatilization from moist soil surfaces is not likely to occur(SRC).

Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method.
NIOSH (NOES Survey 1981-1983) has statistically estimated that 91,001 workers (38,251 of these were female) were potentially exposed to Lauryl amine oxide in the US.
Occupational exposure may occur through dermal contact with this compound at workplaces where Lauryl amine oxide is produced or used. The general population may be exposed to Lauryl amine oxide via dermal contact with this compound and consumer products containing Lauryl amine oxide(SRC).

Lauryl amine Oxide is a nonionic/amphoteric surfactant which is compatible with all surfactant classes: anionic, nonionic, amphoteric, and cationic.
Lauryl amine oxide provides high foaming and thickening properties and is stable at most pH ranges, including, stability in peroxide and hypochlorite solutions.
In addition, Lauryl amine Oxide can mitigate the irritation effects of anionic surfactants.
Major market segments for this product include home care, personal care, oil & gas, and agrochemicals.


LAURAMINE OXIDE is classified as :
-Antistatic
-Cleansing
-Foam boosting
-Hair conditioning
-Hydrotrope
-Surfactant
-Viscosity controlling
-Perfuming

Amine N-oxides are active components in body care products such as shampoo, bubble bath, and hand-soap formulations in combination with alkyl or olefin sulfates.
In acidic media, they are cationic and can act as a mild conditioner.
In neutral or weak basic media, they are featured as excellent foam stabilizer and viscosity building provider.
Lauryl amine oxide is used as a foam enhancer, stabilizer and viscosity builder.

Lauryl amine oxide is used in light duty liquid detergents, drain cleaners, fabric washer.
Dye dispersant, wetting agent, emulsifier, lubricant.
Formulation with anionic, nonionic and cationic materials.

Amphoteric surfactants have dual functional groups (both acidic and basic groups) in the same molecule.
They are polar solvents that have a high solubility in water but a poor solubility in most organic solvents.
They are electrically neutral but carries positive and negative charges on different atoms in an aqueous solution.

Depending on the composition and conditions of pH value, the substances can have anionic or cationic properties.
In the presence of acids, they will accept the hydrogen ions but they will donate hydrogen ions to the solution in the presence of bases, which balances the pH.

Such actions make buffer solutions which resist change to the pH.
In the detergency ability amphoteric surfactants which change their charge according to the pH of the solution affects properties of foaming, wetting and detergentcy through a surface action that exerts both hydrophilic and hydrophobic properties.
In biochemistry amphoteric surfactant is used as a detergent for purifying, cleansing and antimicrobial effects.
Alkylbetains and aminoxides are amphoteric surfactants.
Learn all about lauryl amine oxide, including how Lauryl amine oxide's made, and why Puracy uses lauramine oxide in our products.

FUNCTIONS:
Lauryl amine oxide is an Amine N-oxide, an active component primarily found in shampoo, bubble bath and hand soap thanks to its foam building properties (Source).
Because Lauryl amine oxide has dual functional groups in the same molecule (both asidic and basic groups), Lauryl amine oxide is very versatile.

Lauryl amine oxide can have high solubility in some solutions and low in others; Lauryl amine oxide creates positive charges and negative charges on different atoms; Lauryl amine oxide carries anionic or cationic properties depending on pH value.
Therefore although Lauryl amine oxide is seen most frequently as a foam builder in beauty products, Lauryl amine oxide can also be used as a dye dispersant, wetting agent, emulsifier, lubricant, surfactant, anti-static agent, and viscosity controlling agent, according to research.

Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions.
Occupational exposure to Lauryl amine oxide may occur through dermal contact with this compound at workplaces where Lauryl amine oxide is produced or used.
The general population may be exposed to Lauryl amine oxide via dermal contact with this compound in consumer products containing Lauryl amine oxide.

Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in Lauryl amine oxides release to the environment through various waste streams(SRC).
Based on a classification scheme, an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L and a regression-derived equation, indicates that Lauryl amine oxide is expected to have very high mobility in soil(SRC).
Volatilization of Lauryl amine oxide from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated

Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method.
Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method.
In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil is an important fate process(SRC).

PROPERTIES:
Appearance: Clear Liquid
Odor: Characteristic
Color: Colorless to Pale Yellow
pH (10% Solution W/V): 5.5 – 7.5
Assay, % by mass: 27 – 29
Free Amine, %: 0.5 max
Microbial Count (Plate Method), cfu/mL: < 10
Molecular Weight: 240

How Lauryl amine oxide Is Made:
Lauryl amine oxide is a surfactant, meaning it breaks surface tension in liquids, allowing things to become clean.
Lauryl amine oxide is also a foam builder, stabilizer, viscosity enhancer, emollient and condition
Lauryl amine oxide can be found in personal care products such as shampoo, facial cleansers, body wash, sunscreen, and a variety of other produc
Lauryl amine oxide is a surfactant, meaning Lauryl amine oxide breaks surface tension in liquids, allowing things to become clean.

Lauryl amine oxide is also a foam builder, stabilizer, viscosity enhancer, emollient and conditioner.
Lauryl amine oxide can be found in personal care products such as shampoo, facial cleansers, body wash, sunscreen, and a variety of other products.
We use Lauryl amine oxide as a surfactant and cleanser.
The Cosmetics Ingredient Review has deemed the ingredient safe for use in cosmetic products and in leave-on products in which the concentration is limited to 3.7%.

Research shows the ingredient is typically not a skin or eye irritant.
Commercial production of Lauryl amine oxide occurs largely by mixing the amine with 35% hydrogen peroxide at 60 degrees Celsius.
The mixture is heated to 75 degrees Celsius and sodium sulfite or manganese dioxide are added.
The mixture is then filtered to get rid of extra peroxide.

Lauryl amine oxide and Stearamine Oxide are aliphatic tertiary amine oxides that are used mostly in hair care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents.
Both compounds are susceptible to nitrosation and can form nitrosamines in the presence of nitrosating agents.
In rats, up to 40% of Lauryl amine oxide applied to the skin was absorbed.
In two human volunteers, 92% of the dose applied to the skin was recovered from the skin.

The oral LD50 in rats for a formulation containing 0.3% Lauryl amine oxide was estimated to be >20 g/kg.
At a concentration of 30%, Lauryl amine oxide produced severe dermal reactions in rabbits, but at 0.3% only slight to moderate erythema with slight edema, Assuring, and slight to moderate epithelial desquamation were found.

Stearamine Oxide applied to rabbit skin at 5% did not cause irritation.
Both ingredients caused mild, transient ocular irritation in rabbits.
Clinical data showed dermal exposure to 3.7% Lauryl amine oxide to be a mild irritant, with a slight potential for mild cumulative skin irritation at concentrations as low as 2%. At 0.3%, Lauryl amine oxide was not a sensitizer in clinical studies.

Lauryl amine oxide was nonmutagenic in the Ames assay, but was mutagenic after nitrosation.
Lauryl amine oxide at 0.1% in drinking water was not carcinogenic in rats, but at 0.1% with 0.2% sodium nitrate did increase the incidence of liver neoplasms.

Based on this animal data, neither ingredient should contain N-ni-troso compounds nor be used in formulations containing nitrosating agents.
On the basis of the available animal and clinical data, it is concluded that Lauryl amine oxide and Stearamine Oxide are safe as cosmetic ingredients for rinse-off products, but that the concentration in Lauryl amine oxide leave-on products should be limited to 3.7% and that of Stearamine Oxide limited to 5%.

Lauryl amine oxide and Stearamine Oxide are aliphatic tertiary amine oxides that are used mostly in hair care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents.
Both compounds are susceptible to nitrosation and can form nitrosamines in the presence of nitrosating agents.
In rats, up to 40% of Lauryl amine oxide applied to the skin was absorbed.
In two human volunteers, 92% of the dose applied to the skin was recovered from the skin.

The oral LD,, in rats for a formulation containing 0.3% Lauryl amine oxide was estimated to be >20 &g.
At a concentration of 30%, Lauryl amine oxide produced severe dermal reactions in rabbits, but at 0.3% only slight to moderate erythema with slight edema, fissuring, and slight to moderate epithelial desquamation were found.
Stearamine Oxide applied to rabbit skin at 5% did not cause irritation.
Both ingredients caused mild, transient ocular irritation in rabbits.
Clinical data showed dermal exposure to 3.7% Lauryl amine oxide to be a mild initant, with a slight potential for mild cumulative skin initation at concentrations as low as 2%. At 0.3%, Lauryl amine oxide was not a sensitizer in clinical studies.

Lauryl amine oxide is compatible with most with nonionic, anionic and cationic surfactants.
Works well in neutrral, acid, and alkaline formulations.
Lauryl amine oxide is effective, plus Lauryl amine oxide is an environmentally responsible surfactant that can often replace ngredient that replaces products that are petroleum based, and you may see added performance.

SYNONYM:
Lauryl amine oxide
Dodecyldimethylamine oxide
Lauryldimethylamine N-oxide
LDAO
1-Dodecanamine, N,N-dimethyl-, N-oxide
Dimethyldodecylamine oxide
Ammonyx AO
Ammonyx LO
Empigen OB
Aromox DMCD

About Lauryl amine oxide Helpful information:
Lauryl amine oxide is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 to < 1 000 tonnes per annum.
Lauryl amine oxide is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Consumer Uses of Lauryl amine oxide:
Lauryl amine oxide is used in the following products: washing & cleaning products and cosmetics and personal care products.
Other release to the environment of Lauryl amine oxide is likely to occur from: indoor use as processing aid.

Article service life of Lauryl amine oxide:
ECHA has no public registered data on the routes by which Lauryl amine oxide is most likely to be released to the environment.
ECHA has no public registered data indicating whether or into which articles Lauryl amine oxide might have been processed.

Widespread uses by professional workers of Lauryl amine oxide:
Lauryl amine oxide is used in the following products: laboratory chemicals, polishes and waxes, washing & cleaning products, cosmetics and personal care products and pH regulators and water treatment products. This substance is used in the following areas: health services and scientific research and development. Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

Formulation or re-packing of Lauryl amine oxide:
Lauryl amine oxide is used in the following products: laboratory chemicals, metal working fluids, polishes and waxes, washing & cleaning products, water treatment chemicals and cosmetics and personal care products.
Release to the environment of Lauryl amine oxide can occur from industrial use: formulation of mixtures.

Uses at industrial sites of Lauryl amine oxide:
Lauryl amine oxide is used in the following products: metal working fluids, washing & cleaning products, water treatment chemicals, pH regulators and water treatment products and laboratory chemicals.
Lauryl amine oxide is used in the following areas: health services and scientific research and development.
Lauryl amine oxide is used for the manufacture of: chemicals.
Release to the environment of Lauryl amine oxide can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and as processing aid.

Manufacture of Lauryl amine oxide:
Release to the environment of Lauryl amine oxide can occur from industrial use: manufacturing of the substance.

Regulatory process names
Dodecyldimethylamine oxide
dodecyldimethylamine oxide
1-Dodecanamine, N,N-dimethyl-, N-oxide
1-Dodecanamine, N,N-dimethyl-, N-oxide
ColaLux LG
dodecyl(dimethyl) amine oxide
dodecyl(dimethyl)amine oxide
Dodecyldimethylamine oxide
dodecyldimethylamine oxide
dodecyldimethylamine oxide
Lauramine oxide
LAURYLDIMETHYLAMINE OXIDE
N,N-Dimethyldodecan-1-amine oxide
N,N-dimethyldodecan-1-amine oxide
N,N-dimethyldodecanamine oxide
N,N-Dimethyldodecylamine N-oxide
N,N-Dimethyldodecylamine N-oxide, Lauryldimethylamine N-oxide, DDAO, LDAO
135526-66-8
160714-02-3
1616935-99-9
163221-07-6
1643-20-5
177162-47-9
209122-49-6
244235-92-5
311814-25-2
607690-42-6
73502-08-6

