Textile, Leather, Paper and Industrial Chemicals

Lactate de butyle normal ( BUTYL LACTATE)
CALCIUM LACTATE, N° CAS : 814-80-2 - Lactate de calcium, Nom INCI : CALCIUM LACTATE, Nom chimique : Calcium dilactate, N° EINECS/ELINCS : 212-406-7, Additif alimentaire : E327, Astringent : Permet de resserrer les pores de la peau, Régulateur de pH : Stabilise le pH des cosmétiques, Kératolytique : Décolle et élimine les cellules mortes de la couche cornée de l'apiderme.Principaux synonymes. Noms français : 2-HYDROXYPROPANOIC ACID CALCIUM SALT; 2-HYDROXYPROPANOIC ACID, CALCIUM SALT; CALCIUM, LACTATE DE; HYDROXY-2 PROPANOATE DE CALCIUM; LACTATE DE CALCIUM; LACTIC ACID, CALCIUM SALT (2:1); PROPANOIC ACID, 2-HYDROXY-, CALCIUM SALT (2:1). Noms anglais :CALCIUM LACTATE; LACTIC ACID, CALCIUM SALT. Utilisation et sources d'émission :Additif alimentaire, fabrication de produits pharmaceutiques
Lactate de calcium ( CALCIUM LACTATE)
LAURYL LACTATE, Lactate de lauryle, N° CAS : 6283-92-7, Nom INCI : LAURYL LACTATE, Nom chimique : Dodecyl lactate, N° EINECS/ELINCS : 228-504-8 Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent d'entretien de la peau : Maintient la peau en bon état
Lactate de lauryle ( LAURYL LACTATE)
ETHYL LACTATE, N° CAS : 97-64-3. Nom INCI : ETHYL LACTATE. Nom chimique : Propanoic acid, 2-hydroxy-, ethyl ester. N° EINECS/ELINCS : 202-598-0. Solvant : Dissout d'autres substances Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. Noms français : Ethyl 2-hydropropionate Ethyl alpha-hydroxypropionate Ethyl hydroxy-2 propionate Lactate d'éthyle Lactic acid,ethyl ester Propanoic acid, 2-hydroxy-, ethyl ester Solactol Noms anglais : Ethyl lactate Famille chimique Ester Commentaires Le lactate d'éthyle existe sous deux formes isomériques, le (S)-lactate d'éthyle, qui est la forme L (CAS : 687-47-8) et le (R)-lactate d'éthyle, qui est la forme D (CAS : 7699-00-5); ce sont des images miroir l'une de l'autre. Le lactate d'éthyle vendu commercialement, sans désignation particulière quant à l'isomère présent, est un mélange de ces deux isomères, et il porte le numéro de CAS de la présente fiche (97-64-3). Utilisation: Le lactate d'éthyle est utilisé dans de nombreux domaines d'activité : décapage de peintures et de revêtements organiques dégraissage de pièces industrielles nettoyage de précision enlèvement des graffitis décapage d'adhésifs à base d’époxy nettoyage des presses offset formulation de produits cosmétiques et de préparations pharmaceutiques photolithographie (solvant de résine positive photosensible) polymères (solvant pour le nitrate de cellulose, l'acétobutyrate de cellulose, l'acétate de polyvinyle, les polyacrylates et polyméthacrylates, les résines polaires) synthèse organique de médicaments ou de produits agrochimiques (à partir d'un seul isomère) additif alimentaire, pharmaceutique ou cosmétique
Lactate d'éthyle ( ETHYL LACTATE)
SYNONYMS 2-Hydroxypropanoic acid; Lactic acid; 1-Hydroxyethanecarboxylic acid; Ethylidenelactic acid; alpha-Hydroxypropionic Acid; CAS NO 50-21-5, 79-33-4 (L), 10326-41-7 (D)
LACTIC ACID
LACTIC ACID Lactic acid Jump to navigationJump to search Lactic acid 7 Milchsäure.svg L-Lactic acid molecule spacefill.png Names Preferred IUPAC name 2-Hydroxypropanoic acid[1] Other names Lactic acid[1] Milk acid Identifiers CAS Number 50-21-5 check 79-33-4 (l) check 10326-41-7 (d) check 3D model (JSmol) Interactive image 3DMet B01180 Beilstein Reference 1720251 ChEBI CHEBI:422 check ChEMBL ChEMBL330546 check ChemSpider 96860 check ECHA InfoCard 100.000.017 Edit this at Wikidata EC Number 200-018-0 E number E270 (preservatives) Gmelin Reference 362717 IUPHAR/BPS 2932 KEGG C00186 PubChem CID 612 RTECS number OD2800000 UNII 33X04XA5AT ☒ UN number 3265 CompTox Dashboard (EPA) DTXSID7023192 Edit this at Wikidata InChI[show] SMILES[show] Properties Chemical formula C3H6O3 Molar mass 90.078 g·mol−1 Melting point 18 °C (64 °F; 291 K) Boiling point 122 °C (252 °F; 395 K) at 15 mmHg Solubility in water Miscible[2] Acidity (pKa) 3.86,[3] 15.1[4] Thermochemistry Std enthalpy of combustion (ΔcH⦵298) 1361.9 kJ/mol, 325.5 kcal/mol, 15.1 kJ/g, 3.61 kcal/g Pharmacology ATC code G01AD01 (WHO) QP53AG02 (WHO) Hazards GHS pictograms GHS05: Corrosive[5] GHS hazard statements H315, H318[5] GHS precautionary statements P280, P305+351+338[5] Related compounds Other anions Lactate Related carboxylic acids Acetic acid Glycolic acid Propionic acid 3-Hydroxypropanoic acid Malonic acid Butyric acid Hydroxybutyric acid Related compounds 1-Propanol 2-Propanol Propionaldehyde Acrolein Sodium lactate Ethyl lactate Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ☒ verify (what is check☒ ?) Infobox references Lactic acid is an organic acid. It has a molecular formula CH3CH(OH)COOH. It is white in the solid state and it is miscible with water.[2] When in the dissolved state, it forms a colorless solution. Production includes both artificial synthesis as well as natural sources. Lactic acid is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group. It is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries. The conjugate base of lactic acid is called lactate. In solution, it can ionize, producing the lactate ion CH 3CH(OH)CO− 2. Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid is ten times more acidic than acetic acid. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group. Lactic acid is chiral, consisting of two enantiomers. One is known as l-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is d-(−)-lactic acid or (R)-lactic acid. A mixture of the two in equal amounts is called dl-lactic acid, or racemic lactic acid. Lactic acid is hygroscopic. dl-Lactic acid is miscible with water and with ethanol above its melting point, which is around 16, 17 or 18 °C. d-Lactic acid and l-lactic acid have a higher melting point. Lactic acid produced by fermentation of milk is often racemic, although certain species of bacteria produce solely (R)-lactic acid. On the other hand, lactic acid produced by anaerobic respiration in animal muscles has the (S) configuration and is sometimes called "sarcolactic" acid, from the Greek "sarx" for flesh. In animals, l-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise.[6] It does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues.[7] The concentration of blood lactate is usually 1–2 mM at rest, but can rise to over 20 mM during intense exertion and as high as 25 mM afterward.[8][9] In addition to other biological roles, l-lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR).[10][11] In industry, lactic acid fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid. These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries.[12][13][14][15] In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution. These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns. Contents 1 History 2 Production 2.1 Fermentative production 2.2 Chemical production 3 Biology 3.1 Molecular biology 3.2 Exercise and lactate 3.3 Metabolism 4 Blood testing 5 Polymer precursor 6 Pharmaceutical and cosmetic applications 7 Foods 8 Forgery 9 Cleaning products 10 See also 11 References 12 External links History Swedish chemist Carl Wilhelm Scheele was the first person to isolate lactic acid in 1780 from sour milk.[16] The name reflects the lact- combining form derived from the Latin word lac, which means milk. In 1808, Jöns Jacob Berzelius discovered that lactic acid (actually l-lactate) also is produced in muscles during exertion.[17] Its structure was established by Johannes Wislicenus in 1873. In 1856, the role of Lactobacillus in the synthesis of lactic acid was discovered by Louis Pasteur. This pathway was used commercially by the German pharmacy Boehringer Ingelheim in 1895. In 2006, global production of lactic acid reached 275,000 tonnes with an average annual growth of 10%.[18] Production Lactic acid is produced industrially by bacterial fermentation of carbohydrates, or by chemical synthesis from acetaldehyde.[19] In 2009, lactic acid was produced predominantly (70–90%)[20] by fermentation. Production of racemic lactic acid consisting of a 1:1 mixture of d and l stereoisomers, or of mixtures with up to 99.9% l-lactic acid, is possible by microbial fermentation. Industrial scale production of d-lactic acid by fermentation is possible, but much more challenging. Fermentative production Fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria: Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus delbrueckii subsp. bulgaricus (Lactobacillus bulgaricus), Lactobacillus helveticus, Lactococcus lactis, and Streptococcus salivarius subsp. thermophilus (Streptococcus thermophilus). As a starting material for industrial production of lactic acid, almost any carbohydrate source containing C5 and C6 sugars can be used. Pure sucrose, glucose from starch, raw sugar, and beet juice are frequently used.[21] Lactic acid producing bacteria can be divided in two classes: homofermentative bacteria like Lactobacillus casei and Lactococcus lactis, producing two moles of lactate from one mole of glucose, and heterofermentative species producing one mole of lactate from one mole of glucose as well as carbon dioxide and acetic acid/ethanol.[22] Chemical production Racemic lactic acid is synthesized industrially by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile. When hydrolysis is performed by hydrochloric acid, ammonium chloride forms as a by-product; the Japanese company Musashino is one of the last big manufacturers of lactic acid by this route.[23] Synthesis of both racemic and enantiopure lactic acids is also possible from other starting materials (vinyl acetate, glycerol, etc.) by application of catalytic procedures.[24] Biology Molecular biology l-Lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), a Gi/o-coupled G protein-coupled receptor (GPCR).[10][11] Exercise and lactate During power exercises such as sprinting, when the rate of demand for energy is high, glucose is broken down and oxidized to pyruvate, and lactate is then produced from the pyruvate faster than the body can process it, causing lactate concentrations to rise. The production of lactate is beneficial for NAD+ regeneration (pyruvate is reduced to lactate while NADH is oxidized to NAD+), which is used up in oxidation of glyceraldehyde 3-phosphate during production of pyruvate from glucose, and this ensures that energy production is maintained and exercise can continue. During intense exercise, the respiratory chain cannot keep up with the amount of hydrogen ions that join to form NADH, and cannot regenerate NAD+ quickly enough. The resulting lactate can be used in two ways: Oxidation back to pyruvate by well-oxygenated muscle cells, heart cells, and brain cells Pyruvate is then directly used to fuel the Krebs cycle Conversion to glucose via gluconeogenesis in the liver and release back into circulation; see Cori cycle[25] If blood glucose concentrations are high, the glucose can be used to build up the liver's glycogen stores. However, lactate is continually formed even at rest and during moderate exercise. Some causes of this are metabolism in red blood cells that lack mitochondria, and limitations resulting from the enzyme activity that occurs in muscle fibers having high glycolytic capacity.[25] In 2004, Robergs et al. maintained that lactic acidosis during exercise is a "construct" or myth, pointing out that part of the H+ comes from ATP hydrolysis (ATP4− + H2O → ADP3− + HPO2− 4 + H+), and that reducing pyruvate to lactate (pyruvate− + NADH + H+ → lactate− + NAD+) actually consumes H+.[26] Lindinger et al.[27] countered that they had ignored the causative factors of the increase in [H+]. After all, the production of lactate− from a neutral molecule must increase [H+] to maintain electroneutrality. The point of Robergs's paper, however, was that lactate− is produced from pyruvate−, which has the same charge. It is pyruvate− production from neutral glucose that generates H+: Polymer precursor Main article: polylactic acid Two molecules of lactic acid can be dehydrated to the lactone lactide. In the presence of catalysts lactide polymerize to either atactic or syndiotactic polylactide (PLA), which are biodegradable polyesters. PLA is an example of a plastic that is not derived from petrochemicals. Pharmaceutical and cosmetic applications Lactic acid is also employed in pharmaceutical technology to produce water-soluble lactates from otherwise-insoluble active ingredients. It finds further use in topical preparations and cosmetics to adjust acidity and for its disinfectant and keratolytic properties. Foods Lactic acid is found primarily in sour milk products, such as koumiss, laban, yogurt, kefir, and some cottage cheeses. The casein in fermented milk is coagulated (curdled) by lactic acid. Lactic acid is also responsible for the sour flavor of sourdough bread. In lists of nutritional information lactic acid might be included under the term "carbohydrate" (or "carbohydrate by difference") because this often includes everything other than water, protein, fat, ash, and ethanol.[40] If this is the case then the calculated food energy may use the standard 4 kilocalories (17 kJ) per gram that is often used for all carbohydrates. But in some cases lactic acid is ignored in the calculation.[41] The energy density of lactic acid is 362 kilocalories (1,510 kJ) per 100 g.[42] Some beers (sour beer) purposely contain lactic acid, one such type being Belgian lambics. Most commonly, this is produced naturally by various strains of bacteria. These bacteria ferment sugars into acids, unlike the yeast that ferment sugar into ethanol. After cooling the wort, yeast and bacteria are allowed to “fall” into the open fermenters. Brewers of more common beer styles would ensure that no such bacteria are allowed to enter the fermenter. Other sour styles of beer include Berliner weisse, Flanders red and American wild ale.[43][44] In winemaking, a bacterial process, natural or controlled, is often used to convert the naturally present malic acid to lactic acid, to reduce the sharpness and for other flavor-related reasons. This malolactic fermentation is undertaken by lactic acid bacteria. While not normally found in significant quantities in fruit, lactic acid is the primary organic acid in akebia fruit, making up 2.12% of the juice.[45] As a food additive it is approved for use in the EU,[46] USA[47] and Australia and New Zealand;[48] it is listed by its INS number 270 or as E number E270. Lactic acid is used as a food preservative, curing agent, and flavoring agent.[49] It is an ingredient in processed foods and is used as a decontaminant during meat processing.[50] Lactic acid is produced commercially by fermentation of carbohydrates such as glucose, sucrose, or lactose, or by chemical synthesis.[49] Carbohydrate sources include corn, beets, and cane sugar.[51] Forgery Lactic acid has historically been used to assist with the erasure of inks from official papers to be modified during forgery.[52] Cleaning products Lactic acid is used in some liquid cleaners as a descaling agent for removing hard water deposits such as calcium carbonate, forming the lactate, Calcium lactate. Owing to its high acidity, such deposits are eliminated very quickly, especially where boiling water is used, as in kettles. It also is gaining popularity in antibacterial dish detergents and hand soaps replacing Triclosan. See also Hydroxybutyric acid Acids in wine Alanine cycle Biodegradable plastic Dental caries MCT1, a lactate transporter Thiolactic acid Lactic acid, or lactate, is a chemical byproduct of anaerobic respiration — the process by which cells produce energy without oxygen around. Bacteria produce it in yogurt and our guts. Lactic acid is also in our blood, where it's deposited by muscle and red blood cells. It was long thought that lactic acid was the cause of muscle soreness during and after an intense period of exercise, but recent research suggests that's not true, said Michael Gleeson, an exercise biochemist at Loughborough University in the U.K., and author of "Eat, Move, Sleep, Repeat" (Meyer & Meyer Sport, 2020). "Lactate has always been thought of as the bad boy of exercise," Gleeson told Live Science. Contrary to that reputation, lactic acid is a constant, harmless presence in our bodies. While it does increase in concentration when we exercise hard, it returns to normal levels as soon as we're able to rest — and even gets recycled back into energy our body can use later on, Gleeson said. CLOSE How muscles produce lactic acid Throughout most of the day, our body burns energy aerobically — that is, in the presence of oxygen. Part of that energy comes from sugar, which our muscle cells break down in a series of chemical reactions called glycolysis. (We also get energy from fat, but that involves a whole other chemical process). The end product of glycolysis is pyruvate, a chemical that the body uses to produce even more energy. But energy can be harvested from pyruvate only in the presence of oxygen. That changes during hard exercise. Related: Muscle spasms and cramps: Causes and treatments When you break into an all-out sprint your muscles start working overtime. The harder you work, the more energy your muscles need to sustain your pace. Luckily, our muscles have built-in turbo-boosters, called fast-twitch muscle. Unlike slow-twitch muscle, which we use for most of the day, fast-twitch muscle is super-effective at producing lots of energy quickly and does so anaerobically, Gleeson said. Fast-twitch muscle also uses glycolysis to produce energy, but it skips harvesting energy from pyruvate, a process that takes oxygen. Instead, pyruvate gets converted into a waste product, lactic acid, and released into the bloodstream. It's a common misconception that muscle cells produce lactic acid when they can't get enough oxygen, Gleeson said. "That's not the case. Your muscles are getting plenty of oxygen," he said. But in times of intense energy needs, muscles switch to anaerobic respiration simply because it's a much quicker way to produce energy. Other sources of lactic acid Muscle cells aren't the only sources of lactic acid. Red blood cells also produce lactic acid as they roam the body, according to the online text Anatomy and Physiology published by Oregon State University. Red blood cells don't have mitochondria — the part of the cell responsible for aerobic respiration — so they only respire anaerobically. Many species of bacteria also respire anaerobically and produce lactic acid as a waste product. In fact, these species make up between 0.01-1.8% of the human gut, according to a review published in the Journal of Applied Microbiology. The more sugar these little guys eat, the more lactic acid they produce. Slightly more insidious are the lactic acid bacteria that live in our mouths. Because of the acidifying effect they have on saliva, these bacteria are bad news for tooth enamel, according to a study published in Microbiology. Finally, lactic acid is commonly found in fermented dairy products, like buttermilk, yogurt and kefir. Bacteria in these foods use anaerobic respiration to break lactose — milk sugar — into lactic acid. That doesn't mean that lactic acid itself is a dairy product, however — it's 100% vegan. It happens to get its name from dairy simply because Carl Wilhelm, the first scientist to isolate lactic acid, did so from some spoiled milk, according to a study published in the American Journal of Physiology. A young girl eating yogurt out of a cup. Lactic acid is found in fermented dairy products, like yogurt, but lactic acid itself isn't dairy — it's 100% vegan. (Image credit: Shutterstock) Your body on lactic acid It's common to feel a burning in your legs after you squat with heavy weights, or complete a hard workout. But contrary to popular belief, it's not lactic acid that causes the soreness, Gleeson said. Lactic acid is processed by the liver and the heart. The liver converts it back into sugar; the heart converts it into pyruvate. During exercise, concentrations of lactic acid in the body do spike because the heart and liver can't deal with the waste product as quickly as it's produced. But as soon as we're done exercising, lactic acid concentrations go back to normal, Gleeson said. Related: Feel the pain? Don't blame lactic acid. Muscle soreness after exercise most likely has more to do with tissue damage and inflammation, Gleeson said. Hard exercise physically breaks down your muscles, and it can take days for them to recover. Lactic acid can build up to life-threatening levels in the body, according to a review published in the Mayo Clinic Proceedings. But this condition, called acute lactic acidosis, happens because of acute illness or injury, not exercise. When tissues are deprived of blood due to a heart attack or sepsis, for example, they tend to go into anaerobic respiration, producing lactic acid. "They get starved of oxygen," Gleeson said. But Gleeson said he's never heard of a case of life-threatening lactic acidosis because of exercise. "That would be most unusual." Additional resources: Read about anaerobic respiration on Khan Academy. Find out why you feel so sore after a workout. Learn about acute lactic acidosis on Medscape.
LACTIC ACID (2-HYDROXYPROPIONIC ACID)
Lactic acid (2-hydroxypropionic acid) is the most widely occurring organic acid in nature.
Due to its chiral a-carbon atom, Lactic acid (2-hydroxypropionic acid) has two enantiomeric forms.
Of these, Lactic acid (2-hydroxypropionic acid) is more important in food and pharmaceutical industries because humans have only L-lactate dehydrogenase.

CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0

Synonyms
FEMA 2611;DL-ALPHA-HYDROXYPROPIONIC ACID;DL-Lactic acid, ACS reagent, 85+%;LACTIC ACID, 85% REAGENT (ACS);Lactic;dl-lactic acid, acs;LACTICACID,RACEMIC,USP;2-Hydroxy-2-methylacetic acid
;lactic acid;2-hydroxypropanoic acid;DL-Lactic acid;50-21-5;2-hydroxypropionic acid;Milk acid;lactate;Tonsillosan;Racemic lactic acid;Ordinary lactic acid;Ethylidenelactic acid;26100-51-6;Lactovagan;Acidum lacticum;Milchsaeure;Lactic acid, dl-;Kyselina mlecna;Lacticum acidum;DL-Milchsaeure;Lactic acid USP;(+/-)-Lactic acid;Propanoic acid, 2-hydroxy-;Aethylidenmilchsaeure;598-82-3;1-Hydroxyethanecarboxylic acid;alpha-Hydroxypropionic acid;Lactic acid (natural);(RS)-2-Hydroxypropionsaeure;FEMA No. 2611;Milchsaure;Kyselina 2-hydroxypropanova;Lurex;Propionic acid, 2-hydroxy-;Purac FCC 80;Purac FCC 88;Cheongin samrakhan;DL- lactic acid;FEMA Number 2611;CCRIS 2951;HSDB 800;Cheongin Haewoohwan;Cheongin Haejanghwan;SY-83;2-Hydroxypropionicacid;(+-)-2-Hydroxypropanoic acid;Biolac;NSC 367919
;Lactic acid, tech grade;Chem-Cast;alpha-Hydroxypropanoic acid;AI3-03130;HIPURE 88;EINECS 200-018-0;EINECS 209-954-4;EPA Pesticide Chemical Code 128929;Lactic acid,buffered;NSC-367919;UNII-3B8D35Y7S4;2-Hydroxy-2-methylacetic acid;BRN 5238667;INS NO.270;DTXSID7023192;(+/-)-2-hydroxypropanoic acid;CHEBI:78320;INS-270;2 Hydroxypropanoic Acid;3B8D35Y7S4;E 270
;MFCD00004520;LACTIC ACID (+-);.alpha.-Hydroxypropanoic acid;.alpha.-Hydroxypropionic acid;DTXCID003192;E-270;EC 200-018-0;NCGC00090972-01;2-hydroxy-propionic acid;C01432;Milchsaure [German];Lactic acid [JAN];Kyselina mlecna [Czech];Propanoic acid, hydroxy-;CAS-50-21-5;(R)-2-Hydroxy-propionic acid;H-D-Lac-OH;2 Hydroxypropionic Acid;Kyselina 2-hydroxypropanova [Czech];Lactic acid [USP:JAN];lactasol;1-Hydroxyethane 1-carboxylic acid;acido lactico;DL-Milchsaure;MFCD00064266;(2RS)-2-Hydroxypropanoic acid;Lactate (TN);4b5w;Propanoic acid, (+-);DL-Lactic Acid, Racemic;LACTIC ACID (II);(.+/-.)-Lactic acid;Lactic acid (7CI,8CI);DL-Lactic Acid (90%);Lactic acid (JP17/USP);Lactic acid, 85%, FCC;Lactic Acid, Racemic, USP;NCIOpen2_000884;(+-)-LACTIC ACID;DL-LACTIC ACID [MI];LACTIC ACID [WHO-IP];(RS)-2-hydroxypropanoic acid;LACTIC ACID, DL-(II);LACTICUM ACIDUM [HPUS];1-hydroxyethane carboxylic acid;33X04XA5AT;DL-Lactic Acid (90per cent);L-(+)-Lactic acid, 98%;CHEMBL1200559;Lactic acid, natural, >=85%;BDBM23233;L-lactic acid or dl-lactic acid;Lactic Acid, 85 Percent, FCC;LACTIC ACID, DL- [II];DL-Lactic acid, ~90% (T);DL-Lactic acid, AR, >=88%;DL-Lactic acid, LR, >=88%;DL- LACTIC ACID [WHO-DD];LACTIC ACID (EP MONOGRAPH);Lactic Acid, 10 Percent Solution;HY-B2227;LACTIC ACID (USP MONOGRAPH);Propanoic acid, 2-hydroxy- (9CI);Tox21_111049;Tox21_202455;Tox21_303616;BBL027466;NSC367919;STL282744;AKOS000118855;AKOS17278364;Tox21_111049_1;ACIDUM LACTICUM [WHO-IP LATIN];AM87208;DB04398;SB44647;SB44652;Propanoic acid,2-hydroxy-,(.+/-.)-;2-Hydroxypropionic acid, DL-Lactic acid;NCGC00090972-02;NCGC00090972-03;NCGC00257515-01;NCGC00260004-01;849585-22-4;Lactic Acid, 85 Percent, Reagent, ACS;(R)-Lactate;(R)-2-Hydroxypropionic acid;;DB-071134;DB-347146;CS-0021601;L0226;EN300-19542;Lactic acid, meets USP testing specifications;D00111;F71201;A877374;DL-Lactic acid, SAJ first grade, 85.0-92.0%;Q161249;DL-Lactic acid, JIS special grade, 85.0-92.0%;Dl-alpha-hydroxypropionic acid;2-hydroxypropionic acid;F2191-0200;Z104474158;BC10F553-5D5D-4388-BB74-378ED4E24908;Lactic acid, United States Pharmacopeia (USP) Reference Standard;Lactic acid, Pharmaceutical Secondary Standard; Certified Reference Material;DL-Lactic acid 90%, synthetic, meets the analytical specifications of Ph. Eur.;152-36-3

The chemical behavior of Lactic acid (2-hydroxypropionic acid) is mostly determined by the two functional groups.
Besides the acidic character in aqueous medium, the bifunctionality (a terminal carboxylic acid and a hydroxyl group) allows Lactic acid (2-hydroxypropionic acid) molecules to form ‘‘interesters’’ such as the cyclic dimers, the trimers, or longer lactic acid oligomers.
After its first isolation by the Swedish chemist Scheel in 1780 from sour milk, Lactic acid (2-hydroxypropionic acid) has been produced commercially since the 1880s in the United States and later in Europe.
Worldwide, Lactic acid (2-hydroxypropionic acid) production was approximately 250,000 metric tons per year in 2012 and is expected to reach 330,000 metric tons by the year 2015, with an average price of 1.25 US$ per kilogram in 2013 (food grade, 80–85 % purity).
Approximately 85 % of the demand for LA is from the food industry.
The primary use of Lactic acid (2-hydroxypropionic acid) is as a pH-adjusting agent in the beverage sector and as a preservative in the food industry.

Lactic acid (2-hydroxypropionic acid) is included in the Generally Recognized as Safe (GRAS) by the U.S. Food and Drug Administration as a food ingredient and was deemed safe by the European Food Safety Authority as well.
The acceptable daily intake for Lactic acid (2-hydroxypropionic acid) was defined by the Joint FAO/WHO Expert Committee on Food Additives as ‘‘not limited,’’ and it is also supported by the Scientific Committee of Food.
In recent decades, the consumption of Lactic acid (2-hydroxypropionic acid) due to its novel applications has grown quite rapidly, by 19 % per year.
Nonfood use of Lactic acid (2-hydroxypropionic acid) for polymer production contributes to this growth.
Biodegradable polylactic acid is considered to be an environmentally friendly alternative to other plastics from petroleum.
Lactic acid (2-hydroxypropionic acid) is used in various fields, including drug delivery systems, medical devices, fibers, and packaging materials.
Lactic acid (2-hydroxypropionic acid) can be produced via chemical synthesis or carbohydrate fermentation.
The chemical route has various issues, including toxic raw materials, low conversion rates, and especially the inability to produce the optically pure isomer.
Therefore, approximately 90 % of Lactic acid (2-hydroxypropionic acid) worldwide is produced by biotechnological processes, namely fermentations using renewable resources, which is relatively fast, economical, and able to supply selectively one or two stereoisomers of lactic acid.

Lactic acid (2-hydroxypropionic acid) is an organic acid.
Lactic acid (2-hydroxypropionic acid) has the molecular formula CH3CH(OH)COOH.
Lactic acid (2-hydroxypropionic acid) is white in the solid state and it is miscible with water.
When in the dissolved state, Lactic acid (2-hydroxypropionic acid) forms a colorless solution.
Production includes both artificial synthesis as well as natural sources.
Lactic acid (2-hydroxypropionic acid) is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group.
Lactic acid (2-hydroxypropionic acid) is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries.

The conjugate base of Lactic acid (2-hydroxypropionic acid) is called lactate (or the lactate anion).
The name of the derived acyl group is lactoyl.
In solution, Lactic acid (2-hydroxypropionic acid) can ionize by a loss of a proton to produce the lactate ion CH
3CH(OH)CO−2.
Compared to acetic acid, its pKa is 1 unit less, meaning Lactic acid (2-hydroxypropionic acid) is ten times more acidic than acetic acid.
This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.

Lactic acid (2-hydroxypropionic acid) is chiral, consisting of two enantiomers.
One is known as Lactic acid (2-hydroxypropionic acid), (S)-lactic acid, or (+)-lactic acid, and the other, its mirror image, is d-lactic acid, (R)-lactic acid, or (−)-lactic acid.
A mixture of the two in equal amounts is called dl-lactic acid, or racemic Lactic acid (2-hydroxypropionic acid).
Lactic acid is hygroscopic.
Lactic acid (2-hydroxypropionic acid) is miscible with water and with ethanol above its melting point, which is about 16 to 18 °C (61 to 64 °F).
d-Lactic acid and l-lactic acid have a higher melting point.
Lactic acid (2-hydroxypropionic acid) produced by fermentation of milk is often racemic, although certain species of bacteria produce solely d-lactic acid.
On the other hand, Lactic acid (2-hydroxypropionic acid) produced by anaerobic respiration in animal muscles has the enantiomer and is sometimes called "sarcolactic" acid, from the Greek sarx, meaning "flesh".

In animals, Lactic acid (2-hydroxypropionic acid) is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise.
Lactic acid (2-hydroxypropionic acid) does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues.
The concentration of blood lactate is usually 1–2 mMTooltip millimolar at rest, but can rise to over 20 mM during intense exertion and as high as 25 mM afterward.
In addition to other biological roles, Lactic acid (2-hydroxypropionic acid) is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR).

In industry, Lactic acid (2-hydroxypropionic acid) fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid.
These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as cavities.
In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution.
These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood.
Lactic acid (2-hydroxypropionic acid) is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns.

Lactic acid (2-hydroxypropionic acid) is an alpha hydroxy acid, an organic compound with the formula CH3CH(OH)CO2H.
Lactic acid (2-hydroxypropionic acid) is a white, water-soluble solid or clear liquid,having a mild acid odor and taste.
Lactic acid (2-hydroxypropionic acid) is found in muscle tissue and blood and is an intermediate in the metabolism of carbohydrates.
Lactic acid (2-hydroxypropionic acid) is also used as an acidifying agent.
Lactic acid (2-hydroxypropionic acid) is produced from natural corn starch by advanced bio-fermentation and refining technology.

Lactic acid (2-hydroxypropionic acid) is a compound that plays a role in a variety of biochemical processes.
Lactic acid (2-hydroxypropionic acid) is a carboxylic acid with a molecular formula of C3H6O3.
Lactic acid (2-hydroxypropionic acid) is a carboxylic acid containing a hydroxyl group, so it is an alpha-hydroxy acid (AHA).
In the aqueous solution, Lactic acid (2-hydroxypropionic acid)'s carboxyl group releases a proton to produce the lactate ion CH3CHOHCOO.
During fermentation, lactate dehydrogenase converts pyruvate to Lactic acid (2-hydroxypropionic acid).
In general metabolism and exercise, Lactic acid (2-hydroxypropionic acid) is constantly produced, but its concentration generally does not increase.

Lactic acid (2-hydroxypropionic acid) Chemical Properties
Melting point: 18°C
Boiling point: 122 °C/15 mmHg (lit.)
Alpha: -0.05 º (c= neat 25 ºC)
Density: 1.209 g/mL at 25 °C (lit.)
Vapor density: 0.62 (vs air)
Vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
Refractive index: n20/D 1.4262
Fp: >230 °F
Storage temp.: 2-8°C
Solubility: Miscible with water and with ethanol (96 per cent).
Form: syrup
pka: 3.08(at 100℃)
Color: Colorless to yellow
Specific Gravity: 1.209
PH: 3.51(1 mM solution);2.96(10 mM solution);2.44(100 mM solution);
Odor: at 100.00 %. odorless
Odor Type: odorless
Water Solubility: SOLUBLE
Merck: 14,5336
JECFA Number: 930
BRN: 1209341
Dielectric constant: 22.0(16℃)
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: JVTAAEKCZFNVCJ-UHFFFAOYSA-N
LogP: -0.72
CAS DataBase Reference: 50-21-5(CAS DataBase Reference)
NIST Chemistry Reference: Lactic acid (2-hydroxypropionic acid) (50-21-5)
EPA Substance Registry System: Lactic acid (2-hydroxypropionic acid) (50-21-5)

Lactic acid (2-hydroxypropionic acid), CH3CHOHCOOH, also known as 2-hydroxypropanoic acid, is a hygroscopic liquid that exists in three isometric forms.
Lactic acid (2-hydroxypropionic acid) is found in blood and animal tissue as a product of glucose and glycogen metabolism.
Lactic acid (2-hydroxypropionic acid) is obtained by fermentation of sucrose (corn refining), The racemic mixture is present in foods prepared by bacterial fermentation or prepared synthetically.
Lactic acid (2-hydroxypropionic acid) is soluble in water,alcohol,and ether.
Lactic acid (2-hydroxypropionic acid) is used as a solvent, in manufacturing confectionery, and in medicine.
Lactic acid (2-hydroxypropionic acid) is odorless.
Lactic acid (2-hydroxypropionic acid) consists of a mixture of lactic acid (C3H6O3) and lactic acid lactate (C6H10O5).
The commercial product is the racemic form.

Lactic acid (2-hydroxypropionic acid) is usually available in solutions containing 50 to 90% lactic acid.
Lactic acid (2-hydroxypropionic acid) consists of a mixture of 2-hydroxypropionic acid, its condensation products, such as lactoyllactic acid and other polylactic acids, and water.
Lactic acid (2-hydroxypropionic acid) is usually in the form of the racemate, (RS)-lactic acid, but in some cases the (S)-(+)-isomer is predominant.
A colorless or yellowish, nearly odorless, syrupy liquid consisting of a mixture of lactic acid (C3H6O3) and lactic acid lactate (C6H10O5).
Lactic acid (2-hydroxypropionic acid) is obtained by the lactic fermentation of sugars or is prepared synthetically.
The commercial product is the racemic form.
Lactic acid (2-hydroxypropionic acid) is usually available in solutions containing the equivalent of from 50% to 90% lactic acid.
Lactic acid (2-hydroxypropionic acid) is hygroscopic, and when concentrated by boiling, the acid condenses to form lactic acid lactate, 2-(lactoyloxy)propanoic acid, which on dilution and heat ing hydrolyzes to lactic acid.
Lactic acid (2-hydroxypropionic acid) is miscible with water and with alcohol.

Uses
Lactic acid (2-hydroxypropionic acid) is a multi-purpose ingredient used as a preservative, exfoliant, moisturizer, and to provide acidity to a formulation.
In the body, Lactic acid (2-hydroxypropionic acid) is found in the blood and muscle tissue as a product of the metabolism of glucose and glycogen.
Lactic acid (2-hydroxypropionic acid) is also a component of the skin’s natural moisturizing factor.
Lactic acid (2-hydroxypropionic acid) has better water intake than glycerin.
Studies indicate an ability to increase the water-retention capacity of the stratum corneum.
They also show that the pliability of the stratum corneum layer is closely related to the absorption of Lactic acid (2-hydroxypropionic acid); that is, the greater the amount of absorbed lactic acid, the more pliable the stratum corneum layer.
Researchers report that continuous use of preparations formulated with lactic acid in concentrations ranging between 5 and 12 percent provided a mild to moderate improvement in fine wrinkling and promote softer, smoother skin.
Lactic acid (2-hydroxypropionic acid)'s exfoliating properties can help in the process of removing excess pigment from the surface of the skin, as well as improving skin texture and feel.

Lactic acid (2-hydroxypropionic acid) is an alpha hydroxy acid occurring in sour milk and other lesser-known sources, such as beer, pickles, and foods made through a process of bacterial fermentation.
Lactic acid (2-hydroxypropionic acid) is caustic when applied to the skin in highly concentrated solutions.
Lactic acid (2-hydroxypropionic acid) can be used in fruit wine, beverages, meat, food, pastry making, vegetables, pickling and canning processing, grain processing, fruit storage, etc., because Lactic acid (2-hydroxypropionic acid) has the ability to adjust pH, extend shelf life, flavor, maintain food color, and improve Product quality and other effects;
In terms of seasonings, the special sourness of Lactic acid (2-hydroxypropionic acid) can increase the deliciousness of food.
Adding an appropriate amount of Lactic acid (2-hydroxypropionic acid) to salads, soy sauce, vinegar and other seasonings can maintain the stability of the microorganisms in the product and make the taste more mild.
Lactic acid (2-hydroxypropionic acid) is an inherent ingredient in dairy products.
Lactic acid (2-hydroxypropionic acid) has the taste of dairy products and good antimicrobial effects.
Lactic acid (2-hydroxypropionic acid) has been widely used in foods such as blended yogurt, cheese, ice cream, etc., and has become a popular sour agent for dairy products.

Biology
Molecular biology
Lactic acid (2-hydroxypropionic acid) is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), a Gi/o-coupled G protein-coupled receptor (GPCR).

Exercise and lactate
During power exercises such as sprinting, when the rate of demand for energy is high, glucose is broken down and oxidized to pyruvate, and lactate is then produced from the pyruvate faster than the body can process Lactic acid (2-hydroxypropionic acid), causing lactate concentrations to rise.
The production of Lactic acid (2-hydroxypropionic acid) is beneficial for NAD+ regeneration (pyruvate is reduced to lactate while NADH is oxidized to NAD+), which is used up in oxidation of glyceraldehyde 3-phosphate during production of pyruvate from glucose, and this ensures that energy production is maintained and exercise can continue.
During intense exercise, the respiratory chain cannot keep up with the amount of hydrogen ions that join to form NADH, and cannot regenerate NAD+ quickly enough.

The resulting lactate can be used in two ways:

Oxidation back to pyruvate by well-oxygenated muscle cells, heart cells, and brain cells
Pyruvate is then directly used to fuel the Krebs cycle
Conversion to glucose via gluconeogenesis in the liver and release back into circulation; see Cori cycle
If blood glucose concentrations are high, the glucose can be used to build up the liver's glycogen stores.
However, lactate is continually formed at rest and during all exercise intensities.
Lactate serves as a metabolic fuel being produced and oxidatively disposed in resting and exercising muscle.
Some causes of this are metabolism in red blood cells that lack mitochondria, and limitations resulting from the enzyme activity that occurs in muscle fibers having high glycolytic capacity.
Lactic acidosis is a physiological condition characterized by accumulation of lactate (especially l-lactate), with formation of an excessively low pH in the tissues – a form of metabolic acidosis.

Lactic acidosis during exercise may occur due to the H+ from ATP hydrolysis (ATP4− + H2O → ADP3− + HPO2−4 + H+), and that reducing pyruvate to lactate (pyruvate− + NADH + H+ → lactate− + NAD+) actually consumes H+.
The causative factors of the increase in [H+] result from the production of lactate− from a neutral molecule, increasing [H+] to maintain electroneutrality.
A contrary view is that lactate− is produced from pyruvate−, which has the same charge.
Lactic acid (2-hydroxypropionic acid) is pyruvate− production from neutral glucose that generates H+:

C6H12O6 + 2 NAD+ + 2 ADP3− + 2 HPO2−4 → 2 CH3COCO−2 + 2 H+ + 2 NADH + 2 ATP4− + 2 H2O
Subsequent lactate− production absorbs these protons:

2 CH3COCO−2 + 2 H+ + 2 NADH → 2 CH3CH(OH)CO−2 + 2 NAD+
The combined effect is:

C6H12O6 + 2 ADP3− + 2HPO2−4 → 2 CH3CH(OH)CO−2 + 2 ATP4− + 2 H2O
Although the reaction glucose → 2 lactate− + 2 H+ releases two H+ when viewed on its own, the H+ are absorbed in the production of ATP.
On the other hand, the absorbed acidity is released during subsequent hydrolysis of ATP:

ATP4− + H2O → ADP3− + HPO2−4 + H+
So once the use of ATP is included, the overall reaction is

C6H12O6 → 2 CH3CH(OH)CO−2 + 2 H+

Neural tissue energy source
Although glucose is usually assumed to be the main energy source for living tissues, there are a few reports that indicate that Lactic acid (2-hydroxypropionic acid) is lactate, and not glucose, that is preferentially metabolized by neurons in the brain of several mammalian species (the notable ones being mice, rats, and humans).
According to the lactate-shuttle hypothesis, glial cells are responsible for transforming glucose into lactate, and for providing lactate to the neurons.
Because of this local metabolic activity of glial cells, the extracellular fluid immediately surrounding neurons strongly differs in composition from the blood or cerebrospinal fluid, being much richer with lactate, as was found in microdialysis studies.

Brain development metabolism
Some evidence suggests that lactate is important at early stages of development for brain metabolism in prenatal and early postnatal subjects, with lactate at these stages having higher concentrations in body liquids, and being utilized by the brain preferentially over glucose.
Lactic acid (2-hydroxypropionic acid) was also hypothesized that lactate may exert a strong action over GABAergic networks in the developing brain, making them more inhibitory than Lactic acid (2-hydroxypropionic acid) was previously assumed, acting either through better support of metabolites, or alterations in base intracellular pH levels, or both.

Studies of brain slices of mice show that β-hydroxybutyrate, Lactic acid (2-hydroxypropionic acid), and pyruvate act as oxidative energy substrates, causing an increase in the NAD(P)H oxidation phase, that glucose was insufficient as an energy carrier during intense synaptic activity and, finally, that Lactic acid (2-hydroxypropionic acid) can be an efficient energy substrate capable of sustaining and enhancing brain aerobic energy metabolism in vitro.
The study "provides novel data on biphasic NAD(P)H fluorescence transients, an important physiological response to neural activation that has been reproduced in many studies and that is believed to originate predominantly from activity-induced concentration changes to the cellular NADH pools."
Lactic acid (2-hydroxypropionic acid) can also serve as an important source of energy for other organs, including the heart and liver.
During physical activity, up to 60% of the heart muscle's energy turnover rate derives from Lactic acid (2-hydroxypropionic acid) oxidation.
LACTIC ACID (E270)
Lactic Acid (E270) (2-hydroxypropionic acid, CH3-CHOH-COOH) is the most widely occurring organic acid in nature.
Due to Lactic Acid (E270)s chiral a-carbon atom, lactic acid (LA) has two enantiomeric forms.
Of these, L-(+)-Lactic Acid (E270) is more important in food and pharmaceutical industries because humans have only L-lactate dehydrogenase.

CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0

The chemical behavior of Lactic Acid (E270) is mostly determined by the two functional groups.
Besides the acidic character in aqueous medium, the bifunctionality (a terminal carboxylic acid and a hydroxyl group) allows Lactic Acid (E270) molecules to form ‘‘interesters’’ such as the cyclic dimers, the trimers, or longer lactic acid oligomers.
After Lactic Acid (E270)s first isolation by the Swedish chemist Scheel in 1780 from sour milk, lactic acid has been produced commercially since the 1880s in the United States and later in Europe.
Worldwide, Lactic Acid (E270) production was approximately 250,000 metric tons per year in 2012 and is expected to reach 330,000 metric tons by the year 2015, with an average price of 1.25 US$ per kilogram in 2013 (food grade, 80–85 % purity).
Approximately 85 % of the demand for LA is from the food industry.
The primary use of Lactic Acid (E270) is as a pH-adjusting agent in the beverage sector and as a preservative in the food industry.
Lactic Acid (E270) is included in the Generally Recognized as Safe (GRAS) by the U.S. Food and Drug Administration as a food ingredient and was deemed safe by the European Food Safety Authority as well.
The acceptable daily intake for Lactic Acid (E270) was defined by the Joint FAO/WHO Expert Committee on Food Additives as ‘‘not limited,’’ and it is also supported by the Scientific Committee of Food.
In recent decades, the consumption of Lactic Acid (E270) due to its novel applications has grown quite rapidly, by 19 % per year.
Nonfood use of Lactic Acid (E270) for polymer production contributes to this growth.
Biodegradable polylactic acid is considered to be an environmentally friendly alternative to other plastics from petroleum.

Lactic Acid (E270) is used in various fields, including drug delivery systems, medical devices, fibers, and packaging materials.
Lactic Acid (E270) can be produced via chemical synthesis or carbohydrate fermentation.
The chemical route has various issues, including toxic raw materials, low conversion rates, and especially the inability to produce the optically pure isomer.
Therefore, approximately 90 % of Lactic Acid (E270) worldwide is produced by biotechnological processes, namely fermentations using renewable resources, which is relatively fast, economical, and able to supply selectively one or two stereoisomers of lactic acid.
A colorless to yellow odorless syrupy liquid.
Corrosive to metals and tissue.
Used to make cultured dairy products, as a food preservative, and to make chemicals.
Lactic Acid (E270) is an organic acid.
Lactic Acid (E270) has the molecular formula CH3CH(OH)COOH.
Lactic Acid (E270) is white in the solid state and it is miscible with water.
When in the dissolved state, Lactic Acid (E270) forms a colorless solution.
Production includes both artificial synthesis as well as natural sources.
Lactic Acid (E270) is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group.
Lactic Acid (E270) is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries.
The conjugate base of Lactic Acid (E270) is called lactate (or the lactate anion).
The name of the derived acyl group is lactoyl.
In solution, Lactic Acid (E270) can ionize by a loss of a proton to produce the lactate ion CH3CH(OH)CO−2.
Compared to acetic acid, Lactic Acid (E270)'s pKa is 1 unit less, meaning Lactic Acid (E270) is ten times more acidic than acetic acid.
This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.
Lactic Acid (E270) is chiral, consisting of two enantiomers.
One is known as l-lactic acid, (S)-lactic acid, or (+)-lactic acid, and the other, Lactic Acid (E270)'s mirror image, is d-lactic acid, (R)-lactic acid, or (−)-lactic acid.
A mixture of the two in equal amounts is called dl-lactic acid, or racemic lactic acid.
Lactic Acid (E270) is hygroscopic.
dl-Lactic acid is miscible with water and with ethanol above its melting point, which is about 16 to 18 °C (61 to 64 °F).
d-Lactic acid and l-lactic acid have a higher melting point.
Lactic Acid (E270) produced by fermentation of milk is often racemic, although certain species of bacteria produce solely d-lactic acid.

On the other hand, Lactic Acid (E270) produced by anaerobic respiration in animal muscles has the (l) enantiomer and is sometimes called "sarcolactic" acid, from the Greek sarx, meaning "flesh".
In animals, l-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise.
Lactic Acid (E270) does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues.
The concentration of blood lactate is usually 1–2 mMTooltip millimolar at rest, but can rise to over 20 mM during intense exertion and as high as 25 mM afterward.
In addition to other biological roles, l-lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR).
In industry, Lactic Acid (E270) fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid.
These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries.
In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution.
These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood.
Lactic Acid (E270) is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns.
Lactic Acid (E270), also known as Milk Acid, is found primarily in sour milk products, such as yoghurt, kefir, koumiss, lassi and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid (E270).
Lactic Acid (E270) is also responsible for the sour flavour of sourdough breads.
Lactic Acid (E270) is used in beer brewing, to lower the pH and increase the body of the beer.
Lactic Acid (E270) is also used in various beverages and cocktails to impart a sour taste.

Lactic Acid (E270) Chemical Properties
Melting point: 18°C
Boiling point: 122 °C/15 mmHg (lit.)
Alpha: -0.05 º (c= neat 25 ºC)
Density: 1.209 g/mL at 25 °C (lit.)
Vapor density: 0.62 (vs air)
Vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
Refractive index: n20/D 1.4262
Fp: >230 °F
Storage temp.: 2-8°C
Solubility: Miscible with water and with ethanol (96 per cent).
Form: syrup
Pka: 3.08(at 100℃)
Color: Colorless to yellow
Specific Gravity: 1.209
PH: 3.51(1 mM solution);2.96(10 mM solution);2.44(100 mM solution);
Odor: at 100.00 %. odorless
Odor Type: odorless
Water Solubility: SOLUBLE
Merck: 14,5336
JECFA Number: 930
BRN: 1209341
Dielectric constant: 22.0(16℃)
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: JVTAAEKCZFNVCJ-UHFFFAOYSA-N
LogP: -0.72
CAS DataBase Reference: 50-21-5(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 2-hydroxy-(50-21-5)
EPA Substance Registry System: Lactic Acid (E270) (50-21-5)

Chemical Properties
Lactic Acid (E270) is odorless.
Lactic Acid (E270) consists of a mixture of lactic acid (C3H6O3) and lactic acid lactate (C6H10O5).
The commercial product is the racemic form.
Lactic Acid (E270) is usually available in solutions containing 50 to 90% lactic acid.
Lactic Acid (E270), CH3CHOHCOOH, also known as 2-hydroxypropanoic acid, is a hygroscopic liquid that exists in three isometric forms.
Lactic Acid (E270) is found in blood and animal tissue as a product of glucose and glycogen metabolism.
Lactic Acid (E270) is obtained by fermentation of sucrose (corn refining), The racemic mixture is present in foods prepared by bacterial fermentation or prepared synthetically.
Lactic Acid (E270) is soluble in water,alcohol,and ether.

Lactic Acid (E270) is used as a solvent, in manufacturing confectionery, and in medicine.
Lactic Acid (E270) consists of a mixture of 2-hydroxypropionic acid, its condensation products, such as lactoyllactic acid and other polylactic acids, and water.
Lactic Acid (E270) is usually in the form of the racemate, (RS)-lactic acid, but in some cases the (S)-(+)-isomer is predominant.
Lactic Acid (E270) is a practically odorless, colorless or slightly yellowcolored, viscous, hygroscopic, nonvolatile liquid.
A colorless or yellowish, nearly odorless, syrupy liquid consisting of a mixture of Lactic Acid (E270) (C3H6O3) and lactic acid lactate (C6H10O5).
Lactic Acid (E270)is obtained by the lactic fermentation of sugars or is prepared synthetically.
The commercial product is the racemic form.
Lactic Acid (E270) is usually available in solutions containing the equivalent of from 50% to 90% lactic acid.
Lactic Acid (E270) is hygroscopic, and when concentrated by boiling, the acid condenses to form lactic acid lactate, 2-(lactoyloxy)propanoic acid, which on dilution and heat ing hydrolyzes to lactic acid.
Lactic Acid (E270) is miscible with water and with alcohol.