Lauryl Amine Oxide Lauryldimethylamine oxide (Lauryl amine oxide), also known as dodecyldimethylamine oxide (DDAO), is an amine oxide based zwitterionic surfactant, with a C12 (dodecyl) alkyl tail. It is one of the most frequently-used surfactants of this type.[4] Like other amine oxide based surfactants it is antimicrobial, being effective against common bacteria such as S. aureus and E. coli,[1] however it is also non-denaturing and may be used to solubilize proteins. At high concentrations, Lauryl amine oxide forms liquid crystalline phases.[5] Despite having only one polar atom that is able to interact with water – the oxygen atom (the quaternary nitrogen atom is hidden from intermolecular interactions), DDAO is a strongly hydrophilic surfactant: it forms normal micelles and normal liquid crystalline phases. High hydrophilicity of this surfactant can be explained by the fact that it forms very strong hydrogen bonds with water: the energy of DDAO – water hydrogen bond is about 50 kJ/mol. Parameters Specifications Test Methods Appearance Clear Liquid — Odor Characteristic — Color Colorless to Pale Yellow — pH (10% Solution W/V) 5.5 – 7.5 — Assay, % by mass 27 – 29 — Free Amine, % 0.5 max — Microbial Count (Plate Method), cfu/mL < 10 — Molecular Weight 240 — USES & APPLICATIONS Personal Care: Viscosity Modifier and Foam Enhancer for Shampoos and Shower GelsSoaps and Detergents: Foam Enhancer and Detergent in Hard Surface Cleaners, Sanitizing Products, Dishwashing Liquids and Car Wash SystemsSurfactants and Esters: Water Based Nonionic Surfactant Compatible with Anionic and Cationic Systems Lauryl Amine Oxide (LAO) is a standard liquid surfactant. It appears as a clear yellow liquid. This product is used as a viscosity modifier and foam enhancer for shampoos and shower gels. It is also applied as a foam enhancer and detergent in hard surface cleaners, sanitizing products, dishwashing liquids, and car wash systems. In addition, this product is suitable as a water-based nonionic surfactant compatible with anionic and cationic systems. (1-Dodecyl-14C)Lauryl amine oxide (10 mg with 100 uCi of 14C) was applied to the skin of two humans to study cutaneous absorption and metabolism of Lauryl amine oxide. Ninety-two percent of the applied radioactivity was recovered from the skin of the test subjects 8 hr after dosing, and 0.1 and 0.23% of the radioactivity was recovered from the excretion products of the test subjects. The stratum corneum contained <0.2% of the applied dose. Oral administration of a solution containing 50 mg (1-dodecyl-14C)Lauryl amine oxide (100 uCi of 14C) to two humans resulted in excretion patterns of radioactivity similar to that of the other species studied. Fifty percent and 37% of the radioactivity was found in the urine within 24 hr of dosing, and expired 14C02 contained between 18 and 22% of the radioactivity administered. Four Sprague-Dawley rats were given intraperitoneal injections of 22 mg (methyl-14C)Lauryl amine oxide kg (specific activity 1.3 mCi/g). Sixty-seven percent of the total radioactivity was eliminated in the urine, 8% was expired as I4CO2, and 6% was eliminated in the feces within 24 hr. The distribution of radioactivity was essentially the same as that seen in rats given oral doses of Lauryl amine oxide. The conclusion was that "... microbial metabolism by gastrointestinal flora does not play a major role in the absorption and excretion of [Lauryl amine oxide] in rats." Aqueous (methyl-14C)Lauryl amine oxide (10 mg containing 1.3 mCi/g) was applied to the skin of four Sprague-Dawley rats to test metabolism and absorption of the compound. Over 72 hr, 14.2% of the total radioactivity was found in the urine, 2.5% in the CO2, and 1.8% in the feces. Radioactivity was detected in the liver, kidneys, testes, blood, and expired CO2. Characterization of metabolites of Lauryl amine oxide resulted in the positive identification of only one metabolite, N-dimethyl-4-aminobutyric acid N-oxide. Several pathways exist for metabolism of Lauryl amine oxide: omega,beta-oxidation of alkyl chains (the most common pathway for surfactant metabolism), hydroxylation of alkyl chains, and reduction of the amine oxide group. Lauryl amine oxide and stearamine oxide are aliphatic tertiary amine oxides that are used in cosmetics as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents. Acute Exposure/ The ocular irritation potential of formulations containing 0.3% active Lauryl amine oxide was evaluated by instilling 10 uL into the conjunctival sac of New Zealand White rabbits. The eyes of some rabbits were rinsed with distilled water. Irritation was scored according to the method of Draize (maximum possible score: 110). Slight irritation of the conjunctivae was observed in all unrinsed eyes and in two of three rinsed eyes at the 24-hr grading period. The maximum average score was 2.0 for the animals with unrinsed eyes, and 1.3 for those whose eyes were rinsed. All eyes were clear after 48 hr. Acute Exposure/ Liquid droplet aerosol /formulation containing 0.3% active Lauryl amine oxide/ at concentrations of 0.2, 1.0, and 5.2 mg/L were tested on three groups of four male Swiss-Webster mice. Only the heads of the mice were exposed to the aerosol. The average respiratory rate was monitored using plethysmography 5 min before, 10 min during, and 10 min after each exposure, and the percentage change in respiratory rate was calculated. A decrease in respiratory rate was considered a response to upper airway irritation. A transient decrease was observed in the respiratory rate of the 1.0 mg/L exposed group, but this was not considered significant because no signs of irritation were seen at greater exposure concentrations. The groups treated with 1.0 mg/L and 5.2 mg/L had a 6% decrease in their average respiratory rates. However, these decreases were not attributed to upper airway irritation because the respiratory rates were even lower during the postexposure recovery period. No decrease in respiratory rate was observed in the 0.2 mg/L exposed mice. Acute Exposure/ The acute inhalation toxicity of a liquid droplet aerosol formulation containing 0.3% active Lauryl amine oxide was evaluated. Five female and five male albino Sprague-Dawley-derived rats were exposed for 4 hr to this aerosol at a concentration of 5.3 mg/L. The Equivalent Aerodynamic Diameter of the aerosol was 3.6 um with a geometric standard deviation of 1.91. The animals were observed during the exposure and two times daily for 14 days, and body weights were recorded before exposure and on days 1, 3, 7, and 14 postexposure. At necropsy, the major organs in the abdominal and thoracic cavities were weighed and observed. No deaths occurred during the study and all the rats appeared normal. A slight drop in body weight was observed in the males on day 1, but weight was gained normally for the remainder of the study. The weight gain in the females was normal. The organ weights were all within the anticipated normal control ranges for both sexes. No exposure-related pharmacotoxic signs were evident in any of the organs. The 4-hr LD50 for this aerosol was greater than 5.3 mg/L nominal. Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in its release to the environment through various waste streams. If released to air, an estimated vapor pressure of 6.2X10-8 mm Hg at 25 °C indicates Lauryl amine oxide will exist in both the vapor and particulate phases in the atmosphere. Vapor-phase Lauryl amine oxide will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14.1 hours. Particulate-phase Lauryl amine oxide will be removed from the atmosphere by wet or dry deposition. Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight. If released to soil, Lauryl amine oxide is expected to have very high mobility based upon an estimated Koc of 5.5. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole. In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil and water is an important fate process. If released into water, Lauryl amine oxide is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant. An estimated BCF of 0.7 suggests the potential for bioconcentration in aquatic organisms is low. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. Occupational exposure to Lauryl amine oxide may occur through dermal contact with this compound at workplaces where it is produced or used. The general population may be exposed to Lauryl amine oxide via dermal contact with this compound in consumer products containing Lauryl amine oxide. Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap(1), as a foam stabilizer, and textile antistatic agent(2) may result in its release to the environment through various waste streams(SRC). Based on a classification scheme(1), an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L(2) and a regression-derived equation(3), indicates that Lauryl amine oxide is expected to have very high mobility in soil(SRC). Volatilization of Lauryl amine oxide from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method(5). In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry(6), suggesting that biodegradation in soil is an important fate process(SRC). According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), Lauryl amine oxide, which has an estimated vapor pressure of 6.2X10-8 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase Lauryl amine oxide is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 14.1 hours(SRC), calculated from its rate constant of 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3) Particulate-phase Lauryl amine oxide may be removed from the air by wet or dry deposition(SRC). Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). Lauryl amine oxide, present at 100 mg/L, was 100% removed in 4 weeks as measured by liquid chromatography-mass spectrometry, using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(1). An inherent biodegradability test using an activated sludge inoculum at 100 mg/L and Lauryl amine oxide at 30 mg/L showed the compound to reach 88% of its theoretical total organic carbon in 4 weeks(1). The rate constant for the vapor-phase reaction of Lauryl amine oxide with photochemically-produced hydroxyl radicals has been estimated as 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 14.1 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). Lauryl amine oxide is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(2). Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm(2) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). An estimated BCF of 0.7 was calculated for Lauryl amine oxide(SRC), using a water solubility of 190,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC). The Koc of Lauryl amine oxide is estimated as 5.5(SRC), using a water solubility of 190,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that Lauryl amine oxide is expected to have very high mobility in soil. The Henry's Law constant for Lauryl amine oxide is estimated as 6.6X10-11 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that Lauryl amine oxide is expected to be essentially nonvolatile from water surfaces(2). Lauryl amine oxide's Henry's Law constant indicates that volatilization from moist soil surfaces is not likely to occur(SRC). Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method(3). NIOSH (NOES Survey 1981-1983) has statistically estimated that 91,001 workers (38,251 of these were female) were potentially exposed to Lauryl amine oxide in the US(1). Occupational exposure may occur through dermal contact with this compound at workplaces where Lauryl amine oxide is produced or used. The general population may be exposed to Lauryl amine oxide via dermal contact with this compound and consumer products containing Lauryl amine oxide(SRC). Lauryl amine Oxide is a nonionic/amphoteric surfactant which is compatible with all surfactant classes: anionic, nonionic, amphoteric, and cationic. It provides high foaming and thickening properties and is stable at most pH ranges, including, stability in peroxide and hypochlorite solutions. In addition, Lauryl amine Oxide can mitigate the irritation effects of anionic surfactants. Major market segments for this product include home care, personal care, oil & gas, and agrochemicals. LAURAMINE OXIDE is classified as : Antistatic Cleansing Foam boosting Hair conditioning Hydrotrope Surfactant Viscosity controlling Perfuming Amine N-oxides are active components in body care products such as shampoo, bubble bath, and hand-soap formulations in combination with alkyl or olefin sulfates. In acidic media, they are cationic and can act as a mild conditioner. In neutral or weak basic media, they are featured as excellent foam stabilizer and viscosity building provider. Lauryl amine oxide is used as a foam enhancer, stabilizer and viscosity builder. It is used in light duty liquid detergents, drain cleaners, fabric washer. dye dispersant, wetting agent, emulsifier, lubricant. formulation with anionic, nonionic and cationic materials. Amphoteric surfactants have dual functional groups (both acidic and basic groups) in the same molecule. They are polar solvents that have a high solubility in water but a poor solubility in most organic solvents. They are electrically neutral but carries positive and negative charges on different atoms in an aqueous solution. Depending on the composition and conditions of pH value, the substances can have anionic or cationic properties. In the presence of acids, they will accept the hydrogen ions but they will donate hydrogen ions to the solution in the presence of bases, which balances the pH. Such actions make buffer solutions which resist change to the pH. In the detergency ability amphoteric surfactants which change their charge according to the pH of the solution affects properties of foaming, wetting and detergentcy through a surface action that exerts both hydrophilic and hydrophobic properties. In biochemistry amphoteric surfactant is used as a detergent for purifying, cleansing and antimicrobial effects. Alkylbetains and aminoxides are amphoteric surfactants. Learn all about lauryl amine oxide, including how it's made, and why Puracy uses lauramine oxide in our products. Derived from: coconut Pronunciation: (LORA-meen \ˈäk-ˌsīd\) Type: Naturally-derived What Is Lauryl amine oxide? Lauryl amine oxide is a clear, pale-yellow, amine oxide liquid derived from coconut.[1,2,3] Coconuts grow on the cocos nucifera, or coconut palm tree. Coconut palms grow around the world in lowland tropical and subtropical areas where annual precipitation is low.[4,5] Widely cultivated, healthy coconut palms produce 50 nuts per year, and the tree can be used to produce everything from food and drink to fibers, building materials, and natural ingredients.[6,7] What Does Lauryl amine oxide Do in Our products? Lauryl amine oxide is a surfactant, meaning it breaks surface tension in liquids, allowing things to become clean. It is also a foam builder, stabilizer, viscosity enhancer, emollient and conditioner.[8] It can be found in personal care products such as shampoo, facial cleansers, body wash, sunscreen, and a variety of other products.[9,10] Why Puracy Uses Lauryl amine oxide We use Lauryl amine oxide as a surfactant and cleanser. The Cosmetics Ingredient Review has deemed the ingredient safe for use in cosmetic products and in leave-on products in which the concentration is limited to 3.7%.[13] Research shows the ingredient is typically not a skin or eye irritant. How Lauryl amine oxide Is Made Commercial production of Lauryl amine oxide occurs largely by mixing the amine with 35% hydrogen peroxide at 60 degrees Celsius. The mixture is heated to 75 degrees Celsius and sodium sulfite or manganese dioxide are added. The mixture is then filtered to get rid of extra peroxide. Lauryl amine oxide and Stearamine Oxide are aliphatic tertiary amine oxides that are used mostly in hair care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents. Both compounds are susceptible to nitrosation and can form nitrosamines in the presence of nitrosating agents. In rats, up to 40% of Lauryl amine oxide applied to the skin was absorbed. In two human volunteers, 92% of the dose applied to the skin was recovered from the skin. The oral LD50 in rats for a formulation containing 0.3% Lauryl amine oxide was estimated to be >20 g/kg. At a concentration of 30%, Lauryl amine oxide produced severe dermal reactions in rabbits, but at 0.3% only slight to moderate erythema with slight edema, Assuring, and slight to moderate epithelial desquamation were found. Stearamine Oxide applied to rabbit skin at 5% did not cause irritation. Both ingredients caused mild, transient ocular irritation in rabbits. Clinical data showed dermal exposure to 3.7% Lauryl amine oxide to be a mild irritant, with a slight potential for mild cumulative skin irritation at concentrations as low as 2%. At 0.3%, Lauryl amine oxide was not a sensitizer in clinical studies. Lauryl amine oxide was nonmutagenic in the Ames assay, but was mutagenic after nitrosation. Lauryl amine oxide at 0.1% in drinking water was not carcinogenic in rats, but at 0.1% with 0.2% sodium nitrate did increase the incidence of liver neoplasms. Based on this animal data, neither ingredient should contain N-ni-troso compounds nor be used in formulations containing nitrosating agents. On the basis of the available animal and clinical data, it is concluded that Lauryl amine oxide and Stearamine Oxide are safe as cosmetic ingredients for rinse-off products, but that the concentration in Lauryl amine oxide leave-on products should be limited to 3.7% and that of Stearamine Oxide limited to 5%. Lauryl amine oxide and Stearamine Oxide are aliphatic tertiary amine oxides that are used mostly in hair care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents, and wetting agents. Both compounds are susceptible to nitrosation and can form nitrosamines in the presence of nitrosating agents. In rats, up to 40% of Lauryl amine oxide applied to the skin was absorbed. In two human volunteers, 92% of the dose applied to the skin was recovered from the skin. The oral LD,, in rats for a formulation containing 0.3% Lauryl amine oxide was estimated to be >20 &g. At a concentration of 30%, Lauryl amine oxide produced severe dermal reactions in rabbits, but at 0.3% only slight to moderate erythema with slight edema, fissuring, and slight to moderate epithelial desquamation were found. Stearamine Oxide applied to rabbit skin at 5% did not cause irritation. Both ingredients caused mild, transient ocular irritation in rabbits. Clinical data showed dermal exposure to 3.7% Lauryl amine oxide to be a mild initant, with a slight potential for mild cumulative skin initation at concentrations as low as 2%. At 0.3%, Lauryl amine oxide was not a sensitizer in clinical studies. Lauryl amine oxide was nonmutagenic in the Ames assay, but was mutagenic after nitrosation. Lauryl amine oxide at 0.1% in drinking water was not carcinogenic in rats, but at 0.1% with 0.2% sodium nitrate did increase the incidence of liver neoplasms. Based on this animal data, neither ingredient should contain N-nitrow compounds nor be used in formulations containing nitrosating agents. On the basis of the available animal and clinical data, it is concluded that Lauryl amine oxide and Stearamine Oxide are safe as cosmetic ingredients for rinseoff products, but that the concentration in Lauryl amine oxide leave-on products should be limited to 3.7% and that of Stearamine Oxide limited to 5%. Key Words: Safety assessment-Lauryl amine oxide-Stearamine Oxide. Lauryl amine oxide is an excellent, versatile highly efficent surfactant for cleaning, contributing good foam and solubilizing properties to all kinds of cleaners, shampoos, bath and body products, and even detergents and cleaners for hard surfaces and even formulations for washing fine fabrics. Lauryl amine oxide is compatible with most with nonionic, anionic and cationic surfactants. Works well in neutrral, acid, and alkaline formulations. Lauryl amine oxide is effective, plus it is an environmentally responsible surfactant that can often replace ngredient that replaces products that are petroleum based, and you may see added performance. FEATURES & BENEFITS Bleach (Chlorine) & Acid Stable Can be used with a variety of anionic, nonionic & cationic surfactants and co surfactants. USES: Washes and Cleaners Body Washes Conditioners Alkaline and Acid Cleaners Bleach Cleaners Body Washes Bubble Bath Car and Truck Wash Soaps Conditioners Dishwash Detergents Facial Cleansers Foam Booster Green Products Industrial cleaners Roof and House washes What Is It? In cosmetics and personal-care products, Lauramine and Stearamine Oxides are amine oxides that are used mostly in hair-care products as foam builders and stabilizers, viscosity enhancers, emollients, conditioners, emulsifiers, antistatic agents and wetting agents. Lauramine and Steramine Oxides are used mainly in hair-care products such as shampoos, hair rinses, tonics and hair-grooming aids. Why is it used in cosmetics and personal care products? Lauryl amine oxide and Stearamine Oxide enhance the appearance and feel of hair by increasing hair body and volume, suppleness or sheen. These ingrediets may improve the texture of hair that has been damaged physically or by chemical treatment. Lauramine and Steramine Oxides also increase foaming capacity and prevents the buildup of static electricity in hair-care product formulations. Scientific Facts: Lauryl amine oxide and Stearamine Oxides are Amine Oxides. Amine oxides are usually prepared from tertiary Amines by oxidation, usually with hydrogen peroxide. Lauryl amine oxide is an Amine N-oxide, an active component primarily found in shampoo, bubble bath and hand soap thanks to its foam building properties (Source). Because Lauryl amine oxide has dual functional groups in the same molecule (both asidic and basic groups), it is very versatile. Functions: Lauryl amine oxide is an Amine N-oxide, an active component primarily found in shampoo, bubble bath and hand soap thanks to its foam building properties (Source). Because Lauryl amine oxide has dual functional groups in the same molecule (both asidic and basic groups), it is very versatile. It can have high solubility in some solutions and low in others; it creates positive charges and negative charges on different atoms; it carries anionic or cationic properties depending on pH value. Therefore although Lauryl amine oxide is seen most frequently as a foam builder in beauty products, it can also be used as a dye dispersant, wetting agent, emulsifier, lubricant, surfactant, anti-static agent, and viscosity controlling agent, according to research. Safety Measures/Side Effects: Lauryl amine oxide is approved by the CIR for use in cosmetics but with restriction limiting its use to rinse-off products; The International Journal of Toxicology reports skin irritation from Lauryl amine oxide and recommends limiting its use to rinse off products at a maximum of 3.7% concentration. A 1981 study by published in Contact Dermatitis also found Lauryl amine oxide to be a primary skin irritant. Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap, as a foam stabilizer, and textile antistatic agent may result in its release to the environment through various waste streams. If released to air, an estimated vapor pressure of 6.2X10-8 mm Hg at 25 °C indicates Lauryl amine oxide will exist in both the vapor and particulate phases in the atmosphere. Vapor-phase Lauryl amine oxide will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 14.1 hours. Particulate-phase Lauryl amine oxide will be removed from the atmosphere by wet or dry deposition. Lauryl amine oxide does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight. If released to soil, Lauryl amine oxide is expected to have very high mobility based upon an estimated Koc of 5.5. Volatilization from moist soil surfaces is not expected to be an important fate process based upon an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole. In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry, suggesting that biodegradation in soil and water is an important fate process. If released into water, Lauryl amine oxide is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. Volatilization from water surfaces is not expected to be an important fate process based upon this compound's estimated Henry's Law constant. An estimated BCF of 0.7 suggests the potential for bioconcentration in aquatic organisms is low. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. Occupational exposure to Lauryl amine oxide may occur through dermal contact with this compound at workplaces where it is produced or used. The general population may be exposed to Lauryl amine oxide via dermal contact with this compound in consumer products containing Lauryl amine oxide. Lauryl amine oxide's production and use as a surfactant in dishwasher detergent, shampoo and soap(1), as a foam stabilizer, and textile antistatic agent(2) may result in its release to the environment through various waste streams(SRC). Based on a classification scheme(1), an estimated Koc value of 5.5(SRC), determined from a water solubility of 190,000 mg/L(2) and a regression-derived equation(3), indicates that Lauryl amine oxide is expected to have very high mobility in soil(SRC). Volatilization of Lauryl amine oxide from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 6.6X10-11 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Lauryl amine oxide is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 6.2X10-8 mm Hg(SRC), determined from a fragment constant method(5). In aqueous biodegradation screening tests, Lauryl amine oxide was 100% removed after 28 days as measured by liquid chromatography-mass spectrometry(6), suggesting that biodegradation in soil is an important fate process(SRC).