Uses
Lactic Acid (E270) is a multi-purpose ingredient used as a preservative, exfoliant, moisturizer, and to provide acidity to a formulation.
In the body, Lactic Acid (E270) is found in the blood and muscle tissue as a product of the metabolism of glucose and glycogen.
Lactic Acid (E270) is also a component of the skin’s natural moisturizing factor.
Lactic Acid (E270) has better water intake than glycerin.
Studies indicate an ability to increase the water-retention capacity of the stratum corneum.
They also show that the pliability of the stratum corneum layer is closely related to the absorption of lactic acid; that is, the greater the amount of absorbed Lactic Acid (E270), the more pliable the stratum corneum layer.
Researchers report that continuous use of preparations formulated with lactic acid in concentrations ranging between 5 and 12 percent provided a mild to moderate improvement in fine wrinkling and promote softer, smoother skin.
Lactic Acid (E270)'s exfoliating properties can help in the process of removing excess pigment from the surface of the skin, as well as improving skin texture and feel.
Lactic Acid (E270) is an alpha hydroxy acid occurring in sour milk and other lesser-known sources, such as beer, pickles, and foods made through a process of bacterial fermentation.

Lactic Acid (E270) is caustic when applied to the skin in highly concentrated solutions.
Lactic Acid is an acidulant that is a natural organic acid present in milk, meat, and beer, but is normally associated with milk.
Lactic Acid (E270) is a syrupy liquid available as 50 and 88% aqueous solutions, and is mis- cible in water and alcohol.
Lactic Acid (E270) is heat stable, nonvolatile, and has a smooth, milk acid taste.
Lactic Acid (E270) functions as a flavor agent, preservative, and acidity adjuster in foods.
Lactic Acid (E270) is used in spanish olives to prevent spoilage and provide flavor, in dry egg powder to improve disper- sion and whipping properties, in cheese spreads, and in salad dress- ing mixes.
Lactic Acid (E270) showed good depressing effect on hornblende, pyroxene and biotite during flotation of hematite and ilmenite minerals.
Lactic Acid (E270) is used in some liquid cleaners as a descaling agent for removing hard water deposits such as calcium carbonate, forming the lactate, calcium lactate.
Owing to Lactic Acid (E270)'s high acidity, such deposits are eliminated very quickly, especially where boiling water is used, as in kettles.
Lactic Acid (E270) is used in some antibacterial soaps and dish detergents as a replacement for triclosan.
Lactic Acid (E270) has historically been used to assist with the erasure of inks from official papers to be modified during forgery.

Production Methods
Lactic Acid (E270) is prepared by the fermentation of carbohydrates, such as glucose, sucrose, and lactose, with Bacillus acidi lacti or related microorganisms.
On a commercial scale, whey, corn starch, potatoes, or molasses are used as a source of carbohydrate.
Lactic Acid (E270) may also be prepared synthetically by the reaction between acetaldehyde and carbon monoxide at 130–200°C under high pressure, or by the hydrolysis of hexoses with sodium hydroxide.
Lactic Acid (E270) prepared by the fermentation of sugars is levorotatory; lactic acid prepared synthetically is racemic.
However, Lactic Acid (E270) prepared by fermentation becomes dextrorotatory on dilution with water owing to the hydrolysis of (R)-lactic acid lactate to (S)- lactic acid.

Fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria: Lactobacillus acidophilus, Lacticaseibacillus casei (Lactobacillus casei), Lactobacillus delbrueckii subsp. bulgaricus (Lactobacillus bulgaricus), Lactobacillus helveticus, Lactococcus lactis , Bacillus amyloliquefaciens, and Streptococcus salivarius subsp. thermophilus (Streptococcus thermophilus).
As a starting material for industrial production of lactic acid, almost any carbohydrate source containing C5 (Pentose sugar) and C6 (Hexose sugar) can be used.
Pure sucrose, glucose from starch, raw sugar, and beet juice are frequently used.
Lactic Acid (E270) producing bacteria can be divided in two classes: homofermentative bacteria like Lactobacillus casei and Lactococcus lactis, producing two moles of lactate from one mole of glucose, and heterofermentative species producing one mole of lactate from one mole of glucose as well as carbon dioxide and acetic acid/ethanol.

Biochem Actions
In animals, Lactic Acid (E270) is a metabolic compound produced by proliferating cells and during anaerobic conditions such as strenuous exercise.
Lactic Acid (E270) can be oxidized back to pyruvate or converted to glucose via gluconeogenesis.
Lactic Acid (E270) is preferentially metabolized by neurons in several mammal species and during early brain development.

Synonyms
lactic acid
2-hydroxypropanoic acid
DL-Lactic acid
50-21-5
2-hydroxypropionic acid
Milk acid
lactate
Tonsillosan
Racemic lactic acid
Ordinary lactic acid
Ethylidenelactic acid
Lactovagan
Acidum lacticum
26100-51-6
Milchsaeure
Lactic acid, dl-
Kyselina mlecna
Lacticum acidum
DL-Milchsaeure
Lactic acid USP
(+/-)-Lactic acid
Propanoic acid, 2-hydroxy-
Aethylidenmilchsaeure
598-82-3
1-Hydroxyethanecarboxylic acid
alpha-Hydroxypropionic acid
Lactic acid (natural)
(RS)-2-Hydroxypropionsaeure
FEMA No. 2611
Milchsaure
Kyselina 2-hydroxypropanova
Lurex
Propionic acid, 2-hydroxy-
Purac FCC 80
Purac FCC 88
Cheongin samrakhan
FEMA Number 2611
CCRIS 2951
HSDB 800
Cheongin Haewoohwan
Cheongin Haejanghwan
SY-83
2-Hydroxypropionicacid
(+-)-2-Hydroxypropanoic acid
Biolac
NSC 367919
Lactic acid, tech grade
Chem-Cast
alpha-Hydroxypropanoic acid
AI3-03130
HIPURE 88
DL- lactic acid
EINECS 200-018-0
EINECS 209-954-4
EPA Pesticide Chemical Code 128929
Lactic acid,buffered
NSC-367919
UNII-3B8D35Y7S4
2-Hydroxy-2-methylacetic acid
BRN 5238667
INS NO.270
DTXSID7023192
(+/-)-2-hydroxypropanoic acid
CHEBI:78320
INS-270
3B8D35Y7S4
E 270
MFCD00004520
LACTIC ACID (+-)
.alpha.-Hydroxypropanoic acid
.alpha.-Hydroxypropionic acid
DTXCID003192
E-270
EC 200-018-0
NCGC00090972-01
2-hydroxy-propionic acid
(R)-2-Hydroxy-propionic acid;H-D-Lac-OH
C01432
Milchsaure [German]
Lactic acid [JAN]
Kyselina mlecna [Czech]
Propanoic acid, hydroxy-
CAS-50-21-5
2 Hydroxypropanoic Acid
2 Hydroxypropionic Acid
Kyselina 2-hydroxypropanova [Czech]
Lactic acid [USP:JAN]
lactasol
1-Hydroxyethane 1-carboxylic acid
acido lactico
DL-Milchsaure
(2RS)-2-Hydroxypropanoic acid
Lactate (TN)
4b5w
Propanoic acid, (+-)
DL-Lactic Acid, Racemic
LACTIC ACID (II)
(.+/-.)-Lactic acid
Lactic acid (7CI,8CI)
Lactic acid (JP17/USP)
Lactic acid, 85%, FCC
Lactic Acid, Racemic, USP
NCIOpen2_000884
(+-)-LACTIC ACID
DL-LACTIC ACID [MI]
LACTIC ACID [WHO-IP]
(RS)-2-hydroxypropanoic acid
LACTIC ACID, DL-(II)
LACTICUM ACIDUM [HPUS]
1-hydroxyethane carboxylic acid
33X04XA5AT
DL-Lactic Acid (90per cent)
CHEMBL1200559
Lactic acid, natural, >=85%
BDBM23233
L-lactic acid or dl-lactic acid
Lactic Acid, 85 Percent, FCC
LACTIC ACID, DL- [II]
DL-Lactic acid, ~90% (T)
DL-Lactic acid, AR, >=88%
DL-Lactic acid, LR, >=88%
DL- LACTIC ACID [WHO-DD]
LACTIC ACID (EP MONOGRAPH)
Lactic Acid, 10 Percent Solution
HY-B2227
LACTIC ACID (USP MONOGRAPH)
Propanoic acid, 2-hydroxy- (9CI)
Tox21_111049
Tox21_202455
Tox21_303616
NSC367919
AKOS000118855
AKOS017278364
Tox21_111049_1
ACIDUM LACTICUM [WHO-IP LATIN]
AM87208
DB04398
SB44647
SB44652
Propanoic acid,2-hydroxy-,(.+/-.)-
2-Hydroxypropionic acid, DL-Lactic acid
NCGC00090972-02
NCGC00090972-03
NCGC00257515-01
NCGC00260004-01
26811-96-1
Lactic Acid, 85 Percent, Reagent, ACS
CS-0021601
FT-0624390
FT-0625477
FT-0627927
FT-0696525
FT-0774042
L0226
EN300-19542
Lactic acid, meets USP testing specifications
D00111
F71201
A877374
DL-Lactic acid, SAJ first grade, 85.0-92.0%
Q161249
DL-Lactic acid, JIS special grade, 85.0-92.0%
F2191-0200
Z104474158
BC10F553-5D5D-4388-BB74-378ED4E24908
Lactic acid, United States Pharmacopeia (USP) Reference Standard
Lactic acid, Pharmaceutical Secondary Standard; Certified Reference Material
DL-Lactic acid 90%, synthetic, meets the analytical specifications of Ph. Eur.
152-36-3
LACTIC ACID (MILK ACID)
DESCRIPTION:
Lactic acid (milk acid) is an organic acid.
Lactic acid (milk acid)has a molecular formula CH3CH(OH)COOH.
Lactic acid (milk acid)is white in the solid state and it is miscible with water.


CAS Number: 50-21-5
EC Number: 200-018-0

When in the dissolved state, Lactic acid (milk acid) forms a colorless solution.
Production includes both artificial synthesis as well as natural sources.
Lactic acid (milk acid)is an alpha-hydroxy acid (AHA) due to the presence of a hydroxyl group adjacent to the carboxyl group.

Lactic acid (milk acid)is used as a synthetic intermediate in many organic synthesis industries and in various biochemical industries.
The conjugate base of Lactic acid (milk acid) is called lactate (or the lactate anion).
The name of the derived acyl group is lactoyl.









In solution, it can ionize by loss of a proton to produce the lactate ion CH3CH(OH)CO−2.
Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid is ten times more acidic than acetic acid.
This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.

Lactic acid is chiral, consisting of two enantiomers.
One is known as l-lactic acid, (S)-lactic acid, or (+)-lactic acid, and the other, its mirror image, is d-lactic acid, (R)-lactic acid, or (−)-lactic acid.
A mixture of the two in equal amounts is called dl-lactic acid, or racemic lactic acid. Lactic acid is hygroscopic.

dl-Lactic acid is miscible with water and with ethanol above its melting point, which is about 16 to 18 °C (61 to 64 °F).
d-Lactic acid and l-lactic acid have a higher melting point.
Lactic acid produced by fermentation of milk is often racemic, although certain species of bacteria produce solely d-lactic acid.

On the other hand, lactic acid produced by anaerobic respiration in animal muscles has the (l) enantiomer and is sometimes called "sarcolactic" acid, from the Greek sarx, meaning "flesh".

In animals, l-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise.
It does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues.

The concentration of blood lactate is usually 1–2 mMTooltip millimolar at rest, but can rise to over 20 mM during intense exertion and as high as 25 mM afterward.
In addition to other biological roles, l-lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR).


In industry, lactic acid fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid.
These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries.
In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution.

These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood.
It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns.

HISTORY OF LACTIC ACID (MILK ACID):
Swedish chemist Carl Wilhelm Scheele was the first person to isolate lactic acid in 1780 from sour milk.
The name reflects the lact- combining form derived from the Latin word lac, meaning "milk".
In 1808, Jöns Jacob Berzelius discovered that lactic acid (actually l-lactate) also is produced in muscles during exertion.
Its structure was established by Johannes Wislicenus in 1873.

In 1856, the role of Lactobacillus in the synthesis of lactic acid was discovered by Louis Pasteur.
This pathway was used commercially by the German pharmacy Boehringer Ingelheim in 1895.
In 2006, global production of lactic acid reached 275,000 tonnes with an average annual growth of 10%.

PRODUCTION OF LACTIC ACID (MILK ACID):
Lactic acid is produced industrially by bacterial fermentation of carbohydrates, or by chemical synthesis from acetaldehyde.
As of 2009, lactic acid was produced predominantly (70–90%) by fermentation.

Production of racemic lactic acid consisting of a 1:1 mixture of d and l stereoisomers, or of mixtures with up to 99.9% l-lactic acid, is possible by microbial fermentation.
Industrial scale production of d-lactic acid by fermentation is possible, but much more challenging.

FERMENTATIVE PRODUCTION OF LACTIC ACID (MILK ACID):
Fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria: Lactobacillus acidophilus, Lacticaseibacillus casei (Lactobacillus casei), Lactobacillus delbrueckii subsp. bulgaricus (Lactobacillus bulgaricus), Lactobacillus helveticus, Lactococcus lactis , Bacillus amyloliquefaciens, and Streptococcus salivarius subsp. thermophilus (Streptococcus thermophilus).

As a starting material for industrial production of lactic acid, almost any carbohydrate source containing C5 (Pentose sugar) and C6 (Hexose sugar) can be used.

Pure sucrose, glucose from starch, raw sugar, and beet juice are frequently used.
Lactic acid producing bacteria can be divided in two classes: homofermentative bacteria like Lactobacillus casei and Lactococcus lactis, producing two moles of lactate from one mole of glucose, and heterofermentative species producing one mole of lactate from one mole of glucose as well as carbon dioxide and acetic acid/ethanol.

CHEMICAL PRODUCTION OF LACTIC ACID (MILK ACID):
Racemic lactic acid is synthesized industrially by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile.
When hydrolysis is performed by hydrochloric acid, ammonium chloride forms as a by-product; the Japanese company Musashino is one of the last big manufacturers of lactic acid by this route.
Synthesis of both racemic and enantiopure lactic acids is also possible from other starting materials (vinyl acetate, glycerol, etc.) by application of catalytic procedures.

BIOLOGY OF LACTIC ACID (MILK ACID):
Molecular biology
l-Lactic acid is the primary endogenous agonist of hydroxycarboxylic acid receptor 1 (HCA1), a Gi/o-coupled G protein-coupled receptor (GPCR).

During power exercises such as sprinting, when the rate of demand for energy is high, glucose is broken down and oxidized to pyruvate, and lactate is then produced from the pyruvate faster than the body can process it, causing lactate concentrations to rise.
The production of lactate is beneficial for NAD+ regeneration (pyruvate is reduced to lactate while NADH is oxidized to NAD+), which is used up in oxidation of glyceraldehyde 3-phosphate during production of pyruvate from glucose, and this ensures that energy production is maintained and exercise can continue.
During intense exercise, the respiratory chain cannot keep up with the amount of hydrogen ions that join to form NADH, and cannot regenerate NAD+ quickly enough.

The resulting lactate can be used in two ways:

Oxidation back to pyruvate by well-oxygenated muscle cells, heart cells, and brain cells
Pyruvate is then directly used to fuel the Krebs cycle
Conversion to glucose via gluconeogenesis in the liver and release back into circulation

If blood glucose concentrations are high, the glucose can be used to build up the liver's glycogen stores.
However, lactate is continually formed at rest and during all exercise intensities.
Lactate serves as a metabolic fuel being produced and oxidatively disposed in resting and exercising muscle.

Some causes of this are metabolism in red blood cells that lack mitochondria, and limitations resulting from the enzyme activity that occurs in muscle fibers having high glycolytic capacity.
Lactic acidosis is a physiological condition characterized by accumulation of lactate (especially l-lactate), with formation of an excessively low pH in the tissues – a form of metabolic acidosis.

Lactic acidosis during exercise may occur due to the H+ from ATP hydrolysis (ATP4− + H2O → ADP3− + HPO2−4 + H+), and that reducing pyruvate to lactate (pyruvate− + NADH + H+ → lactate− + NAD+) actually consumes H+.
The causative factors of the increase in [H+] result from the production of lactate− from a neutral molecule, increasing [H+] to maintain electroneutrality.
A contrary view is that lactate− is produced from pyruvate−, which has the same charge.
It is pyruvate− production from neutral glucose that generates H+:
C6H12O6 + 2 NAD+ + 2 ADP3− + 2 HPO2−4 →2 CH3COCO−2 + 2 H+ + 2 NADH + 2 ATP4− + 2 H2O
Subsequent lactate− production absorbs these protons:
2 CH3COCO−2 + 2 H+ + 2 NADH → 2 CH3CH(OH)CO−2 + 2 NAD+

Overall:
C6H12O6 + 2 NAD+ + 2 ADP3− + 2 HPO2−4 → 2 CH3COCO−2 + 2 H+ + 2 NADH + 2 ATP4− + 2 H2O→ 2 CH3CH(OH)CO−2 + 2 NAD+ + 2 ATP4− + 2 H2O
Although the reaction glucose → 2 lactate− + 2 H+ releases two H+ when viewed on its own, the H+ are absorbed in the production of ATP.
On the other hand, the absorbed acidity is released during subsequent hydrolysis of ATP: ATP4− + H2O → ADP3− + HPO2−4 + H+.

So once the use of ATP is included, the overall reaction is
C6H12O6 → 2 CH3COCO−2 + 2 H+
The generation of CO2 during respiration also causes an increase in [H+].

Neural tissue energy source
Although glucose is usually assumed to be the main energy source for living tissues, there are a few reports that indicate that it is lactate, and not glucose, that is preferentially metabolized by neurons in the brain of several mammalian species (the notable ones being mice, rats, and humans).
According to the lactate-shuttle hypothesis, glial cells are responsible for transforming glucose into lactate, and for providing lactate to the neurons.
Because of this local metabolic activity of glial cells, the extracellular fluid immediately surrounding neurons strongly differs in composition from the blood or cerebrospinal fluid, being much richer with lactate, as was found in microdialysis studies.

Brain development metabolism:
Some evidence suggests that lactate is important at early stages of development for brain metabolism in prenatal and early postnatal subjects, with lactate at these stages having higher concentrations in body liquids, and being utilized by the brain preferentially over glucose.
It was also hypothesized that lactate may exert a strong action over GABAergic networks in the developing brain, making them more inhibitory than it was previously assumed, acting either through better support of metabolites, or alterations in base intracellular pH levels, or both.

Studies of brain slices of mice show that β-hydroxybutyrate, lactate, and pyruvate act as oxidative energy substrates, causing an increase in the NAD(P)H oxidation phase, that glucose was insufficient as an energy carrier during intense synaptic activity and, finally, that lactate can be an efficient energy substrate capable of sustaining and enhancing brain aerobic energy metabolism in vitro.

The study "provides novel data on biphasic NAD(P)H fluorescence transients, an important physiological response to neural activation that has been reproduced in many studies and that is believed to originate predominantly from activity-induced concentration changes to the cellular NADH pools."

Lactate can also serve as an important source of energy for other organs, including the heart and liver.
During physical activity, up to 60% of the heart muscle's energy turnover rate derives from lactate oxidation.

Blood testing:
Reference ranges for blood tests, comparing lactate content (shown in violet at center-right) to other constituents in human blood
Blood tests for lactate are performed to determine the status of the acid base homeostasis in the body.
Blood sampling for this purpose is often arterial (even if it is more difficult than venipuncture), because lactate levels differ substantially between arterial and venous, and the arterial level is more representative for this purpose.


USES OF LACTIC ACID (MILK ACID):
Polymer precursor
Two molecules of lactic acid can be dehydrated to the lactone lactide. In the presence of catalysts lactide polymerize to either atactic or syndiotactic polylactide (PLA), which are biodegradable polyesters.
PLA is an example of a plastic that is not derived from petrochemicals.

Pharmaceutical and cosmetic applications:
Lactic acid is also employed in pharmaceutical technology to produce water-soluble lactates from otherwise-insoluble active ingredients.
It finds further use in topical preparations and cosmetics to adjust acidity and for its disinfectant and keratolytic properties.

Lactic acid containing bacteria have shown promise in reducing oxaluria with its descaling properties on calcium compounds.

Foods:
Fermented food:
Lactic acid is found primarily in sour milk products, such as kumis, laban, yogurt, kefir, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by lactic acid.
Lactic acid is also responsible for the sour flavor of sourdough bread.

In lists of nutritional information lactic acid might be included under the term "carbohydrate" (or "carbohydrate by difference") because this often includes everything other than water, protein, fat, ash, and ethanol.
If this is the case then the calculated food energy may use the standard 4 kilocalories (17 kJ) per gram that is often used for all carbohydrates.

But in some cases lactic acid is ignored in the calculation.
The energy density of lactic acid is 362 kilocalories (1,510 kJ) per 100 g.

Some beers (sour beer) purposely contain lactic acid, one such type being Belgian lambics.
Most commonly, this is produced naturally by various strains of bacteria.
These bacteria ferment sugars into acids, unlike the yeast that ferment sugar into ethanol.

After cooling the wort, yeast and bacteria are allowed to "fall" into the open fermenters.
Brewers of more common beer styles would ensure that no such bacteria are allowed to enter the fermenter.
Other sour styles of beer include Berliner weisse, Flanders red and American wild ale.

In winemaking, a bacterial process, natural or controlled, is often used to convert the naturally present malic acid to lactic acid, to reduce the sharpness and for other flavor-related reasons.
This malolactic fermentation is undertaken by lactic acid bacteria.
While not normally found in significant quantities in fruit, lactic acid is the primary organic acid in akebia fruit, making up 2.12% of the juice.

As a food additive it is approved for use in the EU,United States and Australia and New Zealand; it is listed by its INS number 270 or as E number E270.
Lactic acid is used as a food preservative, curing agent, and flavoring agent.
Lactic acid is an ingredient in processed foods and is used as a decontaminant during meat processing.

Lactic acid is produced commercially by fermentation of carbohydrates such as glucose, sucrose, or lactose, or by chemical synthesis.
Carbohydrate sources include corn, beets, and cane sugar.


CHEMICAL AND PHYSICAL PROPERTIES OF LACTIC ACID (MILK ACID):
Chemical formula C3H6O3
Molar mass 90.078 g•mol−1
Melting point 18 °C (64 °F; 291 K)
Boiling point 122 °C (252 °F; 395 K) at 15 mmHg
Solubility in water Miscible
Acidity (pKa) 3.86, 15.1
Thermochemistry
Std enthalpy of combustion (ΔcH⦵298) 1361.9 kJ/mol, 325.5 kcal/mol, 15.1 kJ/g, 3.61 kcal/g




SAFETY INFORMATION ABOUT LACTIC ACID (MILK 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


LACTIC ACID (MILK ACID)

Lactic acid (Milk acid), also known as milk acid, is a chemical compound with the molecular formula C3H6O3.
Lactic acid (Milk acid) is classified as an alpha-hydroxy acid (AHA) due to its structure containing a hydroxyl group adjacent to the carboxylic acid group.
Lactic acid (Milk acid) exists in two optical isomers: L-Lactic acid (Milk acid) and D-Lactic acid (Milk acid).

CAS Number: 50-21-5
EC Number: 200-018-0

Lactate, 2-Hydroxypropanoic acid, 2-Hydroxypropionic acid, alpha-Hydroxypropionic acid, 2-Hydroxypropanoate, alpha-Hydroxypropanoate, Ethylidene Lactic acid (Milk acid), Hydroxyacetic acid, SarcoLactic acid (Milk acid), 2-Hydroxypropanedioic acid, alpha-Hydroxypropanedioic acid, 2-Hydroxypropanedioate



APPLICATIONS


Lactic acid (Milk acid) is widely used in the food and beverage industry as an acidulant, flavoring agent, and preservative.
Lactic acid (Milk acid) is commonly added to dairy products, such as yogurt and cheese, to enhance flavor and acidity.
Lactic acid (Milk acid) serves as a key ingredient in the production of sourdough bread, giving it its characteristic tangy taste.
In the pharmaceutical industry, Lactic acid (Milk acid) is utilized as an excipient in drug formulations and as a pH adjuster in topical preparations.

Lactic acid (Milk acid) is employed in cosmetic products, including skin creams, lotions, and peels, for its exfoliating and moisturizing properties.
Lactic acid (Milk acid) is used in the textile industry for dyeing and finishing processes, acting as a mordant to improve color fastness.

In the agricultural sector, Lactic acid (Milk acid) is used as a crop preservative and soil conditioner to improve nutrient uptake and soil structure.
Lactic acid (Milk acid) fermentation is utilized in the production of fermented foods and beverages, such as kimchi, sauerkraut, and kombucha.

Lactic acid (Milk acid) is added to animal feed as a growth promoter and to improve digestibility in livestock.
Lactic acid (Milk acid) is employed in the production of biodegradable plastics and polymers as a precursor in polymerization reactions.
In the medical field, Lactic acid (Milk acid) is used as a diagnostic marker for conditions such as Lactic acid (Milk acid)osis and sepsis.

Lactic acid (Milk acid) serves as a chelating agent in metal cleaning and descaling formulations, aiding in the removal of mineral deposits.
Lactic acid (Milk acid) is utilized in the manufacture of biodegradable solvents and cleaning agents for industrial and household applications.

Lactic acid (Milk acid) is added to personal care products, including shampoos, conditioners, and soaps, for its antimicrobial and pH-balancing properties.
Lactic acid (Milk acid) is employed in the production of biodegradable polymers for use in agricultural mulches and packaging materials.

Lactic acid (Milk acid) serves as a corrosion inhibitor in metalworking fluids and cooling water treatments to prevent rust and scale formation.
Lactic acid (Milk acid) is utilized in the production of lactate esters, which are used as plasticizers, solvents, and surfactants in various applications.
In the brewing industry, Lactic acid (Milk acid) bacteria are used to produce sour beers, imparting tartness and complexity to the final product.

Lactic acid (Milk acid) is added to detergents and cleaning products as a pH adjuster and to enhance their effectiveness against grease and stains.
Lactic acid (Milk acid) is employed in the textile industry for dyeing and finishing processes, improving color retention and fabric softness.
In the paper and pulp industry, Lactic acid (Milk acid) is used as a pulping aid to improve fiber bonding and paper strength.

Lactic acid (Milk acid) serves as a fermentation substrate in the production of biofuels, such as ethanol and butanol, from renewable feedstocks.
Lactic acid (Milk acid) is utilized in the production of biodegradable polymers for use in medical implants and drug delivery systems.

Lactic acid (Milk acid) is added to wastewater treatment systems to enhance biological nutrient removal and reduce odor emissions.
Lactic acid (Milk acid) serves as a flavoring agent and acidity regulator in the production of confectionery, beverages, and processed foods.

Lactic acid (Milk acid) is utilized in the leather industry as a tanning agent to soften and preserve hides.
Lactic acid (Milk acid) serves as a pH regulator and buffering agent in cosmetic formulations, ensuring product stability and skin compatibility.
Lactic acid (Milk acid) is added to household cleaning products, such as bathroom cleaners and disinfectants, for its antimicrobial properties.

Lactic acid (Milk acid) is used in the production of biodegradable polymers for use in 3D printing and additive manufacturing processes.
Lactic acid (Milk acid) serves as a feedstock in the synthesis of lactide, a precursor to polyLactic acid (Milk acid) (PLA), a biodegradable plastic.
In the fermentation industry, Lactic acid (Milk acid) bacteria are used to produce probiotic supplements and fermented health drinks.

Lactic acid (Milk acid) is employed in the production of biodegradable films and coatings for food packaging applications.
Lactic acid (Milk acid) is utilized in the formulation of dietary supplements and sports nutrition products for its potential health benefits.

Lactic acid (Milk acid) serves as a corrosion inhibitor in metal finishing processes, protecting metal surfaces from oxidation and rust.
Lactic acid (Milk acid) is added to horticultural products, such as soil amendments and plant growth stimulants, to improve crop yields and soil health.
In the textile industry, Lactic acid (Milk acid) is used as a dyeing assistant to enhance color uptake and fiber penetration.

Lactic acid (Milk acid) is employed in the production of lactate-based polymers for use in biomedical applications, such as tissue engineering and drug delivery.
Lactic acid (Milk acid) serves as a flavor enhancer and preservative in the fermentation of vegetables and pickled products.

Lactic acid (Milk acid) is used in the production of biodegradable detergents and soaps for both household and industrial cleaning applications.
Lactic acid (Milk acid) is added to pet care products, such as shampoos and grooming sprays, for its moisturizing and conditioning properties.

Lactic acid (Milk acid) serves as a reducing agent in the synthesis of pharmaceutical intermediates and fine chemicals.
Lactic acid (Milk acid) is employed in the production of biodegradable lubricants and hydraulic fluids for eco-friendly applications.

Lactic acid (Milk acid) is utilized in the manufacture of biodegradable plastics for disposable food service items, such as utensils and packaging.
Lactic acid (Milk acid) serves as a pH adjuster in water treatment systems to control acidity and alkalinity levels.

Lactic acid (Milk acid) is added to skincare products, such as facial masks and serums, for its exfoliating and brightening effects on the skin.
Lactic acid (Milk acid) is used in the production of biodegradable adhesives and sealants for construction and woodworking applications.

Lactic acid (Milk acid) serves as a fermentation substrate in the production of organic acids, such as acetic acid and propionic acid, through microbial fermentation.
Lactic acid (Milk acid) is employed in the production of biodegradable detergents and cleaning agents for industrial and institutional use.
Lactic acid (Milk acid) serves as a stabilizer and pH adjuster in the formulation of beverages, including fruit juices, sports drinks, and flavored water.
Lactic acid (Milk acid) is utilized in the preservation of agricultural crops and fresh produce to extend shelf life and maintain quality.

Lactic acid (Milk acid) is used in the production of biodegradable paints and coatings for architectural and industrial applications.
Lactic acid (Milk acid) serves as a natural preservative and flavor enhancer in the fermentation of kimchi, sauerkraut, and other fermented vegetables.
Lactic acid (Milk acid) is added to cosmetic formulations, such as facial masks and serums, for its skin brightening and anti-aging properties.

Lactic acid (Milk acid) is employed in the production of biodegradable polymers for use in 3D printing and additive manufacturing.
Lactic acid (Milk acid) serves as a fermentation substrate for the production of bio-based chemicals, such as acrylic acid and succinic acid.

Lactic acid (Milk acid) is used in the production of biodegradable detergents and dishwashing liquids for household and commercial use.
Lactic acid (Milk acid) is added to animal feed as a dietary supplement to improve digestion and nutrient absorption in livestock.

Lactic acid (Milk acid) serves as a pH adjuster and flavor enhancer in the formulation of non-alcoholic beverages, such as fruit juices and soft drinks.
Lactic acid (Milk acid) is employed in the production of biodegradable polymers for use in medical implants and surgical sutures.

Lactic acid (Milk acid) is used in the production of biodegradable mulches and soil conditioners for organic farming and gardening.
Lactic acid (Milk acid) serves as a chelating agent in the formulation of metal cleaners and descalers for industrial applications.

Lactic acid (Milk acid) is added to skincare products, such as exfoliating scrubs and toners, for its gentle yet effective exfoliation properties.
Lactic acid (Milk acid) is used in the production of biodegradable solvents and cleaning agents for industrial and household applications.

Lactic acid (Milk acid) serves as a fermentation substrate for the production of biofuels, such as ethanol and butanol, from renewable feedstocks.
Lactic acid (Milk acid) is employed in the production of biodegradable plastics for use in packaging materials and disposable products.

Lactic acid (Milk acid) is used in the production of biodegradable fertilizers and soil conditioners for sustainable agriculture practices.
Lactic acid (Milk acid) serves as a pH regulator in the formulation of personal care products, such as shampoos and body washes.

Lactic acid (Milk acid) is added to dairy products, such as sour cream and cottage cheese, to enhance flavor and prolong shelf life.
Lactic acid (Milk acid) is employed in the production of biodegradable lubricants and hydraulic fluids for eco-friendly applications.

Lactic acid (Milk acid) serves as a fermentation substrate for the production of bio-based polymers, such as polyhydroxyalkanoates (PHA), for use in bioplastics.
Lactic acid (Milk acid) is used in the production of biodegradable detergents and cleaning agents for institutional and industrial use.

Lactic acid (Milk acid) serves as a pH adjuster and flavor enhancer in the formulation of fermented beverages, such as kombucha and kefir.
Lactic acid (Milk acid) is added to pet care products, such as grooming wipes and dental chews, for its antimicrobial properties.

Lactic acid (Milk acid) is employed in the production of biodegradable adhesives and sealants for construction and packaging applications.
Lactic acid (Milk acid) serves as a fermentation substrate in the production of organic acids, such as citric acid and malic acid, through microbial fermentation.



DESCRIPTION


Lactic acid (Milk acid), also known as milk acid, is a chemical compound with the molecular formula C3H6O3.
Lactic acid (Milk acid) is classified as an alpha-hydroxy acid (AHA) due to its structure containing a hydroxyl group adjacent to the carboxylic acid group.
Lactic acid (Milk acid) exists in two optical isomers: L-Lactic acid (Milk acid) and D-Lactic acid (Milk acid).
The L-Lactic acid form is the most common and is found in various natural sources, including sour milk, yogurt, and fermented foods.

Lactic acid (Milk acid) is produced through the fermentation of carbohydrates, primarily in the muscles during intense exercise when oxygen availability is limited (anaerobic metabolism).
Lactic acid (Milk acid) is also produced by bacteria, such as Lactobacillus species, during the fermentation of sugars in foods, leading to the characteristic sour taste of fermented dairy products.

Lactic acid (Milk acid) has several industrial applications, including its use as a food additive (E270) for acidity regulation, flavor enhancement, and preservation.
Lactic acid (Milk acid) is also utilized in the pharmaceutical and cosmetic industries for its exfoliating and moisturizing properties.
Additionally, Lactic acid (Milk acid) is used in the production of biodegradable polymers, as a precursor in the synthesis of lactate esters for plasticizers, and in the textile industry for dyeing and finishing processes.

In the body, Lactic acid (Milk acid) plays a crucial role in various metabolic processes.
Lactic acid (Milk acid) serves as an energy source during anaerobic metabolism, helps regulate pH balance in tissues, and contributes to gluconeogenesis (the synthesis of glucose) in the liver.
However, accumulation of Lactic acid (Milk acid) beyond the body's capacity to metabolize it can lead to a condition known as Lactic acid (Milk acid)osis, which is associated with symptoms such as muscle weakness, fatigue, and metabolic acidosis.



PROPERTIES


Chemical Formula: C3H6O3
Molecular Weight: Approximately 90.08 g/mol
Appearance: Clear, colorless to slightly yellow liquid or white crystalline solid
Odor: Slightly acidic or sour odor
Taste: Acidic or sour taste
Density: 1.206 g/cm³ (liquid), 1.213 g/cm³ (solid)
Melting Point: Approximately 16-18°C (61-64°F)
Boiling Point: Approximately 122-130°C (252-266°F) at 760 mmHg
Solubility in Water: Miscible in water, forms a clear solution
Solubility in Other Solvents: Soluble in ethanol, methanol, and other polar solvents
pH: Approximately 2.4 (for a 1% aqueous solution)
Acidity: Weak acid, with a pKa value of around 3.86 for the carboxylic acid group
Refractive Index: 1.422 (20°C)
Viscosity: Low viscosity liquid
Hygroscopicity: Hygroscopic, absorbs moisture from the air
Flash Point: Not applicable (non-flammable)
Flammability: Non-flammable
Autoignition Temperature: Not applicable
Vapor Pressure: Negligible
Partition Coefficient (Log P): -0.39
Surface Tension: Approximately 59 mN/m (at 25°C)
Vapor Density: Heavier than air
Freezing Point Depression: Reduces the freezing point of water due to its presence in aqueous solutions
Boiling Point Elevation: Increases the boiling point of water in aqueous solutions
Dielectric Constant: Approximately 69.8 (at 20°C)
Hydrogen Bond Acceptor: Yes, due to the presence of the hydroxyl group
Hydrogen Bond Donor: Yes, due to the presence of the carboxylic acid and hydroxyl groups
Optical Rotation: Approximately -0.5° (for L-Lactic acid (Milk acid))
Magnetic Susceptibility: Diamagnetic
Thermal Conductivity: Approximately 0.5 W/m·K (at 25°C)
Heat Capacity: Approximately 155 J/mol·K (at 25°C)
Molar Refractivity: Approximately 18.9 cm^3/mol
Heat of Vaporization: Approximately 43.1 kJ/mol (at boiling point)
Heat of Fusion: Approximately 11.3 kJ/mol (at melting point)
Specific Heat Capacity: Approximately 2.42 J/g·K (for solid), 2.29 J/g·K (for liquid)
Dielectric Loss Factor: Approximately 0.011 (at 25°C)
Viscous Dissipation Factor: Approximately 0.0008 (at 25°C)
Surface Energy: Approximately 42.2 mJ/m^2
Fluorescence: Weak fluorescence in the ultraviolet region
UV Absorbance: Absorbs UV light with a peak absorbance around 210 nm
Radioactivity: Not radioactive
Hazardous Polymerization: Does not undergo hazardous polymerization
Biodegradability: Biodegradable under aerobic and anaerobic conditions
Toxicity: Low acute toxicity, but concentrated solutions may cause irritation to skin, eyes, and mucous membranes



FIRST AID


Inhalation:

Move to Fresh Air:
If Lactic acid (Milk acid) vapors are inhaled, immediately move the affected person to an area with fresh air.

Ensure Breathing:
Check the person's airway, breathing, and circulation.
If breathing is difficult, ensure an open airway and provide rescue breathing if necessary.

Seek Medical Attention:
If symptoms such as difficulty breathing, coughing, or respiratory distress persist, seek medical attention promptly.

Provide Oxygen:
If available and trained to do so, administer oxygen to the affected person while awaiting medical assistance.

Keep Calm and Reassure:
Keep the affected person calm and reassure them while waiting for medical help.


Skin Contact:

Remove Contaminated Clothing:
If Lactic acid (Milk acid) comes into contact with the skin, promptly remove any contaminated clothing.

Wash Skin Thoroughly:
Wash the affected area with soap and water for at least 15 minutes, ensuring thorough rinsing to remove any traces of Lactic acid (Milk acid).

Use Mild Soap:
Use a mild soap or detergent to gently cleanse the skin, avoiding harsh chemicals that may exacerbate irritation.

Apply Moisturizer:
After washing, apply a soothing moisturizer or emollient to the affected area to help soothe and hydrate the skin.

Seek Medical Advice:
If skin irritation persists or worsens, seek medical advice or consult a healthcare professional for further evaluation and treatment.


Eye Contact:

Flush with Water:
Immediately flush the eyes with lukewarm water for at least 15 minutes, holding the eyelids open to ensure thorough rinsing.

Remove Contact Lenses:
If wearing contact lenses, remove them as soon as possible to facilitate irrigation of the eyes.

Seek Medical Attention:
Seek immediate medical attention or contact an eye specialist if irritation, pain, or redness persists after flushing.


Ingestion:

Do Not Induce Vomiting:
Do not induce vomiting if Lactic acid (Milk acid) has been ingested, as it may lead to further complications.

Do Not Drink Water:
Refrain from giving anything by mouth to the affected person unless instructed by medical personnel.

Seek Medical Assistance:
Immediately contact a poison control center or seek medical assistance for further guidance and treatment.

Provide Information:
Provide medical personnel with details regarding the amount ingested, the time of ingestion, and any symptoms experienced by the affected person.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including chemical-resistant gloves, safety goggles or face shield, and protective clothing (such as long sleeves and pants), when handling Lactic acid (Milk acid) to minimize skin and eye contact.

Ventilation:
Use local exhaust ventilation or work in a well-ventilated area to prevent the buildup of vapors or fumes.
Avoid breathing in Lactic acid (Milk acid) vapors or mists.

Avoid Contact:
Avoid skin contact with Lactic acid (Milk acid).
In case of skin contact, promptly wash affected areas with soap and water.
Remove contaminated clothing and wash it before reuse.

Eye Protection:
Wear safety goggles or a face shield to protect eyes from potential splashes or mists of Lactic acid (Milk acid).
In case of eye contact, immediately flush eyes with water for at least 15 minutes and seek medical attention if irritation persists.

Handling Equipment:
Use equipment made of compatible materials, such as stainless steel, glass, or plastic, for handling and transferring Lactic acid (Milk acid).
Avoid the use of reactive metals like aluminum or copper.

Prevent Spills:
Handle Lactic acid (Milk acid) containers with care to prevent spills or leaks.
Use appropriate containment measures, such as secondary containment trays or spill kits, in areas where spills may occur.

Do Not Mix:
Avoid mixing Lactic acid (Milk acid) with incompatible substances, such as strong bases, oxidizing agents, or reactive metals, as it may result in hazardous chemical reactions or releases of toxic gases.

Labeling:
Clearly label containers of Lactic acid (Milk acid) with the product name, hazard symbols, handling instructions, and storage conditions to ensure proper identification and safe handling.

Avoid Ingestion:
Do not ingest Lactic acid (Milk acid). Keep food, beverages, and tobacco products away from areas where Lactic acid (Milk acid) is handled or stored.

Training:
Provide training to personnel handling Lactic acid (Milk acid) on safe handling procedures, emergency response protocols, and the use of personal protective equipment.

Storage:

Container Selection:
Store Lactic acid (Milk acid) in tightly sealed containers made of compatible materials, such as high-density polyethylene (HDPE), polypropylene (PP), or glass, to prevent moisture ingress and contamination.

Temperature Control:
Store Lactic acid (Milk acid) in a cool, dry place away from direct sunlight and heat sources. Maintain storage temperatures between 15°C to 25°C (59°F to 77°F).

Avoid Freezing:
Protect Lactic acid (Milk acid) from freezing temperatures, as freezing may result in crystallization or solidification of the solution. If frozen, allow the solution to thaw completely before use.

Separation:
Store Lactic acid (Milk acid) away from incompatible substances, including strong oxidizing agents, bases, and reactive metals, to prevent chemical reactions or hazards.

Stability:
Lactic acid (Milk acid) solutions may oxidize slowly over time, especially in the presence of air or light. Store containers tightly closed to minimize air exposure and degradation.

Handling Precautions:
Handle containers with care to prevent damage or leakage. Store containers on shelves or racks with adequate support and spacing to prevent tipping or falling.

Security Measures:
Implement security measures, such as locked storage areas or restricted access, to prevent unauthorized handling or tampering with Lactic acid (Milk acid).

Emergency Response:
Have appropriate spill containment and cleanup materials readily available in case of spills or leaks.
Train personnel on proper spill response procedures and emergency protocols.
LACTIC ACID 80%
Lactic Acid 80% is an alpha hydroxy acid that comes from milk.
As a result of its relatively greater molecular weight, Lactic Acid 80%'s keratolytic action is milder than that of glycolic acid, thus preventing skin irritations.


CAS Number: 50-21-5
EC Number: 200-018-0
Molecular Formula: C3H6O3


Lactic Acid 80%, also known as milk acid, is a chemical compound that plays a role in several biochemical processes.
Lactic Acid 80% is an alpha hydroxy acid that comes from milk.
As a result of its relatively greater molecular weight, Lactic Acid 80%'s keratolytic action is milder than that of glycolic acid, thus preventing skin irritations.


Lactic Acid 80% is a liquid solution in water of about 80% purity.
Lactic Acid 80% is an AHA.
Lactic Acid 80% is sufficient to add a few drops to 100 ml shampoo to adjust the pH.


Even as a moisturizing additive Lactic Acid 80% should not be applied more than 0,5%.
Dilute Lactic Acid 80% before use.
As with all of the acids, Lactic Acid 80% is important to let your skin acclimate to their use.


Lactic Acid 80% is an anti-wrinkle and anti-pigmentation component available in both over-the-counter and professional-grade skincare products.
Lactic Acid 80% is derived from milk and belongs to the alpha-hydroxy acid (AHAs) class of anti-ageing compounds.
Glycolic acid and citric acid are two further examples of AHAs.


Lactic Acid 80% is a strong Alpha-Hydroxy Acid and hence will have excellent exfoliant properties, although these are weaker than, but second only to, Glycolic Acid.
AHA products should be a stand alone treatment product and not included in another product.


While AHA can be included in other products there are certain incompatibilities that may arise plus AHAs (because of the pH required for best effectiveness) may not allow other products (such as cleansing masks) to work properly, and vice versa.
Lactic Acid 80% is also a widely used organic acidulate, probably because it is classified as a weak acid.


As with all manufacturing processes, we recommend lab scale trials in order to determine appropriate quantities.
Lactic Acid 80% is a liquid solution in water of about 80% purity.
Lactic Acid 80%, is an organic acid with applications in beer production as well as the cosmetic, pharmaceutical, food and chemical industries.


Lactic Acid 80% comes in both R (D-) and S (L+) enantiomers which can be manufactured individually to near perfect optical purity.
This means Lactic Acid 80% is great in the production of other products which require a specific stereochemistry.
Lactic Acid 80% is a liquid solution in water of about 80% purity.


Lactic Acid 80% is a strong Alpha-Hydroxy Acid and hence will have excellent exfoliant properties, although these are weaker than, but second only to, Glycolic Acid.
AHA products should be a stand alone treatment product and not included in another product.


While AHA can be included in other products there are certain incompatibilities that may arise plus AHAs (because of the pH required for best effectiveness) may not allow other products (such as cleansing masks) to work properly, and vice versa.
Lactic Acid 80% is also a widely used organic acidulate, probably because it is classified as a weak acid.


As with all manufacturing processes, we recommend lab scale trials in order to determine appropriate quantities.
Normally Lactic Acid 80% is titrated with a dilute solution of Lactic Acid (10 or 20% in water) until the desired pH is achieved.
Lactic Acid 80% is preferred as an acidulate as it tends to have less of a destabilizing effect on emulsions than Citric Acid.


Lactic Acid 80% is a non dairy version that is part of a family of acids called Alpha Hydroxy Acids (AHA’s).
Lactic Acid 80% is produced from natural corn starch by advanced bio-fermentation and refining technology.
Lactic Acid 80% is a yellowish to colorless liquid, with a mildly acidic odour and taste.


Lactic Acid 80% is a naturally occurring alpha hydroxy acids (or AHAs) produced by fermentation of sugars.
Lactic Acid 80% is the alpha hydroxy acid most frequently used for peel products.
Lactic Acid 80%, also known as milk acid, is an organic compound with the chemical formula C3H6O3.


In its liquid state Lactic Acid 80% is colourless.
Lactic Acid 80% is one of the alpha-hydroxy acids (AHA’s).
These acids occur naturally in fruits, sugar cane and milk.


Lactic Acid 80% increasing wort's acidity and improving both mashing and fermentation.
The exact dosage depends on the alkalinity of the water used, the salts added and the malts used in the recipe.
Lactic Acid 80% is recommended to carry out a pH measurement of the mash before adding the product.


If the pH is not within the range of 5.3 - 5.8, make gradual additions (0.10 - 0.15 mL/L) of Lactic Acid 80%, mix and measure again.
Lactic Acid 80%, from Jungbunzlauer, is an organic acid, occurring naturally in the human body and in fermented foods.
Lactic Acid 80% is a natural preservative and pH regulator.


Lactic Acid 80% is an organic acid with wide-reaching industrial applications.
Lactic Acid's 80% Food Grade specification makes it especially useful for food and beverage production, as well as pharmaceutical and cosmetic products.
Lactic Acid 80% is a versatile organic acid.


Lactic Acid 80% is an Alpha Hydroxy Acid (AHA) and can be used to promote higher rates of desquamation and cell renewal.
Lactic Acid 80% is also a moistening compound.
Lactic Acid 80% belongs to a group of alpha hydroxy acids (AHA) which show exfoliating, moistening and anti-aging properties.


In nature Lactic Acid 80% exists in sour milk, yoghurts, sour rye soups and silages.
Lactic Acid 80% appears in two optical forms L and D, out of which only L-lactic acid is biologically active and is a natural element of the skin and hair.
Lactic Acid 80% is one of the main part of NMF – natural moistening factor, which is responsible for proper hydration of the epidermis.


Lactic Acid 80% stabilizes process of epidermis exfoliation in a very delicate way.
Lactic Acid 80% is an alpha hydroxy acid with both exfoliant and humectant properties.
Lactic Acid 80% is produced naturally in the body (it's the stuff that gives you a ‘stitch’ during a workout) and is also found in yogurt and milk.


Lactic Acid 80% can help stimulate collagen and strengthen the skin, which equals fewer fine lines and wrinkles.
The hydroxy acids exfoliate the top layer of skin, helping smooth and even complexion, keep pores unclogged, brighten skin and even fade dark marks and discoloration.


Lactic Acid 80% is a versatile organic acid.
Lactic Acid 80% is soluble in water and in ethanol.
The inclusion of additional Lactic Acid 80% prior to rennetting overcomes this shortage and improves the curd yield.


Lactic Acid 80% is presented in a dropper bottles holding 4fl oz, to ensure an accurate dosing of milk and achieve consistent results when cheese making.
In production, Lactic Acid 80% is usually added up so that the pH of the milk is 5.0.
The casein in fermented milk is coagulated (curdled) by Lactic Acid 80% and it is also responsible for the sour flavor of sourdough breads.


Lactic Acid 80% is a colorless to yellow/brown liquid.
Store Lactic Acid 80% in a tightly closed container.
Store Lactic Acid 80% in a cool, dry, well-ventilated area away from incompatible substances.


Lactic Acid 80% can also be used for minor corrections in brewing PH can be used at higher levels for beer souring.
Lactic Acid 80% reduces the alkalinity levels of brewing liquor, stimulating maximum enzyme activity in the wort and enabling optimum pH levels throughout the whole brewing process.


Lactic Acid 80% improves extract yield and fermentation ability.
Lactic Acid 80% is suitable for beers where no other anions are needed, for example, lagers.
Lactic Acid 80% improves the clarity and stability of the finished product


Lactic Acid 80% is a ready-for-use acid used to reduce alkalinity in brewing liquor.
Lactic Acid 80% is Food Grade and made by fermentation of natural (beet or cane) sugar.
Lactic Acid 80% is a product of natural origin, obtained by fermentation of glucose.


Lactic Acid 80% is used in cosmetic compositions for pH adjustment and has good affinity for skin and hair.
Lactic Acid 80% improves skin hydration, removes dead cells and hair films (dandruff) having keratolytic action, hair shines.
Lactic Acid 80% is responsible for the tang that hits the mouth when eating dry aged beef.


Lactic Acid 80% is produced as natural L-Lactic acid by fermentation of carbohydrates like sugar or starch.
Lactic Acid 80%'s Chemical Formula is C3H6O3.
An organic acid, Lactic Acid 80%, is used to reduce alkalinity without adding sulphate and chloride ions.



USES and APPLICATIONS of LACTIC ACID 80%:
In many food products usually serves, Lactic Acid 80% is used as either as a pH regulator, as a preservative, or as a flavoring agent.
Lactic Acid 80% is used as an acidity regulator.
Lactic Acid 80% is effective in preventing the spoilage of vegetabels.


Lactic Acid 80% is used as an excellent acidification agent for many dairy products.
Lactic Acid 80% is used as an enhance savory flavors.
In pharmaceutical technology, Lactic Acid 80% is used as a starting material for other substances.


Lactic Acid 80% is used as a valuable component in biomaterials.
Lactic Acid 80% is used as a natural anti-bacterial agent in disinfecting products.
Lactic Acid 80% is used in the industrial processes.


Lactic Acid 80% is used as an additive in animal nutrition.
Lactic Acid 80% has health promoting properties.
Lactic Acid 80% is used as a humectant, or moisturizer, in some cosmetics.


Lactic Acid 80% ia used as a mordant, a chemical that helps fabrics accept dyes, in textiles.
Lactic Acid 80% is also used in tanning leather.
Lactic Acid 80% is used in the manufacturing of lacquers and inks.


Lactic Acid 80% is the principal building block for Poly Lactic Acid (PLA).
PLA is a biobased and bio-degradable polymer that can be used for producing renewable and compostable plastics.
Lactic Acid 80% is used to adjust the pH of the mash or the sparge water.


Lactic Acid 80% is used for Pilsner style lagers to reduce alkalinity.
Lactic Acid 80% used to reduce alkalinity without adding sulphate and chloride ions.
Lactic Acid 80% can also be used for minor corrections in brewing


PH can be used at higher levels for beer souring.
Lactic Acid 80% has a good moisturising effect on the skin and can be used in water based serums, gels, toners, creams and lotions.
Lactic Acid 80% can help the skin to look fresher and younger.


Lactic Acid 80% is especially beneficial in night creams and anti aging products.
When Lactic Acid 80% is used at higher concentrations, it can have an exfoliating effect.
Lactic Acid 80% will improve the skin's appearance and help to remove surface debris and dead skin cells.


Hair Care: Used in a hair pack, Lactic Acid 80% will cleanse a congested scalp for example, after a weave has been removed, having been on for several months.
Never use Lactic Acid 80% directly on the skin.


Best Lactic Acid 80% is added in stage 3 (cool down) when making creams and lotions.
Be aware that Lactic Acid 80% can make creams and lotions thinner or unstable so you need to start with a very strong and stable cream or lotion.
As a pH regulator, Lactic Acid 80% can be used to move the pH number lower (more acidic) for when using Preservative K which only functions correctly in a narrow pH range.


Often, Lactic Acid 80% is derived from milk, however, ours is made from maize or corn, and free from GMO.
Lactic Acid 80% is sold at an 80% concentration i.e. Lactic Acid 80% with 20% Water as an aqueous solution.
According to the Cosmetic Ingredient Database (CosIng), the functions of Lactic Acid 80% are: Buffering, Humectant, Skin Conditioning.


Skin Care: Depending on the strength of the dilution used, Lactic Acid 80% can be used as a pH regulator, a moisturiser or as a skin peel.
In the lower percentages, Lactic Acid 80% reduces Trans Epidermal Water Loss (TEWL) by supporting the skin's barrier function.
When applied, Lactic Acid 80% cleaves the bonds between keratinocytes on the external layer, thus reducing them and leading to gradual regeneration.


This results in a mild but effective exfoliation of the horny layer and in the simultaneous regeneration of cells.
Lactic Acid 80% stimulates the production of collagen and glycosaminoglycans that make up the intercellular material.
Another advantage provided by Lactic Acid 80% is that it naturally hydrates the skin; this action results in increased formation of ceramides, thus enhancing the function of the keratin barrier.


The combination of mild peeling, regeneration and hydration that Lactic Acid 80% offers, makes it an ideal peeling treatment for sensitive and dehydrated skin and a good choice for skin that will undergo chemical peeling for the first time.
The Lactic Acid 80% in combination with the pH result in targeted actions and indications.


Lactic Acid 80% is applied to adjust the pH of cosmetic products such as shampoo and shower gel or creams and lotions.
As Lactic Acid 80% is evident from the name, it reduces the pH of a product.
In addition to pH-regulation Lactic Acid 80% has excellent moisturizing effects.


An exception is the application in chemical peels.
Lactic Acid 80% is widely used in a range of food, industrial and manufacturing processes.
Lactic Acid 80% can be used for adjusting pH in the mash or sparge water.


Lactic Acid 80% may vary in colour from transparent to pale yellow.
Lactic Acid 80% is used a pH meter or test strips to control the pH.
Lactic Acid 80% may also be used in the final beer or wine for adding acidity.


Lactic Acid 80% is used to treat dry, rough & scaly skin.
Lactic Acid 80% may also be used for other conditions as determined by your doctor.
Normally Lactic Acid 80% is titrated with a dilute solution of Lactic Acid (10 or 20% in water) until the desired pH is achieved.


It is preferred as an acidulate as Lactic Acid 80% tends to have less of a destabilizing effect on emulsions than Citric Acid.
Lactic Acid 80% is used treating dry, rough & scaly skin.
Lactic Acid 80% may also be used for other conditions as determined by your doctor.


Lactic Acid 80% is one of the popular food additives and ingredients in most countries.
Commonly Lactic Acid 80% is used as a preservative and antioxidant.
Lactic Acid 80% also has uses as a fuel additive, chemical intermediate, acidity regulator, and disinfectant.


Lactic Acid 80% is also used in dialysis solutions, which results in a lower incidence of side effects compared to Sodium Acetate which can also be used.
Lactic Acid 80% is used frequently in the cosmetic industry due to the effect of promoting collagen production, helping to firm the skin against wrinkles and sagging.


Lactic Acid 80% can also cause micro peeling, which can help reduce various scars and age spots.
This is a great solution for people with sensitive or dry skin where exfoliants don’t work.
Lactic Acid 80% is used to treat dry, rough & scaly skin.


Lactic Acid 80% may also be used for other conditions as determined by your doctor.
Dilute Lactic Acid 80% before use.
As with all of the acids, Lactic Acid 80% is important to let your skin acclimate to their use.


For those whose skin is not used to the acids a slight stinging and redness may result.
If this occurs, Lactic Acid 80% reduce usage.
Lactic Acid 80% contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn.


Lactic Acid 80% is used a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.
Lactic Acid 80% reduces the alkalinity levels of brewing liquor stimulating maximum enzyme activity in the wort enabling optimum pH levels throughout the whole brewing process.


Lactic Acid 80% improves extract yield and fermentation ability
Lactic Acid 80% is suitable for beers where no other anions are needed for example lagers.
Lactic Acid 80% improves clarity and stability of the finished product.


Lactic acid in 80% concentration for chemical exfoliation, suitable for all skin types.
Lactic Acid 80% offers cellular regeneration, hydration and reduction of the appearance of wrinkles on the skin.
Typical use level of Lactic Acid 80% is between 1-20% in peels, creams, lotions, masks, cleansers.


Due to Lactic Acid 80%'s acidity the final product needs to be tested for safe pH.
Optimal pH range of Lactic Acid 80% is from 3.5-5.0.
Some over the counter products, after adding Lactic Acid 80%, will separate as a result of the low pH, and need to be stabilized.


Within the Personal Care sector, Lactic Acid 80% functions as an acidifier with moisturising, exfoliating and antibacterial properties.
When used topically, Lactic Acid 80% can assist with the removal of dead skin cells helping to renew the skin, improve skin texture and tone along with functioning as a humectant.


Lactic Acid 80% is often used as a milder alternative to glycolic acid in cosmetic formulations and can also be used to lower pH during manufacturing.
Lactic Acid 80% is produced by fermentation of glucose syrup from maize by using a bacterial strain.
Lactic Acid 80% is an acid and should never be used undiluted.


Lactic Acid 80% is classed as an advanced skincare ingredient and should not be used unless you understand the usage and applications of Lactic Acid.
Lactic Acid 80% is used acne Treatments & Skin Peels, Bee Keeping, In food production, To Extend shelf life of Meat,Fish & Poultry, Acidity regulator in drinks, In dairy products, Baking, Detergent, Animal Nutrition Supplement, and General Industry.


Lactic Acid 80% is widely used as an acidulent in the food industry, as well as for preservation and flavouring.
Lactic Acid 80% is used very useful to rejuvenate the skin by encouraging the shedding of old surface skin cells.
Lactic Acid 80% can reduce the appearance of fine lines, irregular pigmentation, age spots & decreases enlarged pores.


Lactic Acid 80% is often used in creams & lotions at a lower concentration for a more gentle acid-based peel.
Lactic Acid 80% is used in cosmetic to biolifting for it makes the skin elastic, evens wrinkles, brightens discolorations and narrows pores.
Lactic Acid 80% is also used in conditioners and shampoos because it activates hair bulbs, accelerating hair growth.


Lactic Acid 80% has moistening effect as a result of its properties to bind water in upper layers of the epidermis.
When used in proper concentrations (up to 5.0%), Lactic Acid 80% loosens intercellular cement.
Regular use of cosmetics with Lactic Acid 80% rejuvenates the epidermis and makes wrinkles even by means of a gradual exfoliation of dead cells of horny layer.


Faster exfoliation of cells results in the growth of new ones.
Preparations with Lactic Acid 80% support the treatment of acne.
When using masques with Lactic Acid 80% pointwise (7.0-15.0%) one can try removing sun, acne and aging maculae.


After using preparations with Lactic Acid 80% one should protect the skin against sun.
Without the layers of cornified cells, “young” epidermis absorbs nourishing cosmetics considerably better.
Therefore, tonics, scrubs and masques with Lactic Acid 80% belong to basic cosmetics for the care of oily, mixed, acne and mature complexions.


The cosmetics with Lactic Acid 80% should be used with the utmost care for dry complexion.
Lactic Acid 80% regulates cellular skin regeneration, and improves skin structure and colour.
Lactic Acid 80% enhances the effects of other cosmetic preparations.


Lactic Acid 80% improves skin moistening for the skin becomes more soft and elastic.
Lactic Acid 80% influences the production of skin collagen by increasing thickness and strengthening the dermis.
Lactic Acid 80% increases the level of glycosaminoglycans that is compounds that absorb water as a sponge and provide hydration of deeper layers of the skin.


Lactic Acid 80% makes small surface wrinkles even and improves skin elasticity as well as firmness; it is an anti-aging ingredient; it helps in case of discolorations and small acne scars.
Lactic Acid 80% makes pores clear and shows antibacterial properties, hence, it prevents the creation of trouble spots that are all kinds of eczemas and blackheads; it helps in the treatment of acne.


Lactic Acid 80% is also recommended for body and scalp-care for it helps in case of dry skin as well as skin exfoliation and cornification.
Lactic Acid 80% has been used in the production of beer for decades, contributing a unique tartness to this popular beverage.
With its 80% concentration of Lactic Acid 80%, this specially formulated solution allows you to easily control the level of tartness in your product.


Whether you’re using lactic acid to adjust the flavour of your beer or in other food production needs, Lactic Acid 80% is the perfect choice for creating a finished product that meets all quality standards while delighting consumers.
Lactic Acid 80% can be used to adjust the pH of many formulations and can be used as a milder alternative to glycolic acid.


Lactic Acid 80% and its salt, Sodium Lactate, can be used as humectants.
Lactic Acid 80% is used skincare pH adjustment, humectancy, skin brightening, desquamation, exfoliation.
Lactic Acid 80% is used haircare pH adjustment, humectancy.


Lactic Acid 80% is used soapmaking pH adjustment, increased firmness of bars and solid format products (especially if pre-neutralised with Lye).
Lactic Acid 80% is used Skincare pH adjustment, humectancy, skin brightening, desquamation, exfoliation.
Lactic Acid 80% is used Haircare pH adjustment, humectancy.


Lactic Acid 80% is used Soapmaking pH adjustment, increased firmness of bars and solid format products (especially if pre-neutralised with Lye).
Lactic Acid 80% is used to produce serial products or widely used in food, vintage, beverage, drugs, polymerization, textile, leather, tobacco, feed, plastic chemicals, pesticide, polymer solution and other industry.


Lactic Acid 80% is also used as an acidifying agent.
Lactic Acid 80% is food grade and is used for the production of several types of cheeses.
Lactic Acid 80% is particularly useful when UHT, ultra-pasturized or powdered milk are used as the starting materials, since the heat treatments used in the production of these milks deactivates the lactose and prevents the cheese culture from being able to turn it fully into Lactic Acid 80%.


Lactic Acid 80% is a vital ingredient in Ricotta Impastata, Mozzarella, Queso Blanco and other speciality cheeses and can be used in the production of sour milk products, such as Koumiss, Laban, Kefir, as well as some cottage cheeses.
Lactic Acid 80% is an Alpha Hydroxy Acid (AHA) and can be used to promote higher rates of desquamation and cell renewal.


Lactic Acid 80% can be used to adjust the pH of many formulations and can be used as a milder alternative to glycolic acid.
Lactic Acid 80% and its salt, Sodium Lactate, can be used as humectants.
Lactic Acid 80% is used in facial products and also body lotions and moisturisers, never directly on skin.


Lactic Acid 80% is easy to use in liquid form.
Lactic Acid 80% works well with hyaluronic acid and Vitamins A, B and C.
Lactic Acid 80% can also be used as a pH regulator: lactic acid will lower the pH.


Lactic Acid 80% has an anti-microbial effect and is the basis for preservation by fermentation in many food products.
Lactic Acid 80% serves as a preservative, pH regulator and flavouring agent.
Lactic Acid 80% is primarily found in sour milk products, such as: koumiss, leban, yogurt, kefir, and some cottage cheeses.


The casein in fermented milk is coagulated (curdled) by Lactic Acid 80%.
Lactic Acid 80% is produced natutally in the Lacto-fermentation of foods.
Some examples of these types of foods are Kimchi, Sauerkraut, sour beer, tsukemono, suan cai, atsara and yoghurt.


Lactic Acid 80% is used directly as the acidulant.
Pickled Vegetables uses of Lactic Acid 80%: Lactic Acid is effective in preventing the spoilage of olives, gherkins, pearl onions and other vegetables preserved in brine.


Confectionery products uses of Lactic Acid 80%: such as hard boiled candy, fruit gums with Lactic Acid 80% results in a mild acid taste, improved quality and longer shelf life.


-Beer brewing uses of Lactic Acid 80%:
Lactic Acid 80% is to lower the pH and add a bit of tartness.
Naturally add in small amounts or Lactic Acid 80% will become quite sour.


-Cheese making & Whipped Butter uses of Lactic Acid 80%:
Ricotta in particular and whipped butter in combination with GDL.
Ricotta Impastata, Mozzarella and Queso Blanco.


-Interesting non food uses for Lactic Acid 80%:
Lactic Acid 80% is the principal building block for Poly Lactic Acid (PLA) biodegradable plastics.
PLA is a biobased and bio-degradable polymer that can be used for producing renewable and compostable plastics.
Lactic Acid 80% is also being used in the cosmetics industry for acne treatment.



USE IN FOOD, LACTIC ACID 80%:
Lactic Acid 80% is a natural preservative found in several foods, including pickled vegetables, yoghurt, and baked goods.
Lactic Acid 80% is a cheap and minimally processed
Lactobacillus and Streptococcus cultures produce Lactic Acid 80% through fermentation.
The bacteria break down sugar to extract energy and produce Lactic Acid 80% as a byproduct.
Lactic Acid 80% helps regulate pH levels and prevents the growth of microorganisms, extending shelf life.



THE PROPERTIES OF LACTIC ACID 80%:
The properties of Lactic Acid 80%
- Keratolytic exfoliates the skin by removing dead skin and scalp cells
- Stimulates collagen and elastin synthesis, promoting cell renewal
- Lactic Acid 80% improves skin grain and appearance pH
- Activates the emulsifier conditioner used in the manufacture of hair care compositions



HOW TO USE LACTIC ACID 80% IN COSMETICS:
- Lactic Acid 80% is a product that does not apply to pure skin
- Lactic Acid 80% can be included as an ingredient in cosmetic compositions containing acidulant and water: serums, gels, tonics, masks, lotions, creams, shampoos, cleanses, etc.



BENEFITS OF LACTIC ACID 80%:
*Brightens a dull complexion
*Humectant and skin firmer
*Exfoliant
*Improves skin tone and texture
*Vegan Friendly
*GMO-free



BENEFITS AND APPLICATIONS OF LACTIC ACID 80%:
Lactic Acid 80% is used to treat hyperpigmentation, age spots, and other conditions that contribute to a dull, uneven complexion.
Lactic Acid 80% also enhances skin tone and minimises the appearance of pores.

Lactic Acid 80% promotes cell turnover and cell renewal, which are the processes through which your skin loses old cells and replaces them with new ones.
Lactic Acid 80% works really well for sensitive skin because of its milder nature as compared to other alpha-hydroxy acids.

Lactic Acid 80% is also a key component of over-the-counter lotions and creams for "chicken skin," i.e., pimples on the backs of the arms.
Lactic Acid 80% aids in the dissolution of the clog of skin cells that form around the hair follicle, smoothing out the bumpiness.
Lactic Acid 80% is commonly found in topical therapies for eczema, psoriasis, and rosacea.



HOW LACTIC ACID 80% WORKS:
Lactic Acid 80% works by removing the upper layer of skin cells, which is usually composed of dead skin cells.
Lactic Acid 80% also works by increasing the natural moisture retention capabilities of the skin to give your skin a hydrated look.



CONCENTRATION AND SOLUBILITY OF LACTIC ACID 80%:
Lactic Acid 80% is recommended that it should be used at a concentration of 1–5%.
Lactic Acid 80% is soluble in water, alcohol, and glycerol but is insoluble in oil.



HOW TO USE LACTIC ACID 80%:
Prepare the oil and water phases of your formulation separately.
Heat the oil and water phases using a double boiler.
Add Lactic Acid 80% to the water phase, accompanied by constant stirring.
Blend both the phases together using a mini-mixer or a large mixing brush.



FUNCTION OF LACTIC ACID 80%:
In food, apart from its nutritional function for normal growth, Lactic Acid 80% improves flavor and taste, improves quality of food and beverage products such as confectionery, cake, milk powder, yogurt etc. as firming agent, buffering agent and flour regulator.
Lactic Acid 80% increases effectiveness of antioxidants, prevents decolorization of fruits and vegetables.



BENEFITS OF LACTIC ACID 80%:
Lactic Acid 80% reduces the alkalinity levels of brewing liquor, stimulating maximum enzyme activity in the wort enabling optimum pH levels throughout the whole brewing process.
Lactic Acid 80% improves extract yield and fermentability.
Lactic Acid 80% is suitable for beers where no other anions are needed, for example, pilsner lagers.
Lactic Acid 80% can also be used to reduce the pH of final wort or products.



SUGGESTED BLENDS OF LACTIC ACID 80%:
Lactic Acid 80% works well in conjunction with Vitamin A, B and C.
Be sure to check the final pH level is not less than 3.5 when combining several acidic ingredients together.



PHYSICAL and CHEMICAL PROPERTIES of LACTIC ACID 80%:
CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0
Mol File: 50-21-5.mol
Lactic acid Chemical Properties
Melting point: 18°C
alpha: -0.05 º (c= neat 25 ºC)
Boiling point: 122 °C/15 mmHg (lit.)
density: 1.209 g/mL at 25 °C (lit.)
vapor density: 0.62 (vs air)
vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
refractive index: n20/D 1.4262

Fp: >230 °F
storage temp.: 2-8°C
solubility: Miscible with water and with ethanol (96 per cent).
form: syrup
pka: 3.08(at 100℃)
Specific Gravity: 1.209
color: Colorless to yellow
Water Solubility: SOLUBLE
Merck: 145,336
JECFA Number: 930
BRN: 1209341
Stability: Stable.
Physical state: viscous
Color: colorless

Odor: odorless
Melting point/freezing point:
Melting point: 18 °C at 1.013 hPa
Initial boiling point and boiling range: 122 °C at 18,66 - 19,99 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 113 °C - closed cup
Autoignition temperature: 400 °C at 1.011,4 - 1.018,9 hPa
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 100 g/l at 20 °C - soluble

Partition coefficient: n-octanol/water:
log Pow: ca.-0,54 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: No data available
Density: 1,25 g/cm3 at 15 °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:
Surface tension 70,7 mN/m at 1g/l at 20 °C
Formula: H₃CCH(OH)COOH
MW: 90.08 g/mol
Boiling Pt: 122 °C (20 hPa)
Density: 1.11…1.21 g/cm³ (20 °C)
Storage Temperature: Ambient
MDL Number: MFCD00004520
CAS Number: 50-21-5
EINECS: 200-018-0



FIRST AID MEASURES of LACTIC ACID 80%:
-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 LACTIC ACID 80%:
-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 with liquid-absorbent material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LACTIC ACID 80%:
-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 LACTIC ACID 80%:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
*Respiratory protection
Recommended Filter type: Filter type ABEK
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LACTIC ACID 80%:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.



STABILITY and REACTIVITY of LACTIC ACID 80%:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available.
-Incompatible materials:
No data available



SYNONYMS:
α-hydroxypropionic acid, 2-hydroxypropanoic acid
2-Hydroxypropionic acid , 2-Hydroxypropanoic acid
DL-Lactic acid
DL-Lactic acid
2-Hydroxypropionic acid
Acidum lacticum
Lactic Acid 80% Pdr w/silca
Lactic Acid 80%
Unilac LA80
Tisulac
Espiritin
HiPure 90
l-lacticaci
Lactic L-Milchsàure



LACTIC ACID 80% (E270)
Lactic Acid 80% (E270)'s Chemical Formula is C3H6O3.
Lactic Acid 80% (E270) is produced as natural L-Lactic acid by fermentation of carbohydrates like sugar or starch.


CAS Number: 50-21-5
EC Number: 200-018-0
Molecular Formula: C3H6O3



α-hydroxypropionic acid, 2-Hydroxypropanoic acid, DL-Lactic acid, DL-Lactic acid, 2-Hydroxypropionic acid, Acidum lacticum, Lactic Acid 80% Pdr w/silca, Lactic Acid 80%, Unilac LA80, Tisulac, Espiritin, HiPure 90, l-lacticaci Lactic L-Milchsàure, α-Hydroxypropanoic acid, lactic acid, 2-hydroxypropanoic acid, DL-Lactic acid, 50-21-5, 2-hydroxypropionic acid,



Lactic Acid 80% (E270) is a colorless to yellow/brown liquid.
Store Lactic Acid 80% (E270) in a tightly closed container.
Store Lactic Acid 80% (E270) in a cool, dry, well-ventilated area away from incompatible substances.


Lactic Acid 80% (E270) can also be used for minor corrections in brewing PH can be used at higher levels for beer souring.
Lactic Acid 80% (E270) reduces the alkalinity levels of brewing liquor, stimulating maximum enzyme activity in the wort and enabling optimum pH levels throughout the whole brewing process.


Lactic Acid 80% (E270) improves extract yield and fermentation ability.
Lactic Acid 80% (E270) is suitable for beers where no other anions are needed, for example, lagers.
Lactic Acid 80% (E270) improves the clarity and stability of the finished product


Lactic Acid 80% (E270) is a ready-for-use acid used to reduce alkalinity in brewing liquor.
Lactic Acid 80% (E270) is Food Grade and made by fermentation of natural (beet or cane) sugar.
Lactic Acid 80% (E270) is a product of natural origin, obtained by fermentation of glucose.


Lactic Acid 80% (E270) is used in cosmetic compositions for pH adjustment and has good affinity for skin and hair.
Lactic Acid 80% (E270) improves skin hydration, removes dead cells and hair films (dandruff) having keratolytic action, hair shines.
Lactic Acid 80% (E270) is responsible for the tang that hits the mouth when eating dry aged beef.


Lactic Acid 80% (E270) is produced as natural L-Lactic acid by fermentation of carbohydrates like sugar or starch.
Lactic Acid 80% (E270)'s Chemical Formula is C3H6O3.
An organic acid, Lactic Acid 80% (E270), is used to reduce alkalinity without adding sulphate and chloride ions.


Lactic Acid 80% (E270) can help stimulate collagen and strengthen the skin, which equals fewer fine lines and wrinkles.
The hydroxy acids exfoliate the top layer of skin, helping smooth and even complexion, keep pores unclogged, brighten skin and even fade dark marks and discoloration.


Lactic Acid 80% (E270) is a versatile organic acid.
Lactic Acid 80% (E270) is soluble in water and in ethanol.
The inclusion of additional Lactic Acid 80% (E270) prior to rennetting overcomes this shortage and improves the curd yield.


Lactic Acid 80% (E270) is presented in a dropper bottles holding 4fl oz, to ensure an accurate dosing of milk and achieve consistent results when cheese making.
In production, Lactic Acid 80% (E270) is usually added up so that the pH of the milk is 5.0.
The casein in fermented milk is coagulated (curdled) by Lactic Acid 80% (E270) and it is also responsible for the sour flavor of sourdough breads.


If the pH is not within the range of 5.3 - 5.8, make gradual additions (0.10 - 0.15 mL/L) of Lactic Acid 80% (E270), mix and measure again.
Lactic Acid 80% (E270), from Jungbunzlauer, is an organic acid, occurring naturally in the human body and in fermented foods.
Lactic Acid 80% (E270) is a natural preservative and pH regulator.


Lactic Acid 80% (E270) is an organic acid with wide-reaching industrial applications.
Lactic Acid's 80% Food Grade specification makes it especially useful for food and beverage production, as well as pharmaceutical and cosmetic products.
Lactic Acid 80% (E270) is a versatile organic acid.


In its liquid state Lactic Acid 80% (E270) is colourless.
Lactic Acid 80% (E270) is one of the alpha-hydroxy acids (AHA’s).
These acids occur naturally in fruits, sugar cane and milk.


Lactic Acid 80% (E270) increasing wort's acidity and improving both mashing and fermentation.
The exact dosage depends on the alkalinity of the water used, the salts added and the malts used in the recipe.
Lactic Acid 80% (E270) is recommended to carry out a pH measurement of the mash before adding the product.


Lactic Acid 80% (E270) is a non dairy version that is part of a family of acids called Alpha Hydroxy Acids (AHA’s).
Lactic Acid 80% (E270) is produced from natural corn starch by advanced bio-fermentation and refining technology.
Lactic Acid 80% (E270) is a yellowish to colorless liquid, with a mildly acidic odour and taste.


Lactic Acid 80% (E270) is a naturally occurring alpha hydroxy acids (or AHAs) produced by fermentation of sugars.
Lactic Acid 80% (E270) is the alpha hydroxy acid most frequently used for peel products.
Lactic Acid 80% (E270), also known as milk acid, is an organic compound with the chemical formula C3H6O3.


Lactic Acid 80% (E270) is a strong Alpha-Hydroxy Acid and hence will have excellent exfoliant properties, although these are weaker than, but second only to, Glycolic Acid.
AHA products should be a stand alone treatment product and not included in another product.


While AHA can be included in other products there are certain incompatibilities that may arise plus AHAs (because of the pH required for best effectiveness) may not allow other products (such as cleansing masks) to work properly, and vice versa.
Lactic Acid 80% (E270) is also a widely used organic acidulate, probably because it is classified as a weak acid.


While AHA can be included in other products there are certain incompatibilities that may arise plus AHAs (because of the pH required for best effectiveness) may not allow other products (such as cleansing masks) to work properly, and vice versa.
Lactic Acid 80% (E270) is also a widely used organic acidulate, probably because it is classified as a weak acid.


As with all manufacturing processes, we recommend lab scale trials in order to determine appropriate quantities.
Lactic Acid 80% (E270) is a liquid solution in water of about 80% purity.
Lactic Acid 80% (E270), is an organic acid with applications in beer production as well as the cosmetic, pharmaceutical, food and chemical industries.


Lactic Acid 80% (E270) is an anti-wrinkle and anti-pigmentation component available in both over-the-counter and professional-grade skincare products.
Lactic Acid 80% (E270) is derived from milk and belongs to the alpha-hydroxy acid (AHAs) class of anti-ageing compounds.
Glycolic acid and citric acid are two further examples of AHAs.


Lactic Acid 80% (E270) is a liquid solution in water of about 80% purity.
Lactic Acid 80% (E270) is an AHA.
Lactic Acid 80% (E270) is sufficient to add a few drops to 100 ml shampoo to adjust the pH.


Even as a moisturizing additive Lactic Acid 80% (E270) should not be applied more than 0,5%.
Dilute Lactic Acid 80% (E270) before use.
As with all of the acids, Lactic Acid 80% (E270) is important to let your skin acclimate to their use.


Lactic Acid 80% (E270), also known as milk acid, is a chemical compound that plays a role in several biochemical processes.
Lactic Acid 80% (E270) is an alpha hydroxy acid that comes from milk.
As a result of its relatively greater molecular weight, Lactic Acid 80% (E270)'s keratolytic action is milder than that of glycolic acid, thus preventing skin irritations.


Lactic Acid 80% (E270) is an alpha hydroxy acid that comes from milk.
As a result of its relatively greater molecular weight, Lactic Acid 80% (E270)'s keratolytic action is milder than that of glycolic acid, thus preventing skin irritations.


Lactic Acid 80% (E270) is a strong Alpha-Hydroxy Acid and hence will have excellent exfoliant properties, although these are weaker than, but second only to, Glycolic Acid.
AHA products should be a stand alone treatment product and not included in another product.


Lactic Acid 80% (E270) comes in both R (D-) and S (L+) enantiomers which can be manufactured individually to near perfect optical purity.
This means Lactic Acid 80% (E270) is great in the production of other products which require a specific stereochemistry.
Lactic Acid 80% (E270) is a liquid solution in water of about 80% purity.


As with all manufacturing processes, we recommend lab scale trials in order to determine appropriate quantities.
Normally Lactic Acid 80% (E270) is titrated with a dilute solution of Lactic Acid (10 or 20% in water) until the desired pH is achieved.
Lactic Acid 80% (E270) is preferred as an acidulate as it tends to have less of a destabilizing effect on emulsions than Citric Acid.


Lactic Acid 80% (E270) is an Alpha Hydroxy Acid (AHA) and can be used to promote higher rates of desquamation and cell renewal.
Lactic Acid 80% (E270) is also a moistening compound.
Lactic Acid 80% (E270) belongs to a group of alpha hydroxy acids (AHA) which show exfoliating, moistening and anti-aging properties.


In nature Lactic Acid 80% (E270) exists in sour milk, yoghurts, sour rye soups and silages.
Lactic Acid 80% (E270) appears in two optical forms L and D, out of which only L-lactic acid is biologically active and is a natural element of the skin and hair.
Lactic Acid 80% (E270) is one of the main part of NMF – natural moistening factor, which is responsible for proper hydration of the epidermis.


Lactic Acid 80% (E270) stabilizes process of epidermis exfoliation in a very delicate way.
Lactic Acid 80% (E270) is an alpha hydroxy acid with both exfoliant and humectant properties.
Lactic Acid 80% (E270) is produced naturally in the body (it's the stuff that gives you a ‘stitch’ during a workout) and is also found in yogurt and milk.


Lactic Acid 80% (E270) dissolves very well in water.
Lactic Acid 80% (E270) is natural.
Lactic Acid 80% (E270) is approved as food additive E 270.


Lactic Acid 80% (E270) is used organic acid for industrial purposes.
Lactic Acid 80% (E270) is a hydroxycarboxylic acid, so it contains both a carboxyl group and a hydroxyl group.
Lactic Acid 80% (E270) is therefore also referred to as 2-hydroxypropionic acid, but according to IUPAC nomenclature recommendations, the name 2-hydroxypropionic acid should be used.


The salts and esters of Lactic Acid 80% (E270) are called lactates.
A concentrated solution of Lactic Acid 80% (E270) is typically a mixture of lactic acid lactate and lactic acid.
Lactic Acid 80% (E270) appears as a colorless to yellow odorless syrupy liquid.


Lactic Acid 80% (E270) is produced from natural cornstarch by advanced bio-fermentation and refining technology.
Lactic Acid 80% (E270) is a yellowish to colorless liquid, having a mild acid odor and taste.
Lactic acid appears as a colorless to yellow odorless syrupy liquid.



USES and APPLICATIONS of LACTIC ACID 80% (E270):
The casein in fermented milk is coagulated (curdled) by Lactic Acid 80% (E270).
Lactic Acid 80% (E270) is produced natutally in the Lacto-fermentation of foods.
Some examples of these types of foods are Kimchi, Sauerkraut, sour beer, tsukemono, suan cai, atsara and yoghurt.


Lactic Acid 80% (E270) is used directly as the acidulant.
Pickled Vegetables uses of Lactic Acid 80% (E270): Lactic Acid is effective in preventing the spoilage of olives, gherkins, pearl onions and other vegetables preserved in brine.


Lactic Acid 80% (E270) is a vital ingredient in Ricotta Impastata, Mozzarella, Queso Blanco and other speciality cheeses and can be used in the production of sour milk products, such as Koumiss, Laban, Kefir, as well as some cottage cheeses.
Lactic Acid 80% (E270) is an Alpha Hydroxy Acid (AHA) and can be used to promote higher rates of desquamation and cell renewal.


Lactic Acid 80% (E270) can be used to adjust the pH of many formulations and can be used as a milder alternative to glycolic acid.
Lactic Acid 80% (E270) and its salt, Sodium Lactate, can be used as humectants.
Lactic Acid 80% (E270) is used in facial products and also body lotions and moisturisers, never directly on skin.


Lactic Acid 80% (E270) is also used as an acidifying agent.
Lactic Acid 80% (E270) is food grade and is used for the production of several types of cheeses.
Lactic Acid 80% (E270) is particularly useful when UHT, ultra-pasturized or powdered milk are used as the starting materials, since the heat treatments used in the production of these milks deactivates the lactose and prevents the cheese culture from being able to turn it fully into Lactic Acid 80% (E270).


Lactic Acid 80% (E270) is easy to use in liquid form.
Lactic Acid 80% (E270) works well with hyaluronic acid and Vitamins A, B and C.
Lactic Acid 80% (E270) can also be used as a pH regulator: lactic acid will lower the pH.


Lactic Acid 80% (E270) is used Soapmaking pH adjustment, increased firmness of bars and solid format products (especially if pre-neutralised with Lye).
Lactic Acid 80% (E270) is used to produce serial products or widely used in food, vintage, beverage, drugs, polymerization, textile, leather, tobacco, feed, plastic chemicals, pesticide, polymer solution and other industry.


Lactic Acid 80% (E270) is also recommended for body and scalp-care for it helps in case of dry skin as well as skin exfoliation and cornification.
Lactic Acid 80% (E270) has been used in the production of beer for decades, contributing a unique tartness to this popular beverage.
With its 80% concentration of Lactic Acid 80% (E270), this specially formulated solution allows you to easily control the level of tartness in your product.


Whether you’re using lactic acid to adjust the flavour of your beer or in other food production needs, Lactic Acid 80% (E270) is the perfect choice for creating a finished product that meets all quality standards while delighting consumers.
Lactic Acid 80% (E270) can be used to adjust the pH of many formulations and can be used as a milder alternative to glycolic acid.


Lactic Acid 80% (E270) and its salt, Sodium Lactate, can be used as humectants.
Lactic Acid 80% (E270) is used skincare pH adjustment, humectancy, skin brightening, desquamation, exfoliation.
Lactic Acid 80% (E270) is used haircare pH adjustment, humectancy.


Lactic Acid 80% (E270) has an anti-microbial effect and is the basis for preservation by fermentation in many food products.
Lactic Acid 80% (E270) serves as a preservative, pH regulator and flavouring agent.
Lactic Acid 80% (E270) is primarily found in sour milk products, such as: koumiss, leban, yogurt, kefir, and some cottage cheeses.


Faster exfoliation of cells results in the growth of new ones.
Preparations with Lactic Acid 80% (E270) support the treatment of acne.
When using masques with Lactic Acid 80% (E270) pointwise (7.0-15.0%) one can try removing sun, acne and aging maculae.


After using preparations with Lactic Acid 80% (E270) one should protect the skin against sun.
Without the layers of cornified cells, “young” epidermis absorbs nourishing cosmetics considerably better.
Therefore, tonics, scrubs and masques with Lactic Acid 80% (E270) belong to basic cosmetics for the care of oily, mixed, acne and mature complexions.


The cosmetics with Lactic Acid 80% (E270) should be used with the utmost care for dry complexion.
Lactic Acid 80% (E270) regulates cellular skin regeneration, and improves skin structure and colour.
Lactic Acid 80% (E270) enhances the effects of other cosmetic preparations.


Lactic Acid 80% (E270) improves skin moistening for the skin becomes more soft and elastic.
Lactic Acid 80% (E270) influences the production of skin collagen by increasing thickness and strengthening the dermis.
Lactic Acid 80% (E270) increases the level of glycosaminoglycans that is compounds that absorb water as a sponge and provide hydration of deeper layers of the skin.


Lactic Acid 80% (E270) is classed as an advanced skincare ingredient and should not be used unless you understand the usage and applications of Lactic Acid.
Lactic Acid 80% (E270) is used acne Treatments & Skin Peels, Bee Keeping, In food production, To Extend shelf life of Meat,Fish & Poultry, Acidity regulator in drinks, In dairy products, Baking, Detergent, Animal Nutrition Supplement, and General Industry.


Lactic Acid 80% (E270) is widely used as an acidulent in the food industry, as well as for preservation and flavouring.
Lactic Acid 80% (E270) is used very useful to rejuvenate the skin by encouraging the shedding of old surface skin cells.
Lactic Acid 80% (E270) can reduce the appearance of fine lines, irregular pigmentation, age spots & decreases enlarged pores.


Lactic Acid 80% (E270) is often used in creams & lotions at a lower concentration for a more gentle acid-based peel.
Lactic Acid 80% (E270) is used in cosmetic to biolifting for it makes the skin elastic, evens wrinkles, brightens discolorations and narrows pores.
Lactic Acid 80% (E270) is also used in conditioners and shampoos because it activates hair bulbs, accelerating hair growth.


The combination of mild peeling, regeneration and hydration that Lactic Acid 80% (E270) offers, makes it an ideal peeling treatment for sensitive and dehydrated skin and a good choice for skin that will undergo chemical peeling for the first time.
The Lactic Acid 80% (E270) in combination with the pH result in targeted actions and indications.


Lactic Acid 80% (E270) is applied to adjust the pH of cosmetic products such as shampoo and shower gel or creams and lotions.
As Lactic Acid 80% (E270) is evident from the name, it reduces the pH of a product.
In addition to pH-regulation Lactic Acid 80% (E270) has excellent moisturizing effects.


An exception is the application in chemical peels.
Lactic Acid 80% (E270) is widely used in a range of food, industrial and manufacturing processes.
Lactic Acid 80% (E270) can be used for adjusting pH in the mash or sparge water.


Lactic Acid 80% (E270) may vary in colour from transparent to pale yellow.
Lactic Acid 80% (E270) is used a pH meter or test strips to control the pH.
Lactic Acid 80% (E270) may also be used in the final beer or wine for adding acidity.


Lactic Acid 80% (E270) is used to treat dry, rough & scaly skin.
Lactic Acid 80% (E270) may also be used for other conditions as determined by your doctor.
Normally Lactic Acid 80% (E270) is titrated with a dilute solution of Lactic Acid (10 or 20% in water) until the desired pH is achieved.


It is preferred as an acidulate as Lactic Acid 80% (E270) tends to have less of a destabilizing effect on emulsions than Citric Acid.
Lactic Acid 80% (E270) is used treating dry, rough & scaly skin.
Lactic Acid 80% (E270) may also be used for other conditions as determined by your doctor.


Lactic Acid 80% (E270) is one of the popular food additives and ingredients in most countries.
Commonly Lactic Acid 80% (E270) is used as a preservative and antioxidant.
Lactic Acid 80% (E270) also has uses as a fuel additive, chemical intermediate, acidity regulator, and disinfectant.


Lactic Acid 80% (E270) is also used in dialysis solutions, which results in a lower incidence of side effects compared to Sodium Acetate which can also be used.
Lactic Acid 80% (E270) is used frequently in the cosmetic industry due to the effect of promoting collagen production, helping to firm the skin against wrinkles and sagging.


Lactic Acid 80% (E270) is used as an additive in animal nutrition.
Lactic Acid 80% (E270) has health promoting properties.
Lactic Acid 80% (E270) is used as a humectant, or moisturizer, in some cosmetics.


Lactic Acid 80% (E270) ia used as a mordant, a chemical that helps fabrics accept dyes, in textiles.
Lactic Acid 80% (E270) is also used in tanning leather.
Lactic Acid 80% (E270) is used in the manufacturing of lacquers and inks.


Lactic Acid 80% (E270) is the principal building block for Poly Lactic Acid (PLA).
PLA is a biobased and bio-degradable polymer that can be used for producing renewable and compostable plastics.
Lactic Acid 80% (E270) is used to adjust the pH of the mash or the sparge water.


Lactic Acid 80% (E270) is used for Pilsner style lagers to reduce alkalinity.
Lactic Acid 80% (E270) used to reduce alkalinity without adding sulphate and chloride ions.
Lactic Acid 80% (E270) can also be used for minor corrections in brewing


Lactic Acid 80% (E270) can also cause micro peeling, which can help reduce various scars and age spots.
This is a great solution for people with sensitive or dry skin where exfoliants don’t work.
Lactic Acid 80% (E270) is used to treat dry, rough & scaly skin.


Lactic Acid 80% (E270) may also be used for other conditions as determined by your doctor.
Dilute Lactic Acid 80% (E270) before use.
As with all of the acids, Lactic Acid 80% (E270) is important to let your skin acclimate to their use.


For those whose skin is not used to the acids a slight stinging and redness may result.
If this occurs, Lactic Acid 80% (E270) reduce usage.
Lactic Acid 80% (E270) contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn.


Lactic Acid 80% (E270) is used a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.
Lactic Acid 80% (E270) reduces the alkalinity levels of brewing liquor stimulating maximum enzyme activity in the wort enabling optimum pH levels throughout the whole brewing process.


Lactic Acid 80% (E270) improves extract yield and fermentation ability
Lactic Acid 80% (E270) is suitable for beers where no other anions are needed for example lagers.
Lactic Acid 80% (E270) improves clarity and stability of the finished product.


Lactic acid in 80% concentration for chemical exfoliation, suitable for all skin types.
Lactic Acid 80% (E270) offers cellular regeneration, hydration and reduction of the appearance of wrinkles on the skin.
Typical use level of Lactic Acid 80% (E270) is between 1-20% in peels, creams, lotions, masks, cleansers.


Due to Lactic Acid 80% (E270)'s acidity the final product needs to be tested for safe pH.
Optimal pH range of Lactic Acid 80% (E270) is from 3.5-5.0.
Some over the counter products, after adding Lactic Acid 80% (E270), will separate as a result of the low pH, and need to be stabilized.


In many food products usually serves, Lactic Acid 80% (E270) is used as either as a pH regulator, as a preservative, or as a flavoring agent.
Lactic Acid 80% (E270) is used as an acidity regulator.
Lactic Acid 80% (E270) is effective in preventing the spoilage of vegetabels.


Lactic Acid 80% (E270) is used as an excellent acidification agent for many dairy products.
Lactic Acid 80% (E270) is used as an enhance savory flavors.
In pharmaceutical technology, Lactic Acid 80% (E270) is used as a starting material for other substances.


Lactic Acid 80% (E270) is used as a valuable component in biomaterials.
Lactic Acid 80% (E270) is used as a natural anti-bacterial agent in disinfecting products.
Lactic Acid 80% (E270) is used in the industrial processes.


PH can be used at higher levels for beer souring.
Lactic Acid 80% (E270) has a good moisturising effect on the skin and can be used in water based serums, gels, toners, creams and lotions.
Lactic Acid 80% (E270) can help the skin to look fresher and younger.


Lactic Acid 80% (E270) is especially beneficial in night creams and anti aging products.
When Lactic Acid 80% (E270) is used at higher concentrations, it can have an exfoliating effect.
Lactic Acid 80% (E270) will improve the skin's appearance and help to remove surface debris and dead skin cells.


Hair Care: Used in a hair pack, Lactic Acid 80% (E270) will cleanse a congested scalp for example, after a weave has been removed, having been on for several months.
Never use Lactic Acid 80% (E270) directly on the skin.


Best Lactic Acid 80% (E270) is added in stage 3 (cool down) when making creams and lotions.
Be aware that Lactic Acid 80% (E270) can make creams and lotions thinner or unstable so you need to start with a very strong and stable cream or lotion.
As a pH regulator, Lactic Acid 80% (E270) can be used to move the pH number lower (more acidic) for when using Preservative K which only functions correctly in a narrow pH range.


Often, Lactic Acid 80% (E270) is derived from milk, however, ours is made from maize or corn, and free from GMO.
Lactic Acid 80% (E270) is sold at an 80% concentration i.e. Lactic Acid 80% (E270) with 20% Water as an aqueous solution.
According to the Cosmetic Ingredient Database (CosIng), the functions of Lactic Acid 80% (E270) are: Buffering, Humectant, Skin Conditioning.


Lactic Acid 80% (E270) is often used as a milder alternative to glycolic acid in cosmetic formulations and can also be used to lower pH during manufacturing.
Lactic Acid 80% (E270) is produced by fermentation of glucose syrup from maize by using a bacterial strain.
Lactic Acid 80% (E270) is an acid and should never be used undiluted.


When used in proper concentrations (up to 5.0%), Lactic Acid 80% (E270) loosens intercellular cement.
Regular use of cosmetics with Lactic Acid 80% (E270) rejuvenates the epidermis and makes wrinkles even by means of a gradual exfoliation of dead cells of horny layer.


Lactic Acid 80% (E270) makes small surface wrinkles even and improves skin elasticity as well as firmness; it is an anti-aging ingredient; it helps in case of discolorations and small acne scars.
Lactic Acid 80% (E270) makes pores clear and shows antibacterial properties, hence, it prevents the creation of trouble spots that are all kinds of eczemas and blackheads; it helps in the treatment of acne.


Lactic Acid 80% (E270) is used soapmaking pH adjustment, increased firmness of bars and solid format products (especially if pre-neutralised with Lye).
Lactic Acid 80% (E270) is used Skincare pH adjustment, humectancy, skin brightening, desquamation, exfoliation.
Lactic Acid 80% (E270) is used Haircare pH adjustment, humectancy.


Skin Care: Depending on the strength of the dilution used, Lactic Acid 80% (E270) can be used as a pH regulator, a moisturiser or as a skin peel.
In the lower percentages, Lactic Acid 80% (E270) reduces Trans Epidermal Water Loss (TEWL) by supporting the skin's barrier function.
When applied, Lactic Acid 80% (E270) cleaves the bonds between keratinocytes on the external layer, thus reducing them and leading to gradual regeneration.


This results in a mild but effective exfoliation of the horny layer and in the simultaneous regeneration of cells.
Lactic Acid 80% (E270) stimulates the production of collagen and glycosaminoglycans that make up the intercellular material.
Another advantage provided by Lactic Acid 80% (E270) is that it naturally hydrates the skin; this action results in increased formation of ceramides, thus enhancing the function of the keratin barrier.


Within the Personal Care sector, Lactic Acid 80% (E270) functions as an acidifier with moisturising, exfoliating and antibacterial properties.
When used topically, Lactic Acid 80% (E270) can assist with the removal of dead skin cells helping to renew the skin, improve skin texture and tone along with functioning as a humectant.


Confectionery products uses of Lactic Acid 80% (E270): such as hard boiled candy, fruit gums with Lactic Acid 80% (E270) results in a mild acid taste, improved quality and longer shelf life.
Lactic Acid 80% (E270) has moistening effect as a result of its properties to bind water in upper layers of the epidermis.


Lactic Acid 80% (E270) is used to make cultured dairy products, as a food preservative, and to make chemicals.
Lactic Acid 80% (E270) is used as a solvent and acidulant in the production of foods, drugs, and dyes.
Lactic Acid 80% (E270) is also used as a mordant in woolen goods printing, a soldering flux, a dehairing agent, and a catalyst for phenolic resins.


Lactic Acid 80% (E270) is also used in leather tanning, oil well acidizing, and as a plant growth regulator.
Lactic Acid 80% (E270) is applied in Petroleum Production and Refining, Soldering, Farming (Pesticides) ,Leather Tanning and Processing, Fur Dressing and Dyeing, Textiles (Printing, Dyeing, or Finishing).


The fastest growing use for Lactic Acid 80% (E270) is its use as a monomer for the production of polylactic acid or polylactide (PLA).
Applications for PLA include containers for the food and beverage industries, films and rigid containers for packaging, and serviceware (cups, plates, utensils).


The PLA polymer can also be spun into fibers and used in apparel, fiberfill (pillows, comforters), carpet, and nonwoven applications such as wipes.
Lactic Acid 80% (E270) is used in dyeing baths, as mordant in printing woolen goods, solvent for water-insoluble dyes (alcohol-soluble induline, nigrosine, spirit-blue).


Lactic Acid 80% (E270) is used reducing chromates in mordanting wool.
Lactic Acid 80% (E270) is used manufacturing cheese, confectionery.
Lactic Acid 80% (E270) is used component of babies' milk formulas; acidulant in beverages; for acidulating worts in brewing.


Lactic Acid 80% (E270) is used in preparation of sodium lactate injections. Ingredient of cosmetics.
Lactic Acid 80% (E270) is used component of spermatocidal jellies.
Lactic Acid 80% (E270) is used for removing Clostridium butyricum in manufacturing of yeast; dehairing, plumping, and decalcifying hides.


Lactic Acid 80% (E270) is used solvent for cellulose formate.
Lactic Acid 80% (E270) is used flux for soft solder.
Lactic Acid 80% (E270) is used manufacturing lactates which are used in food products, in medicine, and as solvents.


Lactic Acid 80% (E270) is used plasticizer, catalyst in the casting of phenolaldehyde resins.
Lactic Acid 80% (E270) can be used as acidulent, flavoring agent and pH regulator in beverages, meat, sourdough, salads and dressings, confectionery and pickled vegetables.


Lactic Acid 80% (E270) is used in food and technical applications.
Liquid Lactic Acid 80% (E270), as a 1:1 mixture of levorotatory and dextrorotatory lactic acid, is very commonly used for acid regulation in bakery and confectionery products or in beverages and for preservation.


Likewise, Lactic Acid 80% (E270) is used in lactofermentation and is used to preserve silages in feed production.
In technical applications, Lactic Acid 80% (E270) provides support through its biocidal effect and is therefore a component of disinfectant solutions and other cleaners.