lauryl amine oxide; Lauryldimethylamine oxide; N,N-Dimethyldodecan-1-amine oxide; Lauramine oxide; Dodecyldimethylamine oxide; Dimethyldodecylamine-N-oxide cas no: 61788-90-7; 1643-20-5; 332-27-2

Benzyl(dodecyl)dimethylammonium; Lauryl dimethyl benzyl ammonium chloride; LAURALKONIUM CHLORIDE; N° CAS : 139-07-1; Nom INCI : LAURALKONIUM CHLORIDE, Nom chimique : Benzyldodecyldimethylammonium chloride, N° EINECS/ELINCS : 205-351-5, Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Noms français : Chlorure de N-benzyl N,N-diméthyl N-dodécyl ammonium; Chlorure de N-benzyl N,N-diméthyl N-lauryl ammonium. Noms anglais : BENZENEMETHANAMINIUM, N-DODECYL-N,N-DIMETHYL-, CHLORIDE; BENZYLDIMETHYLDODECYLAMMONIUM CHLORIDE; BENZYLDIMETHYLLAURYLAMMONIUM CHLORIDE; DODECYLBENZYLDIMETHYLAMMONIUM CHLORIDE DODECYLDIMETHYLBENZYLAMMONIUM CHLORIDE; Lauryl dimethyl benzyl ammonium chloride; LAURYLBENZYLDIMETHYLAMMONIUM CHLORIDE; LAURYLDIMETHYLBENZYLAMMONIUM CHLORIDE; N-BENZYL N,N-DIMETHYL N-DODECYL AMMONIUM CHLORIDE; N-BENZYL N,N-DIMETHYL N-LAURYL AMMONIUM CHLORIDE N-DODECYL N-BENZYL N,N-DIMETHYLAMMONIUM CHLORIDE. Utilisation et sources d'émission : Germicide. 72 139-07-1 [RN] 205-351-5 [EINECS] Benzenemethanaminium, N-dodecyl-N,N-dimethyl-, chloride (1:1) [ACD/Index Name] benzododecinii chloridum [Latin] benzododecinium chloride Benzyldimethyldodecylammonium chloride benzyldodecyldimethylammonium chloride Benzyllauryldimethylammonium chloride chlorure de benzododécinium [French] Chlorure de N-benzyl-N,N-diméthyl-1-dodécanaminium [French] [ACD/IUPAC Name] cloruro de benzododecinio [Spanish] Cloruro de cetalconio [Spanish] MFCD00137276 [MDL number] N-Benzyl-N,N-dimethyl-1-dodecanaminium chloride [ACD/IUPAC Name] N-Benzyl-N,N-dimethyl-1-dodecanaminiumchlorid [German] [ACD/IUPAC Name] N-Benzyl-N,N-dimethyldodecan-1-aminium chloride N-Benzyl-N,N-dimethyldodecan-1-aminiumchlorid N-Dodecyl-N,N-dimethylbenzenemethanaminium chloride Y5A751G47H бензододециния хлорид [Russian] كلوريد بنزودوديسينيوم [Arabic] 苯度氯铵 [Chinese] [139-07-1] [2-(2-methyltetradecan-2-yl)phenyl]ammonium chloride 1/7/139 10328-34-4 [RN] 10328-35-5 [RN] 107397-84-2 [RN] 122-18-9 [RN] 51796-11-3 [RN] 53516-76-0 [RN] 60484-28-8 [RN] 67377-59-7 [RN] 78565-22-7 [RN] 8038-88-8 [RN] 89004-36-4 [RN] 95078-12-9 [RN] Acinol ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE Alkyldimethylbenzylammonium chloride Ammonium, benzyldimethyldodecyl-, chloride Ammonium, benzyldimethylhexadecyl-, chloride Ammonium, benzyldodecyldimethyl-, chloride Ammonium, benzyldodecyldimethyl-, chloride (8CI) Ammonium, benzylhexadecyldimethyl-, chloride Ammonium, benzylhexadecyldimethyl-, chloride (8CI) ammonyx Ammonyx G Ammonyx T Amoryl BR 1244 Baktonium Banicol benirol Benzaletas Benzenemethanaminium, N,N-dimethyl-N-dodecyl-, chloride Benzenemethanaminium, N-dodecyl-N,N-dimethyl-, chloride Benzenemethanaminium, N-hexadecyl, N,N-dimethyl-, chloride Benzenemethanaminium, N-hexadecyl-N,N-dimethyl-, chloride Benzododecinii Chloridum Benzododecinii chloridum [INN-Latin] Benzododecinio cloruro [DCIT] Benzododecinium chloride BENZYL DIMETHYL DODECYL AMMONIUM CHLORIDE benzyl(dodecyl)dimethylazanium chloride benzyl-cetyl-dimethyl-ammonium chloride Benzylcetyldimethylammonium chloride Benzyldimethylcetylammonium chloride Benzyldimethyllaurylammonium chloride Benzyldimethyl-n-dodecylammonium chloride benzyl-dodecyl-dimethylammonium chloride benzyl-dodecyl-dimethyl-ammonium chloride Benzyldodecyldimethylammoniumchloride benzyl-dodecyl-dimethylazanium benzyl-dodecyl-dimethylazanium and chloride benzyl-dodecyl-dimethylazanium chloride benzyl-dodecyl-dimethylazanium;chloride benzyl-hexadecyl-dimethylammonium chloride benzyl-hexadecyl-dimethyl-ammonium chloride benzyl-hexadecyl-dimethylazanium chloride benzyl-lauryl-dimethyl-ammonium chloride Benzyl-lauryldimethylammonium chloride Bicetonium BKC Bonjela [Wiki] Catigene OM Catinal CB 50 Catiogen PAN Catiolite BC 50 Cdbac cequartryl Cequartyl A Cetylbenzyldimethylammonium chloride Cetylon Chloride [ACD/IUPAC Name] [Wiki] Chlorure de Benzododecinium Chlorure de benzododecinium [INN-French] Chlorure de cetalkonium [INN-French] Cloruro de Benzododecinio Cloruro de benzododecinio [INN-Spanish] D-Dodecyl-N,N-dimethylbenzenemethanaminium chloride Dehyquart CBB Dehyquart CDB Dimethylbenzylcetylammonium chloride Dimethylbenzyldodecylammonium chloride Dimethylbenzylhexadecylammonium chloride Dimethylbenzyllaurylammonium chloride dimethyldodecylbenzylammonium chloride Dmcbac Dodecyl dimethyl benzyl ammonium chloride Dodecylbenzyldimethylammonium chloride dodecyl-dimethyl-(phenylmethyl)azanium chloride dodecyldimethylbenzylamine, chloride Dodecyldimethylbenzylammonium chloride Dodecyl-dimethyl-benzylammonium chloride Dodecyldimethylbenzylammonium chloride (ACN) Dodecyldimethylbenzylammoniumchloride drapolene EINECS 204-526-3 EINECS 205-351-5 Enuclene germitol gesminol Hexadecylbenzyldimethylammonium chloride hexadecyl-dimethyl-(phenylmethyl)azanium chloride Hexadecyldimethylbenzylammonium chloride Lauralkonium chloride Lauryl dimethyl benzyl ammonium chloride Laurylbenzalkonium chloride Laurylbenzyldimethylammonium chloride Lauryldimethylbenzoammonium chloride Lauryldimethylbenzylammonium chloride Loraquat B 50 Marinol mefarol N,N-Dimethyl-N-dodecylbenzenemethanaminium chloride N-Benzyl-N,N-dimethyl-1-dodecanaminiumchloride N-Benzyl-N,N-dimethyldodecylammonium chloride N-Benzyl-N-cetyldimethylammonium chloride N-Benzyl-N-dodecyl-N,N-dimethylammonium chloride N-Dodecyldimethylbenzylammonium chloride n-Dodecyl-n,n-Dimethyl-Benzenemethanaminium Chloride N-Dodecyl-N,N-dimethyl-N-benzylammonium chloride n-Hexadecyldimethylbenzylammonium chloride N-Hexadecyl-N,N-dimethylbenzenemethanaminium chloride N-HEXADECYL-N,N-DIMETHYLBENZENEMETHANAMINIUM CL N-Lauryldimethylbenzylammonium chloride Noramium DA 50 Orthosan HM osvan paralkan parasterol Pharycidin concentrate Retarder N Rewoquat B 50 Rodalon Rolcril Spilan Swanol CA 100 Swanol CA 101 Tetranil BC 80 Tetraseptan Texnol R 5 Triton K60 UNII:Y5A751G47H UNII-F5UM2KM3W7 UNII-Y5A751G47H VANTOC CL Winzer solution zephiran chloride Zephirol Zettyn Zettyn (TN) Zettyn chloride

CAS number: 683-10-3
Molecular Formula: C16H33NO2
Molecular Weight: 271.44

Lauryl betaine, derived from vegetables, is a clear or pale yellow liquid that was first discovered as a sugar beet extract.
Lauryl betaine is a mild surfactant (or surfactant) commonly considered a hair and skin conditioner.
Lauryl betaine is a mild ingredient and has skin and hair conditioning properties, making it an excellent ingredient to use in products.
Lauryl betaine is a hair and skin conditioner, a mild surfactant (surfactant) that works well with shampoo, shower gel, or any cleanser.
Lauryl betaine is a mild ingredient and has skin and hair conditioning properties, this makes it an excellent ingredient to use in products.
Lauryl betaine is a hair and skin conditioner, a mild surface-active agent (surfactant) and works well in shampoo, shower gel or any cleansing product.

Lauryl betaine helps separate grease from water, making it useful in shampoos and soaps.
Lauryl betaine’s often used as a surfactant in organic and natural cosmetics such as shampoo, shower gel and skin cleansers as it’s considered more natural and gentle than some other surfactants.
Many natural cosmetics companies add lauryl betaine to their products as an alternative to one particular surfactant called sodium lauryl sulphate (SLS).
Lauryl betaine dissolves easily in water or oil and helps create a rich lather that makes it easier for products to cut through oil and dirt, while leaving skin soft.
Derived from vegetables, lauryl betaine is a clear or pale yellow liquid used that was first discovered as an extract of sugar beets.
Lauryl betaine's a mild surfactant that is commonly considered a hair and skin conditioner.

Lauryl betaine has good washing and foaming effect.
Lauryl betaine is able to be widely used as surfactants with good compatibility.
Laury dimethylaminoacetic acid betaine, (Carboxylatomethyl)dodecyldimethylammonium is an important raw material for shampoo, shower gel, soap, detergent and some other chemical products.
Lauryl-Betaine has a good soft, antistatic, dispersion, disinfection abilities.
This product could be utilized as fiber, fabric softener, blending wool rinsing agent commodities.

Lauryl betaine can be used to manufacture personal washing products, such as shampoo, bubble bath, facial cleanser, etc.
Lauryl betaine is especially suitable for application in baby shampoo, baby bubble bath and baby skin care products.
In hair and skin care formulations Lauryl betaine is an excellent soft conditioner.
Lauryl betaine is a clear or light-yellow liquid which is derived from vegetables.
Lauryl betaine’s often used as a surfactant in organic, natural, vegan, zero-waste or plastic-free cosmetics such as shampoo, shower gel and skin cleansers.
Lauryl betaine has Antistatic, Surfactant, Hair conditioning, Skin conditioning, Cleansing properties.
Unlike SLS, lauryl betaine is considered to be much safer, gentler, and can actually help nourish the skin and hair instead of stripping away the goodness.

Lauryl betaine is an excellent viscosity builder and gelling agent.
Lauryl betaine has hard water tolerance permits equally good foaming in hard and soft water.
Lauryl betaine is stable in high-electrolyte solutions and will help solubilize other surfactants into these systems.
Lauryl betaine is also stable in acidic and alkaline conditions, functioning as cationic in acid media and as anionic in alkaline.
Lauryl betaine is a mild amphoteric surfactant and is compatible with anionic, cationic and non-ionic surfactants.
Lauryl betaine has skin and hair conditioning properties, and creates excellent, stable foam.
Derived from vegetables, lauryl betaine is a clear or pale yellow liquid that dissolves easily in water or oil, and helps create a rich lather that makes it easier for products to cut through oil and dirt.
Lauryl Betaine is a surfactant used in cleaning and personal care products for its ability to clean soils, as well as thicken cleaning formulas and stabilize foam.

Characteristics:
-excellent emulsifying, dispersing, foaming, foam stabilizing, antistatic, solubilizing, wetting, permeating abilities.
-Mild surfactant.
-Can reduce the irritation of the other surfactants.
-Resistance to hard water.
-Excellent compatibility.