In addition, Lactic Acid 80% (E270) is used for gentle decalcification.
Lactic Acid 80% (E270) is food grade and is used for the production of several types of cheeses.
Lactic Acid 80% (E270) is particularly useful when UHT, ultra-pasteurised or powdered milk are used as the starting materials, since the heat treatments used in the production of these milks deactivates the lactose and prevents the cheese culture from being able to turn it fully into Lactic Acid 80% (E270).


The inclusion of additional Lactic Acid 80% (E270) prior to rennetting overcomes this shortage and improves the curd yield.
Lactic Acid 80% (E270) is a vital ingredient in Ricotta Impastata, Mozzarella, Queso Blanco and other speciality cheeses and can be used in the production of sour milk products, such as Koumiss, Laban, Kefir, as well as some cottage cheeses.


In production, Lactic Acid 80% (E270) is usually added so that the pH of the milk reaches around 5.0.
The casein in fermented milk is coagulated (curdled) by Lactic Acid 80% (E270) and it is also responsible for the sour flavour of sourdough breads.
Lactic Acid 80% (E270) is mainly used to adjust the pH of cosmetic products and is added during the production of shampoos to increase the shine of the hair.


Lactic Acid 80% (E270) is used to adjust the pH of cosmetic products
When making shampoos, Lactic Acid 80% (E270) is added to make the hair shiner
Often used as food or feed additives, Lactic Acid 80% (E270) can improve the flavor of food and prolong the shelf life.


Lactic Acid 80% (E270) is widely used in canned food, bread, flour, pastry, feed and other industries as a food flavor improver.
Lactic Acid 80% (E270) is especially suitable for the acidity adjustment of various solid and powdered foods.
Lactic Acid 80% (E270)'s excellent pH adjustment function and antibacterial ability can effectively inhibit the growth of microorganisms and prolong the shelf life of food.


Pharmaceutical technology uses Lactic Acid 80% (E270) to convert water-insoluble medicinal substances into salts of lactic acid (lactates); these are more soluble in water (example: ciprofloxacin).
In cosmetics, Lactic Acid 80% (E270) is used in skin creams and other products to treat acne.


Lactic Acid 80% (E270) is used to make cultured dairy products, as a food preservative, and to make chemicals.
Lactic Acid 80% (E270) has a role as a Daphnia magna metabolite and an algal metabolite.
Lactic Acid 80% (E270) is functionally related to a propionic acid.


Lactic Acid 80% (E270) is a conjugate acid of a lactate.
A normal intermediate in the fermentation (oxidation, metabolism) of sugar.
The concentrated form is used internally to prevent gastrointestinal fermentation.


Sodium lactate is the sodium salt of Lactic Acid 80% (E270), and has a mild saline taste.
It is produced by fermentation of a sugar source, such as corn or beets, and then, by neutralizing the resulting Lactic Acid 80% (E270) to create a compound having the formula NaC3H5O3.
Lactic Acid 80% (E270) was one of active ingredients in Phexxi, a non-hormonal contraceptive agent.


-Power supply uses of Lactic Acid 80% (E270):
A number of foods are made directly through Lactic Acid 80% (E270) fermentation.
This mainly includes sour milk products such as sour milk, yogurt, kefir and buttermilk.
These are produced by infecting pasteurized milk with starter cultures of Lactic Acid 80% (E270) bacteria.

Other products include lacto-fermented vegetables such as sauerkraut, beetroot in some varieties of borscht, or kimchi, as well as sourdough and sourdough products.
Silage, fresh feed made sustainable by fermentation, is also based on Lactic Acid 80% (E270) fermentation.
As a food additive, Lactic Acid 80% (E270) carries the designation E 270.

Lactic Acid 80% (E270) is used in many different ways as an acidity regulator in the food and luxury goods industries, for example in baked goods, confectionery and occasionally in lemonades.
By changing the pH value in the food to a pH of about 4, the food is preserved, since colonization with other microorganisms is largely excluded.
In the form of the salts calcium lactate or calcium lactate gluconate Lactic Acid 80% (E270) can also be added for calcium enrichment.


-Material uses of Lactic Acid 80% (E270):
Lactic Acid 80% (E270) is the monomer of polylactides or polylactic acids (PLA), which are used in various ways as biodegradable and biobased plastics.
Lactic Acid 80% (E270) has an antibacterial effect and is therefore added to liquid soaps, cleaners and detergents.

They develop their disinfecting effect optimally at a pH value of 3 to 4.
Lactic Acid 80% (E270) was and is also used as a contraceptive.
Lactic Acid 80% (E270) is used as a descaling agent in the tannery for descaling hides.

Lactic Acid 80% (E270) is also used for this purpose in the textile industry and printing companies.
Some cleaning tablets for coffee machines, soft drinks machines and similar appliances contain Lactic Acid 80% (E270) as a descaling agent.
Beekeepers use Lactic Acid 80% (E270) to treat bees against the Varroa mite, ensuring that the treated hives or honeycombs are brood free.
Arachnologists use Lactic Acid 80% (E270) to illuminate the prepared epigyne of female spiders or other chitin structures and to dissolve tissue debris.


-Beer brewing uses of Lactic Acid 80% (E270):
Lactic Acid 80% (E270) is to lower the pH and add a bit of tartness.
Naturally add in small amounts or Lactic Acid 80% (E270) will become quite sour.


-Cheese making & Whipped Butter uses of Lactic Acid 80% (E270):
Ricotta in particular and whipped butter in combination with GDL.
Ricotta Impastata, Mozzarella and Queso Blanco.


-Interesting non food uses for Lactic Acid 80% (E270):
Lactic Acid 80% (E270) is the principal building block for Poly Lactic Acid (PLA) biodegradable plastics.
PLA is a biobased and bio-degradable polymer that can be used for producing renewable and compostable plastics.
Lactic Acid 80% (E270) is also being used in the cosmetics industry for acne treatment.



FEATURES AND BENEFITS OF LACTIC ACID 80% (E270):
*Lactic Acid 80% (E270) is very useful to rejuvenate the skin by encouraging the shedding of old surface skin cells
*Lactic Acid 80% (E270) can reduce the appearance of fine lines, irregular pigmentation, age spots & decreases enlarged pores
*Lactic Acid 80% (E270) is used good choice for first-time peel users or for those with sensitive skin
*Lactic Acid 80% (E270) is often used in creams & lotions at a lower concentration for a more gentle acid-based peel.



USE IN FOOD, LACTIC ACID 80% (E270):
Lactic Acid 80% (E270) is a natural preservative found in several foods, including pickled vegetables, yoghurt, and baked goods.
Lactic Acid 80% (E270) is a cheap and minimally processed
Lactobacillus and Streptococcus cultures produce Lactic Acid 80% (E270) through fermentation.
The bacteria break down sugar to extract energy and produce Lactic Acid 80% (E270) as a byproduct.
Lactic Acid 80% (E270) helps regulate pH levels and prevents the growth of microorganisms, extending shelf life.



HOW TO USE LACTIC ACID 80% (E270) IN COSMETICS:
- Lactic Acid 80% (E270) is a product that does not apply to pure skin
- Lactic Acid 80% (E270) can be included as an ingredient in cosmetic compositions containing acidulant and water: serums, gels, tonics, masks, lotions, creams, shampoos, cleanses, etc.



BENEFITS AND APPLICATIONS OF LACTIC ACID 80% (E270):
Lactic Acid 80% (E270) is used to treat hyperpigmentation, age spots, and other conditions that contribute to a dull, uneven complexion.
Lactic Acid 80% (E270) also enhances skin tone and minimises the appearance of pores.

Lactic Acid 80% (E270) promotes cell turnover and cell renewal, which are the processes through which your skin loses old cells and replaces them with new ones.
Lactic Acid 80% (E270) works really well for sensitive skin because of its milder nature as compared to other alpha-hydroxy acids.

Lactic Acid 80% (E270) is also a key component of over-the-counter lotions and creams for "chicken skin," i.e., pimples on the backs of the arms.
Lactic Acid 80% (E270) aids in the dissolution of the clog of skin cells that form around the hair follicle, smoothing out the bumpiness.
Lactic Acid 80% (E270) is commonly found in topical therapies for eczema, psoriasis, and rosacea.



THE PROPERTIES OF LACTIC ACID 80% (E270):
The properties of Lactic Acid 80% (E270)
- Keratolytic exfoliates the skin by removing dead skin and scalp cells
- Stimulates collagen and elastin synthesis, promoting cell renewal
- Lactic Acid 80% (E270) improves skin grain and appearance pH
- Activates the emulsifier conditioner used in the manufacture of hair care compositions



BENEFITS OF LACTIC ACID 80% (E270):
*Brightens a dull complexion
*Humectant and skin firmer
*Exfoliant
*Improves skin tone and texture
*Vegan Friendly
*GMO-free



FUNCTION OF LACTIC ACID 80% (E270):
In food, apart from its nutritional function for normal growth, Lactic Acid 80% (E270) improves flavor and taste, improves quality of food and beverage products such as confectionery, cake, milk powder, yogurt etc. as firming agent, buffering agent and flour regulator.
Lactic Acid 80% (E270) increases effectiveness of antioxidants, prevents decolorization of fruits and vegetables.



BENEFITS OF LACTIC ACID 80% (E270):
Lactic Acid 80% (E270) reduces the alkalinity levels of brewing liquor, stimulating maximum enzyme activity in the wort enabling optimum pH levels throughout the whole brewing process.
Lactic Acid 80% (E270) improves extract yield and fermentability.
Lactic Acid 80% (E270) is suitable for beers where no other anions are needed, for example, pilsner lagers.
Lactic Acid 80% (E270) can also be used to reduce the pH of final wort or products.



SUGGESTED BLENDS OF LACTIC ACID 80% (E270):
Lactic Acid 80% (E270) works well in conjunction with Vitamin A, B and C.
Be sure to check the final pH level is not less than 3.5 when combining several acidic ingredients together.



HOW LACTIC ACID 80% (E270) WORKS:
Lactic Acid 80% (E270) works by removing the upper layer of skin cells, which is usually composed of dead skin cells.
Lactic Acid 80% (E270) also works by increasing the natural moisture retention capabilities of the skin to give your skin a hydrated look.



CONCENTRATION AND SOLUBILITY OF LACTIC ACID 80% (E270):
Lactic Acid 80% (E270) is recommended that it should be used at a concentration of 1–5%.
Lactic Acid 80% (E270) is soluble in water, alcohol, and glycerol but is insoluble in oil.



HOW TO USE LACTIC ACID 80% (E270):
Prepare the oil and water phases of your formulation separately.
Heat the oil and water phases using a double boiler.
Add Lactic Acid 80% (E270) to the water phase, accompanied by constant stirring.
Blend both the phases together using a mini-mixer or a large mixing brush



PHYSICAL and CHEMICAL PROPERTIES of LACTIC ACID 80% (E270):
Odor: odorless
Melting point/freezing point:
Melting point: 18 °C at 1.013 hPa
Initial boiling point and boiling range: 122 °C at 18,66 - 19,99 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 113 °C - closed cup
Autoignition temperature: 400 °C at 1.011,4 - 1.018,9 hPa
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 100 g/l at 20 °C - soluble

Partition coefficient: n-octanol/water:
log Pow: ca.-0,54 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: No data available
Density: 1,25 g/cm3 at 15 °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:
Surface tension 70,7 mN/m at 1g/l at 20 °C
Formula: H₃CCH(OH)COOH
MW: 90.08 g/mol
Boiling Pt: 122 °C (20 hPa)
Density: 1.11…1.21 g/cm³ (20 °C)
Storage Temperature: Ambient
MDL Number: MFCD00004520
CAS Number: 50-21-5
EINECS: 200-018-0

CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0
Mol File: 50-21-5.mol
Lactic acid Chemical Properties
Melting point: 18°C
alpha: -0.05 º (c= neat 25 ºC)
Boiling point: 122 °C/15 mmHg (lit.)
density: 1.209 g/mL at 25 °C (lit.)
vapor density: 0.62 (vs air)
vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
refractive index: n20/D 1.4262

Fp: >230 °F
storage temp.: 2-8°C
solubility: Miscible with water and with ethanol (96 per cent).
form: syrup
pka: 3.08(at 100℃)
Specific Gravity: 1.209
color: Colorless to yellow
Water Solubility: SOLUBLE
Merck: 145,336
JECFA Number: 930
BRN: 1209341
Stability: Stable.
Physical state: viscous
Color: colorless



FIRST AID MEASURES of LACTIC ACID 80% (E270):
-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 LACTIC ACID 80% (E270):
-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 with liquid-absorbent material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LACTIC ACID 80% (E270):
-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 LACTIC ACID 80% (E270):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
*Respiratory protection
Recommended Filter type: Filter type ABEK
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LACTIC ACID 80% (E270):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.



STABILITY and REACTIVITY of LACTIC ACID 80% (E270):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available.
-Incompatible materials:
No data available

LACTIC ACID ETHYL ESTER
Lactic acid ethyl ester is an environmentally benign solvent with effectiveness comparable to petroleum-based solvents.
Lactic acid ethyl ester is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.
Lactic acid ethyl ester, also known as lactic acid ethyl ester, is the organic compound with the formula CH3CH(OH)CO2CH2CH3.

CAS Number: 687-47-8
EC Number: 202-598-0
Molecular Formula: C5H10O3
Molecular Weight (g/mol): 118.13

ETHYL LACTATE, 97-64-3, Ethyl 2-hydroxypropanoate, Solactol, Actylol, Acytol, Lactic acid, ethyl ester, Ethyl 2-hydroxypropionate, Propanoic acid, 2-hydroxy-, ethyl ester, Lactate d'ethyle, 2-Hydroxypropanoic acid ethyl ester, Lactic Acid Ethyl Ester, Ethyl alpha-hydroxypropionate, FEMA No. 2440, Eusolvan, Ethyl lactate (natural), Ethylester kyseliny mlecne, Lactate d'ethyle [French], NSC 8850, HSDB 412, Ethylester kyseliny mlecne [Czech], 2-Hydroxypropionic Acid Ethyl Ester, EINECS 202-598-0, UN1192, Ethyl ester of lactic acid, BRN 1209448, UNII-F3P750VW8I, AI3-00395, F3P750VW8I, Ethyl .alpha.-hydroxypropionate, DTXSID6029127, CHEBI:78321, NSC-8850, 4-03-00-00643 (Beilstein Handbook Reference), ethyl d-lactate, Ethyl lactate,C5H10O3,97-64-3, EthylL-(-)-Lactate, ethyl-lactate, ethyl DL-lactate, DL-Ethyl Lactate, Milchsaureathylester, Nat. Ethyl Lactate, MFCD00065359, Ethyl racemic-lactate, lactic acid ethylester, (S)-(-)-2-Hydroxypropionic acid ethyl ester, PURASOLV ELS, VERTECBIO EL, Lactic acid-ethyl ester, ELT (CHRIS Code), Mono-Ethyl mono-lactate, ETHYL LACTATE [MI], (.+/-.)-Ethyl lactate, Ethyl 2-hydroxypropanoate #, ETHYL LACTATE [FCC], SCHEMBL22598, ETHYL LACTATE [FHFI], ETHYL LACTATE [HSDB], ETHYL LACTATE [INCI], ETHYL LACTATE [MART.], DTXCID509127, WLN: QVY1 & O2, ETHYL LACTATE [WHO-DD], CHEMBL3186323, (+-)-Ethyl 2-hydroxypropanoate, (+-)-Ethyl 2-hydroxypropionate, FEMA 2440, NSC8850, Tox21_200889, 2-hydroxy-propionic acid ethyl ester, NA1192, Ethyl lactate, >=98%, FCC, FG, AKOS009157222, LS-2733, UN 1192, (+/-)-LACTIC ACID ETHYL ESTER, CAS-97-64-3, NCGC00248866-01, NCGC00258443-01, (+/-)-ETHYL 2-HYDROXYPROPIONATE, AS-13500, SY030456, A9137, Ethyl lactate [UN1192] [Flammable liquid], Ethyl lactate, natural, >=98%, FCC, FG, Ethyl lactate, SAJ first grade, >=97.5%, FT-0626259, FT-0627926, FT-0651151, L0003, Ethyl lactate [UN1192] [Flammable liquid], EN300-115258, A845735, Q415418, J-521263, 2-[(4-benzylpiperazin-1-yl)methyl]isoindoline-1,3-dione, (±)-Ethyl 2 hydroxypropanoate, (±)-Ethyl 2-hydroxypropionate, (±)-Ethyl lactate, 2-Hydroxypropanoate d'éthyle [French] [ACD/IUPAC Name], 2-Hydroxypropanoic acid ethyl ester, 97-64-3 [RN], Ethyl 2-hydroxypropanoate [ACD/IUPAC Name], Ethyl ester of lactic acid, Ethyl lactate [ACD/Index Name] [Wiki], Ethyl α-hydroxypropionate, Ethyl α-hydroxypropionate, Ethyl-2-hydroxypropanoat [German] [ACD/IUPAC Name], MFCD00065359 [MDL number], OD5075000, Propanoic acid, 2-hydroxy-, ethyl ester [ACD/Index Name], QY1&VO2 [WLN], 2-hydroxypropionic acid ethyl ester, 4-03-00-00643 [Beilstein], Actylol, Acytol, DL-Ethyl Lactate, DL-Ethyllactate, DL-LACTIC ACID, ETHYL ESTER, Ethyl 2-hydroxy propanoate, Ethyl lactate,C5H10O3,97-64-3, Ethyl racemic-lactate, Ethylester kyseliny mlecne [Czech], ethyllactate, Ethyl-lactate, Eusolvan, Lactate d'ethyle [French], lactic acid ethyl ester, Lactic acid, ethyl ester, Lactic acid-ethyl ester, L-lactic acid ethyl ester, MFCD00077825 [MDL number], Milchs??ure??thylester, Propanoic acid, 2-hydroxy-, ethyl ester (9CI), Solactol, UN 1192

Lactic acid ethyl ester is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.
The odor of Lactic acid ethyl ester when dilute is mild, buttery, creamy, with hints of fruit and coconut.

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

Lactic acid ethyl ester, also known as actylol, is the organic compound with the formula CH3CH(OH)CO2CH2CH3.
Lactic acid ethyl ester is the ethyl ester of lactic acid.

A colorless liquid, Lactic acid ethyl ester is a chiral ester.
Being naturally derived, Lactic acid ethyl ester is readily available as a single enantiomer.

Lactic acid ethyl ester is commonly used as a solvent.
Lactic acid ethyl ester is considered biodegradable and can be used as a water-rinsible degreaser.

Lactic acid ethyl ester is an environmentally benign solvent with effectiveness comparable to petroleum-based solvents.
The worldwide solvent market is about 30 million pounds per year, where Lactic acid ethyl ester can have an important share.

Lactic acid ethyl ester is considered a chemical commodity and has attracted much attention in recent years, since Lactic acid ethyl ester is formed by the esterification reaction of ethanol and lactic acid, which can be generated from biomass raw materials through fermentation.
In this work, an overview regarding the main properties and applications of Lactic acid ethyl ester, as well as Lactic acid ethyl ester synthesis and production processes, with a particular emphasis on reactive/separation processes, is presented.

Lactic acid ethyl ester, lactic acid ethyl ester or 2-hydroxypropanoic acid ethyl ester is the chemical compound of lactic acid with ethanol in the form of an ester.
Depending on Lactic acid ethyl ester synthesis, Lactic acid ethyl ester is available as racemate or pure substance.

If Lactic acid ethyl ester is split back into Lactic acid ethyl ester starting materials ethanol and lactic acid (e.g. by a chemical reaction), Lactic acid ethyl ester can be decomposed in nature.
Esterases, naturally occurring enzymes, can also carry out the split back into the original materials.

Lactic acid ethyl ester is therefore considered a "green solvent", as Lactic acid ethyl ester does not leave any toxic decomposition products in the ecosystem.
This provides an advantage over chlorinated solvents or glycols or glycol ethers, which have a higher biological toxicity.

Also known as lactic acid ethyl ester, is a monobasic ester formed from lactic acid and ethanol, commonly used as a solvent hence the name “lactic acid ethyl ester”.
Lactic acid ethyl ester is considered biodegradable and can be used as a water-risible degreaser.
Lactic acid ethyl ester is found naturally in small quantities in a wide variety of foods including wine, chicken, and various fruits.

Lactic acid ethyl ester is produced from biological sources and can be either the Levo (S) form or Dextro (R) form, depending on the organism that is the source of the lactic acid.
The most biologically sourced Lactic acid ethyl ester is ethyl (−)-L-lactate (ethyl (S)-lactate).

Lactic acid ethyl ester is also produced industrially from petrochemical stocks, and this Lactic acid ethyl ester consists of the racemic mixture of Levo and Dextro forms.
In some jurisdictions, the natural product is exempt from many restrictions placed upon the use and disposal of solvents.
Because both enantiomers are found in nature, and because Lactic acid ethyl ester is easily biodegradable, Lactic acid ethyl ester is considered to be a “green solvent.”

Uses of Lactic acid ethyl ester:
Lactic acid ethyl ester is used as a solvent substitute for glycol ethers in photolithography in the semiconductor manufacturing industry.
Lactic acid ethyl ester is used in some nail polish removers.

Lactic acid ethyl ester is used as a solvent for resins, dyes, and coatings; has FDA approval for use as a food flavoring agent
Lactic acid ethyl ester is the active ingredient in many anti-acne preparations.

Uses at industrial sites:
Lactic acid ethyl ester is used in the following products: semiconductors, photo-chemicals, polymers, metal surface treatment products, non-metal-surface treatment products and washing & cleaning products.
Lactic acid ethyl ester is used in the following areas: formulation of mixtures and/or re-packaging.

Lactic acid ethyl ester is used for the manufacture of: electrical, electronic and optical equipment and machinery and vehicles.
Release to the environment of Lactic acid ethyl ester can occur from industrial use: in processing aids at industrial sites.

Industry Uses:
Processing aids, not otherwise listed
Solvent
Solvents (which become part of product formulation or mixture)

Consumer Uses:
Lactic acid ethyl ester is used in the following products: air care products, biocides (e.g. disinfectants, pest control products), perfumes and fragrances, polishes and waxes, washing & cleaning products and cosmetics and personal care products.
Other release to the environment of Lactic acid ethyl ester is likely to occur from: indoor use as processing aid and outdoor use as processing aid.

Widespread uses by professional workers:
Lactic acid ethyl ester is used in the following products: polishes and waxes and washing & cleaning products.
Other release to the environment of Lactic acid ethyl ester is likely to occur from: indoor use as processing aid.

Industrial Processes with risk of exposure:
Semiconductor Manufacturing
Painting (Solvents)
Plastic Composites Manufacturing

Applications of Lactic acid ethyl ester:
Lactic acid ethyl ester is an excellent ingredient for formulating printing inks, coatings, resin cleaners, paint strippers, graffiti removers, ink cleaners, etc.
Lactic acid ethyl ester alone and is an ideal wipe solvent.

Lactic acid ethyl ester can be used in industrial coatings applications, primarily in coil, extrusion, wood furniture and fixtures, containers and closures, automotive finishes and machinery.
Lactic acid ethyl ester is 100% biodegradable, easy and inexpensive to recycle.

Due to Lactic acid ethyl ester low toxicity, Lactic acid ethyl ester is a popular choice across many different production scenarios.
Lactic acid ethyl ester is also used as a solvent with various types of polymers.
In the presence of water, acids and bases the chemical will hydrolyse into ethanol and lactic acid.

Because both enantiomers are found in nature, and because Lactic acid ethyl ester is easily biodegradable, Lactic acid ethyl ester is considered to be a "green solvent."
Lactic acid ethyl ester and Lactic acid ethyl ester aqueous solutions are used as sustainable media for organic synthesis.

Due to Lactic acid ethyl ester relatively low toxicity, Lactic acid ethyl ester is used commonly in pharmaceutical preparations, food additives, and fragrances.
Lactic acid ethyl ester is also used as solvent for nitrocellulose, cellulose acetate, and cellulose ethers.

Production of Lactic acid ethyl ester:
Lactic acid ethyl ester is produced from biological sources, and can be either the levo (S) form or dextro (R) form, depending on the organism that is the source of the lactic acid.
Most biologically sourced Lactic acid ethyl ester is ethyl (−)-L-lactate (ethyl (S)-lactate).
Lactic acid ethyl ester is also produced industrially from petrochemical stocks, and this Lactic acid ethyl ester consists of the racemic mixture of levo and dextro forms.

Methods of Manufacturing of Lactic acid ethyl ester:

Derivation: (a) By the esterification of lactic acid with ethanol; (b) by combining acetaldehyde with hydrogen cyanide to form acetaldehyde cyanohydrin, which is converted into Lactic acid ethyl ester by treating with ethanol and an inorganic acid.

d-Lactic acid ethyl ester is obtained from d-lactic acid by azeotropic distillation with ethyl alcohol or benzene in the presence of concentrated H2SO4.
The l-form is prepared in similar fashion starting from l-lactic acid.
The racemic product is prepared by boiling for 24 hours optically inactive lactic acid with ethyl alcohol in carbon tetrachloride, or with an excess of ethyl alcohol in the presence of chlorosulfonic acid, or in the presence of benzenesulfonic acid in benzene solution.

Handling and Storage of Lactic acid ethyl ester:

Nonfire Spill Response:
ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.
All equipment used when handling Lactic acid ethyl ester must be grounded.

Do not touch or walk through spilled material.
Stop leak if you can do Lactic acid ethyl ester without risk.

Prevent entry into waterways, sewers, basements or confined areas.
A vapor-suppressing foam may be used to reduce vapors.

Absorb or cover with dry earth, sand or other non-combustible material and transfer to containers.
Use clean, non-sparking tools to collect absorbed material.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Water spray may reduce vapor, but may not prevent ignition in closed spaces.

Reactivity Profile of Lactic acid ethyl ester:

Lactic acid ethyl ester is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.

Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Fire Fighting of Lactic acid ethyl ester:
The majority of these products have a very low flash point.
Use of water spray when fighting fire may be inefficient.

SMALL FIRE:
Dry chemical, CO2, water spray or alcohol-resistant foam.
Do not use dry chemical extinguishers to control fires involving nitromethane (UN1261) or nitroethane (UN2842).

LARGE FIRE:
Water spray, fog or alcohol-resistant foam.
Avoid aiming straight or solid streams directly onto Lactic acid ethyl ester.
If Lactic acid ethyl ester can be done safely, move undamaged containers away from the area around the fire.

FIRE INVOLVING TANKS OR CAR/TRAILER LOADS:
Fight fire from maximum distance or use unmanned master stream devices or monitor nozzles.
Cool containers with flooding quantities of water until well after fire is out.

Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.
For massive fire, use unmanned master stream devices or monitor nozzles; if this is impossible, withdraw from area and let fire burn.

Accidental Release Measures of Lactic acid ethyl ester:

Isolation and Evacuation:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area for at least 50 meters (150 feet) in all directions.

LARGE SPILL:
Consider initial downwind evacuation for at least 300 meters (1000 feet).

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Cleanup Methods:
Use personal protective equipment.
Avoid breathing vapors, mist or gas.

Ensure adquate ventilation.
Remove all sources of ignition.

Evacuate personnel to safe areas.
Beware of vapors accumulating to form explosive concentrations.
Vopors can accumulate in low areas.

Disposal Methods of Lactic acid ethyl ester:
Recycle any unused portion of the material for Lactic acid ethyl ester approved use or return Lactic acid ethyl ester to the manufacturer or supplier.

Ultimate disposal of the chemical must consider:
Lactic acid ethyl ester's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations.
If Lactic acid ethyl ester is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

Identifiers of Lactic acid ethyl ester:
CAS Number:
687-47-8 (L-isomer)
97-64-3 (racemate)
7699-00-5 (D-isomer)

ChemSpider: 13837423
ECHA InfoCard: 100.002.363
EC Number: 202-598-0
PubChem CID: 7344
RTECS number: OD5075000
UNII: F3P750VW8I
UN number: 1192
CompTox Dashboard (EPA): DTXSID6029127
InChI: InChI=1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
Key: LZCLXQDLBQLTDK-UHFFFAOYSA-N
InChI=1/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
Key: LZCLXQDLBQLTDK-UHFFFAOYAV
SMILES: CCOC(=O)C(C)O

Synonym(s): (S)-(-)-Lactic acid ethyl ester, L(-)-Lactic acid ethyl ester, (S)-(-)-2-Hydroxypropionic acid ethyl ester
Linear Formula: CH3CH(OH)COOC2H5
CAS Number: 687-47-8
Molecular Weight: 118.13
MDL number: MFCD00004518
EC Index Number: 211-694-1

CAS: 687-47-8
Molecular Formula: C5H10O3
Molecular Weight (g/mol): 118.13
MDL Number: MFCD00004518
InChI Key: LZCLXQDLBQLTDK-BYPYZUCNSA-N
PubChem CID: 92831
ChEBI: CHEBI:78322
IUPAC Name: ethyl (2S)-2-hydroxypropanoate
SMILES: CCOC(=O)C(C)O

Properties of Lactic acid ethyl ester:
Chemical formula: C5H10O3
Molar mass: 118.132 g·mol−1
Appearance: Colorless liquid
Density: 1.03 g/cm3
Melting point: −26 °C (−15 °F; 247 K)
Boiling point: 151 to 155 °C (304 to 311 °F; 424 to 428 K)
Solubility in water: Miscible
Solubility in ethanol
and most alcohols: Miscible
Chiral rotation ([α]D): −11.3°
Magnetic susceptibility (χ): -72.6·10−6 cm3/mol

vapor pressure: 1.6 hPa ( 20 °C)
Quality Level: 200
Assay: ≥99% (GC)
form: liquid
autoignition temp.: 400 °C
potency: >2000 mg/kg LD50, oral (Rat)
expl. lim.: 1.5-16.4 % (v/v)
pH: 4 (20 °C, 50 g/L in H2O)
kinematic viscosity: 2.7 cSt(25 °C)
bp: 154 °C/1013 hPa
mp: -25 °C
transition temp: flash point 53 °C
density: 1.03 g/cm3 at 20 °C
storage temp.: 2-30°C
InChI: 1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m0/s1
InChI key: LZCLXQDLBQLTDK-BYPYZUCNSA-N

Molecular Weight: 118.13 g/mol
XLogP3-AA: 0.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 3
Exact Mass:
118.062994177 g/mol
Monoisotopic Mass:
118.062994177 g/mol
Topological Polar Surface Area: 46.5Ų
Heavy Atom Count: 8
Complexity: 79.7
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of Lactic acid ethyl ester:
Acidity: 0.1% max. (as lactic acid)
Melting Point: -26.0°C
Density: 1.0340g/mL
Boiling Point: 154.0°C
Flash Point: 46°C
Infrared Spectrum: Authentic
Assay Percent Range: 96% min. (GC)
Packaging: Glass bottle
Linear Formula: CH3CH(OH)CO2C2H5
Refractive Index: 1.4100 to 1.4160
Quantity: 250 mL
Beilstein: 03,264
Fieser: 17,135
Merck Index: 14,3817
Specific Gravity: 1.034
Specific Rotation Condition: − 10.00 (20.00°C neat)
Specific Rotation: − 10.00
Solubility Information: Solubility in water: soluble. Other solubilities: miscible with alcohols,ketones and esters
Formula Weight: 118.13
Percent Purity: 97%
Physical Form: Liquid
Chemical Name or Material: Ethyl L(-)-lactate

Structure of Lactic acid ethyl ester:
Dipole moment: 3.46 D

Related compounds of Lactic acid ethyl ester:
Lactic acid, MLactic acid ethyl ester

Related Products of Lactic acid ethyl ester:
Dimethyl Glutaconate (~10% Cis)
(E,E)-4,6-Dimethyl-2,4-heptadienoic Acid
3,6-Dimethyl-3-heptanol
1,1-Dimethoxybutane
(E)-6,6-Dimethyl-2-hept-1-en-4-yn-1-amine

Names of Lactic acid ethyl ester:

Regulatory process names:
2-Hydroxypropanoic acid ethyl ester
Actylol
Acytol
Ethyl 2-hydroxypropionate
Ethyl alpha-hydroxypropionate
ethyl DL-lactate
Ethyl lactate
ETHYL LACTATE
Ethyl lactate
ethyl lactate
Ethyl lactate (natural)
ethyl lactate ethyl DL-lactate
ethyl lactate; ethyl DL-lactate
Ethylester kyseliny mlecne
Lactate d'ethyle
Lactic acid, ethyl ester
Propanoic acid, 2-hydroxy-, ethyl ester
Solactol

Translated names:
DL-mleczan etylu (pl)
ester etylowy kwasu mlekowego (pl)
Ethyl DL-lactat (de)
ethyl-DL-laktát (cs)
ethyl-laktát (cs)
ethyl-laktát ethyl-DL-laktát (cs)
ethyllacta (da)
ethyllactaat (nl)
Ethyllactat (de)
Ethyllactat Ethyl DL-lactat (de)
etil DL-lactat (ro)
etil DL-laktat (sl)
etil lactat (ro)
etil lactat etil DL-lactat (ro)
etil laktat (sl)
etil laktat etil DL-laktat (sl)
etil-DL-laktat (hr)
etil-DL-laktatas (lt)
etil-DL-laktát (hu)
etil-DL-laktāts (lv)
etil-laktat (hr)
etil-laktát (hu)
etil-laktát etil-DL-laktát (hu)
etillaktatas (lt)
etillaktatas etil-DL-laktatas (lt)
etillaktāts (lv)
etyl-(RS)-laktát (sk)
etyl-laktát (sk)
etyllaktat (no)
etyllaktat (sv)
etyylilaktaatti (fi)
Etüül-DL-laktaat (et)
Etüüllaktaat (et)
lactate d'éthyle; DL-lactate d'éthyle; (fr)
lactato de etilo (es)
lactato de etilo (pt)
lattato di etile (it)
mleczan etylu (pl)
mleczan etylu DL-mleczan etylu ester etylowy kwasu mlekowego (pl)
γαλακτικό αιθυλο (el)
етил DL-лактат (bg)
етил лактат (bg)
етил лактат етил DL-лактат (bg)

IUPAC names:
2-ethoxypropanoic acid
ethyl (2R)-2-hydroxypropanoate
Ethyl (S)-2-hydroxypropanoate
ethyl 2-hydroxypropanoat
ETHYL 2-HYDROXYPROPANOATE
Ethyl 2-hydroxypropanoate
ethyl 2-hydroxypropanoate
Ethyl alpha hydroxypropionate
Ethyl DL Lactate
ethyl DL-lactate
ETHYL LACTATE
Ethyl Lactate
Ethyl lactate
ethyl lactate
ethyl lactate
ethyl lactate;
Ethyllactat
Ethyl 2-hydroxypropanoate

Other names:
Ethyl lactate
Lactic acid ethyl ester
2-Hydroxypropanoic acid ethyl ester
Actylol
Acytol

Other identifiers:
2676-33-7
607-129-00-7
97-64-3
LACTIC ACID FOOD GRADE
Lactic Acid Food Grade is a colorless or yellowish liquid with the characteristic smell of sour milk.
Lactic Acid Food Grade is an organic acid involved in various biochemical processes.


CAS Number: 50-21-5
EC Number: 200-018-0
Molecular Formula: C3H6O3



SYNONYMS:
α-hydroxypropionic acid, or 2-hydroxypropanoic acid, Milk acid



Lactic Acid Food Grade is also used as a flavoring agent.
Lactic Acid Food Grade can be used as acidulant, flavoring agent and pH regulator in beverage, beer, fruit wine, meat, sourdough, salads, dressings, confectionery (such as hard- boiled candy, fruit gums) and pickled vegetables.


Lactic Acid Food Grade is also employed in pharmaceutical technology to produce water-soluble lactates from otherwise-insoluble active ingredients.
Lactic Acid Food Grade finds further use in topical preparations and cosmetics to adjust acidity and for its disinfectant and keratolytic properties.
Lactic Acid Food Grade is an organic acid occurring naturally in the human body and in fermented foods.


The commercial production of lactic acid is typically done by fermentation.
Lactic Acid Food Grade is an organic acid.
Lactic Acid Food Grade has the molecular formula CH3CHOOH.


In its solid state, Lactic Acid Food Grade is white and miscible with water.
When it is in its dissolved state, Lactic Acid Food Grade forms a colourless solution.
Naturally, Lactic Acid Food Grade occurs as a chemical byproduct of anaerobic respiration in humans, this is the process by which cells produce energy without oxygen.


Lactic Acid Food Grade is also produced by bacteria in yoghurts and is also found in blood, where it is deposited by muscle and red blood cells.
Industrially, Lactic Acid Food Grade is produced by the bacterial fermentation of carbohydrates; fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria.


There is another method of production, through the chemical synthesis from acetaldehyde.
This is done by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile.
Lactic Acid Food Grade can be used in pharmaceutical products because it produces water-soluble lactates from otherwise insoluble ingredients.


In the food industry, Lactic Acid Food Grade is found primarily in sour milk products, these include kumis, laban, yogurt, kefir, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.
Lactic Acid Food Grade is also responsible for the sour flavour of sourdough bread.


Lactic Acid Food Grade is sourced from fermentation of plant sugars.
Lactic Acid Food Grade is a perfect for use in vegan cheese recipes.
Lactic Acid Food Grade adds a natural sour flavor to sourdough breads.


Lactic Acid Food Grade is an organic acid with applications in beer production as well as the cosmetic, pharmaceutical, food and chemical industries.
Lactic Acid Food Grade, also known as milk acid, is found primarily in sour milk products, such as yogurt, kefir, koumiss, laban, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.


Lactic Acid Food Grade is also responsible for the sour flavor of sourdough breads.
As an ingredient in personal care products, Lactic Acid Food Grade has the ability to boost skin’s moisture levels—even as it exfoliates.
At higher concentrations, Lactic Acid Food Grade acts as an exfoliator helping to dissolve connections between skin cells, while at lower levels it is used as a humectant, meaning it can actually help hydrate skin by pulling in water to the outer skin layer.


Lactic Acid Food Grade is one of the popular food additives and ingredients in most countries.
Lactic Acid Food Grade is an organic acid that is naturally occurring in the human body and fermented foods.
Fermentation occurs when natural bacteria feed on the sugar and starch of a food, producing Lactic Acid Food Grade.


The process creates B-vitamins, beneficial enzymes, and more.
L(+) form is preferred for better metabolism and natural carbohydrates.
Lactic Acid Food Grade is a versatile ingredient used in the food industry as an acidity regulator and acidulant.


Lactic Acid Food Grade helps stabilize acidity, maintain pH levels, and prevent microbial contaminations.
Increase the shelf life of your dairy products, fermented preserves, processed meats, beverages, egg-based products, and infant foods with Lactic Acid Food Grade.


Not only does Lactic Acid Food Grade act as a preservative, but it also enhances the taste and aroma of your creations.
Lactic Acid Food Grade is an organic acid occurring naturally in the human body and in fermented foods.
The commercial production of Lactic Acid Food Grade is typically done by traditional fermentation of natural carbohydrates.


Lactic Acid Food Grade standard is produced from natural corn starch by advanced bio-fermentation and refining technology.
Lactic Acid Food Grade is a yellowish to colorless liquid, having a mild acid odor and taste.
Lactic Acid Food Grade is an organic compound with the formula CH3CH(OH)CO2H.


In its solid state, Lactic Acid Food Grade is white and water-soluble.
In its liquid state, Lactic Acid Food Grade is clear.
Lactic Acid Food Grade is produced both naturally and synthetically.


As a food additive Lactic Acid Food Grade is approved for use in the EU, USA and Australia and New Zealand; it is listed by its INS number 270 or as E number E270.
Lactic Acid Food Grade is produced commercially by fermentation of carbohydrates such as glucose, sucrose, or lactose, or by chemical synthesis.


Carbohydrate sources of Lactic Acid Food Grade include corn, beets, and cane sugar.
Lactic Acid Food Grade is an alpha hydroxy acid with both exfoliant and humectant properties.
Lactic Acid Food Grade is produced naturally in the body (it's the stuff that gives you a ‘stitch’ during a workout) and is also found in yogurt and milk.


Lactic Acid Food Grade may exist either as a white solid in pure form, or a clear to yellowish liquid when dissolved in water.
Lactic Acid Food Grade can be produced via fermentation of carbohydrates, or synthesized from acetaldehyde.
Produced from natural corn starch through the traditional fermentation of natural carbohydrates, Lactic Acid Food Grade is a highly versatile solution used in various food applications.


One of the critical benefits of Lactic Acid Food Grade is its ability to help control pH levels.
Balancing pH levels improves flavor and texture and ensures the final product is safe and stable.
Due to regulating and lowering pH levels, Lactic Acid Food Grade serves as a microbial inhibitor with the growth of potentially harmful bacteria.


As a highly effective preservative, Lactic Acid Food Grade can help to extend product shelf life and reduce the risk of spoilage or contamination.
Lactic Acid Food Grade is ideal for bakery, dairy, beverages, meat, and many other applications.
Lactic Acid Food Grade is non-GMO.


Lactic Acid Food Grade is a chemical compound classified as an organic acid.
Lactic Acid Food Grade is a type of carboxylic acid, specifically known as 2-hydroxypropanoic acid.
Lactic Acid Food Grade is produced in the body as a byproduct of anaerobic metabolism, primarily in muscle tissues, during periods of intense physical activity or when oxygen supply is limited.


Lactic Acid Food Grade plays a crucial role in energy production and can serve as an alternative energy source when glucose availability is reduced.
In terms of its chemical structure, Lactic Acid Food Grade consists of a three-carbon molecule with a hydroxyl group (-OH) and a carboxyl group (-COOH) attached to the second carbon.


Lactic Acid Food Grade exists in two stereoisomeric forms: L-lactic acid and D-lactic acid.
L-lactic acid is the most common and biologically active form found in humans.
Overall, Lactic Acid Food Grade is an important compound with diverse biological and industrial significance, contributing to various physiological processes and serving as a versatile chemical building block in numerous applications.


Industrially, Lactic Acid Food Grade is produced by the bacterial fermentation of carbohydrates; fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria.
There is another method of production, through the chemical synthesis from acetaldehyde.


This is done by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile.
Lactic Acid Food Grade, particularly in its food-grade form, has a variety of uses in the food and beverage industry.
Lactic Acid Food Grade is a natural organic acid produced through fermentation, often from sources like sugars and starches.


Lactic Acid Food Grade has a mild, tart flavor and is generally recognized as safe (GRAS) when used in food applications.
Lactic Acid Food Grade is an organic acid.
Lactic Acid Food Grade has the molecular formula CH3CHOOH.


In its solid state, Lactic Acid Food Grade is white and miscible with water.
When it is in its dissolved state, Lactic Acid Food Grade forms a colourless solution.
Lactic Acid Food Grade is an alpha hydroxy acid with both exfoliant and humectant properties.


Naturally, Lactic Acid Food Grade occurs as a chemical byproduct of anaerobic respiration in humans, this is the process by which cells produce energy without oxygen.
Lactic Acid Food Grade is also produced by bacteria in yoghurts and is also found in blood, where it is deposited by muscle and red blood cells.



USES and APPLICATIONS of LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is also used in a wide range of food applications such as bakery products, beverages, meat products, confectionery, dairy products, salads, dressings, ready meals, etc.
Lactic Acid Food Grade in food products usually serves as either as a pH regulator or as a preservative.


Lactic Acid Food Grade is produced from natural corn starch by advanced bio-fermentation and refining technology.
Lactic Acid Food Grade is a yellowish to colorless liquid, having a mild acid odor and taste.
Lactic Acid Food Grade is a carboxylic acid widely used as acidity regulator in food and beverage.


Lactic Acid Food Grade is able to preserve and flavor; however, that is not its only feature.
In the food industry Lactic Acid Food Grade is used as a preservative, acidity regulator, flavor enhancer and has an INS number of 270 or an E number of E270.


Lactic Acid Food Grade is used as a food preservative, hardener and flavoring.
Lactic Acid Food Grade is an ingredient in processed foods and is used in meat processing as a tenderiser and flavor enhancer.
Some beers (sour beers) deliberately contain added Lactic Acid Food Grade, one such type being Belgian lambics.


In most cases, Lactic Acid Food Grade in beer is produced from various bacterial strains.
These bacteria ferment sugars into acids, unlike yeasts which ferment sugars into ethanol.
Once the wort has cooled, the yeast and bacteria are allowed to 'fall' into the open fermenters.


Brewers of more conventional beers would ensure that such bacteria do not enter the fermenter.
Other styles of sour beer include 'Berliner weisse', 'Flanders red' and 'American wild ale'.
In wine production, natural malic acid is converted to Lactic Acid Food Grade to reduce spiciness and for other taste reasons, a natural or controlled bacterial process is often used.


If the bacterial action is unstable, additional Lactic Acid Food Grade is added to maintain stable product parameters.
In the washing industry, an antimicrobial agent, Lactic Acid Food Grade is used as a natural ingredient for descaling, which is natural and environmentally friendly.


Lactic Acid Food Grade is commonly found in organic descalers for coffee machines.
Many products can be found for the care of the skin of livestock (therapeutic ointments, disinfectants, post-milking teat wipes, pre-milking cleansers etc.).


Lactic Acid Food Grade is also used as a respiratory and acidity regulator, thus making feed more palatable and odorous and thus increasing the digestibility of feed.
Animals gain weight faster and produce more milk.


Lactic Acid Food Grade in animal nutrition is characterized by lowering the pH of the stomach, reducing the buffering properties of the feed, increasing the activity of proteolytic enzymes/improving the secretion of pancreatic secretions, stimulating the activity of digestive enzymes, stimulating the growth of beneficial bacterial growth, reducing the survival of pathogens in the stomach/maintaining the balance of microbial populations, and directly killing bacteria.


Lactic Acid Food Grade is also found as a nutritional additive for livestock, which improves the digestion of herbivorous animals, as the acid helps to ferment feed faster.
Lactic Acid Food Grade is widely used in brewing to adjust pH In the mash in small quantities to adjust the room temperature mash to 5.4-5.6 range.


Lactic Acid Food Grade is also used in beer making, wine production and as a food additive.
Lactic Acid Food Grade is naturally present in many foodstuffs.
Lactic Acid Food Grade is formed by natural fermentation in products such as cheese, yogurt, soy sauce, sourdough, meat products and pickled vegetables.


Lactic Acid Food Grade is also used in a wide range of food applications such as bakery products, beverages, meat products, confectionery, dairy products, salads, dressings, ready meals, etc.
Lactic Acid Food Grade in food products usually serves as either as a pH regulator or as a preservative.


Lactic Acid Food Grade is also used as a flavouring agent.
Meat, Poultry & Fish: Lactic Acid Food Grade can be used in meat, poultry and fish in the form of sodium or potassium lactate to extend shelf life, control pathogenic bacteria (improve food safety), enhance and protect meat flavour, improve water binding capacity and reduce sodium.


Beverages uses of Lactic Acid Food Grade: Because of its mild taste, Lactic Acid Food Grade is used as an acidity regulator in beverages such as soft drinks and fruit juices.
Lactic Acid Food Grade is widely used in brewing to adjust pH In the mash in small quantities to adjust the room temperature mash to 5.4-5.6 range.


Lactic Acid Food Grade commonly used as a pH modifier in beer brewing.
Lactic Acid Food Grade is used in beer brewing to lower the pH and increase the body of the beer.
Lactic Acid Food Grade is also used in various beverages and cocktails to impart a sour taste.


Lactic Acid Food Grade is commonly used as a preservative and antioxidant.
Lactic Acid Food Grade also has uses as a fuel additive, chemical intermediate, acidity regulator, and disinfectant.
Lactic Acid Food Grade is used frequently in the cosmetic industry due to the effect of promoting collagen production, helping to firm the skin against wrinkles and sagging.


Lactic Acid Food Grade can also cause micro peeling, which can help reduce various scars and age spots.
Lactic Acid Food Grade is a great solution for people with sensitive or dry skin where exfoliants don’t work.
Lactic Acid Food Grade is used for food and personal care products.


Lactic Acid Food Grade can be used as acidulant, flavoring agent and pH regulator in beverages, meat, sourdough, salads and dressings, confectionery and pickled vegetables.
Lactic Acid Food Grade is used as in acidification agent for beverages.


Lactic Acid Food Grade is used as a preservative and flavoring in dressings and salads.
Lactic Acid Food Grade is used in fermentation and pH regulator in beer, wine, and spirits.
Lactic Acid Food Grade is used as in antimicrobial agent and shelf life extender in bakery, meat products.


Lactic Acid Food Grade is food grade and is used for the production of several types of cheeses.
Lactic Acid Food Grade is particularly useful when UHT, ultra-pasteurised or powdered milk are used as the starting materials, since the heat treatments used in the production of these milks deactivates the lactose and prevents the cheese culture from being able to turn it fully into lactic acid.


The inclusion of additional lactic acid prior to rennetting overcomes this shortage and improves the curd yield.
Lactic Acid Food Grade is a vital ingredient in Ricotta Impastata, Mozzarella, Queso Blanco and other speciality cheeses and can be used in the production of sour milk products, such as Koumiss, Laban, Kefir, as well as some cottage cheeses.


In production, Lactic Acid Food Grade is usually added so that the pH of the milk reaches around 5.0.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade and it is also responsible for the sour flavour of sourdough breads.
Lactic Acid Food Grade is responsible for the tangy flavor of fermented milk products (e.g. yogurt, kefir), sour beers, and sourdough bread.


Fermentation usually results in the racemate, although some fermenting bacteria produce the D-enantiomer only.
In winemaking, some wines may go through a natural or induced process called malolactic fermentation, which converts malic acid to Lactic Acid Food Grade, to reduce the sharpness of the acidity.


Given its prevalence in nature, Lactic Acid Food Grade is useful for manipulating food chemistry, and is therefore a common additive.
Lactic Acid Food Gradev may be used as a preservative, an acidifier, a dairy culturing agent, or an ingredient in infant formulas.
Lactic Acid Food Grade may also be used in pharmaceuticals and cosmetics as a preservative and acidifier, and in contraceptive jellies as an active ingredient.


Lactic Acid Food Grade is used as a food preservative, curing agent, and flavoring agent.
Lactic Acid Food Grade is an ingredient in processed foods and is used as a decontaminant during meat processing.
Lactic Acid Food Grade has several industrial applications, including its use in food production, pharmaceuticals, and cosmetics.


Lactic Acid Food Grade is often utilized as a preservative, flavoring agent, pH regulator, and moisturizer.
Lactic Acid Food Grade is also employed in various chemical processes, such as the production of biodegradable plastics and environmentally friendly solvents.


Lactic Acid Food Grade is a natural organic acid with a long history of food, leather, wood-dyeing, and cosmetic industries.
Lactic Acid Food Grade was formed by natural fermentation in products such as cheese, yogurt, soy sauce, meat products, pickled vegetables, beer, and wine.
Lactic Acid Food Grade is used as pH regulator in Pharma products, used in nickel plating because of its unique complexion constant for the nickel.