Lauryl betaine (LB) as an amphoteric surfactant carries both positive and negative charges and should be able to generate stable foam through electrostatic interaction with nanoparticles and co-surfactants.
Lauryl betaine is a mild ingredient and has skin and hair conditioning properties, this makes it an excellent ingredient to use in personal care products.
Lauryl betaine is a hair and skin conditioner, a mild surface-active agent (surfactant) and works well in shampoo, shower gel or any cleansing product.
Derived from vegetables, lauryl betaine is a clear or pale yellow liquid that was first discovered as an extract of sugar beets.
Lauryl betaine is a mild surface-active agent (or surfactant) that is commonly considered a hair and skin conditioner.

Surfactants are partly soluble in water and partly in oil, which allows the oil and water to disperse.
Lauryl Betaine also helps create a thick foam by improving the quality and stability of the foam, making it easier to pass through oil and dirt.
Surfactants help cleanse your skin and hair by mixing water with oil and dirt so it can be washed off.
In this respect, they act as detergents (soaps) and are therefore found in bath products, skin cleansers, and hair care products such as shampoos, conditioners and sprays.

Lauryl betaine contains lauryl alcohol (1-dodecanol) as an alcoholic component.
Betaines are organic compounds (amphoteric surfactants) that have both a positive and a negative charge in their molecular structure; are therefore uncharged on the outside.
Lauryl betaine is a mild amphoteric surfactant and is compatible with anionic, cationic and non-ionic surfactants.
Lauryl betaine has skin and hair conditioning properties, and creates excellent, stable foam.
Derived from vegetables, lauryl betaine is a clear or pale yellow liquid that dissolves easily in water or oil, and helps create a rich lather that makes it easier for products to cut through oil and dirt.

Amphoteric surfactants have dual functional groups (both acidic and basic groups) in the same molecule.
Lauryl betaines are polar solvents that have a high solubility in water but a poor solubility in most organic solvents.
Lauryl betaines are electrically neutral but carries positive and negative charges on different atoms in an aqueous solution.
Depending on the composition and conditions of pH value, the substances can have anionic or cationic properties.
In the presence of acids, they will accept the hydrogen ions but they will donate hydrogen ions to the solution in the presence of bases, which balances the pH. Such actions make buffer solutions which resist change to the pH.
In the detergency ability amphoteric surfactants which change their charge according to the pH of the solution affects properties of foaming, wetting and detergentcy through a surface action that exerts both hydrophilic and hydrophobic properties.
In biochemistry amphoteric surfactant is used as a detergent for purifying, cleansing and antimicrobial effects.
Alkylbetains and aminoxides are amphoteric surfactants.

Characteristics:
-Good compatibility with anionic, cationic, nonionic and other amphoteric surfactants.
-Good softness, rich and stable foam.
-Perfect decontamination, conditioning, antistatic performance, good adjustment of viscosity.
-Lauryl betaine retains stable within a wide range of pH values, and low irritation to skin and eye.
-Added in shampoo, Lauryl betaine is matched with other active matter, and brings forth obvious conditioning and thickening effects.

Product Features:
-resistant to alkali, high temperature, in the 240-320g lye rapid wetting and penetration
-can enhance the luster of the long-lasting fabric
-This product can be used as a penetrant for other strong alkali media.

Surfactants are part water-soluble and part oil-soluble, allowing the oil and water to become dispersed.
Lauryl Betaine also assists in creating a rich lather, improving the quality and stability of foam making it easier for it to cut through oil and dirt.
Lauryl betaine is a clear or light-yellow liquid which is derived from vegetables.
Lauryl betaine was first discovered when it was extracted from sugar beet.

In chemical terms, lauryl betaine is a zwitterion, or an inner salt.
Lauryl betaine has the molecular formula C16H33ClNNaO2 and is known by several other names including laurylbetain, lauryldimethyl betaine, lauryldimethylbetaine and sodium dodecyldimethylbetaine.
Lauryl betaines CAS number is 683-10-3.

Lauryl betaine is usually used as a surface agent, or surfactant.
Surfactants are compounds which are used in many personal body care products as they lower the surface tension between two liquids or between a liquid and a solid, allowing you to wash away dirt, makeup, pollution, skin oils and fats from your skin.

Laryl Betaine is a gentle surfactant, nourishes the skin and hair, so it is an effective component of shampoos, shower gels and any skin cleansing products.
Lauryl betaine improves the quality and stability of the foam.
Lauryl Betaine is mainly used in shampoos, personal care products and shower gels.

USES:
Antistatic: Reduces static electricity by neutralizing electrical charge on a surface
Cleaning Agent: Helps keep a clean surface
Hair conditioner: Leaves hair manageable, supple, soft and shiny and / or confers volume, lightness and shine
Skin care agent: Keeps the skin in good condition
Surfactant: Reduces the surface tension of cosmetics and contributes to the uniform distribution of the product during its use
antistatic agent, hair conditioning agent, skin-conditioning agent - miscellaneous;surfactant - cleansing agent, surfactant - foam booster, viscosity increasing agent - aqueous, antistatic, cleansing, hair conditioning, skin conditioning, and surfactant

Lauryl Betaine is an amphoteric surfactant derived from N-dodecyl-N,N-dialkanol amine with protein denaturing potency.
Lauryl Betaine is mainly used in shampoo, personal hygiene products and oil field chemicals
lauryl betaine is a skin-conditioning agent.
In hair care, it is used as an anti-static conditioning agent and a foam booster.

Cosmetic use: Low irritation to skin and eye with high foam ability and good foam stability.
-Good stability in hard water.
-No dry tact after shampooing.
-Good compatibility with other surfactants.

Cosmetic use: Low irritation to skin and eye with high foam ability and good foam stability.
Good stability in hard water.
No dry tact after shampooing.
Good compatibility with other surfactants.

Lauryl Betaine is an amphoteric surfactant derived from N-dodecyl-N,N-dialkanol amine with protein denaturing potency.
Lauryl Betaine is mainly used in shampoo, personal hygiene products and oil field chemicals.
Lauryl betaine is widely used in middle and high grade shampoos and body washes; it is the main ingredient for preparing mild baby shampoos, baby foam baths, and baby skin care products; it is an excellent soft conditioner in hair care and skin care formulations; it can also be used as a detergent , Wetting agent, thickener, antistatic agent and bactericide, etc.

Typical applications:
-emulsifying agent, dispersing agent.
-foaming agent, foam stabilizing agent.
-thickening agent.
-antistatic agent.

Personal care products:
Conditioning agent, antistatic agent, cleansing agent, foam boosting agent, viscosity controlling agent in personal care products.

Textile:
Antistatic agent, softening agent in textile, leather, fiber.

Household detergents:
Thickening agent, foaming agent, foam stabilizing agent in household cleaning.

Industrial cleaning:
Thickening agent, foaming agent, foam stabilizing agent in industrial cleaning, vehicle cleaning.Disodium Cocoamphodiacetate / Lauryl Betaine is used for Hair dye, Hair cleansing, Skin cleansing and other conditions.
Lauryl betaine is widely used in middle and high grade shampoos and body washes; it is the main ingredient for preparing mild baby shampoos, baby foam baths, and baby skin care products; it is an excellent soft conditioner in hair care and skin care formulations; it can also be used as a detergent , Wetting agent, thickener, antistatic agent and bactericide, etc.
This ingredient has several functions, most often it is:

an ANTISTATIC AGENT , Lauryl betaines role is to avoid and / or reduce static electricity.
Lauryl betaine as a SKIN CARE AGENT , Lauryl betaines role is to keep the skin in good condition.
Lauryl betaine as a CLEANSING AGENT , Lauryl betaines role is to clean the skin or hair.
Lauryl betaine as a HAIR CONDITIONER , Lauryl betaines role is to improve the appearance and feel of the hair, leaving the hair easy to comb, supple, soft and shiny and / or giving volume, light, shine, texture, etc. ..
Lauryl betaine as a SURFACTANT , Lauryl betaines role is to help other ingredients, which normally do not mix, to dissolve or disperse into each other in order to evenly distribute the product during its use.

emulsifier, component enabling the formation of an emulsion.
Emulsion is a physicochemical form that is created by combining (mixing) the water phase with the oil phase.
Examples of cosmetic emulsions are creams, lotions, lotions.
Foaming substance, stabilizing and improving the quality of foam in a mixture with anionic surfactants.
Lauryl betaine acts as a rheology modifier (i.e. improves the consistency causing an increase in viscosity) in washing preparations containing anionic surfactants, thanks to the formation of the so-called mixed micelles.
Solubilizer, enables the introduction of substances insoluble or sparingly soluble in water into the aqueous solution, e.g. fragrances, plant extracts, fatty substances

Lauryl betaine soothes the possible irritating effects of anionic surfactants on the skin.
Lauryl betaine has an antistatic effect on the hair, prevents static. Thanks to this, it conditions, i.e. softens and smoothes the hair.
The moisturizing substance facilitates the contact of the cleaned surface with the washing solution, which facilitates the removal of impurities from the surface of the skin and hair.
A washing substance, removes impurities from the surface of the hair and skin

Works well in shampoos and conditioners, shower gels and other cleansing products
Has anti-static properties
Lauryl betaine is a superb viscosity builder and rheological modifier
Lauryl betaine is able to withstand high water hardness and allows equally good foaming in both hard and soft water formulations.
Lauryl betaine is stable in high-electrolyte solutions and functions as solubilizer for other surfactants into these formulations.
Made from vegetable sources
Environmentally safe

SYNONYMS:
2-(Dodecyldimethylammonio)acetate
683-10-3
Lauryl betaine
Dodecylbetaine
Laurylbetain
Lauryl-N-betaine
Lauryldimethylbetaine
N-dodecyl-N,N-dimethylbetaine
(Carboxylatomethyl)dodecyldimethylammonium
UNII-Y4P927Q133
Lauryl dimethyl glycine
1-Dodecanaminium, N-(carboxymethyl)-N,N-dimethyl-, inner salt
N-DODECYL-N,N-DIMETHYLGLYCINATE
C16H33NO2
Y4P927Q133
Culveram cdg
Anfoterico LB
Obazoline LB
Desimex I
Genagen LAB
Product DDN
Bister ML
Nissan Anon BL
Amipol 6S
Empigen BB/L
Amphitol 20BS
Amphitol 24B
Anon BL
Rewoteric AM-DML
Ambiteric D 40
Anhitol 24B
Dimethyllaurylbetaine
Dodecyldimethylbetaine
Anon BL-SF
Betadet DM 20
Nissan Anon BL-SF
Rikabion A 100
Swanol AM 301
Lauryl-N-methylsarcosine
Rewoteric AM-DML 35
Lauryldimethylammonioacetate
N,N-Dimethyldodecylbetaine
C12BET
BS 12 (betaine surfactant)
(Dodecyldimethylammonio)acetate
N,N-Dimethyl-N-dodecylglycine
Lauryldimethylaminoacetic betaine
(Dodecyldimethylammonio)ethanoate
Betaine lauryldimethylaminoacetate
Dimethyllaurylaminoacetate betaine
BS 12
EINECS 211-669-5
N-Lauryl-N,N-dimethyl-alpha-betaine
2-[dodecyl(dimethyl)azaniumyl]acetate
Glycine, dodecyldimethylbetaine (6CI)
BRN 3670807
N,n-Dimethyl-N-laurylglycine inner salt
alpha-(Dodecyldimethylammonio)-omega-acetate
DSSTox_CID_21266
DSSTox_RID_82033
DSSTox_GSID_46978
(Lauryldimethylammonio)Acetate
SCHEMBL594518
CHEMBL1232088
DTXSID6041266
N-Carboxymethyl-N,N-dimethyl-1-dodecanaminium inner salt
[dodecyl(dimethyl)ammonio]acetate
(Carboxymethyl)dodecyldimethylammonium hydroxide inner salt
2-(dodecyldimethylazaniumyl)acetate
N-(Carboxymethyl)-N-lauryldimethylammonium hydroxide inner salt
Tox21_301433
0534AC
MFCD00084742
1-Dodecanaminium, N-(carboxymethyl)-N,N-dimethyl-, hydroxide, inner salt
AKOS016010279
CS-W010094
DB07631
NCGC00256099-01
CAS-66455-29-6
FT-0670748
V1522
EN300-41676
(Lauryldimethylammonio)acetate, >=95% (HPLC)
N-(Alkyl C10-C16)-N,N-dimethylglycine betaine
EMPIGEN(R) BB detergent, ~30% active substance
W-109593
Q27096852
EMPIGEN(R) BB detergent, ~35% active substance in H2O
UNII-03DH2IZ3FY component DVEKCXOJTLDBFE-UHFFFAOYSA-N
N,N-Dimethyl-N-dodecylglycine betaine, 30% active substance in H2O
Ammonium, (carboxymethyl)dodecyldimethyl-, hydroxide, inner salt (7CI,8CI)

No CAS 9004-82-4, No Cas : 3088-31-1. LES, Texapon, Sodium Lauryl Ether Sulfate. Le lauryl éther sulfate de sodium ou laureth sulfate de sodium (SLES), plus connu sous sa dénomination INCI sodium laureth sulfate (SLES), est un détergent et surfactant ionique fort. Il est utilisé comme ingrédient actifs dans divers produits de soins (savons, shampooings, pâtes dentifrices, etc.) et est un agent moussant très efficace. Concentration : 28 % & 70%. Le lauryl éther sulfate de sodium ou laureth sulfate de sodium (SLES), plus connu sous sa dénomination INCI sodium laureth sulfate (SLES), est un détergent et tensioactif ionique fort, couramment utilisé en biochimie et biologie moléculaire.Le lauryl éther sulfate de sodium est une petite molécule amphiphile composée d'un corps hydrophobe et d'une tête hydrophile, il désagrège les bicouches lipidiques membranaires par rupture des associations hydrophobes. Il dénature les protéines, sans rompre les ponts disulfures. Il confère aux protéines une charge globale négative. On le retrouve dans divers produits ménagers et cosmétiques (savons, shampooings, pâtes dentifrices, etc.). Il est peu onéreux et est un agent moussant très efficace. No Cas : 9004-82-4 2, -dodecoxyethyl hydrogen sulfate; Alkyl ether sulfate, 2-dodecoxyethyl hydrogen sulfate; Dodecan-1-ol, ethoxylated, sulfates, sodium salts (1 - 2.5 mol EO); Dodecyloxypoly(ethyleneoxy) ethyl sulfate, sodium salt;Fatty Alcohols C12 C14 ethoxylated 3 EO sulfates, sodium salts; Poly(oxy-1,2-ethanediyl), .alpha.-sulfo-.omega.-(dodecyloxy)-, sodium salt (2EO); Poly(oxy-1,2-ethanediyl), a-sulfo-w-(dodecyloxy)-, sodium salt (1:1); Poly(oxy-1,2-ethanediyl), alpha-sulfo-omega-(dodecyloxy)-, sodium salt; Poly(oxy-1,2-ethanediyl), α-sulfo-ω-(dodecyloxy)-, sodium salt; Poly(oxy-1,2-ethanediyl)-alpha-sulfo-omega-(dodecyloxy)-sodium salt; sodium 2 dodecoxyethyl sulfate; sodium 2-(2-dodecoxyethoxy)ethyl sulfate; Sodium 2-(dodecyloxy)ethyl sulfate; sodium alkoxy ethyl sulfate; Sodium dodecyl poly(oxyethylene) sulphate ; Sodium dodecylpoly(oxyethylene) sulfate; Sodium Laureth Sulfate; sodium laureth sulfate, ethoxylated (EO > 2.5); Sodium laureth sulphate; Sodium lauryl ether; Sodium Lauryl Ether Sulfate; Sodium lauryl ether sulphate; Sodium laurylether sulfate; Sodium laurylether sulphate; Sodium Poly(oxyethylene) Lauryl Ether Sulfate; Sodium polyoxyethylene lauryl ether sulfate; sulfate or polyoxyethene glycol ether. No Cas : 68585-34-2; Alcohols, C10-16, ethoxylated, sulfates, sodium salts; .alpha.-Alkyl (C10-16) .omega.-hydroxypoly (oxyethylene) sulfate, sodium salt; 2-(2-dodecyloxyethoxy)ethyl sulphate ; 2-[bis(2-hydroxyethyl)amino]ethan-1-ol; 4-(tridecan-3-yl)benzene-1-sulfonic acid; 2-[bis(2-hydroxyethyl)amino]ethanol; 4-tridecan-3-ylbenzenesulfonic acid; Alcohols, C10-14, ethoxylated, sulfates, sodium salts; Alcohols, C10-16, ethoxylated, sulfates, sodium salts; alkyl C10-16 ether sulfate, sodium salt; Alkyl ether sulfate C10-16, sodium salt; linear alkybenzene sulphonic acid; Poly(oxy-1,2-ethanediyl), .alpha.-sulfo-.omega.-hydroxy-, C10-16-alkyl ethers, sodium salts; Poly(oxy-1,2-ethanediyl), a-sulfo-w-hydroxy-, C10-16-alkyl ethers, sodium salts; Polyethylene glycol mono-C10-16-alkyl ether sulfate sodium; Sel sodique du sulfate d'alkyle (C10-C16) éthoxylé; sodium 2-(2-dodecyloxyethoxy)ethyl sulphate; Sodium alkyl(C10-C16)ether sulphate; sodium alkylether sulphate; Sodium Laureth Sulfate; sodium lauryl ether sulfate; sodium lauryl ether sulphate; SODIUM LAURYL ETHOXYSULPHATE No Cas : 68891-38-3; Alcohols, C12-14, ethoxylated, sulfates, sodium salts; Alcohols C12-14 (even numbered) ethoxylated (<2.5 EO) sulfates sodium salts; Alcohols C12-14 ethoxylated sulfates sodium salts; Alcohols C12-14, ethoxylated (1-2,5 EO) sulphated, sodium salts; Alcohols C12-14, ethoxylated sulphated, sodium salts (< 2.5 EO); Alcohols, C12-14 (even numbered), ethoxylated (<2.5 EO), sulfates, sodium salts; Alcohols, C12-14 (even numbered), ethoxylated < 2.5 EO, sulfates, sodium salts; Alcohols, C12-14 (even numbered), ethoxylated <2.5 EO, sulfates, sodium salts; Alcohols, C12-14 (even numbered), ethoxylated, sulfates, sodium salts (< 2.5 EO); Alcohols, C12-14 (even numbered), ethoxylated, sulfates, sodium salts (< 2.5EO); Alcohols, C12-14 (even numbered), ethoxylated, sulfates, sodium salts (<2.5 EO); Alcohols, C12-14(Even numbered) , ethoxylated, sulfates, sodium salts; Alcohols, C12-14(even numbered), ethoxylated (1-2,5 EO) sulphated, sodium; Alcohols, C12-14(even numbered), ethoxylated (1-2,5 EO) sulphated, sodium salts; Alcohols, C12-14(even numbered), ethoxylated < 2.5 EO, sulfates, sodium salts; Alcohols, C12-14(even numbered), ethoxylated <2.5 EO, sulfates, sodium salts; Alcohols, C12-14(even numbered), ethoxylated, sulfates, sodium salts; Alcohols, C12-14(even numbered), ethoxylated, sulfates, sodium salts (< 2.5EO); Alcohols, C12-14(even numbered), ethoxylated<2.5EO, sulfates, sodium salts; Alcohols, C12-14, ethoxylated < 2.5 EO, sulfates, sodium salts; Alcohols, C12-14, ethoxylated, sulfates, sodium sal; Alcohols, C12-14, ethoxylated, sulfates, sodium salts (1 - 2.5 mol EO); Alcohols, C12-14, ethoxylated, sulfates, sodium salts (1 - 2.5 moles ethoxylated); Alcohols, C12-14, ethoxylated, sulfates, sodium salts (3 EO); Alcohols, C12-14, ethoxylated, sulfates, sodium salts (< 2.5EO); Alcohols, C12-C14-(even numbered), ethoxylated, sulphates, sodium salts; Alkyl ether sulfate C12-14, sodium salt; C12-14-Alkyl ether sulfates; FETTALKOHOLETHERSULFAT, NA-SALZ C12-14 2 EO; Hansanol NS 242; POLU(OXY-1,2-EHTANEDIYL), ALPHA-SULFA-OMEGA-HYDROXY-C12-C14 ALKYL ETHERS, SODIUM SALTS; Poly(oxy-1,2-ethanediyl), .alpha.-sulfo-.omega.-hydroxy-,C12-14-alkyl ethers, sodium salts (GRS); Poly(oxy-1,2-ethanediyl), a-sulfo-w-hydroxy-, C12-14-alkyl ethers, sodium salts; Poly(oxy-1,2-ethanediyl), alpha-sulfo-omega-hydroxy-, C12-14-alkyl ethers, sodium salts; Primary Alcohols C12-14(even, numbered) , ethoxylated (1-2.5 EO), sulphated, sodium salts; SLES; sodium 2-(2-dodecyloxyethoxy)ethyl sulphate; Sodium C12-14 Alkyl Ether Sulphate (AES) 1+2 EO; Sodium C12-14 diglycol ether sulfate; Sodium dodecyl sulphate; Sodium Laureth Sulfate; sodium laureth sulphate; Sodium Lauryl Ether Sulfate; sodium {2-[2-(dodecyloxy)ethoxy]ethyl} sulfate No Cas : 98112-64-2; Poly(oxy-1,2-ethanediyl), α-sulfo-ω-(dodecyloxy)-, sodium salt (1:1); Poly(oxy-1,2-ethanediyl), α-sulfo-ω-(dodecyloxy)-, sodium salt (1:1); sodium 1-(2-sulfonatooxyethoxy)dodecane; Sodium Lauryl Ether Sulfate

Lauryl polyglucose D-Glucopyranose; Oligomeric; C10-16-Alkyl Glycosides D-Glucopyranose; Oligomeric,C10-C16-Alkylglycosides Alkyl D-Glucopyranoside (C10-16)Alkyl D-Glycopyranoside cas no: 110615-47-9

Synonyms: LAURYL GLUCOSIDE;APG0814;D-Glucopyranose, oligomeric, C10-16-alkyl glycosides;D-GLUCOPYRANOSE,OLIGOMERIC,C10-C16-ALKYLGLYCOSIDES;ALKYL D-GLUCOPYRANOSIDE;(C10-16)alkyl D-glycopyranoside;Glucopyranose, oligometric, C10-16-alkyl glycosides;D-Glucopyranoside, C10-16-alkyl, oligomeric CAS: 110615-47-9

Lauryl glucoside is a type of non-ionic surfactant that belongs to the class of alkyl polyglucosides (APGs).
Lauryl glucoside is commonly used in various personal care and household products.
The chemical structure of lauryl glucoside consists of a lauryl (C12) alkyl chain attached to a glucose molecule.
This combination of a fatty alcohol and a sugar unit results in a surfactant with both hydrophilic (water-attracting) and lipophilic (oil-attracting) properties.

CAS Number: 59122-55-3
EC Number: 261-614-4



APPLICATIONS


Lauryl glucoside is commonly used in the formulation of mild and gentle facial cleansers.
Lauryl glucoside is a key ingredient in sulfate-free shampoos, providing effective cleansing without causing scalp irritation.
Lauryl glucoside is utilized in baby shampoos and body washes due to its mild and non-irritating nature.

Lauryl glucoside contributes to the formulation of eco-friendly and biodegradable dishwashing liquids.
Lauryl glucoside is an essential component in natural and organic hand soaps, aligning with the demand for cleaner and greener products.

Lauryl glucoside is employed in the production of gentle and moisturizing shower gels.
Lauryl glucoside enhances the foaming properties of bubble baths, creating a luxurious and enjoyable bathing experience.
Lauryl glucoside is used in sulfate-free toothpaste formulations for its mild cleaning action on teeth and gums.

Lauryl glucoside is found in facial cleansing wipes, providing an effective solution for makeup removal.
Lauryl glucoside contributes to the formulation of natural and environmentally friendly laundry detergents.
Lauryl glucoside is employed in the production of pet shampoos, offering a gentle cleansing solution for animals.
Lauryl glucoside is utilized in the formulation of mild and hypoallergenic body lotions for sensitive skin.

Lauryl glucoside is an ingredient in natural and organic sunscreen formulations, ensuring a gentle application on the skin.
Lauryl glucoside is used in the production of mild and tear-free baby wipes, suitable for delicate skin.
Lauryl glucoside is found in eco-friendly and sustainable multi-surface cleaners for household use.

Lauryl glucoside is employed in the formulation of sulfate-free and natural hand sanitizers.
Lauryl glucoside contributes to the creation of mild and gentle shaving creams for both men and women.
Lauryl glucoside is utilized in the production of natural and organic facial masks for a soothing and cleansing experience.
Lauryl glucoside is a component in mild and non-stripping hair conditioners for smooth and manageable hair.

Lauryl glucoside is used in the formulation of sulfate-free and natural deodorants, meeting the demand for clean and skin-friendly options.
Lauryl glucoside is found in eco-friendly and biodegradable household cleaning wipes.
Lauryl glucoside contributes to the formulation of sulfate-free and natural body scrubs for exfoliation.
Lauryl glucoside is utilized in the production of mild and non-drying hand foams for effective hand hygiene.
Lauryl glucoside is found in eco-friendly and biodegradable floor cleaners for household use.
Lauryl glucoside is employed in the formulation of gentle and hydrating foaming face washes for daily skincare routines.

Lauryl glucoside is a versatile ingredient in the formulation of sulfate-free and mild body washes, providing a gentle cleansing experience.
Lauryl glucoside is used in the production of natural and eco-friendly hand foams for public spaces and personal use.
The surfactant is found in sulfate-free and environmentally friendly shaving gels, contributing to a smooth and comfortable shaving experience.

Lauryl glucoside is employed in the formulation of sulfate-free and gentle intimate washes, catering to sensitive areas.
Lauryl glucoside is a key component in the production of mild and tear-free baby shampoos, ensuring a soothing and safe bath time.
Lauryl glucoside is utilized in the formulation of sulfate-free and natural facial cleansers for a refreshing and non-irritating cleanse.

Lauryl glucoside contributes to the creation of sulfate-free and environmentally friendly dish soaps, addressing the demand for greener alternatives.
Lauryl glucoside is used in the production of natural and mild hand exfoliants for a gentle removal of dead skin cells.
Lauryl glucoside is found in sulfate-free and eco-friendly hair styling products, offering a balance between hold and mildness.

Lauryl glucoside is employed in the formulation of sulfate-free and natural body mists for a light and refreshing fragrance.
Lauryl glucoside contributes to the production of natural and gentle makeup removers, effectively lifting away makeup without harshness.
Lauryl glucoside is utilized in the formulation of sulfate-free and mild foot scrubs for exfoliation and softening.
Lauryl glucoside is a component in sulfate-free and natural insect repellents, providing an eco-friendly alternative to chemical-based repellents.
Lauryl glucoside is found in sulfate-free and environmentally friendly fabric softeners, contributing to soft and fresh laundry.
Lauryl glucoside is employed in the formulation of sulfate-free and natural pet shampoos for gentle cleansing of fur and skin.

Lauryl glucoside is used in the production of sulfate-free and mild foam cleansers for makeup brushes and beauty tools.
Lauryl glucoside contributes to the creation of sulfate-free and natural mouthwashes, offering a gentle solution for oral hygiene.

Lauryl glucoside is found in sulfate-free and eco-friendly carpet cleaners for household use.
Lauryl glucoside is employed in the formulation of sulfate-free and natural cuticle oils for nail care.
Lauryl glucoside is a key component in sulfate-free and environmentally friendly sunless tanners, ensuring an even and natural-looking tan.
Lauryl glucoside contributes to sulfate-free and gentle pre-shave oils, preparing the skin for a comfortable shave.
Lauryl glucoside is used in the production of sulfate-free and mild foaming body polishes for smooth and revitalized skin.

Lauryl glucoside is found in sulfate-free and eco-friendly surface disinfectants for household and commercial use.
Lauryl glucoside is employed in the formulation of sulfate-free and natural wound care cleansers, providing a gentle antiseptic solution.
Lauryl glucoside is a component in sulfate-free and mild facial toners, contributing to a balanced and refreshed complexion.

Lauryl glucoside is commonly used in the formulation of sulfate-free and gentle exfoliating scrubs for both face and body.
Lauryl glucoside is a key ingredient in sulfate-free and natural hair masks, providing deep conditioning without weighing down the hair.
Lauryl glucoside is employed in sulfate-free and eco-friendly pet wipes for convenient and mild pet grooming.

Lauryl glucoside contributes to the formulation of sulfate-free and natural cuticle removers, aiding in nail care.
Lauryl glucoside is used in sulfate-free and mild hand sanitizers, providing effective cleansing without over-drying the skin.
Lauryl glucoside is found in sulfate-free and eco-friendly aromatherapy sprays, offering a soothing and natural fragrance.
Lauryl glucoside is a component in sulfate-free and gentle foot creams for softening and moisturizing the feet.

Lauryl glucoside contributes to sulfate-free and natural antiperspirants, providing a mild and skin-friendly alternative.
Lauryl glucoside is employed in the formulation of sulfate-free and eco-friendly makeup setting sprays for a long-lasting finish.
Lauryl glucoside is used in sulfate-free and mild exfoliating foot scrubs for removing rough skin.
Lauryl glucoside is found in sulfate-free and natural cuticle balms, providing hydration and nourishment to the nails.

Lauryl glucoside contributes to sulfate-free and eco-friendly cuticle softeners, promoting healthy nail beds.
Lauryl glucoside is commonly used in sulfate-free and gentle facial tonics for a refreshing and balanced complexion.
Lauryl glucoside is a key ingredient in sulfate-free and natural deodorizing sprays for personal and household use.

The surfactant is employed in sulfate-free and eco-friendly rust removers, addressing household cleaning needs.
Lauryl glucoside contributes to sulfate-free and mild foot sprays, providing a cooling and revitalizing sensation.

Lauryl glucoside is used in sulfate-free and natural leather cleaners for gentle and effective maintenance.
Lauryl glucoside is found in sulfate-free and eco-friendly jewelry cleaners, ensuring a mild yet thorough clean.
Lauryl glucoside is commonly used in sulfate-free and gentle fabric fresheners for a subtle and natural fragrance.
Lauryl glucoside contributes to sulfate-free and natural stain removers, providing an effective yet mild solution for laundry.
Lauryl glucoside is employed in the formulation of sulfate-free and eco-friendly carpet spot cleaners for household use.