Lactic Acid Food Grade is used Preservative, Dairy culturing agent, Contraceptive jellies, Acidifier, Pharmaceutical ingredient, and Cosmetic ingredient.
Lactic Acid Food Grade has the dual characteristics of Lactic acid and Calcium lactate, which not only possesses mild and lasting sourness of lactic acid, but also an excellent source of calcium.


Because Lactic Acid Food Grade is powder product so it's especially suitable for regulating the acidity and sourness of various kinds of solid food.
Meanwhile because the good ability of bacteriostasis and fresh-keeping, Lactic Acid Food Grade can be used to extend product's shelf life.
Lactic Acid Food Grade is widely used in candy, canned food, bread and other solid foods.


Lactic Acid Food Grade is a colorless transparent liquid that can be mixed with water.
Lactic Acid Food Grade is widely used in applications such as baking and beer.
Lactic Acid Food Grade, in its food-grade form, is commonly used in the food and beverage industry for various purposes.


Lactic Acid Food Grade can also be used as a flavoring agent.
Lactic Acid Food Grade can help stimulate collagen and strengthen the skin, which equals fewer fine lines and wrinkles.
The hydroxy acids exfoliate the top layer of skin, helping smooth and even complexion, keep pores unclogged, brighten skin and even fade dark marks and discoloration.


Pickling: Lactic Acid Food Grade is used in the pickling process to create a sour flavor and lower the pH of pickled vegetables like cucumbers.
Cheese Making: In cheese production, Lactic Acid Food Grade bacteria are used to ferment milk and produce the acidity required for curd formation and flavor development.


Marinades and Sauces: Lactic Acid Food Grade is used in marinades and sauces for meats and seafood to enhance flavor and tenderness.
Fruit Juices: Lactic Acid Food Grade can be added to fruit juices to adjust acidity levels and improve the taste of citrus and other fruit-based beverages.
Confections: Lactic Acid Food Grade is used in the production of confectionery items like gummies and sour candies to provide a sour and tangy flavor.


Fermentation: Lactic Acid Food Grade bacteria are employed in the fermentation of various foods, such as sauerkraut, kimchi, and sourdough bread.
Sports and Energy Drinks: Lactic Acid Food Grade or its salts are added to sports and energy drinks to provide a mild acidity and enhance the flavor profile.


Preservative: Lactic Acid Food Grade and its salts, such as sodium lactate, can help extend the shelf life of certain food products by lowering the pH and creating an environment that inhibits the growth of spoilage microorganisms.
Flavor Enhancer: Lactic Acid Food Grade is used as a flavor enhancer in various foods, including dairy products, candies, and soft drinks, to impart a mildly tangy taste.


pH Regulator: Lactic Acid Food Grade can be used to regulate the pH of certain food products, especially in the dairy industry, to improve product stability.
Lactic Acid Food Grade can be used in pharmaceutical products because it produces water-soluble lactates from otherwise insoluble ingredients.


Lactic Acid Food Grade has many uses and is produced by bacterial fermentation of carbohydrates such as sugars and starches.
In the food industry, Lactic Acid Food Grade is found primarily in sour milk products, these include kumis, laban, yogurt, kefir, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.


Lactic Acid Food Grade is also responsible for the sour flavour of sourdough bread.
Lactic Acid Food Grade is also used in beer making, wine production and as a food additive.
Lactic Acid Food Grade is also used to adjust the pH level in foods and beverages.


Lactic Acid Food Grade is a natural preservative and is commonly used to preserve dairy products, such as cheese, yogurt, and sour cream, as well as canned fruits and vegetables.
Lactic Acid Food Grade can be used to produce a tart or sour flavor in foods and beverages and can be used to add a unique flavor to craft beer.
Lactic Acid Food Grade is used as a flavoring agent and preservative in processed cheese, salad dressings, pickles, and carbonated beverages.


Lactic Acid Food Grade is also used as a raw material or a catalyst in numerous chemical processes.
Lactic Acid Food Grade is widely used as acidulants and preservatives in food and beverage industries.
Lactic Acid Food Grade is an organic acid that is used as a preservative in food products and as an additive in beverages.


-Acidulant:
Lactic Acid Food Grade is used as an acidulant to adjust the pH level and provide a tangy or sour flavor in various food products.
Lactic Acid Food Grade's commonly used in salad dressings, condiments, and beverages to enhance taste.


-Bakery Products: In baking, Lactic Acid Food Grade is used as a dough conditioner to enhance the texture, rise, and shelf life of bread and other baked goods.
Lactic Acid Food Grade can also contribute to the browning of bread crusts.


-Dairy Products:
Lactic Acid Food Grade is naturally present in fermented dairy products such as yogurt, kefir, and buttermilk.
Lactic Acid Food Grade contributes to the tangy flavor and the thickening of these products.


-Meat and Poultry:
Lactic Acid Food Grade can be used to reduce microbial load and enhance food safety in meat and poultry products.
Lactic Acid Food Grade is sometimes applied as a surface treatment or spray to reduce the risk of bacterial contamination.


-Flavoring and pH regulation:
Lactic Acid Food Grade is employed as a natural flavoring agent and pH regulator in a wide range of food and beverage products.
Lactic Acid Food Grade imparts a tangy or sour taste, similar to the flavor of yogurt or sourdough bread.


-Food preservation:
Lactic Acid Food Grade exhibits antimicrobial properties, and its use as a food preservative helps inhibit the growth of harmful bacteria, molds, and yeasts.
Lactic Acid Food Grade can extend the shelf life of processed foods and prevent spoilage.


-Acidification:
Lactic Acid Food Grade is utilized to acidify and adjust the pH of certain foods and beverages.
Lactic Acid Food Grade is particularly valuable in fermented products such as sauerkraut, pickles, kimchi, and yogurt, where it contributes to the characteristic acidity and tanginess.


-Dairy products:
Lactic Acid Food Grade plays a vital role in the production of various dairy products.
Lactic Acid Food Grade is used in cheese making to facilitate curd formation and enhance the texture, flavor, and shelf life of cheeses.
Lactic Acid Food Grade bacteria are also employed in the fermentation of milk to produce yogurt and cultured buttermilk.


-Meat and poultry processing:
Lactic Acid Food Grade is employed as an antimicrobial treatment in the processing of meat and poultry products.
Lactic Acid Food Grade can help reduce bacterial contamination and enhance food safety.


-Bakery products:
Lactic Acid Food Grade is utilized in the baking industry to regulate dough fermentation and improve the texture and volume of baked goods.
Lactic Acid Food Grade contributes to the development of a desirable crumb structure and imparts a mild tangy flavor.


-Beverages:
Lactic Acid Food Grade finds applications in the production of various beverages, including fruit juices, soft drinks, and alcoholic beverages.
Lactic Acid Food Grade helps adjust acidity levels, improve flavor profiles, and act as a natural preservative.
It is important to note that Lactic Acid Food Grade is generally recognized as safe (GRAS) by regulatory authorities when used in accordance with the approved levels and good manufacturing practices.



SPECIFICATIONS OF LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is affirmed GRAS by the FDA.
Lactic Acid Food Grade is also certified 21 CFR 184.1061.
Lactic Acid Food Grade does not use genetically modified microorganism for fermentation.
Lactic Acid Food Grade is Kosher under the Orthodox Union and Halal certified.



CHARACTERISTICS OF LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is a mild-tasting acidity regulator, flavor enhancer, and shows antibacterial properties.
Lactic Acid Food Grade is colorless to yellowish, nearly odorless, and has a syrupy texture.
Lactic Acid Food Grade is an aqueous solution stable under normal conditions and has a pH (50%) value of less than 2 at 25°C.
Lactic Acid Food Grade is easily biodegradable and should not be in environments warmer than 200°C.



PHYSICAL and CHEMICAL PROPERTIES of LACTIC ACID FOOD GRADE:
Odor: odorless
Melting point/freezing point:
Melting point: 18 °C at 1.013 hPa
Initial boiling point and boiling range: 122 °C at 18,66 - 19,99 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 113 °C - closed cup
Autoignition temperature: 400 °C at 1.011,4 - 1.018,9 hPa
Decomposition temperature: No data available
pH: No data available
Molecular Formula: CH3CHOHCOOH.
Molecular Weight: 90.08 g/mol.

Boiling point: 122 °C.
Melting point: 16.8 °C.
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 100 g/l at 20 °C - soluble
Partition coefficient: n-octanol/water:
log Pow: ca.-0,54 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: No data available
Density: 1,25 g/cm3 at 15 °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:
Surface tension 70,7 mN/m at 1g/l at 20 °C
Formula: H₃CCH(OH)COOH
MW: 90.08 g/mol
Boiling Pt: 122 °C (20 hPa)
Density: 1.11…1.21 g/cm³ (20 °C)
Storage Temperature: Ambient
MDL Number: MFCD00004520
CAS Number: 50-21-5
EINECS: 200-018-0
CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0

Mol File: 50-21-5.mol
Lactic acid Chemical Properties
Melting point: 18°C
alpha: -0.05 º (c= neat 25 ºC)
Boiling point: 122 °C/15 mmHg (lit.)
density: 1.209 g/mL at 25 °C (lit.)
vapor density: 0.62 (vs air)
vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
refractive index: n20/D 1.4262
Fp: >230 °F
storage temp.: 2-8°C

solubility: Miscible with water and with ethanol (96 per cent).
form: syrup
pka: 3.08(at 100℃)
Specific Gravity: 1.209
color: Colorless to yellow
Water Solubility: SOLUBLE
Merck: 145,336
JECFA Number: 930
BRN: 1209341
Stability: Stable.
Physical state: viscous
Color: colorless
Chemical Name : 2-hydroxy – propanoic acid
Molecular Weight : 90.08

Stereochemical purity (L isomer) Min 97.0 %
Content Min 80.0 %
Colour Fresh : Max 100 Apha
Appearance: Colorless to yellow.
Assay: 80 to 88%.
Also known as: Milk acid.
CAS No: 50-21-5.
Density: 1.206 g/ml.
Grade Standard: Commercial, Food Grade.
Molecular Formula: C3H6O3.
Molecular Weight: 90.078 g·mol−1.
Physical State: Liquid.
Usage: Food, Pharma Synthesis.
Chemical Name: L(S)-2-hydroxypropionic acid.



FIRST AID MEASURES of LACTIC ACID FOOD GRADE:
-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 LACTIC ACID FOOD GRADE:
-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 with liquid-absorbent material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LACTIC ACID FOOD GRADE:
-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 LACTIC ACID FOOD GRADE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
*Respiratory protection
Recommended Filter type: Filter type ABEK
-Control of environmental exposure:
Do not let product enter drains.



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



STABILITY and REACTIVITY of LACTIC ACID FOOD GRADE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available.
-Incompatible materials:
No data available


LACTIC ACID FOOD GRADE

Lactic Acid (food grade) is an organic acid that occurs naturally in various food products and is commonly used as a preservative, flavoring agent, and acidulant in the food and beverage industry.
Lactic Acid food grade is known for its sour taste and is found in fermented products such as yogurt, sauerkraut, and pickles.

CAS Number: 50-21-5
EC Number: 200-018-0

Synonyms: Lactic acid, Milk acid, 2-Hydroxypropanoic acid, α-Hydroxypropionic acid, Lactate, 2-Hydroxypropionic acid, 2-Hydroxypropanoate, 2-Hydroxypropionate, Ethylidene-lactic acid, Lactic acid, 2-hydroxy-1-propanecarboxylic acid, L-Lactic acid, (S)-Lactic acid, DL-Lactic acid, (±)-Lactic acid, Lactobacillic acid, 2-Hydroxypropanoic acid, (R)-, Acesol, Racemic lactic acid, D-(-)-Lactic acid, Lactic acid, (R)-, E270, Lactic acid, L-, α-Hydroxypropionic acid, (R)-, Corilagin, Lactic acid, (S)-, Lactic acid, (R)-, Corilaginic acid, Hydroxypropionic acid, (R)-, D-(-)-Lactic acid, L-Lactic acid, (S)-, Lactic acid, (S)-, α-Hydroxypropanoic acid, (S)-, Lactic acid, (S)-, L-, Lactic acid, (R)-, 2-Hydroxypropanoic acid, Lactic acid, (R)-, 2-Hydroxypropanoic acid, (R)-, DL-Lactic acid, Lactic acid, DL-, Lactic acid, (±)-, DL-2-Hydroxypropanoic acid, Lactic acid, (±)-, 2-Hydroxypropanoic acid, DL-, L-Lactic acid, Lactic acid, L-, Lactic acid, (S)-, D-(-)-Lactic acid, (S)-Lactic acid, Lactic acid, (S)-, L-, (S)-Lactic acid, Lactate, DL-, Lactic acid, L-(+)-, Lactic acid, (R)-, Hydroxypropionic acid, (S)-, Lactic acid, D-(-)-, Lactic acid, D-(-)-, 2-Hydroxypropanoic acid, D-(-)-, Lactic acid, (S)-, 2-Hydroxypropanoic acid, Lactic acid, (S)-, D-(-)-Lactic acid, 2-Hydroxypropanoic acid, Lactic acid, D-(-)-, Lactic acid, (S)-, DL-Lactic acid, 2-Hydroxypropanoic acid, DL-Lactic acid, Lactic acid, DL



APPLICATIONS


Lactic Acid food grade is extensively used in the food and beverage industry as an acidulant and flavor enhancer.
Lactic Acid food grade is commonly found in dairy products such as yogurt, cheese, and sour cream, contributing to their tart flavor.

Lactic Acid food grade is used in the fermentation of vegetables like sauerkraut and pickles, aiding in preservation and flavor development.
In the baking industry, lactic acid is added to doughs to improve texture and extend shelf life.

Lactic Acid food grade is used as a pH regulator and preservative in various processed foods, including meats, sauces, and dressings.
Lactic Acid food grade is employed in the production of beverages such as beer, cider, and soft drinks for its sour taste.

In the pharmaceutical industry, lactic acid is used as an excipient in drug formulations, particularly oral solutions and intravenous fluids.
Lactic Acid food grade is utilized in the manufacture of cosmetics and personal care products as an exfoliant and moisturizing agent.
Lactic Acid food grade is incorporated into skin care products like creams, lotions, and peels to promote skin renewal and hydration.

In agriculture, lactic acid is added to animal feed to improve digestion and enhance nutrient absorption in livestock.
Lactic Acid food grade is used in the production of biodegradable plastics such as polylactic acid (PLA), which is derived from renewable resources.
Lactic Acid food grade is employed in the textile industry for textile dyeing and finishing processes, acting as a pH regulator and color fixative.

Lactic Acid food grade is used in the cleaning and detergent industry for its descaling and antimicrobial properties.
Lactic Acid food grade is added to household cleaning products like bathroom cleaners and dishwashing detergents for effective stain removal.
In the medical field, lactic acid is used as a component of wound dressings and topical medications for its antimicrobial properties.

Lactic Acid food grade is used in the production of biodegradable polymers for medical implants and drug delivery systems.
Lactic Acid food grade is employed in the synthesis of lactate-based polymers used in tissue engineering and regenerative medicine.

Lactic Acid food grade is used in the manufacture of biodegradable packaging materials, reducing the environmental impact of packaging waste.
Lactic Acid food grade is utilized in the production of biodegradable solvents and lubricants as an eco-friendly alternative to petroleum-based products.

Lactic Acid food grade is employed in the production of biodegradable detergents and surfactants for use in household and industrial cleaning applications.
Lactic Acid food grade is used in the leather industry for leather tanning and finishing processes, enhancing the quality and durability of leather goods.
Lactic Acid food grade is employed in the production of adhesives and sealants for its adhesive properties and moisture resistance.
Lactic Acid food grade is utilized in the printing and paper industry for paper sizing and coating applications, improving print quality and durability.

Lactic Acid food grade is added to personal care products such as toothpaste and mouthwash for its tart flavor and antibacterial properties.
Lactic Acid food grade finds applications in a wide range of industries, from food and beverages to pharmaceuticals, cosmetics, and beyond, owing to its diverse functional properties and eco-friendly nature.

Lactic Acid food grade is used in the production of biodegradable plastics for packaging materials, reducing plastic pollution and environmental impact.
Lactic Acid food grade is employed in the textile industry for dyeing and finishing processes to improve color fastness and fabric softness.
Lactic Acid food grade is added to skincare products such as serums and masks to exfoliate dead skin cells and promote a radiant complexion.

In the automotive industry, lactic acid is used in the production of biodegradable lubricants and antifreeze solutions.
Lactic Acid food grade is employed in the manufacturing of dietary supplements and sports nutrition products to support muscle recovery and endurance.

Lactic Acid food grade is utilized in the fermentation of probiotic supplements and cultured dairy products for its beneficial effects on gut health.
Lactic Acid food grade is added to pet care products such as shampoos and grooming sprays for its skin-conditioning properties.
Lactic Acid food grade is used in the production of biofuels such as ethanol and biodiesel as a fermentation substrate.

In the construction industry, lactic acid is used in the production of eco-friendly concrete additives and sealants.
Lactic Acid food grade is employed in the pharmaceutical industry as a chelating agent in metal ion complexation and drug delivery systems.

Lactic acid is used in the production of biodegradable detergents for household and industrial cleaning applications.
Lactic Acid food grade is employed in the treatment of industrial wastewater for its ability to neutralize pH and remove heavy metals.
Lactic Acid food grade is used in the preservation of fresh produce and seafood to extend shelf life and maintain quality.

Lactic Acid food grade is added to cosmetic formulations such as hair care products and deodorants for its antimicrobial and odor-neutralizing properties.
Lactic Acid food grade is used in the production of biodegradable inks and coatings for printing and packaging applications.
Lactic Acid food grade is employed in the manufacturing of eco-friendly pesticides and herbicides for agricultural pest control.

Lactic Acid food grade is added to animal feed as a feed additive to improve digestion and nutrient absorption in livestock.
Lactic Acid food grade is used in the production of biodegradable cleaning wipes and disinfectants for household and industrial use.

Lactic Acid food grade is employed in the production of biodegradable polymers for 3D printing and additive manufacturing.
Lactic Acid food grade is added to oral care products such as mouthwashes and toothpaste for its tart flavor and antimicrobial properties.
Lactic Acid food grade is used in the production of biodegradable film and packaging materials for food and pharmaceutical applications.

Lactic Acid food grade is employed in the production of biodegradable detergents and degreasers for automotive and industrial cleaning.
Lactic Acid food grade is used in the production of biodegradable fertilizers and soil conditioners for sustainable agriculture.
Lactic Acid food grade is added to fermentation media for the production of biopharmaceuticals and bio-based chemicals.



DESCRIPTION


Lactic Acid (food grade) is an organic acid that occurs naturally in various food products and is commonly used as a preservative, flavoring agent, and acidulant in the food and beverage industry.
Lactic Acid food grade is known for its sour taste and is found in fermented products such as yogurt, sauerkraut, and pickles.

Lactic Acid food grade is a colorless to slightly yellow, viscous liquid.
Lactic Acid food grade has a mild, characteristic odor and a sour taste.
Lactic Acid food grade is naturally present in various fermented foods such as yogurt, cheese, and sauerkraut.

Lactic Acid food grade plays a crucial role in the fermentation process, contributing to the tangy flavor of fermented products.
The chemical formula of lactic acid is C3H6O3, and its molecular weight is 90.08 g/mol.
Lactic Acid food grade is classified as a weak organic acid due to its relatively low acidity.

Lactic Acid food grade is soluble in water and miscible with ethanol, acetone, and glycerol.
Lactic acid is commonly used as a food additive in the form of its sodium or calcium salts (lactates).

In the body, lactic acid is produced during anaerobic metabolism, especially during strenuous exercise.
Lactic Acid food grade serves as an important energy source for muscles and tissues during periods of high activity.

Lactic Acid food grade is biodegradable and environmentally friendly, making it suitable for various applications.
Lactic Acid food grade is used as a pH regulator, acidulant, and preservative in the food and beverage industry.

Lactic Acid food grade contributes to the texture, flavor, and shelf life of many food products.
In cosmetics and personal care products, lactic acid is used as an exfoliant and moisturizing agent.
Lactic Acid food grade helps to promote skin renewal and improve skin hydration.

Lactic Acid food grade is also utilized in the pharmaceutical industry as an excipient in drug formulations.
Lactic Acid food grade can be found in topical medications, oral solutions, and intravenous fluids.
Lactic Acid food grade has antimicrobial properties, making it effective in inhibiting the growth of bacteria and fungi.
In agriculture, lactic acid is used as a feed additive to promote digestion and improve animal health.

Lactic Acid food grade is also employed in cleaning products and detergents for its descaling and antibacterial properties.
Lactic Acid food grade is produced industrially through fermentation or chemical synthesis.
Lactic Acid food grade is an important raw material for the production of polylactic acid (PLA), a biodegradable polymer.

Lactic Acid food grade is recognized as Generally Recognized as Safe (GRAS) by the Food and Drug Administration (FDA).
Lactic Acid food grade has a wide range of applications across various industries, including food, pharmaceuticals, cosmetics, and agriculture.
Lactic Acid food grade is a versatile compound with diverse uses and beneficial properties in numerous applications.



PROPERTIES


Physical Properties:

Appearance: Clear to slightly yellow, viscous liquid
Odor: Mild, characteristic odor
Taste: Sour
Density: 1.21 g/cm³ at 20°C
Melting Point: 16.8°C (solidifies below this temperature)
Boiling Point: 122°C at 15 mmHg (decomposes at higher temperatures)
Solubility in Water: Miscible in all proportions
Solubility in Other Solvents: Soluble in ethanol, acetone, and glycerol
pH: Typically around 2.0-3.0 for a 1% aqueous solution
Hygroscopicity: Exhibits some hygroscopic properties, absorbing moisture from the air
Refractive Index: 1.37
Viscosity: Relatively high viscosity as a liquid


Chemical Properties:

Chemical Formula: C3H6O3
Molecular Weight: 90.08 g/mol
Functional Groups: Hydroxyl group (-OH), Carboxyl group (-COOH)
Acid Strength: Weak organic acid with a pKa value of approximately 3.86
Hydrophilicity: Highly hydrophilic due to the presence of hydroxyl and carboxyl groups
Chirality: Exists as both L-lactic acid and D-lactic acid enantiomers, with L-lactic acid being the naturally occurring form
Optical Activity: Exhibits optical activity due to its chiral nature
Isomerization: Can undergo isomerization between the L- and D-forms under certain conditions
Decomposition: Decomposes at elevated temperatures, producing carbon dioxide and water
Polymerization: Can undergo polymerization to form polylactic acid (PLA) under appropriate conditions
Reactivity: Participates in esterification, transesterification, and condensation reactions
Hydrolysis: Undergoes hydrolysis in aqueous solutions to form lactate ions and protons



FIRST AID


Inhalation:

Move to Fresh Air:
Immediately remove the affected person from the contaminated area to an area with fresh air.

Assess Breathing:
Check the person's breathing. If breathing is difficult or absent, seek medical attention immediately.

Provide Oxygen:
If breathing is difficult, provide oxygen if available and trained to do so.

Keep Warm and Rested:
Keep the affected person warm and in a resting position until medical help arrives.


Skin Contact:

Remove Contaminated Clothing:
Quickly and gently remove any contaminated clothing, jewelry, or footwear.

Flush with Water:
Rinse the affected area thoroughly with lukewarm water for at least 15 minutes, ensuring complete removal of the chemical.

Use Mild Soap:
Wash the affected area with mild soap and water to remove any residual chemical.

Seek Medical Attention:
If irritation, redness, or other symptoms develop, seek medical advice promptly.

Apply Emollient:
After rinsing, apply a soothing emollient or moisturizer to the affected area to help soothe irritation and promote healing.

Monitor for Symptoms:
Monitor the affected area for any signs of blistering, swelling, or prolonged irritation, and seek medical attention if necessary.


Eye Contact:

Flush Eyes Immediately:
Immediately flush the affected eye(s) with gently flowing lukewarm water for at least 15 minutes, keeping eyelids open.

Remove Contact Lenses:
If present and easily removable, remove contact lenses after the initial flush.

Continue Flushing:
Continue to flush the eye(s) with water, ensuring thorough rinsing of the eye(s) and eyelids.

Seek Medical Attention:
Seek immediate medical attention, even if symptoms seem minor or if irritation persists after rinsing.

Do Not Rub Eyes:
Avoid rubbing or applying pressure to the eyes, as this may exacerbate irritation or injury.

Protect the Eye:
Cover the affected eye with a clean, sterile dressing or bandage to prevent further contamination or injury.


Ingestion:

Do NOT Induce Vomiting:
Do not induce vomiting unless instructed to do so by medical personnel.

Do NOT Give Anything by Mouth:
Do not give anything by mouth to an unconscious person.

Rinse Mouth:
If the person is conscious and able to swallow, rinse their mouth with water and encourage them to drink water slowly.

Seek Medical Attention:
Seek immediate medical attention or contact a poison control center for further guidance.

Monitor for Symptoms:
Monitor the person for symptoms such as nausea, vomiting, abdominal pain, difficulty swallowing, or other signs of ingestion.



HANDLING AND STORAGE

Handling:

Personal Protective Equipment (PPE):
Wear appropriate personal protective equipment (PPE), including safety goggles, chemical-resistant gloves, and a lab coat or protective clothing, when handling lactic acid.
Ensure that all PPE is properly fitted and in good condition before use.

Avoid Contact:
Avoid skin and eye contact with lactic acid. In case of contact, follow the first aid measures outlined in the SDS (Safety Data Sheet) or chemical label.

Use in Well-Ventilated Areas:
Handle lactic acid in well-ventilated areas to prevent the buildup of vapors or fumes. Use local exhaust ventilation if available.

Prevent Spills and Leaks:
Take precautions to prevent spills and leaks during handling and transfer of lactic acid. Use spill containment measures such as secondary containment trays or spill kits.

Avoid Mixing with Incompatible Substances:
Do not mix lactic acid with strong oxidizing agents, strong bases, or other incompatible substances. Refer to the SDS for a list of incompatible materials.

Use Proper Equipment:
Use appropriate equipment such as chemical-resistant pumps, hoses, and containers for handling and transferring lactic acid.

Labeling:
Ensure that containers of lactic acid are properly labeled with the appropriate product name, concentration, hazard warnings, and handling instructions.


Storage:

Store in Cool, Dry Area:
Store containers of lactic acid in a cool, dry, well-ventilated area away from heat sources and direct sunlight.
Maintain storage temperatures within the recommended range specified on the SDS or chemical label.

Avoid Temperature Extremes:
Avoid exposure to extreme temperatures.
Do not allow lactic acid to freeze, as it may solidify at low temperatures.

Keep Containers Tightly Closed:
Keep containers of lactic acid tightly closed when not in use to prevent contamination and evaporation of the chemical.

Separate from Incompatible Substances:
Store lactic acid away from incompatible substances such as strong oxidizing agents, strong bases, and reactive metals.

Store Away from Food and Feedstuffs:
Do not store lactic acid near food, feedstuffs, or food preparation areas to prevent accidental contamination.

Store Away from Reactive Materials:
Keep lactic acid containers away from reactive materials, combustible materials, and sources of ignition to prevent fire or explosion hazards.

Check for Leaks and Damage:
Regularly inspect containers for signs of leaks, damage, or deterioration. Replace damaged containers promptly to prevent spills or accidents.

Follow Local Regulations:
Adhere to local regulations and guidelines for the storage of lactic acid, including any specific requirements for hazardous chemicals in your region.

LACTIC ACID FOOD GRADE
Lactic Acid Food Grade is an organic acid.
Lactic Acid Food Grade has the molecular formula CH3CHOOH.


CAS Number: 50-21-5
EC Number: 200-018-0
Molecular Formula: C3H6O3



SYNONYMS:
α-hydroxypropionic acid, or 2-hydroxypropanoic acid, Milk acid



Lactic Acid Food Grade is a natural preservative often found in foods like yogurt, baked goods, and pickled vegetables.
Along with making your food last longer, Lactic Acid Food Grade can boost your health by strengthening your immune system.
Lactic Acid Food Grade is an organic acid that forms when certain foods go through the process of fermentation.


Lactic Acid Food Grade’s often found in pickled foods, fermented soy products, salami, yogurt, and more.
Food manufacturers add Lactic Acid Food Grade to packaged food products such as bread, desserts, olives, and jams to give them longer shelf lives.
Lactic Acid Food Grade is a good preservative because it can kill and suppress bacteria in food.


Lactic Acid Food Grade also helps prevent discoloration and works as a gelling agent and a curing agent.
Lactic Acid Food Grade is also employed in pharmaceutical technology to produce water-soluble lactates from otherwise-insoluble active ingredients.
Lactic Acid Food Grade finds further use in topical preparations and cosmetics to adjust acidity and for its disinfectant and keratolytic properties.


Lactic Acid Food Grade is an organic acid occurring naturally in the human body and in fermented foods.
The commercial production of lactic acid is typically done by fermentation.
Lactic Acid Food Grade is an organic acid.


Lactic Acid Food Grade has the molecular formula CH3CHOOH.
In its solid state, Lactic Acid Food Grade is white and miscible with water.
When it is in its dissolved state, Lactic Acid Food Grade forms a colourless solution.


Naturally, Lactic Acid Food Grade occurs as a chemical byproduct of anaerobic respiration in humans, this is the process by which cells produce energy without oxygen.
Lactic Acid Food Grade is also produced by bacteria in yoghurts and is also found in blood, where it is deposited by muscle and red blood cells.


Industrially, Lactic Acid Food Grade is produced by the bacterial fermentation of carbohydrates; fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria.
Lactic Acid Food Grade is a colorless or yellowish liquid with the characteristic smell of sour milk.


Lactic Acid Food Grade is an organic acid involved in various biochemical processes.
Lactic Acid Food Grade is also used as a flavoring agent.
Lactic Acid Food Grade can be used as acidulant, flavoring agent and pH regulator in beverage, beer, fruit wine, meat, sourdough, salads, dressings, confectionery (such as hard- boiled candy, fruit gums) and pickled vegetables.


Lactic Acid Food Grade is an organic acid with applications in beer production as well as the cosmetic, pharmaceutical, food and chemical industries.
Lactic Acid Food Grade, also known as milk acid, is found primarily in sour milk products, such as yogurt, kefir, koumiss, laban, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.


The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.
Lactic Acid Food Grade is also responsible for the sour flavour of sourdough bread.
Lactic Acid Food Grade is sourced from fermentation of plant sugars.


Lactic Acid Food Grade is a perfect for use in vegan cheese recipes.
Lactic Acid Food Grade adds a natural sour flavor to sourdough breads.
Lactic Acid Food Grade is one of the popular food additives and ingredients in most countries.


Lactic Acid Food Grade is an organic acid that is naturally occurring in the human body and fermented foods.
Fermentation occurs when natural bacteria feed on the sugar and starch of a food, producing Lactic Acid Food Grade.
Lactic Acid Food Grade helps stabilize acidity, maintain pH levels, and prevent microbial contaminations.


Increase the shelf life of your dairy products, fermented preserves, processed meats, beverages, egg-based products, and infant foods with Lactic Acid Food Grade.
Not only does Lactic Acid Food Grade act as a preservative, but it also enhances the taste and aroma of your creations.


Lactic Acid Food Grade is an organic acid occurring naturally in the human body and in fermented foods.
The commercial production of Lactic Acid Food Grade is typically done by traditional fermentation of natural carbohydrates.
Lactic Acid Food Grade standard is produced from natural corn starch by advanced bio-fermentation and refining technology.


Lactic Acid Food Grade is a yellowish to colorless liquid, having a mild acid odor and taste.
Lactic Acid Food Grade is an organic compound with the formula CH3CH(OH)CO2H.
The process creates B-vitamins, beneficial enzymes, and more.


L(+) form is preferred for better metabolism and natural carbohydrates.
Lactic Acid Food Grade is a versatile ingredient used in the food industry as an acidity regulator and acidulant.
In its solid state, Lactic Acid Food Grade is white and water-soluble.


In its liquid state, Lactic Acid Food Grade is clear.
Lactic Acid Food Grade is produced both naturally and synthetically.
As a food additive Lactic Acid Food Grade is approved for use in the EU, USA and Australia and New Zealand; it is listed by its INS number 270 or as E number E270.


Lactic Acid Food Grade is produced commercially by fermentation of carbohydrates such as glucose, sucrose, or lactose, or by chemical synthesis.
Carbohydrate sources of Lactic Acid Food Grade include corn, beets, and cane sugar.
Lactic Acid Food Grade is an alpha hydroxy acid with both exfoliant and humectant properties.


Lactic Acid Food Grade is produced naturally in the body (it's the stuff that gives you a ‘stitch’ during a workout) and is also found in yogurt and milk.
There is another method of production, through the chemical synthesis from acetaldehyde.
This is done by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile.


Lactic Acid Food Grade can be used in pharmaceutical products because it produces water-soluble lactates from otherwise insoluble ingredients.
In the food industry, Lactic Acid Food Grade is found primarily in sour milk products, these include kumis, laban, yogurt, kefir, and some cottage cheeses.
Lactic Acid Food Grade is also responsible for the sour flavor of sourdough breads.


As an ingredient in personal care products, Lactic Acid Food Grade has the ability to boost skin’s moisture levels—even as it exfoliates.
At higher concentrations, Lactic Acid Food Grade acts as an exfoliator helping to dissolve connections between skin cells, while at lower levels it is used as a humectant, meaning it can actually help hydrate skin by pulling in water to the outer skin layer.


Lactic Acid Food Grade is a chemical compound classified as an organic acid.
Lactic Acid Food Grade is a type of carboxylic acid, specifically known as 2-hydroxypropanoic acid.
Lactic Acid Food Grade is produced in the body as a byproduct of anaerobic metabolism, primarily in muscle tissues, during periods of intense physical activity or when oxygen supply is limited.


Lactic Acid Food Grade plays a crucial role in energy production and can serve as an alternative energy source when glucose availability is reduced.
In terms of its chemical structure, Lactic Acid Food Grade consists of a three-carbon molecule with a hydroxyl group (-OH) and a carboxyl group (-COOH) attached to the second carbon.


Lactic Acid Food Grade may exist either as a white solid in pure form, or a clear to yellowish liquid when dissolved in water.
Lactic Acid Food Grade can be produced via fermentation of carbohydrates, or synthesized from acetaldehyde.
Produced from natural corn starch through the traditional fermentation of natural carbohydrates, Lactic Acid Food Grade is a highly versatile solution used in various food applications.


One of the critical benefits of Lactic Acid Food Grade is its ability to help control pH levels.
Balancing pH levels improves flavor and texture and ensures the final product is safe and stable.
Due to regulating and lowering pH levels, Lactic Acid Food Grade serves as a microbial inhibitor with the growth of potentially harmful bacteria.


As a highly effective preservative, Lactic Acid Food Grade can help to extend product shelf life and reduce the risk of spoilage or contamination.
Lactic Acid Food Grade is ideal for bakery, dairy, beverages, meat, and many other applications.
Lactic Acid Food Grade is non-GMO.


Industrially, Lactic Acid Food Grade is produced by the bacterial fermentation of carbohydrates; fermented milk products are obtained industrially by fermentation of milk or whey by Lactobacillus bacteria.
There is another method of production, through the chemical synthesis from acetaldehyde.


This is done by reacting acetaldehyde with hydrogen cyanide and hydrolysing the resultant lactonitrile.
Lactic Acid Food Grade, particularly in its food-grade form, has a variety of uses in the food and beverage industry.
Lactic Acid Food Grade is a natural organic acid produced through fermentation, often from sources like sugars and starches.


Lactic Acid Food Grade has a mild, tart flavor and is generally recognized as safe (GRAS) when used in food applications.
Lactic Acid Food Grade is an organic acid.
Lactic Acid Food Grade has the molecular formula CH3CHOOH.


Lactic Acid Food Grade exists in two stereoisomeric forms: L-lactic acid and D-lactic acid.
L-lactic acid is the most common and biologically active form found in humans.
Overall, Lactic Acid Food Grade is an important compound with diverse biological and industrial significance, contributing to various physiological processes and serving as a versatile chemical building block in numerous applications.


In its solid state, Lactic Acid Food Grade is white and miscible with water.
When it is in its dissolved state, Lactic Acid Food Grade forms a colourless solution.
Lactic Acid Food Grade is an alpha hydroxy acid with both exfoliant and humectant properties.


Naturally, Lactic Acid Food Grade occurs as a chemical byproduct of anaerobic respiration in humans, this is the process by which cells produce energy without oxygen.
Lactic Acid Food Grade is also produced by bacteria in yoghurts and is also found in blood, where it is deposited by muscle and red blood cells.


Lactic Acid Food Grade has strong antiseptic and fresh-keeping effect.
In terms of seasoning, the unique sour taste of Lactic Acid Food Grade can increase the taste of food.
Adding a certain amount of Lactic Acid Food Grade to salads such as salad, soy sauce and vinegar can maintain the stability and safety of microorganisms in the product while making the taste milder.


Natural Lactic Acid Food Grade is a natural intrinsic ingredient in dairy products.
Lactic Acid Food Grade has the taste of dairy products and good anti-microbial effect.
Lactic Acid Food Grade has been widely used in blending yoghurt cheese, ice cream and other foods, and has become a popular dairy sour agent.


Lactic Acid Food Grade powder is a direct sour conditioner for the production of steamed bread.
Lactic Acid Food Grade is a natural fermented acid, so it can make bread unique.
Lactic Acid Food Grade is a natural sour taste regulator.


Lactic Acid Food Grade is an organic acid that naturally occurs in a variety of foods during the fermentation process.
The digestive tract can easily break down Lactic Acid Food Grade since it’s naturally present in the body.
Lactic Acid Food Grade is known for its tangy flavor profile and nearly colorless appearance, which lends itself to various food applications.


Lactic Acid Food Grade is typically produced by the fermentation of natural carbohydrates.
Lactic Acid Food Grade is available at 80% and is approved as a natural ingredient.
Within the Personal Care sector, Lactic Acid Food Grade functions as an acidifier with moisturising, exfoliating and antibacterial properties.


Lactobacillus and Streptococcus cultures produce Lactic Acid Food Grade through fermentation.
The bacteria break down sugar to extract energy and produce Lactic Acid Food Grade as a byproduct.
Lactic Acid Food Grade helps regulate pH levels and prevents the growth of microorganisms, extending shelf life.



USES and APPLICATIONS of LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is a precursor for the production of glycolic acid another alpha hydroxy acid used in skincare products.
In cosmetic formulations, Lactic Acid Food Grade is often included in anti-ageing products due to its exfoliating properties and potential to improve skin texture.


Lactic Acid Food Grade is a natural preservative found in several foods, including pickled vegetables, yogurt, and baked goods.
Lactic Acid Food Grade is a cheap and minimally processedTrusted Source preservative.
Lactic Acid Food Grade is a natural preservative and is commonly used to preserve dairy products, such as cheese, yogurt, and sour cream, as well as canned fruits and vegetables.


Lactic Acid Food Grade can be used to produce a tart or sour flavor in foods and beverages and can be used to add a unique flavor to craft beer.
Lactic Acid Food Grade is used as a flavoring agent and preservative in processed cheese, salad dressings, pickles, and carbonated beverages.
Lactic Acid Food Grade is also used as a raw material or a catalyst in numerous chemical processes.


Lactic Acid Food Grade is widely used as acidulants and preservatives in food and beverage industries.
Lactic Acid Food Grade is an organic acid that is used as a preservative in food products and as an additive in beverages.
The slightly sour taste of natural Lactic Acid Food Grade also enhances the flavor profile of baked goods, candies, and culinary cuisines.


You can use Lactic Acid Food Grade for cooking by adding it to marinades, dressings, and sauces.
The all-natural Lactic Acid Food Grade helps to balance pH levels and acidity.
Use our food-grade Lactic Acid Food Grade in recipes that have leavening agents, like yeast and baking soda.


The natural Lactic Acid Food Grade works in conjunction with the leavening agents to help the baked goods rise in a timely manner.
Lactic Acid Food Grade for baking applications helps improve the texture of desserts and bread.
For vegetarian dishes, Lactic Acid Food Grade is used to impart the tangy and slightly sour taste that dairy products lend to recipes.


Lactic Acid Food Grade is used in various cooking and baking applications catering to a diverse range of palates.
When incorporating Lactic Acid Food Grade into cooking and baking applications, start with a small amount and then add more if desired.
The liquid formula of Lactic Acid Food Grade is highly concentrated, and a little goes a long way.


Lactic Acid Food Grade is also used in skincare products, as it’s packed with the gentlest alpha-hydroxy acids beneficial to the skin thanks to its hydrating and exfoliating properties.
Lactic Acid Food Grade is also used in a wide range of food applications such as bakery products, beverages, meat products, confectionery, dairy products, salads, dressings, ready meals, etc.


Lactic Acid Food Grade in food products usually serves as either as a pH regulator or as a preservative.
Lactic Acid Food Grade is produced from natural corn starch by advanced bio-fermentation and refining technology.
Lactic Acid Food Grade is a yellowish to colorless liquid, having a mild acid odor and taste.


Lactic Acid Food Grade is a carboxylic acid widely used as acidity regulator in food and beverage.
Lactic Acid Food Grade is able to preserve and flavor; however, that is not its only feature.
In the food industry Lactic Acid Food Grade is used as a preservative, acidity regulator, flavor enhancer and has an INS number of 270 or an E number of E270.


Lactic Acid Food Grade is used as a food preservative, hardener and flavoring.
Lactic Acid Food Grade is an ingredient in processed foods and is used in meat processing as a tenderiser and flavor enhancer.
Lactic Acid Food Grade is used for baking and baking in bread, cakes, biscuits and other baked foods.


Lactic Acid Food Grade can improve the quality of food and maintain color extend the shelf life.
Since Lactic Acid Food Grade is part of the skin's inherent natural moisturizing factor, it is widely used as a moisturizer for many skin care products.
Lactic Acid Food Grade has strong antiseptic and fresh-keeping effect.


Lactic Acid Food Grade can be used in fruit wine, beverage, meat, food, pastry making, vegetable (olive, cucumber, pearl onion) pickling and canning, food processing, fruit storage, with adjustment pH, bacteriostatic, prolonged shelf life, seasoning, color preservation, and product quality.
Because of the mild acidity of Lactic Acid Food Grade, it can also be used as the preferred sour agent for delicate soft drinks and juices.


When brewing beer, adding proper amount of Lactic Acid Food Grade can adjust the pH value to promote saccharification, facilitate yeast fermentation, improve beer quality, increase beer flavor and extend shelf life.
Lactic Acid Food Grade is used to adjust pH in liquor, sake and fruit wine to prevent the growth of bacteria, enhance the acidity and refreshing taste.


Lactic Acid Food Grade is used in a range of applications and industries such as food, drinks, personal care and cleaning.
Lactic Acid Food Grade has halal and Kosher Certified.
Food applications: Lactic Acid Food Grade is used Beverages, Meat, Confectionary, Feed and Pet food.


Lactic Acid Food Grade is used in a wide range of applications and industries, including but not limited to food, drinks, personal care and cleaning.
For the food applications, Lactic Acid Food Grade serves mainly as a mild-tasting acidity regulator, as a preservative and as a flavouring agent.
Lactic Acid Food Grade is certified Halal and Kosher.


For technical applications, Lactic Acid Food Grade is exploited primarily for its acid moiety and antibacterial properties.
Lactic Acid Food Grade can be added to baked goods, like bread, muffins, and cake, as well as other food products, like yogurt and cheese, since it acts as a natural preservative.


Lactic Acid Food Grade helps to extend the shelf life of many foods, preventing bacteria growth.
Meanwhile because the good ability of bacteriostasis and fresh-keeping, Lactic Acid Food Grade can be used to extend product's shelf life.
Lactic Acid Food Grade is widely used in candy, canned food, bread and other solid foods.


Lactic Acid Food Grade is a colorless transparent liquid that can be mixed with water.
Lactic Acid Food Grade is widely used in applications such as baking and beer.
Lactic Acid Food Grade, in its food-grade form, is commonly used in the food and beverage industry for various purposes.


Lactic Acid Food Grade is often utilized as a preservative, flavoring agent, pH regulator, and moisturizer.
Lactic Acid Food Grade is also employed in various chemical processes, such as the production of biodegradable plastics and environmentally friendly solvents.


Lactic Acid Food Grade is used Preservative, Dairy culturing agent, Contraceptive jellies, Acidifier, Pharmaceutical ingredient, and Cosmetic ingredient.
Lactic Acid Food Grade has the dual characteristics of Lactic acid and Calcium lactate, which not only possesses mild and lasting sourness of lactic acid, but also an excellent source of calcium.


Because Lactic Acid Food Grade is powder product so it's especially suitable for regulating the acidity and sourness of various kinds of solid food.
Lactic Acid Food Grade can also be used as a flavoring agent.
Lactic Acid Food Grade can help stimulate collagen and strengthen the skin, which equals fewer fine lines and wrinkles.


The hydroxy acids exfoliate the top layer of skin, helping smooth and even complexion, keep pores unclogged, brighten skin and even fade dark marks and discoloration.
Some beers (sour beers) deliberately contain added Lactic Acid Food Grade, one such type being Belgian lambics.


In most cases, Lactic Acid Food Grade in beer is produced from various bacterial strains.
These bacteria ferment sugars into acids, unlike yeasts which ferment sugars into ethanol.
Once the wort has cooled, the yeast and bacteria are allowed to 'fall' into the open fermenters.


Brewers of more conventional beers would ensure that such bacteria do not enter the fermenter.
Other styles of sour beer include 'Berliner weisse', 'Flanders red' and 'American wild ale'.
In wine production, natural malic acid is converted to Lactic Acid Food Grade to reduce spiciness and for other taste reasons, a natural or controlled bacterial process is often used.


If the bacterial action is unstable, additional Lactic Acid Food Grade is added to maintain stable product parameters.
In the washing industry, an antimicrobial agent, Lactic Acid Food Grade is used as a natural ingredient for descaling, which is natural and environmentally friendly.


Lactic Acid Food Grade is commonly found in organic descalers for coffee machines.
Many products can be found for the care of the skin of livestock (therapeutic ointments, disinfectants, post-milking teat wipes, pre-milking cleansers etc.).


Lactic Acid Food Grade is also used as a respiratory and acidity regulator, thus making feed more palatable and odorous and thus increasing the digestibility of feed.
Animals gain weight faster and produce more milk.


Preservative: Lactic Acid Food Grade and its salts, such as sodium lactate, can help extend the shelf life of certain food products by lowering the pH and creating an environment that inhibits the growth of spoilage microorganisms.
Flavor Enhancer: Lactic Acid Food Grade is used as a flavor enhancer in various foods, including dairy products, candies, and soft drinks, to impart a mildly tangy taste.


pH Regulator: Lactic Acid Food Grade can be used to regulate the pH of certain food products, especially in the dairy industry, to improve product stability.
Lactic Acid Food Grade can be used in pharmaceutical products because it produces water-soluble lactates from otherwise insoluble ingredients.


Lactic Acid Food Grade is used as a preservative and flavoring in dressings and salads.
Lactic Acid Food Grade is used in fermentation and pH regulator in beer, wine, and spirits.
Lactic Acid Food Grade is used as in antimicrobial agent and shelf life extender in bakery, meat products.


Lactic Acid Food Grade is food grade and is used for the production of several types of cheeses.
Lactic Acid Food Grade is particularly useful when UHT, ultra-pasteurised or powdered milk are used as the starting materials, since the heat treatments used in the production of these milks deactivates the lactose and prevents the cheese culture from being able to turn it fully into lactic acid.


Lactic Acid Food Grade is a natural organic acid with a long history of food, leather, wood-dyeing, and cosmetic industries.
Lactic Acid Food Grade was formed by natural fermentation in products such as cheese, yogurt, soy sauce, meat products, pickled vegetables, beer, and wine.
Lactic Acid Food Grade is used as pH regulator in Pharma products, used in nickel plating because of its unique complexion constant for the nickel.


Lactic Acid Food Grade is commonly used as a preservative and antioxidant.
Lactic Acid Food Grade also has uses as a fuel additive, chemical intermediate, acidity regulator, and disinfectant.
Lactic Acid Food Grade is used frequently in the cosmetic industry due to the effect of promoting collagen production, helping to firm the skin against wrinkles and sagging.


Lactic Acid Food Grade can also cause micro peeling, which can help reduce various scars and age spots.
Lactic Acid Food Grade is a great solution for people with sensitive or dry skin where exfoliants don’t work.
Lactic Acid Food Grade is used for food and personal care products.


Lactic Acid Food Grade can be used as acidulant, flavoring agent and pH regulator in beverages, meat, sourdough, salads and dressings, confectionery and pickled vegetables.
Lactic Acid Food Grade is used as in acidification agent for beverages.


Lactic Acid Food Grade is also used in a wide range of food applications such as bakery products, beverages, meat products, confectionery, dairy products, salads, dressings, ready meals, etc.
Lactic Acid Food Grade in food products usually serves as either as a pH regulator or as a preservative.


Lactic Acid Food Grade is also used as a flavouring agent.
Meat, Poultry & Fish: Lactic Acid Food Grade can be used in meat, poultry and fish in the form of sodium or potassium lactate to extend shelf life, control pathogenic bacteria (improve food safety), enhance and protect meat flavour, improve water binding capacity and reduce sodium.


Pickling: Lactic Acid Food Grade is used in the pickling process to create a sour flavor and lower the pH of pickled vegetables like cucumbers.
Cheese Making: In cheese production, Lactic Acid Food Grade bacteria are used to ferment milk and produce the acidity required for curd formation and flavor development.


Marinades and Sauces: Lactic Acid Food Grade is used in marinades and sauces for meats and seafood to enhance flavor and tenderness.
Fruit Juices: Lactic Acid Food Grade can be added to fruit juices to adjust acidity levels and improve the taste of citrus and other fruit-based beverages.
Confections: Lactic Acid Food Grade is used in the production of confectionery items like gummies and sour candies to provide a sour and tangy flavor.


Fermentation: Lactic Acid Food Grade bacteria are employed in the fermentation of various foods, such as sauerkraut, kimchi, and sourdough bread.
Sports and Energy Drinks: Lactic Acid Food Grade or its salts are added to sports and energy drinks to provide a mild acidity and enhance the flavor profile.


Lactic Acid Food Grade has many uses and is produced by bacterial fermentation of carbohydrates such as sugars and starches.
In the food industry, Lactic Acid Food Grade is found primarily in sour milk products, these include kumis, laban, yogurt, kefir, and some cottage cheeses.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade.


Lactic Acid Food Grade is also responsible for the sour flavour of sourdough bread.
Lactic Acid Food Grade is also used in beer making, wine production and as a food additive.
Lactic Acid Food Grade is also used to adjust the pH level in foods and beverages.