Lauryl glucoside is a component in sulfate-free and mild tattoo cleansers, promoting gentle aftercare.
Lauryl glucoside is found in sulfate-free and natural air fresheners, offering a mild and non-irritating aroma.
Lauryl glucoside contributes to sulfate-free and eco-friendly furniture polishes for gentle and effective cleaning.
Lauryl glucoside is used in sulfate-free and mild insect bite relief products, providing a soothing solution for irritated skin.

Lauryl glucoside finds application in sulfate-free and mild sunscreen formulations, contributing to an even and non-greasy application.
Lauryl glucoside is a key ingredient in sulfate-free and natural hair styling gels, offering hold without stiffness.
Lauryl glucoside is employed in sulfate-free and eco-friendly makeup brush cleansers, ensuring thorough yet gentle cleaning.
Lauryl glucoside contributes to the formulation of sulfate-free and mild bath oils, providing a nourishing and relaxing bathing experience.

Lauryl glucoside is used in sulfate-free and natural intimate wipes, offering gentle cleansing for sensitive areas.
Lauryl glucoside is found in sulfate-free and eco-friendly cuticle conditioners, promoting healthy and hydrated nails.
Lauryl glucoside is commonly used in sulfate-free and mild exfoliating lip scrubs for soft and smooth lips.

Lauryl glucoside is a component in sulfate-free and natural cuticle protectants, offering a barrier against environmental stressors.
Lauryl glucoside contributes to sulfate-free and eco-friendly toilet bowl cleaners for effective and mild sanitation.
Lauryl glucoside is employed in sulfate-free and natural leave-in conditioners for soft and manageable hair.

Lauryl glucoside is used in sulfate-free and mild body powders, providing a silky and non-irritating feel on the skin.
Lauryl glucoside is found in sulfate-free and eco-friendly automotive cleaners for gentle yet efficient vehicle maintenance.
Lauryl glucoside contributes to sulfate-free and natural eye makeup removers, ensuring gentle and effective cleansing.

Lauryl glucoside is commonly used in sulfate-free and mild hand creams for moisturizing without a greasy residue.
Lauryl glucoside is employed in sulfate-free and eco-friendly glass cleaners, promoting streak-free and clear surfaces.
Lauryl glucoside is a key ingredient in sulfate-free and natural carpet deodorizers, offering a fresh and mild fragrance.
Lauryl glucoside is found in sulfate-free and mild surface disinfectant sprays for household and commercial use.

Lauryl glucoside contributes to sulfate-free and eco-friendly air purifiers, ensuring a clean and fresh environment.
Lauryl glucoside is used in sulfate-free and natural hair volumizers, providing lift without product buildup.
Lauryl glucoside is a component in sulfate-free and mild leather conditioners for preserving and softening leather goods.
Lauryl glucoside is commonly employed in sulfate-free and eco-friendly plant insecticides for mild yet effective pest control.

Lauryl glucoside contributes to sulfate-free and natural wound healing balms, providing a soothing and protective layer.
Lauryl glucoside is found in sulfate-free and mild shoe deodorizers, combating odor without harsh chemicals.
Lauryl glucoside is employed in sulfate-free and eco-friendly household grease removers for kitchen surfaces.
Lauryl glucoside is used in sulfate-free and natural bath bombs, providing effervescence and mild skin nourishment.



DESCRIPTION


Lauryl glucoside is a type of non-ionic surfactant that belongs to the class of alkyl polyglucosides (APGs).
Lauryl glucoside is commonly used in various personal care and household products.
The chemical structure of lauryl glucoside consists of a lauryl (C12) alkyl chain attached to a glucose molecule.
This combination of a fatty alcohol and a sugar unit results in a surfactant with both hydrophilic (water-attracting) and lipophilic (oil-attracting) properties.

Lauryl glucoside is a non-ionic surfactant widely used in the formulation of personal care and household products.
Lauryl glucoside is derived from natural sources, combining a lauryl alcohol chain with glucose.
Lauryl glucoside exhibits excellent emulsifying properties, enabling the dispersion of oil and water in various formulations.

The chemical structure of Lauryl Glucoside features a hydrophobic tail and a hydrophilic head, contributing to its surfactant behavior.
Lauryl glucoside is known for its mildness on the skin, making it suitable for use in cosmetic products for sensitive skin types.
Lauryl glucoside is often utilized in shampoo formulations for its ability to create a rich lather while being gentle on the hair and scalp.
Lauryl glucoside is biodegradable, aligning with the growing demand for environmentally friendly and sustainable ingredients.

Lauryl glucoside functions as a detergent, effectively removing dirt and impurities from various surfaces.
Lauryl glucoside is compatible with a wide range of other cosmetic ingredients, contributing to its versatility in formulations.

Lauryl glucoside is commonly found in facial cleansers, body washes, and liquid soaps, providing effective cleansing without causing skin irritation.
Lauryl glucoside contributes to the stability of formulations, ensuring the even distribution of ingredients in products like lotions and creams.
Lauryl glucoside is produced through a green and eco-friendly process, aligning with the increasing demand for natural and sustainable cosmetics.

Lauryl glucoside is an amphiphilic molecule, allowing it to interact with both oil and water phases in formulations.
Lauryl glucoside enhances the foaming properties of products like shower gels, creating a luxurious and satisfying user experience.
Lauryl glucoside is often used in baby care products due to its gentle nature and mild cleansing properties.

Lauryl glucoside can contribute to the overall stability and texture of formulations, improving the feel and appearance of the end product.
Lauryl glucoside is a clear to slightly hazy liquid, making it easy to incorporate into various cosmetic and cleaning formulations.

Lauryl glucoside can be utilized in industrial applications for its emulsifying and dispersing capabilities in manufacturing processes.
Lauryl glucoside is an essential ingredient in sulfate-free formulations, addressing the demand for milder alternatives in personal care products.

Lauryl glucoside is known for its versatility, allowing formulators to create products with different viscosities and textures.
Lauryl glucoside is compatible with a wide pH range, providing stability in formulations with varying acidities or alkalinity.
Lauryl glucoside can contribute to the improvement of the sensorial properties of products, such as their fragrance and feel on the skin.

Lauryl glucoside is a key ingredient in natural and organic formulations, meeting the preferences of consumers seeking cleaner beauty products.
Lauryl glucoside is produced through sustainable practices, often sourced from renewable resources, supporting eco-conscious product development.
Lauryl glucoside exemplifies the balance between effective cleaning properties and a gentle, skin-friendly profile, making it a sought-after ingredient in the cosmetic and cleaning industries.



PROPERTIES


Boiling Point: 301°C at 101.3kPa
Density: 1.16 g/cm3 at 20℃
Vapor Pressure: 0.008Pa at 20°C
Surface Tension: 29.5mN/m at 1g/L and 23°C



FIRST AID


Inhalation:

If inhaled, move the person to fresh air.
If breathing difficulties persist, seek medical attention.


Skin Contact:

Remove contaminated clothing.
Wash the affected area with plenty of water and mild soap.
If irritation persists, seek medical advice.


Eye Contact:

Rinse eyes thoroughly with water for at least 15 minutes, holding eyelids open.
Seek medical attention if irritation or redness persists.


Ingestion:

Rinse mouth with water.
Do not induce vomiting unless directed by medical personnel.
Seek immediate medical attention.


Note to Physicians:

Treat symptomatically based on the individual's condition.
No specific antidote is known.


General Advice:

Ensure that first aid personnel are aware of the substance involved and take precautions to protect themselves.
If symptoms persist or if in doubt, seek medical attention.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment, including gloves and safety glasses or goggles, to minimize skin and eye contact.

Ventilation:
Work in a well-ventilated area or use local exhaust ventilation to control airborne concentrations.

Avoid Contact:
Avoid direct skin and eye contact.
In case of contact, follow first aid measures and rinse affected areas thoroughly.

Hygiene Practices:
Practice good personal hygiene, including washing hands thoroughly after handling Lauryl Glucoside.

Preventive Measures:
Implement measures to prevent the generation of aerosols or dust during handling.

Storage Compatibility:
Store Lauryl Glucoside away from incompatible materials and substances.
Check the compatibility information provided in the safety data sheet (SDS).

Temperature Control:
Store in a cool, dry place, away from heat sources and direct sunlight, to maintain product stability.


Storage:

Temperature:
Store Lauryl Glucoside within the specified temperature range as indicated on the product information or safety data sheet.

Ventilation:
Ensure storage areas are well-ventilated to prevent the buildup of vapors.

Container Integrity:
Store Lauryl Glucoside in containers made of materials compatible with the substance to maintain container integrity.

Incompatible Materials:
Keep Lauryl Glucoside away from incompatible materials, as specified in the safety data sheet.

Segregation:
Segregate Lauryl Glucoside from incompatible substances to prevent chemical reactions or contamination.

Handling Containers:
Handle containers with care to prevent damage or leakage. Follow recommended procedures for lifting and moving containers.

Labeling:
Ensure that containers are labeled correctly with the product name, hazard information, and any necessary precautionary measures.

Emergency Procedures:
Familiarize personnel with emergency procedures, including spill response and proper cleanup methods.



SYNONYMS


Lauryl Polyglucose
D-Glucopyranose, O-Dodecyl and O-Decyl Derivs.
Decyl Glucoside Laurate
Decyl Glucoside Laurate Polyethylene Glycol Ether
Decyl Glucoside Laurate Polyglyceryl-2
Decyl Glucoside Oleate
Dodecyl D-Glucopyranoside
Dodecyl Glucoside
Dodecyl Polyglucose
Glucopyranoside, Lauryl
Lauryl Glucose
Lauryl Polyglucose Carboxylate
Nonyl Glucoside
Octyl D-Glucopyranoside
Octyl Glucoside
Polyethylene Glycol Ether Decyl Glucoside Laurate
Polyethylene Glycol Ether Lauryl Glucoside Laurate
Polyethylene Glycol Ether Octyl Glucoside Laurate
Polyethylene Glycol Ether Undecyl Glucoside Laurate
Polyglyceryl-2 Decyl Glucoside Laurate
Polyglyceryl-2 Dodecyl Glucoside
Polyglyceryl-2 Dodecyl Glucoside Laurate
Polyglyceryl-2 Lauryl Glucoside
Polyglyceryl-2 Octyl Glucoside Laurate
Undecyl Glucoside
2-Dodecyl-D-glucopyranoside
Decyl Glucose
Decyl Polyglucose
Dodecyl Polyglucoside
Glucoside, Lauryl
Glycoside, Lauryl
Lauryl Glucose Carboxylate
Lauryl Oligosaccharide
Polyglyceryl-2 Dodecyl Glucoside
Lauryl Glucoside Laurate
Decyl Glucoside Laurate Polyglyceryl-2
Lauryl Glucoside Laurate Polyglyceryl-2
Dodecyl Glucoside Laurate Polyethylene Glycol Ether
Lauryl Glucoside Laurate Polyethylene Glycol Ether
Decyl Glucoside Laurate
Lauryl Polyglucose Carboxylate
Polyglyceryl-2 Decyl Glucoside Laurate
Lauryl Glucoside Laurate Polyglyceryl-2
Lauryl Glucoside Laurate Polyglyceryl-2 Oleate
Lauryl Glucoside Oleate
Dodecyl Glucoside Laurate
Octyl Glucoside Laurate
Polyglyceryl-2 Octyl Glucoside Laurate
Lauryl Glucoside Laurate Polyglyceryl-2 Oleate
Lauryl Polyglucoside Carboxylate
1-Dodecyl-beta-D-glucopyranoside
Dodecyl β-D-Glucopyranoside
Decyl β-D-Glucopyranoside
D-Glucopyranoside, O-Decyl
Glycoside, Lauryl Poly-
O-Decyl-D-Glucopyranoside
O-Dodecyl-D-Glucopyranoside
Polyoxyethylene (2) Dodecyl Glucoside
2-Dodecyl Glucopyranoside
Decyl Polyglycoside
Lauryl Oligoglucosides
Lauryl Polyglucose Laurate
Polyglyceryl-2 Lauryl Glucoside Oleate
Polyglyceryl-2 Lauryl Glucoside Palmitate
Lauryl Glucoside Palmitate
Polyglyceryl-2 Lauryl Glucoside Linoleate
Polyglyceryl-2 Lauryl Glucoside Linolenate
Lauryl Glucoside Linoleate
Lauryl Glucoside Linolenate
Lauryl Glucoside Oleate Linoleate
Polyglyceryl-2 Lauryl Glucoside Oleate Linoleate
Polyglyceryl-2 Lauryl Glucoside Oleate Linolenate
Lauryl Glucoside Oleate Linolenate
Decyl Glucoside Laurate Polyglyceryl-2 Linoleate
Decyl Glucoside Laurate Polyglyceryl-2 Linolenate

Lauryl Glucoside (APG1214) is a surfactant and cleansing agent used in cosmetics.
Lauryl Glucoside (APG1214) is a glycoside produced from glucose and lauryl alcohol.
Lauryl Glucoside (APG1214) and Octyl glucoside are similar products used in cosmetics.

CAS: 110615-47-9
MF: C18H36O6
MW: 348.47484
EINECS: 600-975-8

Synonyms
D-Glucopyranose, oligomeric, C10-16-alkyl glycosides,110615-47-9,D-Glucopyranose, oligomeric, C10-16-alkyl glycosides (n=1.3),D-Glucopyranose, oligomeric, C10-16-alkyl glycosides (n=1.4),D-glucopyrasone, oligomeric, C10-16-alkyl glycosides,DTXSID50105933

Lauryl Glucoside (APG1214) is a mild and versatile surfactant commonly used in the formulation of personal care and cosmetic products.
Lauryl Glucoside (APG1214) is classified as a non-ionic surfactant and is derived from natural raw materials, making it suitable for various skin types, including sensitive skin.
Lauryl Glucoside (APG1214) is composed of a fatty alcohol (lauryl alcohol) and glucose, resulting in a surfactant that exhibits excellent foaming and emulsifying properties.

Due to its gentle nature, Lauryl Glucoside (APG1214) is often found in products such as shampoos, body washes, facial cleansers, and baby care items.
Lauryl Glucoside (APG1214) ability to produce a stable lather, coupled with its mildness, makes it a preferred choice for formulations that require effective cleansing without causing irritation.
Additionally, Lauryl Glucoside (APG1214) is biodegradable, aligning with the growing demand for environmentally friendly and sustainable cosmetic ingredients.

The synthesis of Lauryl Glucoside (APG1214) involves the reaction between lauryl alcohol, derived from natural sources like coconut or palm kernel oil, and glucose obtained from cornstarch or other plant-based sources.
This process results in a surfactant that meets the criteria for natural and green formulations.
The versatility, mildness, and biodegradability of Lauryl Glucoside (APG1214) contribute to its popularity in the cosmetic industry, where there is a growing emphasis on creating products that are effective, safe, and environmentally conscious.

Lauryl Glucoside (APG1214) Chemical Properties
Boiling point: 301℃ at 101.3kPa
Density: 1.16 at 20℃
Vapor pressure: 0.008Pa at 20℃
Form: Solid
InChI: InChI=1/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18?/s3
InChIKey: PYIDGJJWBIBVIA-KGFPCJIYNA-N
LogP: -0.07 at 20℃
Surface tension: 29.5mN/m at 1g/L and 23℃
EPA Substance Registry System: Lauryl Glucoside (APG1214) (110615-47-9)

Uses
Lauryl Glucoside (APG1214) is a mild surfactant.
Lauryl Glucoside (APG1214) creates an excellent and stable foam.
Lauryl Glucoside (APG1214) is useful in hair care products where it aids hair cleaning abilities without stripping the hair.
Lauryl Glucoside (APG1214) can be used alongside other glucosides to enhance the foam and skin conditioning properties.