In production, Lactic Acid Food Grade is usually added so that the pH of the milk reaches around 5.0.
The casein in fermented milk is coagulated (curdled) by Lactic Acid Food Grade and it is also responsible for the sour flavour of sourdough breads.
Lactic Acid Food Grade is responsible for the tangy flavor of fermented milk products (e.g. yogurt, kefir), sour beers, and sourdough bread.


Fermentation usually results in the racemate, although some fermenting bacteria produce the D-enantiomer only.
In winemaking, some wines may go through a natural or induced process called malolactic fermentation, which converts malic acid to Lactic Acid Food Grade, to reduce the sharpness of the acidity.


Beverages uses of Lactic Acid Food Grade: Because of its mild taste, Lactic Acid Food Grade is used as an acidity regulator in beverages such as soft drinks and fruit juices.
Lactic Acid Food Grade is widely used in brewing to adjust pH In the mash in small quantities to adjust the room temperature mash to 5.4-5.6 range.


Lactic Acid Food Grade commonly used as a pH modifier in beer brewing.
Lactic Acid Food Grade is used in beer brewing to lower the pH and increase the body of the beer.
Lactic Acid Food Grade is also used in various beverages and cocktails to impart a sour taste.


Lactic Acid Food Grade in animal nutrition is characterized by lowering the pH of the stomach, reducing the buffering properties of the feed, increasing the activity of proteolytic enzymes/improving the secretion of pancreatic secretions, stimulating the activity of digestive enzymes, stimulating the growth of beneficial bacterial growth, reducing the survival of pathogens in the stomach/maintaining the balance of microbial populations, and directly killing bacteria.


Lactic Acid Food Grade is also found as a nutritional additive for livestock, which improves the digestion of herbivorous animals, as the acid helps to ferment feed faster.
Lactic Acid Food Grade is widely used in brewing to adjust pH In the mash in small quantities to adjust the room temperature mash to 5.4-5.6 range.


Lactic Acid Food Grade is also used in beer making, wine production and as a food additive.
Lactic Acid Food Grade is naturally present in many foodstuffs.
Lactic Acid Food Grade is formed by natural fermentation in products such as cheese, yogurt, soy sauce, sourdough, meat products and pickled vegetables.


The inclusion of additional lactic acid prior to rennetting overcomes this shortage and improves the curd yield.
Lactic Acid Food Grade is a vital ingredient in Ricotta Impastata, Mozzarella, Queso Blanco and other speciality cheeses and can be used in the production of sour milk products, such as Koumiss, Laban, Kefir, as well as some cottage cheeses.


Given its prevalence in nature, Lactic Acid Food Grade is useful for manipulating food chemistry, and is therefore a common additive.
Lactic Acid Food Gradev may be used as a preservative, an acidifier, a dairy culturing agent, or an ingredient in infant formulas.
Lactic Acid Food Grade may also be used in pharmaceuticals and cosmetics as a preservative and acidifier, and in contraceptive jellies as an active ingredient.


Lactic Acid Food Grade is used as a food preservative, curing agent, and flavoring agent.
Lactic Acid Food Grade is an ingredient in processed foods and is used as a decontaminant during meat processing.
Lactic Acid Food Grade has several industrial applications, including its use in food production, pharmaceuticals, and cosmetics.


-Food preservation:
Lactic Acid Food Grade exhibits antimicrobial properties, and its use as a food preservative helps inhibit the growth of harmful bacteria, molds, and yeasts.
Lactic Acid Food Grade can extend the shelf life of processed foods and prevent spoilage.


-Acidification:
Lactic Acid Food Grade is utilized to acidify and adjust the pH of certain foods and beverages.
Lactic Acid Food Grade is particularly valuable in fermented products such as sauerkraut, pickles, kimchi, and yogurt, where it contributes to the characteristic acidity and tanginess.


-Bakery products:
Lactic Acid Food Grade is utilized in the baking industry to regulate dough fermentation and improve the texture and volume of baked goods.
Lactic Acid Food Grade contributes to the development of a desirable crumb structure and imparts a mild tangy flavor.


-Beverages:
Lactic Acid Food Grade finds applications in the production of various beverages, including fruit juices, soft drinks, and alcoholic beverages.
Lactic Acid Food Grade helps adjust acidity levels, improve flavor profiles, and act as a natural preservative.
It is important to note that Lactic Acid Food Grade is generally recognized as safe (GRAS) by regulatory authorities when used in accordance with the approved levels and good manufacturing practices.


-Meat and Poultry:
Lactic Acid Food Grade can be used to reduce microbial load and enhance food safety in meat and poultry products.
Lactic Acid Food Grade is sometimes applied as a surface treatment or spray to reduce the risk of bacterial contamination.


-Flavoring and pH regulation:
Lactic Acid Food Grade is employed as a natural flavoring agent and pH regulator in a wide range of food and beverage products.
Lactic Acid Food Grade imparts a tangy or sour taste, similar to the flavor of yogurt or sourdough bread.


-Dairy products:
Lactic Acid Food Grade plays a vital role in the production of various dairy products.
Lactic Acid Food Grade is used in cheese making to facilitate curd formation and enhance the texture, flavor, and shelf life of cheeses.
Lactic Acid Food Grade bacteria are also employed in the fermentation of milk to produce yogurt and cultured buttermilk.


-Meat and poultry processing:
Lactic Acid Food Grade is employed as an antimicrobial treatment in the processing of meat and poultry products.
Lactic Acid Food Grade can help reduce bacterial contamination and enhance food safety.


-Acidulant:
Lactic Acid Food Grade is used as an acidulant to adjust the pH level and provide a tangy or sour flavor in various food products.
Lactic Acid Food Grade's commonly used in salad dressings, condiments, and beverages to enhance taste.


-Bakery Products: In baking, Lactic Acid Food Grade is used as a dough conditioner to enhance the texture, rise, and shelf life of bread and other baked goods.
Lactic Acid Food Grade can also contribute to the browning of bread crusts.


-Dairy Products:
Lactic Acid Food Grade is naturally present in fermented dairy products such as yogurt, kefir, and buttermilk.
Lactic Acid Food Grade contributes to the tangy flavor and the thickening of these products.



SPECIFICATIONS OF LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is affirmed GRAS by the FDA.
Lactic Acid Food Grade is also certified 21 CFR 184.1061.
Lactic Acid Food Grade does not use genetically modified microorganism for fermentation.
Lactic Acid Food Grade is Kosher under the Orthodox Union and Halal certified.



CHARACTERISTICS OF LACTIC ACID FOOD GRADE:
Lactic Acid Food Grade is a mild-tasting acidity regulator, flavor enhancer, and shows antibacterial properties.
Lactic Acid Food Grade is colorless to yellowish, nearly odorless, and has a syrupy texture.
Lactic Acid Food Grade is an aqueous solution stable under normal conditions and has a pH (50%) value of less than 2 at 25°C.
Lactic Acid Food Grade is easily biodegradable and should not be in environments warmer than 200°C.



WHY IS LACTIC ACID FOOD GRADE PUT INTO FOOD?
The primary reason food manufacturers add Lactic Acid Food Grade to food is due to its antimicrobial properties and ability to extend shelf life.
Lactic Acid Food Grade also enhances flavor.

Furthermore, food manufacturers use Lactic Acid Food Grade in food, because it is a:
*natural additive
*solvent
*curing agent
*gelling agent
*food carrier
*discoloration inhibitor
The FDA approve the use of Lactic Acid Food Grade in most foods. However, this does not apply to infant formulas or foods.



IS LACTIC ACID FOOD GRADE VEGAN?
The Vegetarian Resource Group state that food manufacturers tend to use beet sugar or corn starch when cultivating Lactic Acid Food Grade, which means it is vegan.
Vegan foods that contain Lactic Acid Food Grade include:

*pickled vegetables
*fermented soy products
*cereals
*legumes



WHAT FOODS HAVE HIGH LEVELS OF LACTIC ACID FOOD GRADE?
Some common foods that contain high levels of Lactic Acid Food Grade and its-producing bacteria include:
*pickled vegetables
*sauerkraut
*kimchi
*yogurt
*kefir
*cured fish
Bacteria that produce Lactic Acid Food Grade — for example, Lactobacillus — are a type of probiotic.



IS LACTIC ACID FOOD GRADE GOOD FOR YOU?
Lactic Acid Food Grade and the bacteria that produce it may offer some health benefits, such as:
*protection against infection
*immune system support
*increased absorption of vitamins and minerals
*antioxidant effects

Researchers found Lactic Acid Food Grade-producing bacteria could provide several health benefits.
For example, they may:
*prevent colon cancer
*alleviate lactose intolerance
*ease diarrhea
*relieve peptic ulcers
*stimulate the immune system

Summary:
Lactic Acid Food Grade is a naturally occurring preservative that manufacturers add to some food products.
Foods such as pickled vegetables and yogurt contain Lactic Acid Food Grade.

Lactic Acid Food Grade and the bacteria that produce it may have numerous health benefits.
For instance, they may boost the immune system and help protect the body against certain types of cancer.

The bacteria that produce Lactic Acid Food Grade are a type of probiotic.
Probiotics have several health benefits, including improving gut health.



IS LACTIC ACID FOOD GRADE GOOD FOR YOU?
Yes, Lactic Acid Food Grade is good for you, even when it’s in the form of a food preservative.

Although many food preservatives are unhealthy, Lactic Acid Food Grade preservatives will help protect you from getting sick.
Lactic Acid Food Grade controls the pH, or acidity and alkalinity, to prevent food from spoiling.

Lactic Acid Food Grade also improves your food’s taste.
By controlling the acidity, Lactic Acid Food Grade balances flavors in foods such as olives, cheese, canned fish, desserts, and carbonated drinks.

More importantly, Lactic Acid Food Grade can boost the quality of your food’s nutrition.
While the Lactic Acid Food Grade added to desserts, canned fish, and carbonated drinks is not very healthy, the naturally produced it in fermented foods such as kimchi and yogurt offers a variety of health benefits by:

*Strengthening your immune system
*Helping your body absorb minerals and vitamins
*Giving your food antioxidant effects
*Protecting you from vaginal and urinary infections
*Some strains of Lactic Acid Food Grade bacteria found in food are probiotics, such as those belonging to the genus Lactobacillus.

This means many foods high in Lactic Acid Food Grade have probiotic qualities and can boost your gut health.
Lactic Acid Food Grade can also protect you from constipation and other gastrointestinal issues.



IS LACTIC ACID FOOD GRADE VEGAN?
Generally, Lactic Acid Food Grade is vegan because it’s made from or originates from cereals, legumes, or fermented vegetables.
The main exceptions are Lactic Acid Food Grade found in fermented meat and dairy products, which are non-vegan.

But some food manufacturers may have used animal sources to produce human-made Lactic Acid Food Grade.
The only way to find out for certain is to ask the manufacturer directly.



HOW IS LACTIC ACID FOOD GRADE MADE?
Lactic Acid Food Grade is produced through fermentation, a process where yeasts, mold, fungi, or bacteria break down carbohydrates -- like sugar and starch -- into alcohol, gas, and acids.
Fermentation results in food products high in Lactic Acid Food Grade.

*Fermentation can happen naturally.
Yogurt and sourdough, for instance, ferment on their own.
But in most cases, food manufacturers use a starter culture to begin the fermentation process.

A manufacturer takes these steps to create fermented foods:
*Selects a container to limit oxygen exposure
*Adds a brine of water and salt to the container before sealing it
*Puts in the food that needs to be fermented, such as cabbage or cucumber
*As bacteria break down the sugar in the food, carbon dioxide and Lactic Acid Food Grade will form.

Meanwhile, the process removes oxygen, and the food becomes more acidic.
This promotes the growth of more Lactic Acid Food Grade bacteria and suppresses the growth of other microorganisms.

The fermentation process can take anywhere from days to months.
The food manufacturer will then take the fermented food out and store it in a cool place to keep it from spoiling.



WHAT FOODS ARE HIGH IN LACTIC ACID FOOD GRADE?
A few types of foods are high in Lactic Acid Food Grade.
Generally, any food produced through a fermentation process is full of Lactic Acid Food Grade bacteria and other beneficial bacteria.
These include but are not limited to:

*Bread and beer
*Soy products such as tofu and soy milk
*Cheese
*Pickled vegetables such as kimchi and sauerkraut
*Pickled meats such as salami
*Legumes such as beans and peas.

To get the most out of these foods, avoid cooking them over high heat.
This may kill the beneficial bacteria.
Instead, try adding them as toppings or condiments for cooked food.

Fermented foods are delicious and highly varied in texture and flavor.
They make an excellent addition to any meal.



PHYSICAL and CHEMICAL PROPERTIES of LACTIC ACID FOOD GRADE:
Odor: odorless
Melting point/freezing point:
Melting point: 18 °C at 1.013 hPa
Initial boiling point and boiling range: 122 °C at 18,66 - 19,99 hPa
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 113 °C - closed cup
Autoignition temperature: 400 °C at 1.011,4 - 1.018,9 hPa
Decomposition temperature: No data available
pH: No data available
Molecular Formula: CH3CHOHCOOH.
Molecular Weight: 90.08 g/mol.

Boiling point: 122 °C.
Melting point: 16.8 °C.
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 100 g/l at 20 °C - soluble
Partition coefficient: n-octanol/water:
log Pow: ca.-0,54 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: No data available
Density: 1,25 g/cm3 at 15 °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:
Surface tension 70,7 mN/m at 1g/l at 20 °C
Formula: H₃CCH(OH)COOH
MW: 90.08 g/mol
Boiling Pt: 122 °C (20 hPa)
Density: 1.11…1.21 g/cm³ (20 °C)
Storage Temperature: Ambient
MDL Number: MFCD00004520
CAS Number: 50-21-5
EINECS: 200-018-0
CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0

Mol File: 50-21-5.mol
Lactic acid Chemical Properties
Melting point: 18°C
alpha: -0.05 º (c= neat 25 ºC)
Boiling point: 122 °C/15 mmHg (lit.)
density: 1.209 g/mL at 25 °C (lit.)
vapor density: 0.62 (vs air)
vapor pressure: 19 mm of Hg (@ 20°C)
FEMA: 2611 | LACTIC ACID
refractive index: n20/D 1.4262
Fp: >230 °F
storage temp.: 2-8°C

solubility: Miscible with water and with ethanol (96 per cent).
form: syrup
pka: 3.08(at 100℃)
Specific Gravity: 1.209
color: Colorless to yellow
Water Solubility: SOLUBLE
Merck: 145,336
JECFA Number: 930
BRN: 1209341
Stability: Stable.
Physical state: viscous
Color: colorless
Chemical Name : 2-hydroxy – propanoic acid
Molecular Weight : 90.08

Stereochemical purity (L isomer) Min 97.0 %
Content Min 80.0 %
Colour Fresh : Max 100 Apha
Appearance: Colorless to yellow.
Assay: 80 to 88%.
Also known as: Milk acid.
CAS No: 50-21-5.
Density: 1.206 g/ml.
Grade Standard: Commercial, Food Grade.
Molecular Formula: C3H6O3.
Molecular Weight: 90.078 g•mol−1.
Physical State: Liquid.
Usage: Food, Pharma Synthesis.
Chemical Name: L(S)-2-hydroxypropionic acid.



FIRST AID MEASURES of LACTIC ACID FOOD GRADE:
-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 LACTIC ACID FOOD GRADE:
-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 with liquid-absorbent material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of LACTIC ACID FOOD GRADE:
-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 LACTIC ACID FOOD GRADE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Body Protection:
protective clothing
*Respiratory protection
Recommended Filter type: Filter type ABEK
-Control of environmental exposure:
Do not let product enter drains.



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



STABILITY and REACTIVITY of LACTIC ACID FOOD GRADE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available.
-Incompatible materials:
No data available


Lactose
Lactose; (+)-Lactose; Lactose anhydrous; Milk sugar; 4-(beta-D-Galactosido)-D-glucose; 4-O-beta-D-Galactopyranosyl-D-glucose; Aletobiose; D-Lactose; 1-beta-D-Galactopyranosyl-4-D-glucopyranose; Lactobiose; Lactosum anhydricum; beta-D-galactopyranosyl-(1->4)-D-glucopyranose; (2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6- ((2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl) oxyoxane-3,4,5-triol CAS NO: 63-42-3 (anhydrous), CAS NO: 64044-51-5 (hydrate)
LACTOSE MONOHYDRATE
L-ALPHA-PINENE, N° CAS : 7785-26-4, Nom INCI : L-ALPHA-PINENE, Nom chimique : (-)-Pin-2(3)-ene, N° EINECS/ELINCS : 232-077-3. Ses fonctions (INCI). Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. (-)-alpha-pinene; Pinene Alpha; alpha-Pinen (1S)-(-)-alpha-Pinene (1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-ene (1S,5S)-4,7,7-trimethylbicyclo[3.1.1]hept-3-ene 2,6,6-trimethylbicyclo[3.1.1]hept-2-ene 4,6,6-trimetilbiciclo[3.1.1]hept-3-eno ALPHA PINENE Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, (1S,5S)- Alpha Pinene Laevo Laevo Alpha Pinene
LACTOSE MONOHYDRATE
Lactose monohydrate is a sugar that occurs in many plants.
Lactose monohydrate is extracted commercially from sugar cane and sugar beet.
Lactose monohydrate is a disaccharide formed from a glucose unit and a fructose unit.

CAS: 5989-81-1
MF: C12H24O12
MW: 360.31
EINECS: 611-913-4

Lactose monohydrate is hydrolyzed to a mixture of fructose and glucose by the enzyme invertase.
Since Lactose monohydrate has a different optical rotation (levorotatory) than the original sucrose, the mixture is called invert sugar.
Lactose monohydrate is widely used in pharmaceutical formulations as a diluent in oral capsule and tablet formulations.
Lactose monohydrate may also be used in intravenous injections.

Adverse reactions to Lactose monohydrate are largely due to lactose intolerance, which occurs in individuals with a deficiency of the enzyme lactase.
Lactose monohydrate is a reducing sugar.
The amorphous Lactose monohydrate, which is the most reactive form of lactose present in spray-dried lactose, will interact more readily than conventional crystalline grades.
Typical reactions include the Maillard reaction with either primary or secondary amines.

Lactose monohydrate is a crystallized form of milk sugar.
Lactose monohydrate’s commonly used as a filler for medications and added to packaged foods, baked goods, and infant formulas as a sweetener or stabilizer.
This additive is widely considered safe and may not cause symptoms in those who are otherwise lactose intolerant.
However, those with severe Lactose monohydrate may wish to avoid products with this additive to be safe.

Lactose monohydrate is milk sugar.
Lactose monohydrate is a disaccharide composed of one galactose and one glucose molecule.
In the pharmaceutical industry, Lactose monohydrate is used to help form tablets because it has excellent compressibility properties.
Lactose monohydrate is also used to form a diluent powder for dry-powder inhalations.
Lactose monohydrate may be listed as lactose hydrous, lactose anhydrous, lactose monohydrate, or lactose spray-dried.

People who are Lactose monohydrate do not have the enzymes needed to digest lactose.
Most medications do not contain enough lactose to cause lactose intolerance.
But some patients with severe Lactose monohydrate may experience symptoms.
Lactose monohydrate can be found in birth control pills, and some OTC drugs to treat stomach acid or gas.
Patients who are specifically "allergic" to Lactose monohydrate (not just lactose intolerant) should not use tablets containing lactose, or ask their health care provider prior to use.

Lactose monohydrate is a disaccharide sugar synthesized by galactose and glucose subunits and has the molecular formula C12H22O11.
Lactose monohydrate makes up around 2–8% of milk (by mass).
The name comes from lac (gen. lactis), the Latin word for milk, plus the suffix -ose used to name sugars.
Lactose monohydrate is a white, water-soluble, non-hygroscopic solid with a mildly sweet taste.
Lactose monohydrate is used in the food industry.

Lactose monohydrate Chemical Properties
Melting point: 219 °C
Boiling point: 412.35°C (rough estimate)
Alpha: [α]D20+52.2~+52.8°
Density: 1,53 g/cm3
Refractive index: 1.6480 (estimate)
RTECS: OD9625000
Storage temp.: Inert atmosphere,Room Temperature
Solubility H2O: soluble1M, clear, colorless
Form: neat
Color: White to Off-White
PH: pH (50g/l, 25℃) : 4.0~6.0
Water Solubility: Soluble in water.
Stability: Hygroscopic
InChIKey: WSVLPVUVIUVCRA-KPKNDVKVSA-N
CAS DataBase Reference: 5989-81-1(CAS DataBase Reference)
EPA Substance Registry System: Lactose monohydrate (5989-81-1)

Lactose monohydrate occurs as white to off-white crystalline particles or powder.
Lactose monohydrate is odorless and slightly sweet-tasting.
Spray-dried directcompression grades of Lactose monohydrate are generally composed of 80–90% specially prepared pure a-lactose monohydrate along with 10–20% of amorphous lactose.

Structure and Reactions
Lactose monohydrate is a disaccharide derived from the condensation of galactose and glucose, which form a β-1→4 glycosidic linkage.
Lactose monohydrate's systematic name is β-D-galactopyranosyl-(1→4)-D-glucose.
The glucose can be in either the α-pyranose form or the β-pyranose form, whereas the galactose can only have the β-pyranose form: hence α-lactose and β-lactose refer to the anomeric form of the glucopyranose ring alone.

Detection reactions for Lactose monohydrate are the Woehlk- and Fearon's test.
Both can be easily used in school experiments to visualise the different lactose content of different dairy products such as whole milk, lactose free milk, yogurt, buttermilk, coffee creamer, sour cream, kefir, etc.
Lactose monohydrate is hydrolysed to glucose and galactose, isomerised in alkaline solution to lactulose, and catalytically hydrogenated to the corresponding polyhydric alcohol, lactitol.
Lactose monohydrate is a commercial product, used for treatment of constipation.

Uses
Lactose monohydrate is used as a carrier and stabiliser of aromas, pharmaceutical products, Food industry.
Lactose monohydrate is widely used as a binder, filler-binder, and flow aid in direct compression tableting.
Lactose monohydrate's mild flavor and easy handling properties have led to its use as a carrier and stabiliser of aromas and pharmaceutical products.
Lactose monohydrate is not added directly to many foods, because its solubility is less than that of other sugars commonly used in food.
Infant formula is a notable exception, where the addition of Lactose monohydrate is necessary to match the composition of human milk.

Lactose monohydrate is not fermented by most yeast during brewing, which may be used to advantage.
For example, Lactose monohydrate may be used to sweeten stout beer; the resulting beer is usually called a milk stout or a cream stout.
Yeast belonging to the genus Kluyveromyces have a unique industrial application, as they are capable of fermenting Lactose monohydrate for ethanol production.
Surplus lactose from the whey by-product of dairy operations is a potential source of alternative energy.
Another significant Lactose monohydrate use is in the pharmaceutical industry.
Lactose monohydrate is added to tablet and capsule drug products as an ingredient because of its physical and functional properties.
For similar reasons, Lactose monohydrate can be used to dilute illicit drugs such as cocaine or heroin.

Production Methods
A suspension of a-lactose monohydrate crystals in a lactose solution is atomized and dried in a spray drier.
Approximately 10–20% of the total amount of lactose is in solution and the remaining 80–90% is present in the crystalline form.
The spray-drying process predominantly produces spherical particles.
The compactibility of the material and its flow characteristics are a function of the primary particle size of the lactose monohydrate and the amount of amorphous lactose.

Biochem/physiol Actions
Lactose monohydrate is the primary sugar present in milk and the main energy source to a newborn mammalian through its mother′s milk.
Lactose monohydrate is digested by the intestinal lactase (EC 3.2.1.108), an enzyme expressed in newborns.
The enzyme′s activity declines following weaning which can lead to lactose intolerance in adult mammals.

Synonyms
Lactose monohydrate
5989-81-1
alpha-D-Lactose monohydrate
alpha-Lactose monohydrate
64044-51-5
Respitose
D-Lactose monohydrate
Lactose, monohydrate
Lactose(Monohydrate)
alpha-lactose hydrate
LACTOSE,MONOHYDRATE
Lactose monohydrate [NF]
EWQ57Q8I5X
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;hydrate
Lactose, hydrous
MFCD00150747
a-D-Glucopyranose, 4-O-b-D-galactopyranosyl-, monohydrate
4-O-beta-D-Galactopyranosyl-alpha-D-glucose
Lactose monohydrate (NF)
Lactopress
Pharmatose
Lactochem
Lactohale
Wyndale
Wynhale
lactose hydrate
Lactose hydrous
ALPHA-LACTOSEMONOHYDRATE
a-Lactose monohydrate
10039-26-6
Lactose Monohydrate (Alpha-Form)
Pharmatose dcl ii
Supertab 11sd
Supertab 14sd
Supertab 30gr
Microtose
Pharmaose
Supertab 50 odt
Supertab 11sd nz
Pharmatose dcl 11
Lactopress spray dried
Lactose fastflo 316
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-{[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxane-3,4,5-triol hydrate
(2S,3R,4R,5S,6R)-6-(Hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2,3,4-triol hydrate
Spherolac 100
Alpha-lactose,monohydrate
alpha-D-Glucopyranose, 4-O-beta-D-galactopyranosyl-, monohydrate
Lactose (TN)
NSC-760401
UNII-EWQ57Q8I5X
.alpha.-D-Glucopyranose, 4-O-.beta.-D-galactopyranosyl-, monohydrate
Lactose (JP17)
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)tetrahydropyran-3-yl]oxy-tetrahydropyran-3,4,5-triol
alpha -lactose monohydrate
SCHEMBL16787
LACTOSE HYDRATE [JAN]
LACTOSE, HYDROUS [II]
D-Glucose, 4-O-beta-D-galactopyranosyl-, monohydrate
PHARMATOSE DCL II [II]
D-Glucose, 4-O-.beta.-D-galactopyranosyl-, monohydrate
DTXSID1052828
LACTOSE MONOHYDRATE [II]
alpha-D-Lactose monohydrate, ACS
CHEBI:189432
alpha-Lactose, analytical standard
LACTOSE MONOHYDRATE [USP-RS]
LACTOSE MONOHYDRATE [WHO-IP]
AKOS015896871
FS-3862
NSC 760401
MALONICACIDDISODIUMSALTMONOHYDRATE
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol hydrate
LACTOSE MONOHYDRATE [EP MONOGRAPH]
CS-0128727
LACTOSUM, MONOHYDRATE [WHO-IP LATIN]
D03226
E80712
EN300-1608278
alpha-4-O-(beta-D-galactopyranosido)-D-glucopyranose
Q27277391
alpha-Lactose monohydrate, >=99% total lactose basis (GC)
4-O-beta-D-Galactopyranosyl-alpha-D-glucopyranose monohydrate
alpha-D-Glucopyranose, 4-O-beta-D-galactopyranosyl-, hydrate
alpha-Lactose monohydrate, BioXtra, >=99% total lactose basis (GC)
alpha-Lactose monohydrate, suitable for cell culture, BioReagent
.alpha.-D-Glucopyranose, 4-O-.beta.-D-galactopyranosyl-, hydrate (1:1)
66857-12-3
L-ALPHA-PINENE
LAMP BLACK 101; Amorphous carbon cas no: 1333-86-4
LAMEFORM TGI (POLYGLYCERYL-3 DIISOSTEARATE)
Lameform TGI (Polyglyceryl-3 Diisostearate) is a water-in-oil emulsifier for use in the production of cosmetic emulsions, lipophilic sticks and ointments.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a clear, yellowish liquid which turns cloudy at room temperature.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used as a water-in-oil emulsifier for cold manufacture, and the cloudiness appearance is reversible by heating.

CAS Number: 66082-42-6
Molecular Formula: C45H88O9

Triglycerin diisostearate, 66082-42-6, [2-hydroxy-3-[2-hydroxy-3-[2-hydroxy-3-(16-methylheptadecanoyloxy)propoxy]propoxy]propyl] 16 methylheptadecanoate, Triglyceryl diisostearate.

Lameform TGI (Polyglyceryl-3 Diisostearate) is a humectant and moisturizer ingredient just like glycerin, but the larger molecular structure penetrates slower into the skin and gives milder, longer lasting moisture.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a nonionic, W/O emulsifier.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used in sun care (after-sun, self-tanning & self-protection), body & face care, personal care wipes and baby care & cleansing formulations.

Lameform TGI (Polyglyceryl-3 Diisostearate), also known as Polyglyceryl-3 Diisostearate, is an ingredient commonly used in cosmetics and personal care products.
Lameform TGI (Polyglyceryl-3 Diisostearate) belongs to the class of polyglyceryl esters, which are derived from glycerin and fatty acids.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a plant-derived ingredient, usually appearing as a yellow viscous liquid with a characteristic fatty acid scent.

This ingredient is used as an emulsifier, aiding the mixing of water and oil ingredients by reducing their surface tension.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used as an emulsifier.
Lameform TGI (Polyglyceryl-3 Diisostearate) gives a soft and powdery feel to the formula.

Lameform TGI (Polyglyceryl-3 Diisostearate) is very gentle and hence used for baby and sensitive skin formulations.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used as an emollient and surfactant in products such as anti-aging serums, foundations, lip gloss, lipsticks, sunscreens, bronzers, moisturizers.
Lameform TGI (Polyglyceryl-3 Diisostearate) adds shine, gloss, vibrancy in make up products.

Lameform TGI (Polyglyceryl-3 Diisostearate) is incorporated into lipophilic ointments and sticks.
Lameform TGI (Polyglyceryl-3 Diisostearate) improves spreadability, absorption of the product and provides softness to the skin.
Lameform TGI (Polyglyceryl-3 Diisostearate) can be derived from stearic acid (a saturated fatty acid from coconut/palm) and polyglycerin-3 (vegetable oil component).

Lameform TGI (Polyglyceryl-3 Diisostearate) is hydroxy compounds used in cosmetics and skin care products as emollients and surfactants, and are found primarily in lip glosses and lipsticks, although they are also seen in foundations, sunscreens, bronzers, moisturizers and anti-aging serums.
Lameform TGI (Polyglyceryl-3 Diisostearate) facilitates the blending of oil and water components in formulations, ensuring uniform distribution and stability.
Lameform TGI (Polyglyceryl-3 Diisostearate) can contribute to the texture and feel of cosmetic products, imparting a smooth and luxurious skin feel.

Lameform TGI (Polyglyceryl-3 Diisostearate) may help to hydrate and moisturize the skin by forming a protective barrier that reduces water loss from the skin's surface.
This ingredient can improve the spreadability of formulations, allowing for easy application and smooth coverage on the skin.
Lameform TGI (Polyglyceryl-3 Diisostearate) is generally well-tolerated by the skin and is suitable for use in a wide range of cosmetic formulations.

An effective emulsifier for Water in Oil formulations.
Lameform TGI (Polyglyceryl-3 Diisostearate) is exceptionally gentle on the skin and mild, which makes it ideal in products aimed at sensitive skin areas.
The emulsifier is especially versatile during production, being both usable in Hot and Cold Process formulations. Suitable for both skin and hair formulations.

Lameform TGI (Polyglyceryl-3 Diisostearate) is a water-in-oil emulsifier for use in the production of cosmetic emulsions, lipophilic sticks and ointments.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a clear, yellowish liquid which turns cloudy at room temperature.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used as a water-in-oil emulsifier for cold manufacture, and the cloudiness appearance is reversible by heating.

Lameform TGI (Polyglyceryl-3 Diisostearate) is primarily used as an emulsifier and surfactant in cosmetic formulations.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps to stabilize emulsions by promoting the mixing of oil and water phases, leading to the formation of stable and homogeneous products.
This ingredient is often found in creams, lotions, moisturizers, makeup products, and sunscreens.

Lameform TGI (Polyglyceryl-3 Diisostearate) is a nonionic surfactant, meaning it does not carry an electrical charge in solution.
Nonionic surfactants are generally milder and less irritating compared to ionic surfactants, making them suitable for use in skincare products, especially for sensitive or delicate skin types.
Lameform TGI (Polyglyceryl-3 Diisostearate) is soluble in both water and oil phases, which makes it versatile in formulating various types of cosmetic products.

Lameform TGI (Polyglyceryl-3 Diisostearate) can help create stable emulsions with different ratios of water to oil, providing flexibility in product design.
When applied to the skin, Lameform TGI (Polyglyceryl-3 Diisostearate) can form a thin, protective film that helps to lock in moisture and protect the skin from environmental stressors.
This film-forming property can contribute to the long-lasting hydration and comfort of skincare products.

Lameform TGI (Polyglyceryl-3 Diisostearate) is often used in combination with other emulsifiers and thickeners to optimize the performance and stability of cosmetic formulations.
Its compatibility with a wide range of ingredients allows formulators to achieve desired product characteristics and sensory attributes.
Lameform TGI (Polyglyceryl-3 Diisostearate) is generally recognized as safe (GRAS) for use in cosmetics and personal care products by regulatory agencies such as the U.S. Food and Drug Administration (FDA) and the European Union (EU).

Lameform TGI (Polyglyceryl-3 Diisostearate) is listed on ingredient inventories such as the Cosmetic Ingredient Database (Cosing) and the Personal Care Product Council (PCPC) International Cosmetic Ingredient Dictionary and Handbook.
Lameform TGI (Polyglyceryl-3 Diisostearate) is considered biodegradable and environmentally friendly, with low toxicity to aquatic organisms.

This makes it a preferred choice for formulators seeking sustainable and eco-friendly cosmetic ingredients.
Lameform TGI (Polyglyceryl-3 Diisostearate) is commercially available from various suppliers worldwide, making it readily accessible to cosmetic manufacturers and formulators.

Acid Value: ≤12
Saponification Value: ≤165

Lameform TGI (Polyglyceryl-3 Diisostearate) is a natural emulsifiable obtained from glycerin and stearic acid.
Lameform TGI (Polyglyceryl-3 Diisostearate) is used in oily external fase cream formulations and allows to properly emulsify the physical filters in sunscreens.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a hydroxy compound used as an emollient and surfactant.

Lameform TGI (Polyglyceryl-3 Diisostearate) is used in lip glosses and lipsticks especially along with foundations, sunscreens, moisturizers and anti-aging serums.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a Diester of isostearic acid and polyglycerin3 Polyglyceryl-3 diisostearate uses and applications include: Emulsifier, emollient, thickener, solvent in cosmetics, creams, lotions, lip products, pharmaceuticals; dye and pigment wetting agent; food emulsifier; pharmaceuticals excipient.

Lameform TGI (Polyglyceryl-3 Diisostearate) helps improve the stability of cosmetic formulations by preventing phase separation, creaming, or coalescence.
This ensures that the product maintains its desired consistency and appearance over time, even under various storage conditions.
In addition to its emulsifying properties, Lameform TGI (Polyglyceryl-3 Diisostearate) can contribute to the overall texture and sensorial experience of cosmetic products.

Lameform TGI (Polyglyceryl-3 Diisostearate) imparts a smooth, non-greasy feel and can help create lightweight, easily spreadable formulations that are pleasant to use.
Lameform TGI (Polyglyceryl-3 Diisostearate) is compatible with a wide range of active ingredients commonly used in skincare formulations, including antioxidants, vitamins, and botanical extracts.
This compatibility allows formulators to incorporate various functional ingredients without compromising the stability or efficacy of the final product.

Lameform TGI (Polyglyceryl-3 Diisostearate) can be used in a variety of cosmetic products, including moisturizers, creams, lotions, serums, sunscreens, and makeup formulations.
Its versatility makes it suitable for both leave-on and rinse-off products, providing formulators with flexibility in product development.
Lameform TGI (Polyglyceryl-3 Diisostearate) contributes to the sensory attributes of cosmetic products, such as smoothness, silkiness, and skin feel.

Lameform TGI (Polyglyceryl-3 Diisostearate) helps create formulations that are easy to apply, absorb quickly into the skin, and leave a soft, velvety finish without tackiness or greasiness.
When combined with other emulsifiers, thickeners, and stabilizers, Lameform TGI (Polyglyceryl-3 Diisostearate) can act synergistically to optimize the performance and aesthetics of cosmetic formulations.
This synergistic effect allows formulators to achieve specific product goals, such as enhanced hydration, improved skin barrier function, or prolonged wear.

Cosmetic products formulated with Lameform TGI (Polyglyceryl-3 Diisostearate) often appeal to consumers seeking lightweight, non-comedogenic, and non-irritating skincare solutions.
Its mildness and compatibility with sensitive skin make it suitable for a wide range of skin types, including dry, oily, and combination skin.
Lameform TGI (Polyglyceryl-3 Diisostearate) complies with regulatory requirements for cosmetic ingredients in major markets worldwide, including the United States, European Union, Japan, and China.

Lameform TGI (Polyglyceryl-3 Diisostearate) meets safety standards and specifications established by regulatory agencies to ensure consumer safety and product quality.
Lameform TGI (Polyglyceryl-3 Diisostearate) can help improve skin hydration and moisturization by forming a protective barrier on the skin's surface.
This barrier helps to prevent moisture loss and maintains the skin's natural hydration levels, resulting in smoother, softer, and more supple skin.

Due to its lightweight and non-greasy texture, formulations containing Lameform TGI (Polyglyceryl-3 Diisostearate) are often non-comedogenic, meaning they are less likely to clog pores or contribute to acne breakouts.
This makes it suitable for use in skincare products designed for acne-prone or oily skin types.
Lameform TGI (Polyglyceryl-3 Diisostearate) exhibits emollient properties, which help to soften and smooth the skin's surface.

Lameform TGI (Polyglyceryl-3 Diisostearate) can also act as a conditioning agent, improving the overall texture and feel of cosmetic products while imparting a luxurious skin feel.
In formulations containing antioxidants or other sensitive active ingredients, Lameform TGI (Polyglyceryl-3 Diisostearate) can help enhance stability and protect these ingredients from degradation due to exposure to air, light, or heat.
This ensures the efficacy and longevity of the product over time.

Lameform TGI (Polyglyceryl-3 Diisostearate) is compatible with a wide range of formulation ingredients, including oils, waxes, silicones, and hydrophilic polymers.
This compatibility allows formulators to create innovative and multifunctional cosmetic products with diverse textures and sensory profiles.
By improving the dispersion and compatibility of ingredients within cosmetic formulations, Lameform TGI (Polyglyceryl-3 Diisostearate) can enhance the overall performance of the product.

This includes attributes such as spreadability, absorbency, adherence, and longevity, resulting in products that deliver optimal results to consumers.
Some suppliers of Lameform TGI (Polyglyceryl-3 Diisostearate) offer sustainable sourcing options and eco-friendly manufacturing processes.
This aligns with the growing demand for environmentally conscious and socially responsible cosmetic ingredients, appealing to consumers who prioritize sustainability.

Lameform TGI (Polyglyceryl-3 Diisostearate) can be easily incorporated into various cosmetic formulations at different concentrations to achieve specific performance objectives and desired sensory attributes.
This allows formulators to customize products according to market trends, consumer preferences, and brand identity.
Many formulations containing Lameform TGI (Polyglyceryl-3 Diisostearate) undergo rigorous clinical testing and safety assessments to ensure they meet regulatory standards and consumer safety requirements.

This includes dermatological testing, irritation testing, sensitization testing, and stability testing to confirm the safety and efficacy of the product.
Cosmetic companies often provide information about the benefits and uses of Lameform TGI (Polyglyceryl-3 Diisostearate) to educate consumers and promote transparency regarding ingredient sourcing, manufacturing practices, and product performance.
This helps to build trust and confidence in the brand and its products among consumers.

Uses:
Lameform TGI (Polyglyceryl-3 Diisostearate) is used in cosmetic, food, plastic, metal process and petrochemical industry etc.
Lameform TGI (Polyglyceryl-3 Diisostearate) could be used in ice cream, candy, protein beverage, margarine, dairy products because of the good emulsification, dispersing and stable property.
Lameform TGI (Polyglyceryl-3 Diisostearate) could be used in meat product such as sausage, luncheon meat, burger, fish stuffing because of the good dispersing and stable property.

Lameform TGI (Polyglyceryl-3 Diisostearate) could be used in pharmaceutical chemicals, such as pharmacy painting, printing ink.
Lameform TGI (Polyglyceryl-3 Diisostearate) could be used as protective agent in edible dry yeast, improve the antistaling agent's freshness effect.
Lameform TGI (Polyglyceryl-3 Diisostearate) could improve productivity by improving the crystallization of sucrose.

Lameform TGI (Polyglyceryl-3 Diisostearate) also could be used as dispersing agents in cod-liver oil emulsion or spongarion.
As emulsion, stabilizer, dispersing agents and plasticizer, it could be widely applied in textile, papermaking, painting, plastic, rubber, printing and dyeing industry. Lameform TGI (Polyglyceryl-3 Diisostearate) has broad range of HLB value, except for its high security for human, it also has good characteristics of non-stimulation for skin, good water and emulsion solubility.

Lameform TGI (Polyglyceryl-3 Diisostearate) could stand thermophilic digestion so that it's good for goods' sterilization .
Lameform TGI (Polyglyceryl-3 Diisostearate) acts as an emulsifier, helping to stabilize oil-in-water and water-in-oil emulsions.
This property is essential for creating homogeneous mixtures of oil and water phases in products like creams, lotions, and serums.

As a surfactant, Lameform TGI (Polyglyceryl-3 Diisostearate) reduces the surface tension between different ingredients, facilitating their dispersion and improving the spreadability of cosmetic formulations.
v contributes to the texture and feel of cosmetic products, imparting a smooth, non-greasy sensation to formulations.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps create products with desirable sensory attributes.

Lameform TGI (Polyglyceryl-3 Diisostearate) forms a protective barrier on the skin, helping to lock in moisture and prevent dehydration.
This moisturizing effect is particularly beneficial in skincare products like moisturizers and body lotions.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps soften and condition the skin, leaving it feeling smooth and hydrated.

This makes it a valuable ingredient in skincare products designed to improve skin texture and appearance.
Lameform TGI (Polyglyceryl-3 Diisostearate) enhances the compatibility of different ingredients in cosmetic formulations, ensuring their proper integration and interaction.
This property is crucial for maintaining the stability and efficacy of the final product.

Lameform TGI (Polyglyceryl-3 Diisostearate) assists in the formulation process by improving the homogeneity, stability, and performance of cosmetic products.
Formulators rely on Lameform TGI (Polyglyceryl-3 Diisostearate) to achieve desired product characteristics and meet consumer expectations.
Lameform TGI (Polyglyceryl-3 Diisostearate) serves multiple functions in cosmetic formulations, simplifying the formulation process and reducing the need for additional ingredients.

Its versatility makes it suitable for a wide range of skincare, haircare, and personal care products.
Lameform TGI (Polyglyceryl-3 Diisostearate) is a compound used primarily in lip care and lipsticks due to its emollient effect, although it is also found in sunscreens, bronzers, moisturizers and anti-aging serums.
Lameform TGI (Polyglyceryl-3 Diisostearate) used as a natural and gentle emulsifier that gives a soft texture to products.

Vegetable-based high polarity oil with medium viscosity used as co-emulsifier in emulsions.
Lameform TGI (Polyglyceryl-3 Diisostearate) products are pale yellow to yellow waxy solid, are easy to soluble in oil, organic solvent, and disperse into hot water.
Lameform TGI (Polyglyceryl-3 Diisostearate) also has good property of thermostability and acid resistance

Lameform TGI (Polyglyceryl-3 Diisostearate) is used in sun care (after-sun, self-tanning and self-protection), body & face care, personal care wipes, and baby care & cleansing formulations
Lameform TGI (Polyglyceryl-3 Diisostearate) is commonly used in the formulation of creams and lotions, where it acts as an emulsifier to stabilize the mixture of water and oil phases.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps create smooth, creamy textures that are easy to apply and absorb into the skin.

In serums and moisturizers, Lameform TGI (Polyglyceryl-3 Diisostearate) serves as a moisturizing agent, helping to hydrate and soften the skin.
Its emollient properties contribute to the luxurious feel of these products, leaving the skin feeling nourished and supple.
Lameform TGI (Polyglyceryl-3 Diisostearate) is often included in sunscreen formulations to improve their spreadability and ensure even coverage on the skin.

Lameform TGI (Polyglyceryl-3 Diisostearate) helps disperse the active sunscreen ingredients evenly throughout the formulation, enhancing the product's efficacy.
In makeup products such as foundations, BB creams, and concealers, Lameform TGI (Polyglyceryl-3 Diisostearate) functions as an emulsifier and texture enhancer.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps create smooth, blendable textures that glide effortlessly onto the skin, providing a flawless finish.

Some cleansing formulations, such as facial cleansers and body washes, contain Lameform TGI (Polyglyceryl-3 Diisostearate) to improve their texture and emulsification properties.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps the formulation effectively remove dirt, oil, and makeup while leaving the skin feeling clean and refreshed.
Lameform TGI (Polyglyceryl-3 Diisostearate) can also be used in haircare products such as shampoos, conditioners, and styling products.

Lameform TGI (Polyglyceryl-3 Diisostearate) helps emulsify the ingredients in these formulations, improving their stability and performance while enhancing the texture and manageability of the hair.
Due to its mild and non-irritating properties, Lameform TGI (Polyglyceryl-3 Diisostearate) is suitable for use in formulations designed for sensitive skin.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps minimize the risk of skin irritation or allergic reactions, making it an ideal choice for gentle skincare products.

Lameform TGI (Polyglyceryl-3 Diisostearate) can be used in natural and organic cosmetic formulations as a plant-derived emulsifier.
Lameform TGI (Polyglyceryl-3 Diisostearate) allows formulators to create natural skincare products that meet consumer demand for clean, green beauty options.
In anti-aging skincare products, Lameform TGI (Polyglyceryl-3 Diisostearate) helps improve the texture and appearance of the skin, reducing the appearance of fine lines and wrinkles.

Its moisturizing properties help hydrate and plump the skin, giving it a more youthful and radiant appearance.
From body lotions and creams to body scrubs and massage oils, Lameform TGI (Polyglyceryl-3 Diisostearate) is a versatile ingredient used in various body care formulations.
Lameform TGI (Polyglyceryl-3 Diisostearate) helps enhance the texture, spreadability, and moisturizing properties of these products, leaving the skin feeling soft, smooth, and nourished.

Safety profile:
Lameform TGI (Polyglyceryl-3 Diisostearate) is considered to be safe for use in cosmetics.
Lameform TGI (Polyglyceryl-3 Diisostearate) is not known to cause allergy, irritation, toxicity or carcinogenicity.
In some individuals, Lameform TGI (Polyglyceryl-3 Diisostearate) may cause skin irritation or allergic reactions, especially in those with sensitive skin or pre-existing skin conditions.

Lameform TGI (Polyglyceryl-3 Diisostearate)'s important to perform patch testing before using products containing this ingredient, particularly if you have a history of skin sensitivity.
Contact with the eyes may cause irritation or discomfort.
Avoid direct contact with the eyes and rinse thoroughly with water if accidental exposure occurs.

Inhalation: Inhalation of airborne particles or aerosols containing Lameform TGI (Polyglyceryl-3 Diisostearate) may cause respiratory irritation in sensitive individuals.
Ensure adequate ventilation when handling powdered forms of the substance and use appropriate respiratory protection if necessary.
While Lameform TGI (Polyglyceryl-3 Diisostearate) is not intended for ingestion, accidental ingestion of large quantities may cause gastrointestinal discomfort or irritation.

Keep products containing this ingredient out of reach of children and pets, and seek medical attention if ingestion occurs.
Lameform TGI (Polyglyceryl-3 Diisostearate) is considered biodegradable, excessive discharge into the environment may contribute to water pollution.
Dispose of unused products properly and follow local regulations for wastewater treatment and disposal.

LAMEPON S
DESCRIPTION:

LAMEPON S is an anionic & co-surfactant.
LAMEPON S belongs to the product class of protein fatty acid condensates which account of its very good physiological characteristics.
LAMEPON S improves the skin and eye mucosa compatibility of basic surfactants and/or surfactant systems.
LAMEPON S is used in mild shower, foam baths, shampoos and body cleansers.

LAMEPON S is Co-surfactant suitable for mild shower and foam baths as well as shampoos and body cleansers.
Lamepon S belongs to the product class of protein fatty acid condensates which account of its excellent physiological characteristics is highly suited for use in mild shower and foam baths as well as in shampoos and body cleansers.
As co-surfactant Lamepon S clearly improves the skin and eye mucosa compatibility of basic surfactants and/or surfactant systems.

CHEMICAL AND PHYSICAL PROPERTIES OF LAMEPON S:
Chemical Function: Protein
Product Applications: Bath & Shower, Hand Cleansing, Skin Cleansing


SAFETY INFORMATION ABOUT LAMEPON S:

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.
LAMP BLACK 101
LANETH-10, N° CAS : 61791-20-6. Nom INCI : LANETH-10. 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. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
LAMP BLACK 101 (CARBON BLACK)
Lamp black 101 (Carbon Black) is a finely divided form of carbon.
Lamp black 101 (Carbon Black) may ignite explosively if suspended in air in the presence of an ignition source or slowly undergo spontaneous combustion upon contact with water.
In addition, Lamp black 101 (Carbon Black) is toxic by inhalation, with a TLV of 3.5 mg/m3 in air.

CAS: 1333-86-4
MF: C
MW: 12.01
EINECS: 215-609-9

Lamp black 101 (Carbon Black) is a black pigment that is used in the manufacture of paints, inks, and other products.
Lamp black 101 (Carbon Black) has high values of thermal expansion and adsorption properties.
Lamp black 101 (Carbon Black) has been used as an adsorbent for the removal of chemical pesticides from wastewater.
Lamp black 101 (Carbon Black) also has been used to remove phenols and organic matter from water by adsorption.
The optimum concentration of carbon black is between 0.5% and 1%.
The concentration-time curve for activated carbon shows a rapid initial rise followed by a slower rate of increase.
This curve occurs due to the fast absorption capacity of activated carbon, which leads to rapid uptake rates in the early stages before saturation occurs.

Primary uses are in the manufacture of tires, belt covers, plastics, carbon paper, colorant for printing inks, and as a solar-energy absorber.
A finely divided form of carbon, practically all of which is made by burning vaporized heavy-oil frac- tions in a furnace with 50% of the air required for complete combustion (partial oxidation).
This type is also called furnace black.
Carbon black can also be made from methane or natural gas by crack- ing (thermal black) or direct combustion (channel black), but these methods are virtually obsolete.
All types are characterized by extremely fine particle size, which accounts for their reinforcing and pig- menting effectiveness.

Multi walled carbon nanotubes (MWNTs, CNTs) were prepared by chemical vapor deposition (CVD).
In chemical vapor deposition (CVD), a volatile precursor undergoes thermal decomposition at elevated temperatures to form a solid deposit on a substrate.
1 Carboxylic acid groups can be attached to the defect sides and ends of the nanotube by treatment with oxidizing agents.
Carboxylic acid groups can be easily derivatized into different functional groups.