Lauryl Glucoside (APG1214) is very effective when used in ionic formulations to add foam depth and emulsifying properties.
Lauryl Glucoside (APG1214) is very useful for Bath Foams, Shower Gel and Shampoo where you wish to increase the foaming ability of the product without a decrease in the natural formulation.
Lauryl Glucoside (APG1214) is biodegradable.

Lauryl Glucoside (Dodecyl Glucoside) is an alkyl polyglucoside (C 12-16 fatty alcohol glucoside), a mild surfactant and skin cleanser with excellent foaming properties derived from natural corn starch, fatty acids, and coconut.


CAS Number: 59122-55-3
EC Number: 261-614-4
Chem/IUPAC Name: Dodecyl β-D-glucopyranoside
Chemical formula: C18H36O6



SYNONYMS:
Dodecyl β-D-glucopyranoside, (2R,3R,4S,5S,6R)-2-(Dodecyloxy)-6-(hydroxymethyl)oxane-3,4,5-triol, Dodecyl glucoside, Lauryl polyglucoside, Dodecyl D-glucoside, lauryl glucoside, 110615-47-9, dodecyl d-glucopyranoside, 27836-64-2, EINECS 248-685-7, UNII-VB00RDE21R, VB00RDE21R, D-Glucopyranoside, dodecyl, EC 600-975-8, (3R,4S,5S,6R)-2-dodecoxy-6-(hydroxymethyl)oxane-3,4,5-triol, UNII-76LN7P7UCU, GLUCOSIDE, DODECYL, D-, dodecyl--d-glucopyranoside, SCHEMBL57535, CLAON ALL 4 CLEANSER, DTXSID30893048, PYIDGJJWBIBVIA-IHAUNJBESA-N, beta-D-GLUCOPYRANOSIDE, DODECYL, DB14746, W-110711, C10-16 Alkyl Glucoside, D-Glucopyranose, Oligomeric, C10-16-Alkyl Glycosides, D-Glucopyranoside, Dodecyl, Dodecyl D-Glucoside, Glucopyranose, Oligomeric, C10-16-Alkyl Glycosides, Lauryl D-Glucopyranoside, Lauryl Glucoside (INCI), 59122-55-3, Dodecyl glucoside, Dodecyl b-D-glucopyranoside, Dodecyl beta-D-glucopyranoside, n-DODECYL-beta-D-GLUCOPYRANOSIDE, C18H36O6, Dodecyl D-glucoside, D-Glucopyranoside, Dodecyl, Lauryl D-glucopyranoside



Lauryl Glucoside (Dodecyl Glucoside) is an alkyl polyglucoside (C 12-16 fatty alcohol glucoside), a mild surfactant and skin cleanser with excellent foaming properties derived from natural corn starch, fatty acids, and coconut.
In addition, Lauryl Glucoside (Dodecyl Glucoside) is non-petrochemical, non-ethoxylated, and readily biodegradable.


Lauryl Glucoside (Dodecyl Glucoside) exhibits superior cleansing efficacy as a minimum outcome.
Lauryl Glucoside (Dodecyl Glucoside) meets cleansing targets in the same way as standard surfactants while also providing the additional benefit of exceptional mildness in personal care formulations.


A deep pore cleansing test shows that cleaning with water does not remove the soil sufficiently from the skin.
In contrast, the cleansing with both Sodium Laureth Sulfate and Lauryl Glucoside (Dodecyl Glucoside) shows excellent cleansing efficacy.
The best-combined results in cleansing and mildness are achieved with this "green" ingredient.


According to a study into the effects of alkyl glucoside on the phenomenon of scale lifting during extension of untreated hair fibers, it was found that treatments with Sodium Laureth Sulfate lead to the more extensive weakening of the scale structure of combed fibers.
At pronounced extension levels, cuticle cells start to separate from underlying cuticles.


By contrast, treatments with Lauryl Glucoside (Dodecyl Glucoside) show less severe scale lifting and reduced angles of scale lifting.
In comparison Sodium Laureth Sulfate, instead, has a strong effect on the hair surface, appearing as the lifting of the cuticle scales.
In terms of cleansing efficacy, the lipometric measurements show the comparable effects of Sodium Laureth Sulfate and Lauryl Glucoside (Dodecyl Glucoside).


Lauryl Glucoside (Dodecyl Glucoside) is a non-ionic surfactant and member of the alkyl glucoside family (e.g. coco glucoside, decyl glucoside) which are substances formed by mixing alcohols and sugar and/or glucose.
Lauryl Glucoside (Dodecyl Glucoside) is usually sustainably sourced from palm kernel oil, corn sugar, or coconut.


Lauryl Glucoside (Dodecyl Glucoside) improves the cleansing process without stripping necessary moisture.
Lauryl Glucoside (Dodecyl Glucoside) is a plant-based surfactant that usually appears as a clear liquid with a mild sweet fatty aroma, and is found in many cleaning products, soaps and cleansers.


Regarding its safety profile, a group of Alkyl Glucosides, including Lauryl Glucoside (Dodecyl Glucoside), were assessed by the Cosmetic Ingredient Review (CIR) Expert Panel in 2013.
They reviewed their safety for dermal exposure in cosmetics and concluded they are “safe in the present practices of use and concentration when formulated to be nonirritating.”


EWG notes studies showing allergic contact dermatitis to decyl and Lauryl Glucoside (Dodecyl Glucoside) exists in a small percentage of the population, and appropriate care should be taken for those with sensitivities.
Lauryl Glucoside (Dodecyl Glucoside) is a surfactant used in cosmetics and laundry detergents.


Lauryl Glucoside (Dodecyl Glucoside) is a glycoside produced from glucose and lauryl alcohol.
Lauryl Glucoside (Dodecyl Glucoside) is biodegradable.
Lauryl Glucoside (Dodecyl Glucoside)'s Molecular Formula is C18H36O6 and Molecular Weight is 348.5.


Lauryl Glucoside (Dodecyl Glucoside) is one of several non-ionic surfactants found within the polyglycoside family.
Lauryl Glucoside (Dodecyl Glucoside)’s obtained from the sugars and fatty alcohols found within coconuts, making it a naturally derived renewable resource.
Lauryl Glucoside (Dodecyl Glucoside)'s these types of ingredients that provide the mild and gentle “sudsing” base for body washes, facial cleansers, shampoos, bubble bath, and other liquid cleansing formulations.


Lauryl Glucoside (Dodecyl Glucoside) holds a thicker texture than decyl glucoside.
Lauryl Glucoside (Dodecyl Glucoside) is sulfate free.
Lauryl Glucoside (Dodecyl Glucoside) is one of several non-ionic surfactants found within the polyglycoside family.


Lauryl Glucoside (Dodecyl Glucoside) is obtained from coconuts, making it a naturally derived renewable resource.
Lauryl Glucoside (Dodecyl Glucoside) holds a thicker texture than decyl glucoside.
Lauryl Glucoside (Dodecyl Glucoside) is a cationic surfactant that has been used in pharmaceutical preparations for the treatment of bacterial vaginosis.


Lauryl Glucoside (Dodecyl Glucoside) is a non-irritating, low-toxicity compound that is effective against most Gram-positive and Gram-negative bacteria.
Lauryl Glucoside (Dodecyl Glucoside) is an alkyl glucoside primarily used as a surfactant in common cosmetic, skincare, and household products.
Lauryl Glucoside (Dodecyl Glucoside) is increasingly used as it is extracted from plant-based sources and considered ecologically safe.


Lauryl Glucoside (Dodecyl Glucoside) is a very mild, non-ionic surfactant that provides gentle cleansing, particularly for oily skin in shampoos, body washes and bubble baths.
Lauryl Glucoside (Dodecyl Glucoside) is considered safer alternative to regular harsh sulfates.


Lauryl Glucoside (Dodecyl Glucoside), also referred to as Lauryl Glucose, is a surfactant of the anionic type.
This cleansing agent, Lauryl Glucoside (Dodecyl Glucoside), is made from glucose and lauryl alcohol.
Lauryl Glucoside (Dodecyl Glucoside) is an odorless liquid that can be light yellow or clear when it comes to appearance.



USES and APPLICATIONS of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Dental Care uses of Lauryl Glucoside (Dodecyl Glucoside): As a surfactant, Lauryl Glucoside (Dodecyl Glucoside) has foaming qualities that make it an effective ingredient in toothpaste and tooth whitening products.
Cosmetics: Lauryl Glucoside (Dodecyl Glucoside) is often used as a cleansing agent and surfactant in cosmetics, including makeup primer, eye makeup remover, BB creams, and eye cream.


Lauryl Glucoside (Dodecyl Glucoside) Uses in Puracy Products: Instead of sulfates, Puracy uses Lauryl Glucoside (Dodecyl Glucoside) as a surfactant and cleanser in many of our foaming products.
Lauryl Glucoside (Dodecyl Glucoside) is used in some of our personal care and cleaning products for its gentle but effective cleansing properties, and general compatibility with sensitive skin.


Lauryl Glucoside (Dodecyl Glucoside) is derived from lauryl alcohol (from coconut or palm) and glucose (from corn or potato).
Lauryl Glucoside (Dodecyl Glucoside)'s what's known as a ‘non-ionic surfactant’, which means the molecules have no charge and help deliver non-streak cleaning.


Lauryl Glucoside (Dodecyl Glucoside) also contributes to lather, wetting and suspension of soils in products like shampoo, body wash, bubble bath, laundry products, facial cleansers and toothpastes.
Lauryl Glucoside (Dodecyl Glucoside) adds high foaming capacity to your foaming product


When combined with other glucosides helps increase foaming and cleansing richness
Lauryl Glucoside (Dodecyl Glucoside) adds high foaming capacity to your foaming product, if you want more foam in your product add it.
Lauryl Glucoside (Dodecyl Glucoside) is a surfactant and cleansing agent used in cosmetics.


Of course, Lauryl Glucoside (Dodecyl Glucoside) all comes down to personal preferences, and I do feel that the majority of surfactants are not suitable for skincare but that doesn’t mean that all are created equally or that all hold the same purposes in the world of cleaning and cleansing.
Since there are limited ways that one can actually “make soap” we must select the option that works best for our formulation.


You can use the lye and water method, or you can use surfactants.
Besides these two forms of soap making there are precious few other ways of making a high-quality sudsing action product.
You are all pretty much covered when selecting Lauryl Glucoside (Dodecyl Glucoside) as your base.


Simple blending techniques are used, just add Lauryl Glucoside (Dodecyl Glucoside) your other water-based additives and stir, adjust the pH of the finished product using either citric acid or lactic acid – thicken if desired and you are finished.
You can add oil-based ingredients to surfactants … however, depending upon the ratio added you will notice a decrease in the lathering ability.


Your own testing will need to be performed as to how much oil your formulation can hold.
Lauryl Glucoside (Dodecyl Glucoside) adds high foaming capacity to your foaming product.
When combined with other glucosides helps increase foaming and cleansing richness.


Lauryl Glucoside (Dodecyl Glucoside) can be used as a foaming agent, conditioner or emulsifier
Lauryl Glucoside (Dodecyl Glucoside) has excellent foaming capacity and good dermatological compatibility
Lauryl Glucoside (Dodecyl Glucoside) is biodegradable


Blend Lauryl Glucoside (Dodecyl Glucoside) with other surfactants to produce a foaming product with skin cleansing abilities.
Lauryl Glucoside (Dodecyl Glucoside) works excellently blended with Cocamidopropyl betaine.
Lauryl Glucoside (Dodecyl Glucoside) is water-soluble and proves to be useful when blended alongside ionic formulas to enhance their emulsifying and foam depths.


This Non-ionic surfactant, Lauryl Glucoside (Dodecyl Glucoside), can be used as an emulsifier, conditioner, or foaming agent.
Lauryl Glucoside (Dodecyl Glucoside) can be used as both co-surfactant and base-surfactant in skin cleansers because it has the best foaming capacity of the glucosides, and it is also dermatologically compatible.


Lauryl Glucoside (Dodecyl Glucoside) assists in enhancing the viscosity and conditioning properties of the final product.
Lauryl Glucoside (Dodecyl Glucoside) works slowly compared to other Glucosides, but it certainly has the best cleansing effect and is stable.
The foam-producing ability makes Lauryl Glucoside (Dodecyl Glucoside) one popular cosmetic raw material in personal care and skincare applications.


Haircare products also use Lauryl Glucoside (Dodecyl Glucoside) since it has deeply cleansed the hair without stripping the natural oils.
Moreover, Lauryl Glucoside (Dodecyl Glucoside) can be used to enhance the foam and skin conditioning properties of products like Bath Foams, Shower Gel, and face washes.


Lauryl Glucoside (Dodecyl Glucoside) is used for external use only.
Lauryl Glucoside (Dodecyl Glucoside) is used great for baby wash, Pet safe shampoo and Sensitive skin formulation.
Lauryl Glucoside (Dodecyl Glucoside) is used body wash, face wash, liquid hand soap, shampoo, baby care, sensitive skin care and wipes


Lauryl Glucoside (Dodecyl Glucoside) has been shown to be an effective antimicrobial agent with an adsorption mechanism based on hydrogen bonding.
Lauryl Glucoside (Dodecyl Glucoside) also has been shown to have skin cancer prevention properties, as it is able to inhibit the proliferation of human skin cells.


Lauryl Glucoside (Dodecyl Glucoside) can also cause allergic reactions or sensitization in some individuals, while diamine tetraacetic acid (DTA) may be used as a stabilizer in products containing lauryl glucoside.


-Skincare Products uses of Lauryl Glucoside (Dodecyl Glucoside):
Foaming, emulsifying and stabilizing abilities of Lauryl Glucoside (Dodecyl Glucoside) are incorporated while making skincare products like face washes, cleansers, toner, and even face masks.
Products containing Lauryl Glucoside (Dodecyl Glucoside) attract the oil, dirt, and other impurities from the skin and rinses off easily.


-Haircare Applications of Lauryl Glucoside (Dodecyl Glucoside):
Potent foaming and cleansing feature of Lauryl Glucoside (Dodecyl Glucoside) is used to make shampoo, hair cleansers, hair masks, and many other hair care products because it effectively removes the filth and grime that gets stuck in the hair without causing any damage to the scalp and hair strands.


-Body Cleanser uses of Lauryl Glucoside (Dodecyl Glucoside):
Lauryl Glucoside (Dodecyl Glucoside) act as a non-ionic surfactant has potent cleansing and purifying function; therefore, it is used to make body cleansers like body wash, shower gels, bubble bath, etc., considering that it cleanses the impurities from the body and at the same time also conditions and nourishes the skin.


-Sunscreen uses of Lauryl Glucoside (Dodecyl Glucoside):
Lauryl Glucoside (Dodecyl Glucoside) is made from sustainable and plant-based ingredients that is why it is added in many leave-on products like sunscreens, face creams, toners, etc. as they benefit the skin in so many ways and apart from that they are also completely safe to apply on the skin.


-Moisturiser and Creams uses of Lauryl Glucoside (Dodecyl Glucoside):
Lauryl Glucoside (Dodecyl Glucoside) is nonionic surfactants that go through the condensation of glucose with a fatty alcohol.
Lauryl Glucoside (Dodecyl Glucoside) is primarily derived from palm, coconut, and rapeseed oil, and thus it is used to make moisturizer, creams, and lotions.