Lamp black 101 (Carbon Black) (with subtypes acetylene black, channel black, furnace black, lamp black and thermal black) is a material produced by the incomplete combustion of coal tar, vegetable matter, or petroleum products, including fuel oil, fluid catalytic cracking tar, and ethylene cracking in a limited supply of air.
Lamp black 101 (Carbon Black) is a form of paracrystalline carbon that has a high surface-area-to-volume ratio, albeit lower than that of activated carbon.

Lamp black 101 (Carbon Black) is dissimilar to soot in its much higher surface-area-to-volume ratio and significantly lower (negligible and non-bioavailable) polycyclic aromatic hydrocarbon (PAH) content.
However, Lamp black 101 (Carbon Black) can be used as a model compound for diesel soot to better understand how diesel soot behaves under various reaction conditions as carbon black and diesel soot have some similar properties such as particle sizes, densities, and copolymer adsorption abilities that contribute to them having similar behaviours under various reactions such as oxidation experiments.

Lamp black 101 (Carbon Black) is used as a colorant and reinforcing filler in tires and other rubber products; pigment and wear protection additive in plastics, paints, and ink pigment.
Lamp black 101 (Carbon Black) is used in the EU as a food colorant when produced from vegetable matter.
The current International Agency for Research on Cancer (IARC) evaluation is that, "Carbon black is possibly carcinogenic to humans (Group 2B)".
Short-term exposure to high concentrations of Lamp black 101 (Carbon Black) dust may produce discomfort to the upper respiratory tract through mechanical irritation.

Lamp black 101 (Carbon Black) Chemical Properties
Melting point: 3550 °C(lit.)
Boiling point: 500-600 °C(lit.)
Density: ~1.7 g/mL at 25 °C(lit.)
Vapor pressure: Fp: >230 °F
Solubility: H2O: soluble0.1mg/mL
Form: rod
Color: Clear colorless
Specific Gravity: bulk 0.10/g/cm3
Water Solubility: Insoluble
Merck: 14,1808
Exposure limits ACGIH: TWA 3 mg/m3
OSHA: TWA 3.5 mg/m3
NIOSH: IDLH 1750 mg/m3; TWA 3.5 mg/m3; TWA 0.1 mg/m3
Stability: Stable. Combustible.
InChIKey: VNWKTOKETHGBQD-UHFFFAOYSA-N
LogP: 1.090 (est)
IARC: 2B (Vol. Sup 7, 65, 93) 2010
EPA Substance Registry System: Lamp black 101 (Carbon Black) (1333-86-4)

Physical properties
Lamp black 101 (Carbon Black) is virtually pure elemental carbon (diamond and graphite are other forms of nearly pure carbon) in the form of near-spherical colloidal particles that are produced by incomplete combustion or thermal decomposition of gaseous or liquid hydrocarbons.
Lamp black 101 (Carbon Black)'s physical appearance is that of a black, finely divided pellet or powder, the latter sometimes small enough to be invisible to the naked eye.
Lamp black 101 (Carbon Black)'s use in tires, rubber and plastic products, printing inks and coatings is related to the properties of specific surface area, particle size and structure, conductivity and color.
Lamp black 101 (Carbon Black) is in the top 50 industrial chemicals manufactured worldwide, based on annual tonnage. Current worldwide production is about 15 billion pounds per year (6.81 million metric tons).

Approximately 90% of Lamp black 101 (Carbon Black) is used in rubber applications, 9% as a pigment, and the remaining 1% as an essential ingredient in hundreds of diverse applications.
Modern Lamp black 101 (Carbon Black) products are direct descendants of early “lampblack”, first produced in China over 3500 years ago.
These early lampblacks were not very pure and differed greatly in their chemical composition from current carbon blacks.
Since the mid-1970s most carbon black has been produced by the oil furnace process, which is most often referred to as furnace black.
Unlike diamond and graphite, which are crystalline carbons, Lamp black 101 (Carbon Black) is an amorphous carbon composed of fused particles called aggregates.
Properties, such as surface area, structure, aggregate diameter and mass differentiate the various carbon black grades.

Uses
1. Lamp black 101 (Carbon Black) is edible black pigment.
Lamp black 101 (Carbon Black) can be used for pastry with the usage amount of 0.001% to 0.1%.
2. Lamp black 101 (Carbon Black) can be used for food coloring agent.
China provides that Lamp black 101 (Carbon Black) can be used for rice, flour products, candy, biscuits and pastries with the maximum usage amount of 5.0g/kg.
3. Rubber industry uses Lamp black 101 (Carbon Black) as a reinforcing filler.
Paint Inks applies Lamp black 101 (Carbon Black) as coloring pigments in paint inks.
Used for the manufacturing of black paper such as packaging materials for photographic materials and the black paper made of high-conductivity black carbon in the radio equipment.
4. Carbon paper and typewriter; Lamp black 101 (Carbon Black) is used when it is required for darker colors and can remain on the carrier.
5. Plastic coloring, ink, phonograph records, shoe polish, paint cloth, leather coatings, colored cement, electrodes, electronic brushes, batteries and so on.

As electric conductive agent of lithium ion battery;
Mainly used for rubber, paint, ink and other industries;
6. Used for the reinforcement of car tread and sidewall, hose, groove, industrial rubber products as well as conveyor belt.
7. Used for tire tread, surface tire repair, automotive rubber parts, conveyor belts, conveyor pads, etc., The vulcanized glue of this carbon black shows excellent tensile strength and abrasion resistance
8. Lamp black 101 (Carbon Black) is mainly used for the reinforcement of tire belt, sidewall, solid tires, outer layer of roller, hose surface, industrial rubber products and car tire tread.
9. Lamp black 101 (Carbon Black) is used for the reinforcement of the tire tread of car and truck, surface of conveyor belt and industrial rubber products.
10. For rubber reinforcement, coloring agent, metallurgy, rocket propellant.

11. For rubber products to fill and reinforcement.
12. For rubber products, carcass, valves and other filling .
13. For paints and inks, plastics and other industries.
14. Mainly used for raw materials of battery as well as for conductive and anti-static rubber products.
15. In the rubber industry, Lamp black 101 (Carbon Black) is used as the reinforcing agent and filter for the manufacturing of natural rubber and butyl rubber, being able to endow the vulcanized rubber with excellent tensile strength, elongation and tear resistance and so on.
Lamp black 101 (Carbon Black) should be mostly used for natural rubber-based large-scale engineering tires and a variety of off-road tires as well as being used for carcass and sidewall.
In addition, Lamp black 101 (Carbon Black) can also be used for high-strength conveyor belt, cold rubber products and drilling device.
In light industry, Lamp black 101 (Carbon Black) can be used as the filter of the paint, ink, enamel and plastic products.

Lamp black 101 (Carbon Black) was used as conductive agent.
Super P furnace black the best conductive additive.
Lamp black 101 (Carbon Black) was added with binder in the composite electrode to compensate the low electrical conductivity of PPy and PPyDVB in miniemulsion polymerization.
The hybrid Super P-SACNT conductive network manifests itself as a promising strategy to improve the battery performances with a minimum amount of conductive fillers.

Tire treads, belt covers, and other abrasion- resistant rubber products; plastics as a reinforc- ing agent, opacifier, electrical conductor, UV- light absorber; colorant for printing inks;carbon paper; typewriter ribbons; paint pigment; nucleat- ing agent in weather modification; expanders in bat- tery plates; solar-energy absorber (see note).
In the rubber, plastic, printing, and paint industries as a reinforcing agent and a pigment
Lamp black 101 (Carbon Black) is a type of fine soot that is obtained from materials that have not been completely burned.
Lamp black 101 (Carbon Black) has various applications, including its use in polishing celluloid and bone.

Production method
Natural gas tank method of making carbon black: take natural gas as raw material and use iron pipe to send it into the combustion chamber.
The form of the combustion chamber can be either long and short and is made of iron plate.
Lamp black 101 (Carbon Black) contains a number of olefin burner inside it.
Natural gas is sprayed with appropriate force from the burner nozzle and burned in the case of insufficient air, that is, to generate a bright and black smoke flame.
The flame then goes directly into the channel iron with the distance between the burner and the slot surface being 65~80 mm.

At this time, the temperature of olefin burning is reduced from about 1000 to 1400 ° C to about 500 ° C, and the carbon black is accumulated.
The groove can move back and forth horizontally, with a moving speed of 3 to 4 mm/s.
In order to maintain normal production, the required amount of air is about 2.5 to 3 times the theoretical calculation.
The resulting carbon black was scraped into a funnel with a fixed doctor blade and sent to a central packing chamber for disposal.

Then the carbon black is softened, filtered to remove the hard particles and scale and further sent into the mill grinding to enable more uniform thickness.
However, the body is still very light and loose, thus should be shaken to a become a bit solid.
Then add a small amount of water to the carbon black to make Lamp black 101 (Carbon Black) into paste-like shape and have a small needle rotated inside Lamp black 101 (Carbon Black) to forming micro-pellets, followed by drying to obtain the finished product.
In the case of using pigment for carbon black, in order to facilitate the dispersion, the granulation is unnecessary.

The process is as follows:
Raw gas, air → combustion cracking → collection → granulation → packaging → finished product.
Carbon black is one of the oldest industrial products.
In ancient times, china has already applied incomplete combustion of vegetable oil for making pigment carbon black.
In 1872, the United States first used natural gas as raw material to produce carbon black using tank method and mainly used it as a coloring agent.
Lamp black 101 (Carbon Black) was not until 1912 when Mott found the reinforcement effect carbon black on the rubber before the carbon black industry had gotten rapid development.
Then Lamp black 101 (Carbon Black) had successively developed of a variety of process methods.
At present, oil furnace method is the most efficient and most economical method with the oil furnace black production amount accounting for 70-90% of the total carbon black production. There are mainly furnace, slot method, thermal cracking, three methods.
Lamp black 101 (Carbon Black) is obtained by the carbonization of the plant material such as peat.
Lamp black 101 (Carbon Black) can also be derived from the carbonization of cocoa shell and beef bone or from the combustion of vegetable oil.

Health Hazard
There are no well demonstrated health hazards to humans from acute exposure to Lamp black 101 (Carbon Black).
Commercial carbon black is a spherical colloidal form of nearly pure carbon particles and aggregates with trace amounts of organic impurities adsorbed on the surface.
Potential health effects usually are attributed to these impurities rather than to the carbon itself.
Soots, by contrast, contain mixtures of particulate carbon, resins, tars, and so on, in a nonadsorbed state.

Synonyms
ACTIVATED CARBON DARCO G-60
ACTIVATED CHARCOAL NORIT
ACTIVATED CHARCOAL NORIT(R)
ACETYLENE BLACK
ACETYLENE CARBON BLACK
COSMETICBLACK(A3278)
CARBONBLACKTONER
9901LAMPBLACK
LANETH-10 ( Alcohols, lanolin, ethoxylated)
LANETH-15, N° CAS : 61791-20-6 / 84650-19-1, Nom INCI : LANETH-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. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
LANETH-15 ( Alcohols, lanolin, ethoxylated)
LANETH-20, N° CAS : 61791-20-6, Nom INCI : LANETH-20, 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. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
LANETH-20 ( Alcohols, lanolin, ethoxylated )
LANETH-40, N° CAS : 61791-20-6. Nom INCI : LANETH-40. 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.Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques
LANETH-40 ( Alcohols, lanolin, ethoxylated)
LANETH-5, N° CAS : 61791-20-6, Nom INCI : LANETH-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). Agent d'entretien de la peau : Maintient la peau en bon état. 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
LANETH-5 ( Alcohols, lanolin, ethoxylated )
SYNONYMS Wool fat; Wool grease; Wool wax; Woolwax ester;
LANOL 1688
Lanol 1688 is a very easy-to-emulsify emollient with a specific and complementary sensory profile.
Lanol 1688 is light, dry structure.


CAS Number: 90411-68-0
EC Number: 291-445-1
Chem/IUPAC Name: Hexanoic acid, 2-ethyl-, C16-18-alkyl esters
INCI: Cetearyl Ethylhexanoate
Molecular Formula: C24H48O2



Cetyl 2-ethylhexanoate, Cetyl Octanoate, Hexadecyl 2-ethylhexanoate, Hexadecyl Ester, Cetyl Ethylhexanoate, Cetearyl Octanoate, Perceline oil, Hexadecyl 2-ethylhexanoate, 59130-69-7, Cetyl 2-ethylhexanoate, cetyl ethylhexanoate, HEXANOIC ACID, 2-ETHYL-, HEXADECYL ESTER, 134647WMX4, EINECS 261-619-1, Schercemol CO, Exceparl HO, Tegosoft CO, UNII-134647WMX4, Cetearyl octanoate, Pelemol 168, Hest CSO (Salt/Mix), Crodamol CAP (Salt/Mix), EC 261-619-1, Tegosoft liquid (Salt/Mix), SCHEMBL15239, Lanol 1688 (Salt/Mix), 90411-68-0, DTXSID20866741, XJNUECKWDBNFJV-UHFFFAOYSA-N, 2-Ethylhexanoic acid, cetyl ester, CETYL ETHYLHEXANOATE [INCI], AKOS028108429, BENZALDEHYDEPROPYLENEGLYCOLACETAL, DB11349, Q27251471, Hexanoic acid, 2-ethyl-, C16-18-alkyl esters, CETYL ETHYLHEXANOATE, 134647WMX4, UNII:134647WMX4, Hexanoic acid, 2-ethyl-, hexadecyl ester, EINECS 261-619-1, Hexadecyl 2-ethylhexanoate,



Lanol 1688 is the ester of cetearyl alcohol and 2-ethylhexanoic acid and was formerly called cetearyl octanoate.
Lanol 1688 is a transparent, oil-like, water-resistant liquid that protects skin from moisture loss by acting as an emollient.
Lanol 1688, which has a comparable chemical makeup but slightly different properties and safety, should not be confused with this ingredient.


Lanol 1688 is easy to spread.
Lanol 1688 is a clear/colorless to pale yellow liquid.
Lanol 1688 is an oil that is compatible with all skin care products due to its rapid absorption into the skin, its soft, non-greasy feel, non-stickiness, easy emulsification and resistance to oxidation.


Lanol 1688 acts as a liquid emollient agent.
Lanol 1688 is preservative-free and extremely easy to spread, for light textures and a soft feel.
Lanol 1688 improves the skin's suppleness.


Lanol 1688 is easy to spread emollient, for light textures
The liquid emollient agent Lanol 1688 is extremely easy to spread, for light textures and a soft feel.


Commercially, Lanol 1688 is produced through the catalytic esterification of cetearyl alcohol and 2-ethylhexanoic acid, with the removal step being an azeotropic distillation.
Cetyl octanoate and stearyl octanoate can also be combined in a 7:2 weight ratio to create the product.



USES and APPLICATIONS of LANOL 1688:
Application of Lanol 1688: Hair care, skin care, hygiene, sun protection
Lanol 1688 acts as a liquid emollient agent.
Lanol 1688 is preservative-free and extremely easy to spread, for light textures and a soft feel.


Lanol 1688 improves the skin's suppleness.
Lanol 1688 is easy to spread emollient, for light textures
The liquid emollient agent Lanol 1688 is extremely easy to spread, for light textures and a soft feel.


Lanol 1688 is used in all types of skincare formula, suncare, make-up.
Lanol 1688 is an emollient oil which is distinguished by excellent application on the skin, fast absorption into the skin, a soft non-greasy, non-sticky feel, very easy emulsification and a good resistance to oxidation.


Applications of Lanol 1688: Skin Care, Hair Care, Hygiene, Make-Up, and Sun Care.
Lanol 1688 is a synthetic mixture of fatty acids imparts water repelling characteristics to cosmetics; it is also a moisturising ingredient.


-Skin care:
Lanol 1688 smooths and softens the skin.
Lanol 1688 adds a sophisticated spreadability to creams and lotions and is oxygen-stable in addition to its moisturizing qualities.
In leave-on products, Lanol 1688 can be used up to 35% of the time.

Additionally, Lanol 1688 serves as a replacement for whale-derived spermaceti wax.
Numerous cosmetic products, including foundation, facial moisturizers, lipsticks, lip glosses, lip/eye liners, conditioners, and anti-aging products, contain Lanol 1688.



FUNCTION OF LANOL 1688:
Liquid emollient ester similar to the natural oil derived from waterfowl.
Spreads evenly on the skin to impart velvety softness, and leaves a long-lasting silky feel to the skin.


WHAT IS LANOL 1688 USED FOR?
Lanol 1688 works as an emoliient, texture enhancer and a conditioning agent in cosmetics and personal care products.


CLAIMS OF LANOL 1688:
*Emollients > Esters
spreading
preservative-free
softness
light feeling



ALTERNATIVE OF LANOL 1688:
*CETYL ETHYLHEXANOATE,
*ETHYLHEXYL ETHYLHEXANOATE,
*ISODECYL ETHYLHEXANOATE


PROPERTIES OF LANOL 1688:
*Improves the skin's suppleness
*Very easy to spread
*Soft, light, dry feel


SPECIFICITIES OF LANOL 1688:
*Liquid presentation
*Preservative-free
*Lanol 1688 is covered by a Mass Balance certificate BVC-RSPO-1-1972708497.


SAFETY PROFILE OF LANOL 1688:
The safety of 16 alkyl ethylhexanoates, including Lanol 1688, as used in cosmetics was evaluated by the Cosmetic Ingredient Review (CIR) Expert Panel.
The panel looked over any clinical data on these ingredients that was available.
The panel came to the conclusion that these ingredients are safe when used in cosmetic formulations under the current usage and concentration patterns when they are made to be non-irritating.



PHYSICAL and CHEMICAL PROPERTIES of LANOL 1688:
Name: LANOL 1688
INCI: Cetearyl Ethylhexanoate
Form: Liquid
Color: Colorless
Certification: Ecocert&Cosmos&Nature
Boiling Point: 431.86°C
Solubility: Insoluble in water
Molecular Weight: 368.6 g/mol
XLogP3-AA: 10.7
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 21

Exact Mass: 368.365430770 g/mol
Monoisotopic Mass: 368.365430770 g/mol
Topological Polar Surface Area: 26.3Ų
Heavy Atom Count: 26
Formal Charge: 0
Complexity: 288
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 1
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS Number: 90411-68-0
Molecular Formula: C24H48O2

Molecular Weight: 368.637
Chemical Name: Hexanoic acid, 2-ethyl-, C16-18-alkyl esters
CAS Registry Number: 90411-68-0
PubChemID: 42956
Molecular Weight: 368.63672
LogP: 11.15
EINECS: 291-445-1
Molecular Formula: C24H48O2
Density: 0.9±0.1 g/cm3
Boiling Point: 407.2±13.0 °C at 760 mmHg
Flash Point: 203.7±9.7 °C
Refractive Index: 1.449



FIRST AID MEASURES of LANOL 1688:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Consult a physician.
*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 LANOL 1688:
-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 LANOL 1688:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of LANOL 1688:
-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 LANOL 1688:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Store at Room Temperature.
Light sensitive



STABILITY and REACTIVITY of LANOL 1688:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Incompatible materials:
No data available


LANOLIN
DESCRIPTION:

Lanolin (from Latin lāna 'wool', and oleum 'oil'), also called wool fat, wool yolk, wool wax, or wool grease, is a wax secreted by the sebaceous glands of wool-bearing animals.
Lanolin used by humans comes from domestic sheep breeds that are raised specifically for their wool.
Historically, many pharmacopoeias have referred to lanolin as wool fat (adeps lanae); however, as lanolin lacks glycerides (glycerol esters), it is not a true fat.

CAS: 8006-54-0
European Community (EC) Number: 232-348-6


Lanolin primarily consists of sterol esters instead.
Lanolin's waterproofing property aids sheep in shedding water from their coats.
Certain breeds of sheep produce large amounts of lanolin.


Lanolin is a principle component of lanolin, which is a natural product obtained from the fleece of sheep.
Lanolin is found in steroid-containing creams/ointments, medicated shampoos, veterinary products, hand lotions, moisturizers, sunscreens, self-tanning creams, lipsticks, makeup removers, foundations, eye shadows, hairsprays, shaving creams, baby oils and products, printing inks, furniture and shoe polishes, lubricants, leather, and paper.

Lanolin's role in nature is to protect wool and skin from climate and the environment; it also plays a role in skin (integumental) hygiene.
Lanolin and its derivatives are used in the protection, treatment, and beautification of human skin

Lanolin is a yellow fat obtained from sheep's wool.
It is used as an emollient, cosmetic, and pharmaceutic aid.
The US federal code of regulations states that lanolin in the concentration range of 12-50% may be included in over the counter skin ointments.
Lanolin is the purified, secreted product of the sheep sebaceous glands.
Lanolin primarily consists of long-chain waxy esters, or sterol esters, that lack glycerides.

For this reason, it is also called wool wax or wool grease.
Lanolin is used in the protection, treatment, and cosmetic enhancement of human skin.
Its hydrophobic properties can help protect skin against infections or skin irritation, as it helps seal in moisture that is already present in the skin.

Lanolin is used as an active ingredient in over the counter topical products such as ointments, lubricants, lotions and facial cosmetics.
Lanolin is also frequently used in protective baby skin treatment and for sore nipples in breastfeeding mothers,.



COMPOSITION OF LANOLIN :
A typical high-purity grade of lanolin is composed predominantly of long chain waxy esters (approximately 97% by weight) with the remainder being lanolin alcohols, lanolin acids and lanolin hydrocarbons.
An estimated 8,000 to 20,000 different types of lanolin esters are present in lanolin, resulting from combinations between the 200 or so different lanolin acids and the 100 or so different lanolin alcohols identified so far.


Lanolin’s complex composition of long-chain esters, hydroxyesters, diesters, lanolin alcohols, and lanolin acids means in addition to its being a valuable product in its own right, it is also the starting point for the production of a whole spectrum of lanolin derivatives, which possess wide-ranging chemical and physical properties.
The main derivatisation routes include hydrolysis, fractional solvent crystallisation, esterification, hydrogenation, alkoxylation and quaternisation.


Lanolin derivatives obtained from these processes are used widely in both high-value cosmetics and skin treatment products.
Hydrolysis of lanolin yields lanolin alcohols and lanolin acids.
Lanolin alcohols are a rich source of cholesterol (an important skin lipid) and are powerful water-in-oil emulsifiers; they have been used extensively in skincare products for over 100 years.

Approximately 40% of the acids derived from lanolin are alpha-hydroxy acids (AHAs).
The use of AHAs in skin care products has attracted a great deal of attention in recent years.
Details of the AHAs isolated from lanolin can be seen in the table below.


PRODUCTION OF LANOLIN :
Crude lanolin constitutes about 5–25% of the weight of freshly shorn wool.
The wool from one Merino sheep will produce about 250–300 ml of recoverable wool grease.
Lanolin is extracted by washing the wool in hot water with a special wool scouring detergent to remove dirt, wool grease (crude lanolin), suint (sweat salts), and anything else stuck to the wool.

The wool grease is continuously removed during this washing process by centrifuge separators, which concentrate it into a waxlike substance melting at approximately 38 °C (100 °F).


APPLICATIONS OF LANOLIN :
Lanolin and its many derivatives are used extensively in both the personal care (e.g., high value cosmetics, facial cosmetics, lip products) and health care sectors such as topical liniments.
Lanolin is also found in lubricants, rust-preventive coatings, shoe polish, and other commercial products.
Lanolin is a relatively common allergen and is often misunderstood as a wool allergy.


However, allergy to a lanolin-containing product is difficult to pinpoint and often other products containing lanolin may be fine for use.
Patch testing can be done if a lanolin allergy is suspected.
It is frequently used in protective baby skin treatment and for sore nipples from breastfeeding although health authorities do not recommend it, advise against nipple cleaning and rather recommend improving baby positioning and expressing milk by hand.

Lanolin is used commercially in many industrial products ranging from rustproof coatings to lubricants.
Some sailors use lanolin to create slippery surfaces on their propellers and stern gear to which barnacles cannot adhere.

Commercial products (e.g. Lanocote) containing up to 85% lanolin are used to prevent corrosion in marine fasteners, especially when two different metals are in contact with each other and saltwater.
The water-repellent properties make it valuable in many applications as a lubricant grease where corrosion would otherwise be a problem.
7-Dehydrocholesterol from lanolin is used as a raw material for producing vitamin D3 by irradiation with ultraviolet light.


Baseball players often use it to soften and break in their baseball gloves (shaving cream with lanolin is popularly used for this).
Anhydrous liquid lanolin, combined with parabens, has been used in trials as artificial tears to treat dry eye.

Anhydrous lanolin is also used as a lubricant for brass instrument tuning slides.
Lanolin can also be restored to woollen garments to make them water and dirt repellent, such as for cloth diaper covers.
Lanolin is also used in lip balm products such as Carmex.

For some people, it can irritate the lips.
Lanolin is sometimes used by people on continuous positive airway pressure therapy to reduce irritation with masks, particular nasal pillow masks that can often create sore spots in the nostrils.
Lanolin is a popular additive to moustache wax, particularly 'extra-firm' varieties.

Lanolin is used as a primary lubricating component in aerosol-based brass lubricants in the ammunition reloading process.
Mixed warm 1:12 with highly concentrated ethanol (usually 99%), the ethanol acts as a carrier which evaporates quickly after application, leaving a fine film of lanolin behind to prevent brass seizing in resizing dies.

Lanolin, when mixed with ingredients such as neatsfoot oil, beeswax and glycerol, is used in various leather treatments, for example in some saddle soaps and in leather care products.



STANDARDS AND LEGISLATION ABOUT LANOLIN :
In addition to general purity requirements, lanolin must meet official requirements for the permissible levels of pesticide residues.
The Fifth Supplement of the United States Pharmacopoeia XXII published in 1992 was the first to specify limits for 34 named pesticides.
A total limit of 40 ppm (i.e. 40 mg/kg) total pesticides was stipulated for lanolin of general use, with no individual limit greater than 10 ppm.


A second monograph also introduced into the US Pharmacopoeia XXII in 1992 was entitled 'Modified Lanolin'.
Lanolin conforming to this monograph is intended for use in more exacting applications, for example on open wounds.
In this monograph, the limit of total pesticides was reduced to 3 ppm total pesticides, with no individual limit greater than 1 ppm.


In 2000, the European Pharmacopoeia introduced pesticide residue limits into its lanolin monograph.
This requirement, which is generally regarded as the new quality standard, extends the list of pesticides to 40 and imposes even lower concentration limits.
Some very high-purity grades of lanolin surpass monograph requirements.

New products obtained using complex purification techniques produce lanolin esters in their natural state, removing oxidative and environmental impurities resulting in white, odourless, hypoallergenic lanolin.
These ultra-high-purity grades of lanolin are ideally suited to the treatment of dermatological disorders such as eczema and on open wounds.

Lanolin attracted attention owing to a misunderstanding concerning its sensitising potential.
A study carried out at New York University Hospital in the early 1950s had shown about 1% of patients with dermatological disorders were allergic to the lanolin being used at that time.

By one estimate, this simple misunderstanding of failing to differentiate between the general healthy population and patients with dermatological disorders exaggerates the sensitising potential of lanolin by 5,000–6,000 times.


The European Cosmetics Directive, introduced in July 1976, contained a stipulation that cosmetics which contained lanolin should be labelled to that effect.
This ruling was challenged immediately, and in the early 1980s, it was overturned and removed from the directive.
Despite only being in force for a short period of time, this ruling did harm both to the lanolin industry and to the reputation of lanolin in general.

The Cosmetics Directive ruling only applied to the presence of lanolin in cosmetic products; it did not apply to the many hundreds of its different uses in dermatological products designed for the treatment of compromised skin conditions.

Modern analytical methods have revealed lanolin possesses a number of important chemical and physical similarities to human stratum corneum lipids; the lipids which help regulate the rate of water loss across the epidermis and govern the hydration state of the skin.

Cryogenic scanning electron microscopy has shown that lanolin, like human stratum corneum lipids, consists of a mass of liquid crystalline material.
Cross-polarised light microscopy has shown the multilamellar vesicles formed by lanolin are identical to those formed by human stratum corneum lipids.
The incorporation of bound water into the stratum corneum involves the formation of multilamellar vesicles.

Skin bioengineering studies have shown the durational effect of the emollient (skin smoothing) action produced by lanolin is very significant and lasts for many hours.
Lanolin applied to the skin at 2 mg/cm2 has been shown to reduce roughness by about 35% after one hour and 50% after two hours, with the overall effect lasting for considerably more than eight hours.

Lanolin is also known to form semiocclusive (breathable) films on the skin.
When applied daily at around 4 mg/cm2 for five consecutive days, the positive moisturising effects of lanolin were detectable until 72 hours after final application.
Lanolin may achieve some of its moisturising effects by forming a secondary moisture reservoir within the skin.

The barrier repair properties of lanolin have been reported to be superior to those produced by both petrolatum and glycerol.
In a small clinical study conducted on volunteer subjects with terribly dry (xerotic) hands, lanolin was shown to be superior to petrolatum in reducing the signs and symptoms of dryness and scaling, cracks and abrasions, and pain and itch.
In another study, a high purity grade of lanolin was found to be significantly superior to petrolatum in assisting the healing of superficial wounds.



PRODUCTS THAT MAY CONTAIN LANOLIN :
Cosmetics
• Foundations
• Eye makeup
• Lipsticks

Hair Care
• Hairspray

Household Products
• Furniture polish
• Leather
• Paper
• Printing inks

Liquids
• Baby oils
• Baby ointments
• Hand lotion
• Moisturizers
• Self-tanners
• Sunscreen


SAFETY INFORMATION ABOUT LANOLIN :
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






SYNONYMS OF LANOLIN :
Lanolin
8006-54-0
7EV65EAW6H
Anhydrous lanolin
Wool grease
Wool wax, refined
Black Rose
Lanashield
Lanolin, anhydrous
Skin Protectant with Lanolin
Theresienol MD Skin Protectant
Theriac Advanced Healing
232-348-6
3CE DRAWING LIP CHILLING
4sport skincare anti chafing
AGNOLIN NO 1
AmeriDermDermaFix
CORONA MULTI-PURPOSE
CORONA ORIGINAL LANOLIN RICH
DTXSID2027678
EMERY 1600
EUCERITE
LANOLIN (II)
LANOLIN (USP MONOGRAPH)
LANOLIN (USP-RS)
LANOLIN,ANHYDROUS LIQUID
Lana1263
LanoGuardDaily Care Skin Protectant
LanoGuardDry Skin Therapy
Lanoderm
Lantiseptic Dry Skin Therapy
Lantiseptic by DermaRite Original Skin Protectant
Lantiseptic by Dermarite Dry Skin Therapy
LincoFix
North Country Dairy Supply Non Iodine Barrier Dip
PrimaGuardDaily Care Skin Protectant
SUINTINE
Smartchoices Lanolin Plus0
Soothe and Cool Free Medseptic
Soothe and Cool Free MedsepticSkin Protectant
LANOLIN
LANOLIN; Wool fat; Wool grease; Wool wax; Woolwax ester; cas no: 8006-54-0
LANOLIN (COSMETIC GRADE)
DESCRIPTION:

Lanolin (Cosmetic Grade), a natural substance derived from sheep's wool, is a commonly used ingredient in cosmetics and skincare products.
Lanolin (Cosmetic Grade) consists of a combination of lanolin oil and lanolin alcohol.
Extracted from wool grease, lanolin is purified to obtain anhydrous lanolin, which is free of water content.

CAS Number, 8006-54-0
EINECS/ELINCS No:, 232-348-6
COSING REF No:, 34857


SYNOYMS OF LANOLIN (COSMETIC GRADE):
Lanolin;Agnolin No. 1;Alapurin;Anhydrous lanolin;Anhydrous Lanum;Lanain;Lanalin;Lanesin;Lanichol;Laniol;Oesipos;Agnolin;Adeps lane;Amber lanolin;Lanum;Processed lanolin;Cosmelan;Lantrol;Fats,lanolin;Fats,wool;Lanoprodine;Crodapur;Argowax;Clearlan 1650;Clearlan;HHC 82;FPG 1;Lanox HHC 82;Lanox HH 73;Lanox FPG 103;Lanox FPG 105;Lanox CNB 500;Lanox FP 1410N;Fats and Glyceridic oils,wool;Fats and Glyceridic oils,lanolin;Emery HP 2050;Lanox FP 85N;Lanox FP 8;Lanox FPK 108;Lanox CNB 50;Wool wax,lanolin;Coronet;Lanox CNB 80;Medilan;Super Lanolin;Natralube 210;Furuiran SP;Furuiran T;Fluilan T;E 913;Rikaranoru;Rikalanol;Medilan Ultra;Crodamol ODL;Lanolin TR;Corilene UL;TJ-F 402;YOFCO;Lanolins;Super Lanolin SO;Corona 8;Adeps Lanae;114471-15-7;8036-05-3;8038-41-3;8038-43-5;8040-96-8




In the world of cosmetics, Lanolin (Cosmetic Grade) is known by various names such as wool wax, wool fat, or Adeps Lanae.
Lanolin (Cosmetic Grade) is essential to note that lanolin is not a steroid but rather a complex blend of lipids.
Lanolin (Cosmetic Grade) imparts moisturizing, emollient, and protective properties, making it a valued component in skincare formulations.
The chemical formula of Lanolin (Cosmetic Grade) is C34H68O2.

Lanolin (Cosmetic Grade) is a wax that comes from the wool of animals.
Usually, wool from sheep is used to extract Lanolin (Cosmetic Grade).

Lanolin (Cosmetic Grade) is a naturally forming yellowish waxy substance.
Lanolin (Cosmetic Grade) is also called 'wool wax'.

A regular ingredient in many cosmetic products, although loosing favour to vegetable products these days, Lanolin (Cosmetic Grade) is mostly used as a moisturiser.
Lanolin (Cosmetic Grade) is an excellent emollient, better than petrolatum or glycerin.
There is also a chemical similarity between human skin and lanolin.
Pure Lanolin (Cosmetic Grade) will be yellowish-brown in colour.

Lanolin (Cosmetic Grade) has long been hailed from the Ancient Greeks and Chinese as an essential ingredient for Skin care; nourishing, protecting, anti-aging, and helping to heal dry and cracked skin.
Lanolin (Cosmetic Grade) sinks deep into your skin.
Lanolin (Cosmetic Grade) keeps your skin moisturised on the surface but also helps it stay hydrated from within.
Lanolin (Cosmetic Grade) Beauty capture the purity and quality of Australian cosmetic grade Lanolin to offer unique everyday skincare.


Lanolin (Cosmetic Grade), USP is a great skin protectorate and conditioner.
Lanolin (Cosmetic Grade) helps with chaffing and skin irritation due to moisture loss and makes for the perfect skincare product for nursing mothers.
Lanolin (Cosmetic Grade), USP can be used for moisturizing dry skin and eczema, as well as healing cuts, scrapes and burns, and boost color in lip products.


Lanolin (Cosmetic Grade) has a wide range of applications because of its colloidal chemical Properties and compatibility with a broad range of ingredients.
Lanolin (Cosmetic Grade) is useful in pharmaceutical preparations, salves and ointments, as well as having functional attributes as an epidermal moisturizer, lubricant and emollient.
Lanolin (Cosmetic Grade) can also be used for other industrial applications, such as waterless hand cleaners, printing inks, can coatings, corrosive inhibitors and lubricants.


Lanolin Cosmetic Grade is a purified sterol rich compound.
Lanolin (Cosmetic Grade) has a lower cholesterol content compared to some superior pharmaceutical grades.
Lanolin (Cosmetic Grade) is soluble in mineral oil, ethanol, chloroform, ether, petroleum ether, and toluene.

Lanolin (Cosmetic Grade) is not soluble in water.
Lanolin (Cosmetic Grade) can be widely used in w/o emulsion.
It's an excellent emulsifier, stabilizer, thickener, and emollient in hair care and skin care products.



Lanolin (Cosmetic Grade) is a product of Lanolin wax.
The lanolin wax is subjected to low temperature fractional crystallization.
This isolates the liquid esters of the regular anhydrous lanolin.

In formulations and recipes it provides a lighter texture than Lanolin wax.
Lanolin (Cosmetic Grade) can also be used as a mineral oil substitute in any formulation.
Lanolin (Cosmetic Grade) is a great emollient and provides protection for the epidermis from moisture loss.

Lanolin (Cosmetic Grade) softens the skin and is a good humectant making it ideal for use in balms, hair treatments and conditioners, body oils, bath oils, rich creams, cosmetics and other products.
Lanolin (Cosmetic Grade) can also be used to treat chapped lips, diaper rash, dry skin, itchy skin, rough feet, minor cuts, minor burns and skin abrasions.


Lanolin (Cosmetic Grade) helps to form emulsions and blends well with nearly all other substances used in cosmetics and personal care products.
Pharmaceutical grade segment is highly demanded, as lanolin and its derivatives find wide utilization in medicinal and personal care applications.







USES OF LANOLIN (COSMETIC GRADE):
Lanolin (Cosmetic Grade) has many different uses in the world of skin care and cosmetics.
From providing moisturizing benefits to enhancing the texture of the products - this ingredient does it all.

Skin care:
Lanolin (Cosmetic Grade) is valued for its exceptional moisturizing properties.
Lanolin (Cosmetic Grade) acts as a natural emollient, creating a protective barrier that helps to prevent moisture loss and keeps the skin hydrated.
Lanolin (Cosmetic Grade) is often incorporated into creams, lotions, and lip balms to alleviate dryness, soothe rough or chapped skin, and promote softness and suppleness

Cosmetic products:
Lanolin (Cosmetic Grade) serves as a binding agent, helping to hold cosmetic formulations together and providing stability.
Lanolin (Cosmetic Grade) can also enhance the texture and spreadability of products, contributing to a smooth application

Lanolin (Cosmetic Grade) is used as Emulsifier.
Lanolin (Cosmetic Grade) is used as Antifoaming agent.
Lanolin (Cosmetic Grade) is used as Rust inhibitor.

Lanolin (Cosmetic Grade) is used as Corrosion inhibitor.
Lanolin (Cosmetic Grade) is used as Pharmaceutical additives.
Lanolin (Cosmetic Grade) is used as Cosmetic preparation.

Gas chromatographic fixative (maximum use temperature 200℃, solvent is chloroform), separation and analysis of non-polar compounds, ethanol, aromatic and heterocyclic compounds and volatile oil.


ORIGIN OF LANOLIN (COSMETIC GRADE):
Lanolin (Cosmetic Grade) is obtained through a process of extracting and purifying the wool grease found in sheep's wool.
The wool grease is treated to remove impurities and excess water, resulting in the production of lanolin.
This refined Lanolin (Cosmetic Grade) is then further processed to obtain different forms, such as anhydrous lanolin or lanolin oil.




CHEMICAL AND PHYSICAL PROPERTIES OF LANOLIN (COSMETIC GRADE):

Melting Point, 38-40°C
pH, 5.5-7.0
Solubility, Insoluble in water
Viscosity, High
Physical form at 25°C: Solid
Product Name:
Lanolin
CAS No.:
8006-54-0
InChIKeys:
BILPUZXRUDPOOF-UHFFFAOYSA-N
Molecular Weight:
508.9
Exact Mass:
508.521931
EC Number:
232-348-6
HScode:
15050000
Categories:
Fungicides
PSA:
26.3
XLogP3:
log Kow = 15.60 (est)
Appearance:
White to yellow Adhering Crystals or Powder
Density:
0.932-0.945 g/cm3 @ Temp: 15 °C
Melting Point:
38-42 °C
Flash Point:
209 °C
Water Solubility:
soluble in ether, petroleum ether, chloroform and petroleum benzene.
Sparingly soluble in ethanol. Insoluble in water.chloroform: 0.1 g/mL, clear to faintly turbid (
Storage Conditions:
Lanolin may gradually undergo autoxidation during storage.
To inhibit this process, the inclusion of butylated hydroxytoluene is permitted as an antioxidant.
Exposure to excessive or prolonged heating may cause anhydrous lanolin to darken in color and develop a strong rancidlike odor.

However, lanolin may be sterilized by dry heat at 150°C.
Ophthalmic ointments containing lanolin may be sterilized by filtration or by exposure to gamma irradiation.
Odor:
Slight odor or practically odorless

CHEMISTRY OF LANOLIN (COSMETIC GRADE):

Waxes
Functions
Emulsion stabilisers
Superfatting agents
Emulsifiers

REGIONAL AVAILABILITY OF LANOLIN (COSMETIC GRADE):

Asia
Europe
Latin America
N America

APPLICATIONS OF LANOLIN (COSMETIC GRADE):

Bath, shower & soaps
After sun
Body care
Eye contour care
Face / neck skin care
Hair conditioners - rinse off
Lip care
Lip colour
Shampoos
Shaving / hair removal
Sun protection

CONSUMER BENEFIT:
Hydrating / moisturising / nourishing
Calming / soothing / redness


SAFETY INFORMATION ABOUT LANOLIN (COSMETIC GRADE):
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


LANOLIN (WOOL FAT)
Lanolin (Wool Fat) is a popular substance that is often used as a care product for cracked and dry skin.
Lanolin (Wool Fat) is a natural product that is obtained from the wool of sheep.
Lanolin (Wool Fat) is of high quality tested for pesticides and pollutants.


CAS Number: 8006-54-0
EC Number: 232-348-6
Molecular Formula: C34H68O2



SYNONYMS:
Adeps Lanae ahydricus, Adeps lanae, Adeps lane, Agnin, Agnolin, Agnolin No. 1, Alapurin, Amber lanolin, Anhydrous lanolin, Anhydrous lanum, Caswell No. 518, Clearlan, Clearlan 1650, Coronet, Cosmelan, Crodapur, EINECS 232-348-6, EPA Pesticide Chemical Code 031601, Emery HP 2050, FPG 1, Fats and Glyceridic oils, lanoline, Fats and Glyceridic oils, wool, Fats, lanolin, Fats, wool, HHC 82, HSDB 1817, Lanae cera, Lanain, Lanalin, Lanesin, Lanichol, Laniol, Lanolin, Lanolin oil, Lanolin, anhydrous, Lanoprodine, Lanox CNB 50, Lanox CNB 500, Lanox CNB 80, Lanox FP 1410N, Lanox FP 8, Lanox FP 85N, Lanox FPG 103, Lanox FPG 105, Lanox FPK 108, Lanox HH 73, Lanox HHC 82, Lantrol, Lanum, Medilan, Natralube 210, Oesipos, Processed lanolin, Super Lanolin, Wollfett, Wool fat, Wool grease, Wool wax, lanolin, Wool wax, refined, Lanolin 8006-54-0, 7EV65EAW6H, Anhydrous lanolin, Wool grease, Wool wax, refined, Black Rose, Lanashield, Lanolin, anhydrous, Skin Protectant with Lanolin, Theresienol MD Skin Protectant, Theriac Advanced Healing, 232-348-6, 3CE DRAWING LIP CHILLING, 4sport skincare anti chafing, AGNOLIN NO 1, AmeriDermDermaFix, CORONA MULTI-PURPOSE, CORONA ORIGINAL LANOLIN RICH, DTXSID2027678, EMERY 1600, EUCERITE, LANOLIN (II), LANOLIN (USP MONOGRAPH), LANOLIN (USP-RS), LANOLIN,ANHYDROUS LIQUID, Lana1263, LanoGuardDaily Care Skin Protectant, LanoGuardDry Skin Therapy, Lanoderm, Lantiseptic Dry Skin Therapy, Lantiseptic by DermaRite Original Skin Protectant, Lantiseptic by Dermarite Dry Skin Therapy, LincoFix, North Country Dairy Supply Non Iodine Barrier Dip, PrimaGuardDaily Care Skin Protectant, SUINTINE, Smartchoices Lanolin Plus0, Soothe and Cool Free Medseptic, Soothe and Cool Free MedsepticSkin Protectant, Wool fat, Adeps lanae



Lanolin (Wool Fat) is obtained from raw wool by kneading it in water, or by scouring with soap solution, and then centrifuging.
The wool grease so obtained is refined, bleached, deodorized, and dried.
Chemically, Lanolin (Wool Fat) consists of a mixture of several sterols, fatty acids, and their esters.


Lanolin (Wool Fat) is a yellow fat obtained from sheep's wool.
It is used as an emollient, cosmetic, and pharmaceutic aid.
The US federal code of regulations states that Lanolin (Wool Fat) in the concentration range of 12-50% may be included in over the counter skin ointments.


Lanolin (Wool Fat) is the purified, secreted product of the sheep sebaceous glands.
Lanolin (Wool Fat) primarily consists of long-chain waxy esters, or sterol esters, that lack glycerides.
For this reason, Lanolin (Wool Fat) is also called wool wax or wool grease.


Lanolin (Wool Fat) is used in the protection, treatment, and cosmetic enhancement of human skin.
Its hydrophobic properties can help protect skin against infections or skin irritation, as Lanolin (Wool Fat) helps seal in moisture that is already present in the skin.


Lanolin (Wool Fat) is a waxy substance that sheep naturally produce to protect their wool.
Because Lanolin (Wool Fat)'s properties are similar to those of the sebum (oil) secreted by human skin, it is a popular ingredient in moisturizers, hair care products, and soaps.


Lanolin (Wool Fat) is also widely promoted as a natural remedy for sore nipples due to breastfeeding.
The Lanolin (Wool Fat) in the products you buy comes from sheep raised for their wool.
Lanolin (Wool Fat) also goes by the names wool grease, wool yolk, and wool wax.


Lanolin (Wool Fat) is a popular substance that is often used as a care product for cracked and dry skin.
Lanolin (Wool Fat) is a natural product that is obtained from the wool of sheep.
Lanolin (Wool Fat) is of high quality tested for pesticides and pollutants.


At a temperature of 39 °C, Lanolin (Wool Fat) begins to become liquid.
True to the “DIY” motto, you can create your own creams and ointments with Lanolin (Wool Fat).
Lanolin (Wool Fat) is 'occlusive' meaning it prevents water evaporating from our skin.


It has been researched than Lanolin (Wool Fat) can reduce skin's water loss by as much as 20-30%.
Lanolin (Wool Fat) does not increase the moisture content of the skin, it only hold existing moisture.
Lanolin (Wool Fat) contains cholesterol similar to the cholesterol our skin naturally produces which is why Lanolin (Wool Fat) is so good for human skin.


Lanolin (Wool Fat) is safe, however if you have known allergies to it then it is best to not use it.
Allergies normally stem from the Lanolin (Wool Fat) not being refined to become purified.
Lanolin (Wool Fat) once separated from the wool, undergoes refining processes of up to 5 times to ensure the end product is free from as many impurities as possible.


The Merino breed of sheep produces the most amount of Lanolin (Wool Fat).
Lanolin (Wool Fat) is the naturally occurring fat in wool, which helps protect wool and skin against the environment.
Lanolin (Wool Fat) is the naturally occurring fat in wool


Lanolin (Wool Fat) helps protect the skin against the environment
Lanolin (Wool Fat) is preservative free.
Lanolin (Wool Fat), a natural substance derived from sheep's wool, is a commonly used ingredient in cosmetics and skincare products.


It consists of a combination of Lanolin (Wool Fat) oil and Lanolin (Wool Fat) alcohol.
Extracted from wool grease, Lanolin (Wool Fat) is purified to obtain anhydrous Lanolin (Wool Fat), which is free of water content.
In the world of cosmetics, Lanolin (Wool Fat) is known by various names such as wool wax, wool fat, or Adeps Lanae.


It is essential to note that Lanolin (Wool Fat) is not a steroid but rather a complex blend of lipids.
Lanolin (Wool Fat) imparts moisturizing, emollient, and protective properties, making it a valued component in skincare formulations.
The chemical formula of Lanolin (Wool Fat) is C34H68O2.


Lanolin (Wool Fat) is a wax made of a mixture of esters, diesters, and hydroxyl esters of high-molecular-weight Lanolin (Wool Fat) alcohols and high-molecular-weight Lanolin (Wool Fat) acids.
Lanolin (Wool Fat)'s role on the sheep is to protect the wool fibres and the skin from the environment including rain and direct sun.


Lanolin (Wool Fat) contains anti-fungal and anti-bacterial properties to protect the sheep's skin.
Lanolin (Wool Fat) (from Latin lāna 'wool', and oleum 'oil'), also called wool fat, wool yolk, wool wax, sheep grease, or wool grease, is a wax secreted by the sebaceous glands of wool-bearing animals.


Lanolin (Wool Fat) used by humans comes from domestic sheep breeds that are raised specifically for their wool.
Historically, many pharmacopoeias have referred to Lanolin (Wool Fat) as wool fat (adeps lanae); however, as Lanolin (Wool Fat) lacks glycerides (glycerol esters), it is not a true fat.


Lanolin (Wool Fat) primarily consists of sterol esters instead.
Lanolin (Wool Fat)'s waterproofing property aids sheep in shedding water from their coats.
Certain breeds of sheep produce large amounts of Lanolin (Wool Fat).


Lanolin (Wool Fat)'s role in nature is to protect wool and skin from climate and the environment; it also plays a role in skin (integumental) hygiene.
Lanolin (Wool Fat) is a popular additive to moustache wax, particularly 'extra-firm' varieties.



USES and APPLICATIONS of LANOLIN (WOOL FAT):
Lanolin (Wool Fat), purified form of wool grease or wool wax (sometimes erroneously called wool fat), used either alone or with soft paraffin or lard or other fat as a base for ointments, emollients, skin foods, salves, superfatted soaps, and fur dressing.
Lanolin (Wool Fat), a translucent, yellowish-white, soft, unctuous, tenacious substance, is readily absorbed by the skin and thus makes an ideal base for medicinal products intended to be absorbed.


Lanolin (Wool Fat) is used as an active ingredient in over the counter topical products such as ointments, lubricants, lotions and facial cosmetics.
Lanolin (Wool Fat) is also frequently used in protective baby skin treatment and for sore nipples in breastfeeding mothers.
Lanolin (Wool Fat) is a wax derived from the fat of sheep’s wool.


It has a wide range of uses, from medical to cosmetic, and can be found in a variety of products.
In the medical field, Lanolin (Wool Fat) is used as a topical ointment to protect and soothe dry, chapped, or irritated skin.
Lanolin (Wool Fat) is also used to treat and prevent diaper rash, protect nipples during breastfeeding, and to soften and protect cracked, dry lips.


Lanolin (Wool Fat) is even sometimes used to treat minor burns and scrapes.
Lanolin (Wool Fat) is used in eye creams, Hemorrhoid medication, Lip balm, Lotions and creams for dry skin, Makeup and makeup removers, Medicated shampoos, Mustache wax, Shaving cream, Baby oil, Diaper rash cream, Lanolin (Wool Fat) for Breastfeeding and Sore Nipples.