-Toothpaste uses of Lauryl Glucoside (Dodecyl Glucoside):
Lauryl Glucoside (Dodecyl Glucoside) is a very mild dispersant or surfactant that is made from natural resources.
Surfactants also have foaming qualities that are important to disperse toothpaste while brushing.
Because Lauryl Glucoside (Dodecyl Glucoside) is made from body-safe ingredients, it is safe for health.


-Shampoos with Lauryl Glucoside (Dodecyl Glucoside):
If chemicals have already damaged the hair, Lauryl Glucoside (Dodecyl Glucoside) can be further weakened by treatments with surfactants.
In other words, sensitive hair such as bleached, colored, permed, weathered, or magnificent hair should be shampooed with gentle-action surfactants.


-Skincare and Body Care uses of Lauryl Glucoside (Dodecyl Glucoside):
As a surfactant and cleansing agent, Lauryl Glucoside (Dodecyl Glucoside) breaks surface tension so dirt and oil are lifted and washed away more easily.
This is a great reason that you can find Lauryl Glucoside (Dodecyl Glucoside) in shampoo, face washes, bubble bath, body wash, and other personal care products.



WHAT IS LAURYL GLUCOSIDE (DODECYL GLUCOSIDE)USED FOR?
*Skin care:
Lauryl Glucoside (Dodecyl Glucoside) can be used alongside other glucosides to enhance the foam and skin conditioning properties.
Lauryl Glucoside (Dodecyl Glucoside) is very effective when used in ionic formulations to add foam depth and emulsifying properties.
Lauryl Glucoside (Dodecyl Glucoside) is very useful for bath foams, shower gel to increase the foaming ability of the product.

*Hair care:
Lauryl Glucoside (Dodecyl Glucoside) creates an excellent and stable foam.
Lauryl Glucoside (Dodecyl Glucoside) is useful in hair care products where it aids hair cleaning abilities without stripping the hair.



HOW TO USE LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Blend Lauryl Glucoside (Dodecyl Glucoside) with other surfactants to produce a foaming product with skin cleansing abilities.
Lauryl Glucoside (Dodecyl Glucoside) works excellently blended with Cocamidopropyl betaine.



USAGE LEVEL OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Recommended Usage Level of Lauryl Glucoside (Dodecyl Glucoside):
10% - 20% (Face Wash)
15% - 30% (Shower Gel / Bath Foam / Shampoo)



INDULGENT HIGH FOAM, LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) is an non-ionic surfactant that can be used as a foaming agent, conditioner or emulsifier.
Lauryl Glucoside (Dodecyl Glucoside) has the best foaming capacity of the glucosides and good dermatological compatibility.
Therefore Lauryl Glucoside (Dodecyl Glucoside) is suitable for use as a base surfactant or a co-surfactant in cosmetic surfactant cleansing preparations.

We recommend adding 5% Lauryl Glucoside (Dodecyl Glucoside) to your glucoside based surfactant formulation to boost foam.
Lauryl Glucoside (Dodecyl Glucoside) aids the viscosity build up of your final product.
Lauryl Glucoside (Dodecyl Glucoside) increases the foaming ability



CHARACTERISTICS OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) creates an excellent and stable foam.
Lauryl Glucoside (Dodecyl Glucoside) is useful in hair care products where it aids hair cleaning abilities without stripping the hair.

Lauryl Glucoside (Dodecyl Glucoside) can be used alongside other glucosides to enhance the foam and skin conditioning properties.
Lauryl Glucoside (Dodecyl Glucoside) is very effective when used in ionic formulations to add foam depth and emulsifying properties.

Lauryl Glucoside (Dodecyl Glucoside) is very useful for Bath Foams, Shower Gel and Shampoo where you wish to increase the foaming ability of the product without a decrease in the natural formulation.
Lauryl Glucoside (Dodecyl Glucoside) is biodegradable.



BENEFITS OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
*Conditioning Properties
Lauryl Glucoside (Dodecyl Glucoside) is a mild and non-ionic surfactant with excellent skin conditioning and nourishing properties.
Lauryl Glucoside (Dodecyl Glucoside) also acts as an emulsifier and stabilizer, which helps to impart moisturization and hydration deeply into the layers of the skin.

*Foaming Ability
Stable foaming ability of Lauryl Glucoside (Dodecyl Glucoside) is used in cleansers because it is very mild and gentle on the skin.
The potential of Lauryl Glucoside (Dodecyl Glucoside) to form copious amounts of foam makes it one of the commonly used ingredients in bath gels, shampoos, and skin cleansers.

*Suitable for Sensitive Skin:
Lauryl Glucoside (Dodecyl Glucoside) is made from natural ingredients, so it does not affect the skin.
You can add products that contain Lauryl Glucoside (Dodecyl Glucoside) to your daily beauty regimen.
Lauryl Glucoside (Dodecyl Glucoside)'s tender composition is perfect for sensitive and acne-prone skin.

*Environmental-Friendly:
Lauryl Glucoside (Dodecyl Glucoside) is biodegradable, which does not threaten the environment during and after use.
Vegans can use Lauryl Glucoside (Dodecyl Glucoside) as components derived from natural resources and completely free from animal-derived ingredients.

*Protects from Skin Damage:
Harsh surfactants and skin cleansers usually result in hyperpigmentation, blemishes, and sometimes even acne in deeper skin tones.
Whereas Lauryl Glucoside (Dodecyl Glucoside) is a safer alternative for Indian skin as it contains only body-safe ingredients for all skin types.

*Deeply Cleanses Scalp:
Haircare products containing Lauryl Glucoside (Dodecyl Glucoside) are known for their cleansing and foaming features.
Lauryl Glucoside (Dodecyl Glucoside) can make the whole product spread easily on the scalp and simultaneously draw all the dirt, grease, and oil from the scalp and hair strands.



WHERE IS LAURYL GLUCOSIDE (DODECYL GLUCOSIDE) FOUND?
Glucosides are used because of their emulsifying and foaming properties.
For this property, Lauryl Glucoside (Dodecyl Glucoside) may be found in:

*Cosmetics
*Hair dyes
*Shampoos and shower gels
*Tanning formulations.

It is also present in leave-on products such as:
*Sunscreens
*Deodorants
*Fragrances.
More recently, alkyl glucosides have been used in wound care products as well.



ORIGIN OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) is a glycoside produced from glucose and lauryl alcohol.
Lauryl Glucoside (Dodecyl Glucoside) is made by combining corn sugar and either coconut oil or palm oil.
Lauryl Glucoside (Dodecyl Glucoside) is derived through natural processes.



WHAT DOES LAURYL GLUCOSIDE (DODECYL GLUCOSIDE) DO IN A FORMULATION?
*Cleansing
*Emulsifying
*Foam boosting
*Skin conditioning
*Surfactant



SAFETY PROFILE OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) is considered quite safe for skin as it is a very mild surfactant, that poses little or no risk of irritation, and therefore used for sensitive skin.

A number of agencies such as the Safe Cosmetics Database, GoodGuide database, EcoCert and the Organic Food Federation consider Lauryl Glucoside (Dodecyl Glucoside) as a safe ingredient.

It is even included in the CIR list of safe ingredients for cosmetics.
10 to 20% Lauryl Glucoside (Dodecyl Glucoside) can be used in facial cleansers while 15 to 30% in shampoos and body washes.
A maximum of 40% of Lauryl Glucoside (Dodecyl Glucoside) is permitted for use in any product.



ALTERNATIVES OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
*DECYL GLUCOSIDE,
*COCOGLUCOSIDE



PROPERTIES OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
*Uncompromising mildness
Lauryl Glucoside (Dodecyl Glucoside) is not only gentle on the skin but can reduce the irritation potential of surfactant mixtures.
Compared to other surfactants, Lauryl Glucoside (Dodecyl Glucoside) is much milder and can be used in effective formulas with outstanding ocular and mucous compatibility without trading performance.
During 3D human cornea equivalent model tests, no damage was observed, further confirming the mildness of LG.


*Excellent daily cleaning
Lauryl Glucoside (Dodecyl Glucoside) shows a lower irritation potential than the other surfactants tested, confirming its excellent suitability for ensuring mildness in body washes.
As a measure of skin barrier integrity, the cumulative irritation potential of surfactants is assessed by transepidermal water loss (TEWL).


*Gentle cleansing with the power of nature
The use of Lauryl Glucoside (Dodecyl Glucoside) in shampoo allows consumers to take advantage of the efficacy of nature in removing chemical residues from the hair.

The analysis of silicone remaining on hair shows that, with one-time washing using a stripping shampoo containing Lauryl Glucoside (Dodecyl Glucoside), silicone can be reduced by 62% on virgin hair and 77% on bleached hair.
After three washes, the deposit reduction on virgin hair is even more significant.

Compared to Sodium Laureth Sulfate shampoos, this represents a marked improvement.
After using a Lauryl Glucoside (Dodecyl Glucoside) shampoo, the hair is better prepared for deep penetrating treatments.


*Excellent foam height
Lauryl Glucoside (Dodecyl Glucoside) improves the foam properties of shampoos, produces good, quantitatively stable foam, and sustains its height.


*Sensory profile
In a sensory test comparison of Cocamidopropyl Betaine and Lauryl Glucoside (Dodecyl Glucoside) as the primary surfactant of shampoo, the results showed no difference in terms of stickiness either in wet hair or during hair drying.
Together with the better-wet combability, better foam properties, and the proven kindness to the skin exhibited by Lauryl Glucoside (Dodecyl Glucoside), this finding confirms the superiority of alkyl polyglucosides in shampoo applications.



HOW LAURYL GLUCOSIDE (DODECYL GLUCOSIDE) IS MADE?
Commercial production of Lauryl Glucoside (Dodecyl Glucoside) generally starts by mixing palm, corn, or coconut alcohol with either sugar, glucose, or a glucose polymer under acidic conditions.



USAGE RATE OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) can be added to formulas as is.
Typical use level 1-25% depending on desired foaming and cleansing effects.



SCIENTIFIC RESEARCH APPLICATIONS OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
*Drug Delivery
Lauryl Glucoside (Dodecyl Glucoside)'s ability to act as a surfactant and its mild nature make it a potential carrier for drug delivery.
Studies have explored its use in:
*Transdermal drug delivery:
Lauryl Glucoside (Dodecyl Glucoside) might improve the penetration of drugs through the skin, potentially aiding in the development of topical drug formulations.

*Antibacterial and Antifungal Properties
Studies suggest Lauryl Glucoside (Dodecyl Glucoside) might exhibit antibacterial and antifungal properties.

Research has shown its potential effectiveness against:
*Gram-positive bacteria:
Lauryl Glucoside (Dodecyl Glucoside) has been shown to be effective against certain gram-positive bacteria, including Staphylococcus aureus.

*Fungi:
Studies indicate Lauryl Glucoside (Dodecyl Glucoside) may possess antifungal activity against Candida albicans



WHY DO WE USE LAURYL GLUCOSIDE (DODECYL GLUCOSIDE) IN FORMULATIONS?
Lauryl Glucoside (Dodecyl Glucoside) is mostly used as an emulsifier, conditioner, or foaming agent in cosmetic products as well as it is one of the mildest and most skin-friendly cosmetic ingredients.



STRENGHTS OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Lauryl Glucoside (Dodecyl Glucoside) is very mild surfactant blend offering excellent ph-independent foaming and cleansing properties


NOTE, LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Vegans can use products containing Lauryl Glucoside (Dodecyl Glucoside) as it does not comprise components that are derived from animals.



BENEFITS OF LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
*Very mild surfactant blend offering excellent ph-independent foaming and cleansing properties
*Can replace sulfates
*Low pH stability - performs well in salicylic acid formulations
*Efficient at low use levels
*EO/PO free
*Suitable for baby products and sensitive skin and scalp



PHYSICAL and CHEMICAL PROPERTIES of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
Molecular Weight: 348.5 g/mol
XLogP3-AA: 3.5
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 13
Exact Mass: 348.25118886 g/mol
Monoisotopic Mass: 348.25118886 g/mol
Topological Polar Surface Area: 99.4 Ų
Heavy Atom Count: 24
Formal Charge: 0
Complexity: 301
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 4
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0

Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Boiling Point: 301°C at 101.3 kPa
Density: 1.16 g/cm³ at 20°C
Vapor Pressure: 0.008 Pa at 20°C
Surface Tension: 29.5 mN/m at 1 g/L and 23°C
Physical state: Powder
Color: White
Odor: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available

Decomposition temperature: No data available
pH: No data available
Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available

Assay: 95.00 to 100.00%
Food Chemicals Codex Listed: No
Soluble in water: 21.19 mg/L @ 25°C (estimated)
Texture: Slippery, detergenty
Scent: No or faint odor
pH: 11-12
Charge: Non-ionic
HLB Value: 13
Appearance: Thick white paste
Solubility: Water
Usage rate: 1 - 25%
Charge: Non-ionic
Active surfactant matter: 50 - 53%
pH range: 4 - 12
Vegan: Yes
Palm oil: Yes*
CAS Number: 59122-55-3

IUPAC Name: Dodecyl β-D-glucopyranoside
INCI Name: Sodium Lauryl Glucose Carboxylate
Molecular Weight: 348.48 g/mol
Specific Gravity: N/A
Boiling Point: 499 ± 45.0 °C
Flash Point: 255.6 ± 28.7 °C
Odor: Faint
pH Level: 5.5 to 6.5
HLB Value: 13
Color: Clear to yellowish
Grade Standard: Technical Grade
Shelf Life: 24 months
Form: Liquid
Alternative Names: Dodecyl glucoside, Lauryl polyglucoside
Solubility: Yes
Applications: Cosmetic

Formula: C18H36O6
MW: 348.47
MDL No.: MFCD00063298
InChI: InChI=1S/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18-/m1/s1
InChI Key: PYIDGJJWBIBVIA-UYTYNIKBSA-N
CAS Number: 59122-55-3
Product Name: Lauryl glucoside
IUPAC Name: (2R,3R,4S,5S,6R)-2-dodecoxy-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular Formula: C18H36O6
Molecular Weight: 348.5 g/mol
InChI: InChI=1S/C18H36O6/c1-2-3-4-5-6-7-8-9-10-11-12-23-18-17(22)16(21)15(20)14(13-19)24-18/h14-22H,2-13H2,1H3/t14-,15-,16+,17-,18-/m1/s1
InChI Key: PYIDGJJWBIBVIA-UYTYNIKBSA-N
SMILES: CCCCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
Synonyms: dodecyl glucopyranoside, dodecyl glucoside, dodecyl-beta-D-glucopyranoside
Canonical SMILES: CCCCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O
Isomeric SMILES: CCCCCCCCCCCCCO[C@H]1C@@HO



FIRST AID MEASURES of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed
No data available



ACCIDENTAL RELEASE MEASURES of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Environmental precautions:
No special environmental precautions required.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Choose body protection in relation to its type.
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
No special environmental precautions required.



HANDLING and STORAGE of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Precautions for safe handling:
*Hygiene measures:
General industrial hygiene practice.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
*Storage stability:
Recommended storage temperature: -20 °C
*Storage class:
Storage class (TRGS 510): 13: Non Combustible Solids



STABILITY and REACTIVITY of LAURYL GLUCOSIDE (DODECYL GLUCOSIDE):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available