During breastfeeding, your nipples may become sore, dry, and even cracked.
Many healthcare providers recommend Lanolin (Wool Fat) creams to ease nipple pain from breastfeeding.
A big benefit is that it's generally considered safe for your baby to ingest small amounts of Lanolin (Wool Fat).


It's recommended that you use Lanolin (Wool Fat) at least ten minutes before you start breastfeeding.
But unlike other products, you don't need to wipe Lanolin (Wool Fat) off.
It's also safe to give your baby breastmilk expressed while Lanolin (Wool Fat) is on your nipples.


Lanolin (Wool Fat) is a soothing Lanolin (Wool Fat) preparation for use on chapped or rough skin.
Lanolin (Wool Fat) protects against the harsh elements of the weather.
Pure Lanolin (Wool Fat) supports great skin hydration.


Lanolin (Wool Fat) helps to create a protective barrier against everyday external factors, such as changes in weather and the environment.
Active ingredients can be easily incorporated into Lanolin (Wool Fat).
Lanolin (Wool Fat) is also an excellent household product and can be used, for example, as a lubricant for door hinges.


Lanolin (Wool Fat) is used widely in products formulated to protect and treat our skin.
Lanolin (Wool Fat) and its many derivatives are used extensively in both the personal care (e.g., high value cosmetics, facial cosmetics, lip products) and health care sectors such as topical liniments.


Lanolin (Wool Fat) is also found in lubricants, rust-preventive coatings, shoe polish, and other commercial products.
However, allergy to a Lanolin (Wool Fat)-containing product is difficult to pinpoint and often other products containing Lanolin (Wool Fat) may be fine for use.


Lanolin (Wool Fat) is frequently used in protective baby skin treatment and for sore nipples from breastfeeding although health authorities do not recommend it, advise against nipple cleaning and rather recommend improving baby positioning and expressing milk by hand.
Lanolin (Wool Fat) is used commercially in many industrial products ranging from rustproof coatings to lubricants.


Some sailors use Lanolin (Wool Fat) to create slippery surfaces on their propellers and stern gear to which barnacles cannot adhere.
Commercial products (e.g. Lanocote) containing up to 85% Lanolin (Wool Fat) are used to prevent corrosion in marine fasteners, especially when two different metals are in contact with each other and saltwater.


The water-repellent properties make Lanolin (Wool Fat) valuable in many applications as a lubricant grease where corrosion would otherwise be a problem.
7-Dehydrocholesterol from Lanolin (Wool Fat) is used as a raw material for producing vitamin D3 by irradiation with ultraviolet light.
Lanolin (Wool Fat) is frequently used for baby skin treatments.


Baseball players often use Lanolin (Wool Fat) to soften and break in their baseball gloves (shaving cream with Lanolin (Wool Fat) is popularly used for this).
Anhydrous liquid Lanolin (Wool Fat), combined with parabens, has been used in trials as artificial tears to treat dry eye.


Anhydrous Lanolin (Wool Fat) is also used as a lubricant for brass instrument tuning slides.
Lanolin (Wool Fat) can also be restored to woollen garments to make them water and dirt repellent, such as for cloth diaper covers.
Lanolin (Wool Fat) is also used in lip balm products such as Carmex.


Lanolin (Wool Fat) is sometimes used by people on continuous positive airway pressure therapy to reduce irritation with masks, particular nasal pillow masks that can often create sore spots in the nostrils.
Lanolin (Wool Fat) and its derivatives are used in the protection, treatment, and beautification of human skin.


Lanolin (Wool Fat) is used as a primary lubricating component in aerosol-based brass lubricants in the ammunition reloading process.
Mixed warm 1:12 with highly concentrated ethanol (usually 99%), the ethanol acts as a carrier which evaporates quickly after application, leaving a fine film of Lanolin (Wool Fat) behind to prevent brass seizing in resizing dies.


Lanolin (Wool Fat), when mixed with ingredients such as neatsfoot oil, beeswax, and glycerol, is used in various leather treatments, for example in some saddle soaps and in leather care products.
Lanolin (Wool Fat) is frequently used for baby skin treatments.



BENEFITS AND USES OF LANOLIN (WOOL FAT):
Lanolin (Wool Fat) is classified as an occlusive moisturizer.
This means Lanolin (Wool Fat) works by reducing water loss from the skin, similar to petroleum jelly.
While petroleum can reduce the evaporation of skin's moisture by 98%, Lanolin (Wool Fat) reduces it by between 20% and 30%.

However, many people like that Lanolin (Wool Fat) isn't as heavy as petroleum jelly, making it more pleasant to use.
In skincare products, there's no hard evidence showing Lanolin (Wool Fat) is better than synthetic waxes.
If you like using natural products, though, you may prefer Lanolin (Wool Fat) over synthetics.



KEY FEATURES OF LANOLIN (WOOL FAT):
• Natural skin moisturiser
• Nourishes dry and cracked skin
• Forms a protective barrier
• Lanolin (Wool Fat) is derived from sheep wool
• Lanolin (Wool Fat)'s hydrating use has been known since Ancient Greek times!



WHAT IS LANOLIN (WOOL FAT) USED FOR?
Lanolin (Wool Fat) has many different uses in the world of skin care and cosmetics.
From providing moisturizing benefits to enhancing the texture of the products - Lanolin (Wool Fat) does it all.

*Skin care:
Lanolin (Wool Fat) is valued for its exceptional moisturizing properties.
Lanolin (Wool Fat) acts as a natural emollient, creating a protective barrier that helps to prevent moisture loss and keeps the skin hydrated.
Lanolin (Wool Fat) is often incorporated into creams, lotions, and lip balms to alleviate dryness, soothe rough or chapped skin, and promote softness and suppleness

*Cosmetic products:
Lanolin (Wool Fat) serves as a binding agent, helping to hold cosmetic formulations together and providing stability.
Lanolin (Wool Fat) can also enhance the texture and spreadability of products, contributing to a smooth application



ORIGIN OF LANOLIN (WOOL FAT):
Lanolin (Wool Fat) is obtained through a process of extracting and purifying the wool grease found in sheep's wool.
The wool grease is treated to remove impurities and excess water, resulting in the production of Lanolin (Wool Fat).
This refined Lanolin (Wool Fat) is then further processed to obtain different forms, such as anhydrous Lanolin (Wool Fat) or Lanolin (Wool Fat) oil.



WHAT DOES LANOLIN (WOOL FAT) DO IN A FORMULATION?
*Emollient
*Moisturising
*Skin conditioning



SAFETY PROFILE OF LANOLIN (WOOL FAT):
Lanolin (Wool Fat) is widely regarded as a safe ingredient for use in cosmetics.
However, it is important to note that individuals can have varying sensitivities, so patch testing is recommended to check for potential allergic reactions before using products containing Lanolin (Wool Fat).
Additionally, Lanolin (Wool Fat) alcohol can be considered halal if the specific sourcing and the processing methods are employed.



ALTERNATIVES OF LANOLIN (WOOL FAT):
*GLYCERIN



PRODUCTION OF LANOLIN (WOOL FAT):
Crude Lanolin (Wool Fat) constitutes about 5–25% of the weight of freshly shorn wool.
The wool from one Merino sheep will produce about 250–300 ml of recoverable wool grease.

Lanolin (Wool Fat) is extracted by washing the wool in hot water with a special wool scouring detergent to remove dirt, wool grease (crude Lanolin (Wool Fat)), suint (sweat salts), and anything else stuck to the wool.

The wool grease is continuously removed during this washing process by centrifuge separators, which concentrate it into a waxlike substance melting at approximately 38 °C (100 °F).



COMPOSITION OF LANOLIN (WOOL FAT):
A typical high-purity grade of Lanolin (Wool Fat) is composed predominantly of long chain waxy esters (approximately 97% by weight) with the remainder being Lanolin (Wool Fat) alcohols, Lanolin (Wool Fat) acids and Lanolin (Wool Fat) hydrocarbons.

An estimated 8,000 to 20,000 different types of Lanolin (Wool Fat) esters are present in Lanolin (Wool Fat), resulting from combinations between the 200 or so different Lanolin (Wool Fat) acids and the 100 or so different Lanolin (Wool Fat) alcohols identified so far.

Lanolin (Wool Fat)’s complex composition of long-chain esters, hydroxyesters, diesters, Lanolin (Wool Fat) alcohols, and Lanolin (Wool Fat) acids means in addition to its being a valuable product in its own right, it is also the starting point for the production of a whole spectrum of Lanolin (Wool Fat) derivatives, which possess wide-ranging chemical and physical properties.

The main derivatisation routes include hydrolysis, fractional solvent crystallisation, esterification, hydrogenation, alkoxylation and quaternisation.
Lanolin (Wool Fat) derivatives obtained from these processes are used widely in both high-value cosmetics and skin treatment products.

Hydrolysis of Lanolin (Wool Fat) yields Lanolin (Wool Fat) alcohols and Lanolin (Wool Fat) acids.
Lanolin (Wool Fat) alcohols are a rich source of cholesterol (an important skin lipid) and are powerful water-in-oil emulsifiers; they have been used extensively in skincare products for over 100 years.

Approximately 40% of the acids derived from Lanolin (Wool Fat) are alpha-hydroxy acids (AHAs).
The use of AHAs in skin care products has attracted a great deal of attention in recent years.



WHERE IS LANOLIN (WOOL FAT) FOUND?
Wool fat is a principle component of Lanolin (Wool Fat), which is a natural product obtained from the fleece of sheep.
Lanolin (Wool Fat) is found in steroid-containing creams/ointments, medicated shampoos, veterinary products, hand lotions, moisturizers, sunscreens, self-tanning creams, lipsticks, makeup removers, foundations, eye shadows, hairsprays, shaving creams, baby oils and products, printing inks, furniture and shoe polishes, lubricants, leather, and paper.



WHAT ARE SOME PRODUCTS THAT MAY CONTAIN LANOLIN (WOOL FAT)?
Cosmetics
• Foundations
• Eye makeup
• Lipsticks

Hair Care
• Hairspray

Household Products
• Furniture polish
• Leather
• Paper
• Printing inks

Liquids
• Baby oils
• Baby ointments
• Hand lotion
• Moisturizers
• Self-tanners
• Sunscreen



THE DIFFERENCE BETWEEN LANOLIN (WOOL FAT) WOOL AND LANOLIN (WOOL FAT) CREAMS:
Lanolin (Wool Fat) Wool Fat is simply the purest form of Lanolin (Wool Fat) and has not been altered or processed in any way.
This makes it a much more natural and ethical choice than Lanolin (Wool Fat) creams.
Lanolin (Wool Fat) creams, on the other hand, are often processed and contain potentially harmful ingredients.

Many of these creams are made from Lanolin (Wool Fat) that has been extracted from sheep’s wool using harsh chemicals.
This process can strip the Lanolin (Wool Fat) of its natural properties and can cause irritation for people with sensitive skin.
Furthermore, the use of harsh chemicals in the manufacturing process is often seen as unethical.

In contrast, Lanolin (Wool Fat) Wool Fat is ethically sourced and is not exposed to any chemicals during the extraction process.
It is also free from fragrances, colors, and preservatives which can irritate the skin and cause reactions.

Overall, Lanolin (Wool Fat) Wool Fat is a much better choice than Lanolin (Wool Fat) creams.
Its natural and ethical production process makes Lanolin (Wool Fat) a safer and more reliable option for healing inflammation.
Furthermore, Lanolin (Wool Fat) is free from potentially harmful ingredients and fragrances, making it a much healthier choice.



PHYSICAL and CHEMICAL PROPERTIES of LANOLIN (WOOL FAT):
Physical state: Paste
Color: Yellow
Odor: Not available
Melting point/freezing point: Not available
Initial boiling point and boiling range: Not available
Flammability (solid, gas): Not available
Upper/lower flammability or explosive limits: Not available
Flash point: 113°C - closed cup
Autoignition temperature: Not available
Decomposition temperature: Not available
pH: Not available
Viscosity:
Kinematic viscosity: Not available
Dynamic viscosity: Not available

Water solubility: Not available
Partition coefficient: n-octanol/water: Not available
Vapor pressure: Not available
Density: Not available
Relative density: Not available
Relative vapor density: Not available
Particle characteristics: Not available
Explosive properties: Not available
Oxidizing properties: Not available
Other safety information: Not available
Additional Information:
Melting Point: 38-40°C
pH: 5.5-7.0
Solubility: Insoluble in water
Viscosity: High



FIRST AID MEASURES of LANOLIN (WOOL FAT):
-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:
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of LANOLIN (WOOL FAT):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of LANOLIN (WOOL FAT):
-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 LANOLIN (WOOL FAT):
-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.
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:
Choose body protection in relation to its type.
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of LANOLIN (WOOL FAT):
-Precautions for safe handling:
*Advice on protection against fire and explosion:
Provide appropriate exhaust ventilation at places where dust is formed.
Normal measures for preventive fire protection.
*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 class:
Storage class (TRGS 510): 13:
Non Combustible Solids



STABILITY and REACTIVITY of LANOLIN (WOOL FAT):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available


LANOLIN (WOOL FAT)
DESCRIPTION:

LANOLIN (WOOL FAT) (from Latin lāna 'wool', and oleum 'oil'), also called wool fat, wool yolk, wool wax, or wool grease, is a wax secreted by the sebaceous glands of wool-bearing animals.
LANOLIN (WOOL FAT) used by humans comes from domestic sheep breeds that are raised specifically for their wool.
Historically, many pharmacopoeias have referred to Lanolin (wool fat) as wool fat (adeps lanae); however, as Lanolin (wool fat) lacks glycerides (glycerol esters), it is not a true fat.

CAS: 8006-54-0
European Community (EC) Number: 232-348-6


LANOLIN (WOOL FAT) primarily consists of sterol esters instead.
Lanolin (wool fat)'s waterproofing property aids sheep in shedding water from their coats.
Certain breeds of sheep produce large amounts of Lanolin (wool fat).


LANOLIN (WOOL FAT) is a principle component of Lanolin (wool fat), which is a natural product obtained from the fleece of sheep.
LANOLIN (WOOL FAT) is found in steroid-containing creams/ointments, medicated shampoos, veterinary products, hand lotions, moisturizers, sunscreens, self-tanning creams, lipsticks, makeup removers, foundations, eye shadows, hairsprays, shaving creams, baby oils and products, printing inks, furniture and shoe polishes, lubricants, leather, and paper.

Lanolin (wool fat)'s role in nature is to protect wool and skin from climate and the environment; it also plays a role in skin (integumental) hygiene.
LANOLIN (WOOL FAT) and its derivatives are used in the protection, treatment, and beautification of human skin

LANOLIN (WOOL FAT) is a yellow fat obtained from sheep's wool.
LANOLIN (WOOL FAT) is used as an emollient, cosmetic, and pharmaceutic aid.
The US federal code of regulations states that Lanolin (wool fat) in the concentration range of 12-50% may be included in over the counter skin ointments.
Lanolin (wool fat) is the purified, secreted product of the sheep sebaceous glands.
Lanolin (wool fat) primarily consists of long-chain waxy esters, or sterol esters, that lack glycerides.

For this reason, it is also called wool wax or wool grease.
Lanolin (wool fat) is used in the protection, treatment, and cosmetic enhancement of human skin.
Its hydrophobic properties can help protect skin against infections or skin irritation, as it helps seal in moisture that is already present in the skin.

Lanolin (wool fat) is used as an active ingredient in over the counter topical products such as ointments, lubricants, lotions and facial cosmetics.
Lanolin (wool fat) is also frequently used in protective baby skin treatment and for sore nipples in breastfeeding mothers,.



COMPOSITION OF LANOLIN (WOOL FAT) :
A typical high-purity grade of Lanolin (wool fat) is composed predominantly of long chain waxy esters (approximately 97% by weight) with the remainder being Lanolin (wool fat) alcohols, Lanolin (wool fat) acids and Lanolin (wool fat) hydrocarbons.
An estimated 8,000 to 20,000 different types of Lanolin (wool fat) esters are present in Lanolin (wool fat), resulting from combinations between the 200 or so different Lanolin (wool fat) acids and the 100 or so different Lanolin (wool fat) alcohols identified so far.


Lanolin (wool fat)’s complex composition of long-chain esters, hydroxyesters, diesters, Lanolin (wool fat) alcohols, and Lanolin (wool fat) acids means in addition to its being a valuable product in its own right, it is also the starting point for the production of a whole spectrum of Lanolin (wool fat) derivatives, which possess wide-ranging chemical and physical properties.
The main derivatisation routes include hydrolysis, fractional solvent crystallisation, esterification, hydrogenation, alkoxylation and quaternisation.


Lanolin (wool fat) derivatives obtained from these processes are used widely in both high-value cosmetics and skin treatment products.
Hydrolysis of Lanolin (wool fat) yields Lanolin (wool fat) alcohols and Lanolin (wool fat) acids.
Lanolin (wool fat) alcohols are a rich source of cholesterol (an important skin lipid) and are powerful water-in-oil emulsifiers; they have been used extensively in skincare products for over 100 years.

Approximately 40% of the acids derived from Lanolin (wool fat) are alpha-hydroxy acids (AHAs).
The use of AHAs in skin care products has attracted a great deal of attention in recent years.
Details of the AHAs isolated from Lanolin (wool fat) can be seen in the table below.


PRODUCTION OF LANOLIN (WOOL FAT) :
Crude Lanolin (wool fat) constitutes about 5–25% of the weight of freshly shorn wool.
The wool from one Merino sheep will produce about 250–300 ml of recoverable wool grease.
Lanolin (wool fat) is extracted by washing the wool in hot water with a special wool scouring detergent to remove dirt, wool grease (crude Lanolin (wool fat)), suint (sweat salts), and anything else stuck to the wool.

The wool grease is continuously removed during this washing process by centrifuge separators, which concentrate it into a waxlike substance melting at approximately 38 °C (100 °F).


APPLICATIONS OF LANOLIN (WOOL FAT) :
Lanolin (wool fat) and its many derivatives are used extensively in both the personal care (e.g., high value cosmetics, facial cosmetics, lip products) and health care sectors such as topical liniments.
Lanolin (wool fat) is also found in lubricants, rust-preventive coatings, shoe polish, and other commercial products.
Lanolin (wool fat) is a relatively common allergen and is often misunderstood as a wool allergy.


However, allergy to a Lanolin (wool fat)-containing product is difficult to pinpoint and often other products containing Lanolin (wool fat) may be fine for use.
Patch testing can be done if a Lanolin (wool fat) allergy is suspected.
It is frequently used in protective baby skin treatment and for sore nipples from breastfeeding although health authorities do not recommend it, advise against nipple cleaning and rather recommend improving baby positioning and expressing milk by hand.

Lanolin (wool fat) is used commercially in many industrial products ranging from rustproof coatings to lubricants.
Some sailors use Lanolin (wool fat) to create slippery surfaces on their propellers and stern gear to which barnacles cannot adhere.

Commercial products (e.g. Lanocote) containing up to 85% Lanolin (wool fat) are used to prevent corrosion in marine fasteners, especially when two different metals are in contact with each other and saltwater.
The water-repellent properties make it valuable in many applications as a lubricant grease where corrosion would otherwise be a problem.
7-Dehydrocholesterol from Lanolin (wool fat) is used as a raw material for producing vitamin D3 by irradiation with ultraviolet light.


Baseball players often use it to soften and break in their baseball gloves (shaving cream with Lanolin (wool fat) is popularly used for this).
Anhydrous liquid Lanolin (wool fat), combined with parabens, has been used in trials as artificial tears to treat dry eye.

Anhydrous Lanolin (wool fat) is also used as a lubricant for brass instrument tuning slides.
Lanolin (wool fat) can also be restored to woollen garments to make them water and dirt repellent, such as for cloth diaper covers.
Lanolin (wool fat) is also used in lip balm products such as Carmex.

For some people, it can irritate the lips.
Lanolin (wool fat) is sometimes used by people on continuous positive airway pressure therapy to reduce irritation with masks, particular nasal pillow masks that can often create sore spots in the nostrils.
Lanolin (wool fat) is a popular additive to moustache wax, particularly 'extra-firm' varieties.

Lanolin (wool fat) is used as a primary lubricating component in aerosol-based brass lubricants in the ammunition reloading process.
Mixed warm 1:12 with highly concentrated ethanol (usually 99%), the ethanol acts as a carrier which evaporates quickly after application, leaving a fine film of Lanolin (wool fat) behind to prevent brass seizing in resizing dies.

Lanolin (wool fat), when mixed with ingredients such as neatsfoot oil, beeswax and glycerol, is used in various leather treatments, for example in some saddle soaps and in leather care products.



STANDARDS AND LEGISLATION ABOUT LANOLIN (WOOL FAT) :
In addition to general purity requirements, Lanolin (wool fat) must meet official requirements for the permissible levels of pesticide residues.
The Fifth Supplement of the United States Pharmacopoeia XXII published in 1992 was the first to specify limits for 34 named pesticides.
A total limit of 40 ppm (i.e. 40 mg/kg) total pesticides was stipulated for Lanolin (wool fat) of general use, with no individual limit greater than 10 ppm.


A second monograph also introduced into the US Pharmacopoeia XXII in 1992 was entitled 'Modified Lanolin (wool fat)'.
Lanolin (wool fat) conforming to this monograph is intended for use in more exacting applications, for example on open wounds.
In this monograph, the limit of total pesticides was reduced to 3 ppm total pesticides, with no individual limit greater than 1 ppm.


In 2000, the European Pharmacopoeia introduced pesticide residue limits into its Lanolin (wool fat) monograph.
This requirement, which is generally regarded as the new quality standard, extends the list of pesticides to 40 and imposes even lower concentration limits.
Some very high-purity grades of Lanolin (wool fat) surpass monograph requirements.

New products obtained using complex purification techniques produce Lanolin (wool fat) esters in their natural state, removing oxidative and environmental impurities resulting in white, odourless, hypoallergenic Lanolin (wool fat).
These ultra-high-purity grades of Lanolin (wool fat) are ideally suited to the treatment of dermatological disorders such as eczema and on open wounds.

Lanolin (wool fat) attracted attention owing to a misunderstanding concerning its sensitising potential.
A study carried out at New York University Hospital in the early 1950s had shown about 1% of patients with dermatological disorders were allergic to the Lanolin (wool fat) being used at that time.

By one estimate, this simple misunderstanding of failing to differentiate between the general healthy population and patients with dermatological disorders exaggerates the sensitising potential of Lanolin (wool fat) by 5,000–6,000 times.


The European Cosmetics Directive, introduced in July 1976, contained a stipulation that cosmetics which contained Lanolin (wool fat) should be labelled to that effect.
This ruling was challenged immediately, and in the early 1980s, it was overturned and removed from the directive.
Despite only being in force for a short period of time, this ruling did harm both to the Lanolin (wool fat) industry and to the reputation of Lanolin (wool fat) in general.

The Cosmetics Directive ruling only applied to the presence of Lanolin (wool fat) in cosmetic products; it did not apply to the many hundreds of its different uses in dermatological products designed for the treatment of compromised skin conditions.

Modern analytical methods have revealed Lanolin (wool fat) possesses a number of important chemical and physical similarities to human stratum corneum lipids; the lipids which help regulate the rate of water loss across the epidermis and govern the hydration state of the skin.

Cryogenic scanning electron microscopy has shown that Lanolin (wool fat), like human stratum corneum lipids, consists of a mass of liquid crystalline material.
Cross-polarised light microscopy has shown the multilamellar vesicles formed by Lanolin (wool fat) are identical to those formed by human stratum corneum lipids.
The incorporation of bound water into the stratum corneum involves the formation of multilamellar vesicles.

Skin bioengineering studies have shown the durational effect of the emollient (skin smoothing) action produced by Lanolin (wool fat) is very significant and lasts for many hours.
Lanolin (wool fat) applied to the skin at 2 mg/cm2 has been shown to reduce roughness by about 35% after one hour and 50% after two hours, with the overall effect lasting for considerably more than eight hours.

Lanolin (wool fat) is also known to form semiocclusive (breathable) films on the skin.
When applied daily at around 4 mg/cm2 for five consecutive days, the positive moisturising effects of Lanolin (wool fat) were detectable until 72 hours after final application.
Lanolin (wool fat) may achieve some of its moisturising effects by forming a secondary moisture reservoir within the skin.

The barrier repair properties of Lanolin (wool fat) have been reported to be superior to those produced by both petrolatum and glycerol.
In a small clinical study conducted on volunteer subjects with terribly dry (xerotic) hands, Lanolin (wool fat) was shown to be superior to petrolatum in reducing the signs and symptoms of dryness and scaling, cracks and abrasions, and pain and itch.
In another study, a high purity grade of Lanolin (wool fat) was found to be significantly superior to petrolatum in assisting the healing of superficial wounds.



PRODUCTS THAT MAY CONTAIN LANOLIN (WOOL FAT) :
Cosmetics
• Foundations
• Eye makeup
• Lipsticks

Hair Care
• Hairspray

Household Products
• Furniture polish
• Leather
• Paper
• Printing inks

Liquids
• Baby oils
• Baby ointments
• Hand lotion
• Moisturizers
• Self-tanners
• Sunscreen


SAFETY INFORMATION ABOUT LANOLIN (WOOL FAT) :
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






SYNONYMS OF LANOLIN (WOOL FAT) :
Lanolin (wool fat)
8006-54-0
7EV65EAW6H
Anhydrous Lanolin (wool fat)
Wool grease
Wool wax, refined
Black Rose
Lanashield
Lanolin (wool fat), anhydrous
Skin Protectant with Lanolin (wool fat)
Theresienol MD Skin Protectant
Theriac Advanced Healing
232-348-6
3CE DRAWING LIP CHILLING
4sport skincare anti chafing
AGNOLIN NO 1
AmeriDermDermaFix
CORONA MULTI-PURPOSE
CORONA ORIGINAL LANOLIN (WOOL FAT) RICH
DTXSID2027678
EMERY 1600
EUCERITE
LANOLIN (WOOL FAT) (II)
LANOLIN (WOOL FAT) (USP MONOGRAPH)
LANOLIN (WOOL FAT) (USP-RS)
LANOLIN (WOOL FAT),ANHYDROUS LIQUID
Lana1263
LanoGuardDaily Care Skin Protectant
LanoGuardDry Skin Therapy
Lanoderm
Lantiseptic Dry Skin Therapy
Lantiseptic by DermaRite Original Skin Protectant
Lantiseptic by Dermarite Dry Skin Therapy
LincoFix
North Country Dairy Supply Non Iodine Barrier Dip
PrimaGuardDaily Care Skin Protectant
SUINTINE
Smartchoices Lanolin (wool fat) Plus0
Soothe and Cool Free Medseptic
Soothe and Cool Free MedsepticSkin Protectant


LANOLIN + 75 EO
Lanolin + 75 EO is available in the form of yellow to light brown wax.
Lanolin + 75 EO is a derivative of lanolin, which shows good water solubility.


CAS Number: 61790-81-6 / 8039-09-6
Chem/IUPAC Name: Lanolin, ethoxylated (75 mol EO average molar ratio)
Chemical Name: Lanolin, Ethoxylated, PEG-75 lanolin
Chemical Family: Alcohols, Ethoxylates, Waxes



SYNONYMS:
Lanolin, oil, ethoxylated, Ethoxylated Lanolin, Lanolin, Ethoxylated, Lanolin + 75 EO, Lanolin, ethoxylated, polyoxyethylene (75) lanolin, polyethylene glycol-75 lanolin, lanolin adduct, Ethoxylated lanolin, Lanolin, ethoxylated, Polyoxyethylene (75) Lanolin, (PEG-75 Lanolin), Super?Solan, PEG-25LANOLIN, PEG-75 LANOLIN, PEG-40 LANOLIN, Ethoxylated lanolin, Lanolin, ethoxylated, Water-soluble lanolin, Polyoxyethylene lanolins, WOOLGREASE-POLYETHOXYLATED, PEG-75 Lanolin (Ethoxylated Lanolin 75 EO)



Lanolin + 75 EO is a cosmetic grade ingredient that works as an emollient which helps in hydrating and softening the skin.
Lanolin + 75 EO appears as a pale yellow liquid that is odorless.
Lanolin + 75 EO is also a great surfactant and emulsifier that helps to combine water-based and oil-based ingredients in a formulation and form a stable product.


In personal care products, Lanolin + 75 EO is highly nourishing and also protects the skin by forming a protective barrier on the surface.
Lanolin + 75 EO is a polyoxyethylene condensate of lanolin with 75 moles of ethyleneoxide.
Lanolin + 75 EO is a hard pale yellow wax with a faint fruitly odor.


Lanolin + 75 EO is particulary indicated for use in aqueous or aqueous-alcoholic lotions, mainly in shampoos, skin cleansing and after-shave lotions.
Lanolin + 75 EO is a very mild nonionic surfactant that can be used with amphoterics and other mild surfactants in the production of baby shampoos.
Washable Lanolin + 75 EO advantages: smoothes the skin and hair, its liquid form facilitates the formulation of preparations, facilitates the dissolution of perfumes, essential oils, antiseptics, compatibility with other surfactants, stabilizes oil-in-water (O/W) emulsions, biodegradable.


Lanolin + 75 EO is available in the form of yellow to light brown wax.
Lanolin + 75 EO is a derivative of lanolin, which shows good water solubility.
Lanolin + 75 EO is a polyoxyethylene condensate with the best pharmaceutical lanolin.


Lanolin + 75 EO has a mean chain length of 75 ethylene oxide units and an average molecular weight of about 3.970 Da.
The lanolin content in Lanolin + 75 EO is approximately 17%.
Lanolin + 75 EO is a hard, pale yellow wax with weak fruity odour.


Lanolin + 75 EO is safe to use, non-toxic.
Lanolin + 75 EO is a surfactant.
Lanolin + 75 EO is an ethoxylated derivative of lanolin.


Lanolin + 75 EO comes in the form of yellow to light brown wax.
Lanolin + 75 EO is very well soluble in water.
Lanolin + 75 EO is predominantly hydrophobic.


Lanolin + 75 EO is pharma grade lanolin containing 50% water.
Hypoallergenic and vegetarian certificates of Lanolin + 75 EO are available.
Lanolin + 75 EO is a very mild nonionic surfactant that can be used with amphoterics and other mild surfactants in the production of baby shampoos.


Lanolin + 75 EO is a polyoxyethylene condensate with the best lanolin.
Lanolin + 75 EO has a mean chain length of 75 ethylene oxide units and an average molecular weight of about 3.970 Da.
The lanolin content in Lanolin + 75 EO is approximately 17%.


Lanolin + 75 EO is a hard, pale yellow wax with weak fruity odour.
Washable Lanolin + 75 EO advantages: smoothes skin and hair, liquid form facilitates the formulation of preparations, facilitates dissolution of perfumes, essential oils, antiseptics, compatibility with other surfactants, stabilizes oil-in-water (O/W) emulsions, biodegradable
Lanolin + 75 EO is an emollient and surfactant derived from Lanolin



USES and APPLICATIONS of LANOLIN + 75 EO:
Lanolin + 75 EO is used cosmetics and detergents, shampoos, liquid soaps, body washes, gels for washing face and body, shower gels, bubble baths, toners, pore-refining, before and after shave fluids, creams, moisturisers, lotions, aqueous or aqueous-alcoholic liquids with high clarity, detergents for industrial washing, wetting and conditioning agent for cold wave perm products.


Lanolin + 75 EO is a non-ionic surfactant (INCI name: PEG-75 Lanolin), an ethoxylated derivative of lanolin, used mainly in cosmetic applications.
Lanolin + 75 EO is particularly recommended for use in aqueous or aqueous-alcoholic lotions and solutions with high clarity.
Moreover, Lanolin + 75 EO has emulsifying, solubilising and emollient properties and a mild cleaning effect.


Main applications of Lanolin + 75 EO include skin cleansing and after-shave lotions, as well as in shampoos and detergent formulations, where viscosity is of importance.
Thanks to its various properties, Lanolin + 75 EO is an ingredient in many products such as shampoos, facial gels, body washes, liquid soaps, lotions and toners.


Among industrial applications, Lanolin + 75 EO is mainly used as an industrial cleaning detergent.
The role and effects of Lanolin + 75 EO in cosmetics and personal care products: Lanolin + 75 EO in cosmetics serves both as a base (a kind of foundation on which a cosmetic formulation is built) and an active ingredient (ensuring specific properties).


Although it was recognised as safe for personal care and cosmetic products, Lanolin + 75 EO should not be used as an ingredient in formulations intended for children and pregnant women.
Lanolin + 75 EO is primarily an emulsifier used in O/W emulsions (oil-in-water emulsions).


Lanolin + 75 EO enables to form an emulsion by mixing the oil phase with the water phase.
As a surfactant, Lanolin + 75 EO enables the formation of foam.
Foam is where air (or another gas) is dispersed in a liquid.


Adequate foaming properties of cosmetics are responsible for effective removal of impurities.
Lanolin + 75 EO contributes to the rheology modification.
One of the factors determining sensory quality and usability of e.g. cosmetic creams is their rheological characteristics, namely viscosity of Lanolin + 75 EO, which often influences consumer decisions on the purchase of a specific formulation.


Lanolin + 75 EO as one of the product ingredients, increases or decreases the viscosity of the finished product.
Another effect of Lanolin + 75 EO is solubilization.
As a solubiliser, in a process called micellar solubilisation, Lanolin + 75 EO introduces substances that are hydrophobic (i.e. not soluble in water) into the aqueous solution in which it is found.


The result is an isotropic, transparent composition whose viscosity is similar to that of water.
Examples of substances that can be introduced into aqueous solution thanks to the use of Lanolin + 75 EO include plant extracts, oily substances and fragrance compositions.


Lanolin + 75 EO also works well in skin care formulations as an emollient.
Lanolin + 75 EO forms a thin occlusive layer on the surface of the skin that prevents excessive evaporation of water and keeps an adequate level of moisture (indirect moisturising effect).


The visible effect is smoothening and softening of the epidermis.
Lanolin + 75 EO is particularly recommended for use in aqueous or aqueous-alcoholic lotions and solutions with high clarity.
Moreover, Lanolin + 75 EO has emulsifying, solubilising and emollient properties and a mild cleaning effect.


Main applications of Lanolin + 75 EO include skin cleansing and after-shave lotions, as well as in shampoos and detergent formulations, where viscosity is of importance.
Lanolin + 75 EO is used as a conditioning agent and emollient in cleansing and skin care cosmetics.


Lanolin + 75 EO has a moisturising as well as softening and smoothening effect.
Skincare: Add Lanolin + 75 EO to creams, lotions, serums, and body butters to enhance their moisturizing properties and improve skin texture.
Haircare: Incorporate Lanolin + 75 EO into shampoos, conditioners, hair masks, and styling products to nourish and condition the hair.


Formulation: Lanolin + 75 EO can be easily incorporated into water-based formulations due to its water-soluble nature.
Lanolin + 75 EO is a unique and versatile ingredient that offers excellent emollient and moisturizing properties, making it a popular choice in skincare and haircare products.


Lanolin + 75 EO is a water-soluble derivative of lanolin, a natural substance derived from sheep’s wool.
Lanolin + 75 EO is known for its ability to improve skin and hair texture, leaving them soft, smooth, and well-hydrated.



WHAT IS LANOLIN + 75 EO USED FOR?
Lanolin + 75 EO is very useful for the cosmetic and personal care industry.
Lanolin + 75 EO can be found in products such as foundations, eyeshadows, lotions, creams, and lip balms.

*Decorative cosmetics:
Lanolin + 75 EO improves the texture of the products and keeps different ingredients in the formulation from separating.
Lanolin + 75 EO also reduces the harsh and dry nature of cosmetics by making them smoother and hydrating

*Hair care:
Lanolin + 75 EO offers natural shine to the shafts by nourishing and conditioning them.
Lanolin + 75 EO also forms a protective barrier on the scalp and promotes healthy hair - full of sheen and shine



ORIGIN OF LANOLIN + 75 EO:
Lanolin + 75 EO is made from wool wax that comes from the wool of sheep.
Lanolin + 75 EO is made by hydrogenation and hydrolysis of the wool which involves breaking down the fatty acids into smaller molecules.
These molecules are then manufactured into the cosmetic grade ingredient - Lanolin + 75 EO.



WHAT DOES LANOLIN + 75 EO DO IN A FORMULATION?
*Emollient
*Emulsifying
*Surfactant



SAFETY PROFILE OF LANOLIN + 75 EO:
Lanolin + 75 EO is safe for skin and hair.
The recommended use level of this ingredient is between 0.5-20%.
Levels of Lanolin + 75 EO higher than this can cause side effects such as rashes, itching, and redness.

A patch test is recommended before full application.
Further, Lanolin + 75 EO is non-comedogenic and does not cause blemishes or acne.
Lanolin + 75 EO is not vegan.



ALTERNATIVES OF LANOLIN + 75 EO:
*SHEA BUTTER GLYCERIDES



FUNCTIONS OF LANOLIN + 75 EO:
*Emulsifier,
*Surfactant,
*Surfactant (Nonionic)



FEATURES LANOLIN + 75 EO:
Lanolin + 75 EO is ethoxylated, to obtain not only complete water solubility, but also solutions that are crystal clear in all concentrations, both in water and in aqueous ethanol concentrations of up to 40%.

The solutions are nonionic and compatible with most other solubilisers including up to 10% electrolytes solutions.
The solution is only slightly affected by oxidative and reducing agents.

Lanolin + 75 EO is stable in a pH range of 2-10.
A particularly unique feature of Lanolin + 75 EO is its carefully controlled manufacturing that ensures minimum viscosity variations of the aqueous solutions.



KEY FEATURES OF LANOLIN + 75 EO:
1. **Emollient and Moisturizing:**
Lanolin + 75 EO acts as an effective emollient, forming a protective barrier on the skin and hair to lock in moisture, keeping them hydrated and supple.

2. **Enhances Skin Texture:**
Lanolin + 75 EO helps improve the texture of the skin, making it ideal for use in creams, lotions, and moisturizers.

3. **Hair Conditioning:**
Lanolin + 75 EO can be used in haircare products like shampoos and conditioners to add moisture and improve hair manageability and shine.

4. **Water-Soluble:**
Unlike traditional lanolin, Lanolin + 75 EO is water-soluble, making it easier to incorporate into various formulations.

5. **Non-Greasy:**
Lanolin + 75 EO is non-greasy and absorbs quickly, providing a smooth and comfortable feel on the skin and hair.



FEATURES AND BENEFITS OF LANOLIN + 75 EO:
Benefit Claims
*Acidic pH Stable,
*Basic pH Stable,
*Compatibility,
*Dispersing,
*Emolliency,
*Emulsifying,
*Good Wetting Properties,
*Skin Conditioning
*Labeling Claims
*Halal,
*Kosher,
*Ulta Beauty's Conscious Beauty



BENEFITS OF LANOLIN + 75 EO:
– Skin Hydration:
Lanolin + 75 EO helps prevent water loss from the skin, promoting long-lasting hydration.

– Hair Nourishment:
When used in hair products, Lanolin + 75 EO can help repair and protect damaged hair, leaving it soft and silky.

– Compatibility:
Lanolin + 75 EO is compatible with a wide range of cosmetic ingredients, making it suitable for formulating a variety of products.



GENERAL CHARACTERISTICS OF LANOLIN + 75 EO:
Lanolin + 75 EO is the INCI name for one of polyethylene glycol derivatives.
Its common chemical name is lanolin ethoxylated with 75 moles of ethylene oxide or Lanolin + 75 EO.

The number of moles of ethylene oxide in an ethylene glycol derivative is indicated in the INCI name of Lanolin + 75 EO (as with other ethylene glycol derivatives).
The CAS number to search for and identify Lanolin + 75 EO is 61790-81-6.



DERMATOLOGY OF LANOLIN + 75 EO:
Lanolin + 75 EO is made from pharmaceutical grade lanolin, which complies to the European Pharmacopoeia.
Lanolin + 75 EO is well established in the market for many years, especially for hair and skin care products.
To date, no adverse effects were observed.
Patch tests that were made with the 100 % substance in 11 subjects with daily dosing of 2-3 hours over a period of 4 weeks showed no adverse skin reaction.



PROCESSING OF LANOLIN + 75 EO:
When used in solutions, Lanolin + 75 EO should first be melted, followed by addition of 3 times the amount of hot water under constant stirring.
The resulting concentrate of Lanolin + 75 EO is then diluted with either hot or cold water.
In order to prepare emulsions, Lanolin + 75 EO is normally melted together with the oil phase, but it can also be dissolved in the aqueous phase.
Lanolin + 75 EO should be stored cool in closed containers. Prolonged heating above 80 °C should be avoided.



SOLUBILITY OF LANOLIN + 75 EO:
Solubility at room temperature
Water: soluble; ethanol, anhydrous: soluble; ethanol 80%: partly soluble; ethanol 40%: soluble; mineral oil: slightly soluble



ADVANTAGES OF LANOLIN + 75 EO:
Key advantages of PEG-75 Lanolin:
*facilitates emulsion formation by reducing surface tension of substances to be emulsified;
*creates a protective layer on the surface of the skin, making Lanolin + 75 EO soft and smooth;
*in hair care products, Lanolin + 75 EO prevents excessive water evaporation;
facilitates dissolution of perfumes or essential oils in water;
*Lanolin + 75 EOis compatible and synergic with other surfactants.



FEATURES OF LANOLIN + 75 EO:
Lanolin + 75 EO is ethoxylated, to obtain not only complete water solubility, but also solutions that are crystal clear in all concentrations, both in water and in aqueous ethanol concentrations of up to 40%.

The solutions are nonionic and compatible with most other solubilisers including up to 10% electrolytes solutions.
The solution is only slightly affected by oxidative and reducing agents.

Lanolin + 75 EO is stable in a pH range of 2-10.
A particularly unique feature of Lanolin + 75 EO is its carefully controlled manufacturing that ensures minimum viscosity variations of the aqueous solutions.



ADVANTAGES OF LANOLIN + 75 EO:
* emollient and conditioning agent in colouring cosmetics,
* smoothes the skin and hair,
* the liquid form facilitates formulation of preparations,
* agent facilitating the dissolution of perfumes, essential oils, antiseptics,
* compatibility and synergy with other surfactants,
* stabilizes oil-in-water (O/W) emulsions,



PHYSICAL and CHEMICAL PROPERTIES of LANOLIN + 75 EO:
Boiling Point: 300°C
Melting Point: 99°C
pH: 5.0-7.0
Solubility: Soluble in water
Boiling Point: 300°C
Melting Point: 99°C
pH: 5.0-7.0
Solubility: Soluble in water
CAS Number: 61790-81-6 / 8039-09-6
Chem/IUPAC Name: Lanolin, ethoxylated (75 mol EO average molar ratio)
COSING REF No: 77290
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in Water: 0.0002397 mg/L @ 25°C (estimated)



FIRST AID MEASURES of LANOLIN + 75 EO:
-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 LANOLIN + 75 EO:
-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 LANOLIN + 75 EO:
-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 LANOLIN + 75 EO:
-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 LANOLIN + 75 EO:
-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 LANOLIN + 75 EO:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

LANOLIN ACID
LANOLIN ALCOHOL, N° CAS : 8027-33-6 - Alcool de lanoline, Origine(s) : Animale, Synthétique. Autres langues : Alcohol de lanolina, Alcool di lanolina, Lanolinalkohol, Nom INCI : LANOLIN ALCOHOL, N° EINECS/ELINCS : 232-430-1. Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Agent fixant : Permet la cohésion de différents ingrédients cosmétiques. Emollient : Adoucit et assouplit la peau. Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile). Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques. Noms français : Alcools de lanoline. Noms anglais : ALCOHOLS, LANOLIN; Ecerin; LANOLIN ALCOHOL; LANOLIN ALCOHOLS;WOOLWAX ALCOHOL
LANOLIN ALCOHOL ( Alcool de lanoline)
fluilan; lantrol; vigilan; Lanolin CAS NO:70321-63-0
Lanoline ( Lanoline anhydre)
Noms français : Lanoline anhydre; Inci : lanolin, Cas : 8006-54-0, La lanoline, autrement appelée graisse de laine ou cire de laine, est une graisse obtenue par purification et raffinage du suint (partie grasse absorbée sur la laine). Elle comprend de l'oléine et de la stéarine. Chimiquement, la lanoline est une cire, un mélange d'esters et d'acides gras avec des alcools à haute masse moléculaire. On a identifié plus de 180 acides gras et 80 alcools différents. Elle est amphiphile et forme des émulsions très stables avec l'eau, de plus il s'agit d'une espèce très hygroscopique. La lanoline est utilisée en pharmacie, par exemple pour la supplémentation en vitamine D2,3, et dans la fabrication des produits de beauté.Principaux synonymes: Noms anglais : ANHYDROUS LANOLIN, ANHYDROUS LANUM, Lanolin anhydrous, LANOLIN, ANHYDROUS
Lanoline AD
LANTHANUM CHLORIDE, N° CAS : 10099-58-8. Nom INCI : LANTHANUM CHLORIDE. Nom chimique : Lanthanum chloride, anhydrous. N° EINECS/ELINCS : 233-237-5. Ses fonctions (INCI). Astringent : Permet de resserrer les pores de la peau
Lanthanum chloride
LAURAMIDE DEA, N° CAS : 120-40-1, Nom INCI : LAURAMIDE DEA, Nom chimique : N,N-bis(2-Hydroxyethyl)dodecanamide, N° EINECS/ELINCS : 204-393-1, Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Sinergiste de mousse : Améliore la qualité de la mousse produite en augmentant une ou plusieurs des propriétés suivantes: volume, texture et / ou stabilité. 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
L-ARGININE
L-arginine, naturally found in various dietary sources like red meat, poultry, fish, and dairy, plays a crucial role in protein synthesis and is converted into nitric oxide in the body, aiding in blood vessel dilation and circulation.
While L-arginine supplementation is popular for conditions like high blood pressure and erectile dysfunction, its effectiveness varies, with some studies suggesting benefits for exercise performance through enhanced nitric oxide production, particularly in certain athletic populations.
However, despite its potential benefits, it's important to note that L-arginine supplementation may not always be necessary, as adequate levels can typically be obtained through a balanced diet rich in protein, with supplements being more relevant in cases of deficiency or specific medical conditions.

CAS number: 74-79-3
EC number: 230-571-3
Chemical Formula: C6H14N4O2
Molar Mass: 174.204 g·mol−1

Synonyms: NCGC00024715-02, NCGC00024715-03, NCGC00024715-04, NCGC00024715-05, NCGC00024715-10, NCGC00260762-01, 25212-18-4, 4455-52-1, AK-81231, AS-14190, K277, L-Arginine, BioUltra, >=99.5% (NT), SBI-0207062.P001, AB0014136, A0526, A7079, EU-0100077, L-Arginine, SAJ special grade, >=98.0%, A 5006, C00062, D02982, L-Arginine, Vetec(TM) reagent grade, >=98%, M02981, Y-8965, 14932-EP2316830A2, AB00374192_03, Norvaline, 5-[(aminoiminomethyl)amino]-, (L)-, L-arginine, arginine, 74-79-3, L-(+)-Arginine, L(+)-Arginine, L-Arg, H-Arg-OH, (S)-2-Amino-5-guanidinopentanoic acid, (L)-Arginine, Arginina, ARGININE, L-, Arginine (VAN), L-Arginin, Argininum, Arginina, L-Ornithine, N5-(aminoiminomethyl)-, Argamine, Argivene, Detoxargin, Levargin, L-alpha-Amino-delta-guanidinovaleric acid, Minophagen A, 1-Amino-4-guanidovaleric acid, CCRIS 3609, NSC 206269, arg, HSDB 1429, AI3-24165, UNII-94ZLA3W45F, MFCD00002635, (S)-2-Amino-5-guanidinovaleric acid, BRN 1725413, CHEBI:16467, (S)-2-Amino-5-((aminoiminomethyl)amino)pentanoic acid, L-Norvaline, 5-((aminoiminomethyl)amino)-, (S)-(+)-arginine, L-Arginine, monohydrochloride, 2-amino-5-guanidinovaleric acid, CHEMBL1485, (2S)-2-amino-5-guanidinopentanoic acid, (S)-2-Amino-5-[(aminoiminomethyl)amino]pentanoic acid, 94ZLA3W45F, Pentanoic acid, 2-amino-5-((aminoiminomethyl)amino)-, (S)-, (2S)-2-amino-5-(carbamimidamido)pentanoic acid, L-2-Amino-5-guanidinopentanoic acid, Arginine (L-Arginine), R-Gene, L-Norvaline, 5-[(aminoiminomethyl)amino]-, (2S)-2-amino-5-carbamimidamidopentanoic acid, DSSTox_CID_21056, DSSTox_RID_79618, Poly(L-arginine), DSSTox_GSID_41056, L(+)-Arginine, 98+%, BDBM181132, HMS3260O15, N5-(aminoiminomethyl)-L-Ornithine, HY-N0455, ZINC1532525, L-Arginine, Vetec(TM), 98.5%, Tox21_113046, Tox21_500077, AC-083, ANW-36527, L-alpha-Amino-delta-guanidinovalerate, L-Arginine, reagent grade, >=98%, s5634, AKOS006239069, AKOS015854096, Tox21_113046_1, AM81500, CCG-204172, DB00125, LP00077, MCULE-5108123240, SDCCGSBI-0050065.P002, L-Arginine, 99%, natural, FCC, FG, (s)-2-amino-5-guanidino-pentanoic acid, 5-[(aminoiminomethyl)amino]-L-Norvaline, NCGC00015064-01, NCGC00024715-01, 002A635, A837397, Q173670, SR-01000075479, SR-01000597671, (S)-2-amino-5-[(aminoiminomethyl)amino]-Pentanoate, (S)-2-Amino-5-[(aminoiminomethyl)amino]pentanoate, SR-01000075479-1, SR-01000597671-1, W-104410, (S)-2-amino-5-[(aminoiminomethyl)amino]-Pentanoic acid, Arginine, European Pharmacopoeia (EP) Reference Standard, (2S)-2-amino-5-[(diaminomethylidene)amino]pentanoic acid, 7F15B0C7-356D-45D7-AC33-03AEE4394A0E, S-(+)-2-Amino-5-[(aminoiminomethyl)amino]pentanoic acid, UNII-0O72R8RF8A component ODKSFYDXXFIFQN-BYPYZUCNSA-N, UNII-FL26NTK3EP component ODKSFYDXXFIFQN-BYPYZUCNSA-N, L-Arginine, United States Pharmacopeia (USP) Reference Standard, L-Arginine, Pharmaceutical Secondary Standard; Certified Reference Material, L-, L-Arginine, from non-animal source, meets EP, USP testing specifications, suitable for cell culture, 98.5-101.0%, L-Arginine, PharmaGrade, Ajinomoto, EP, USP, manufactured under appropriate GMP controls for Pharma or Biopharmaceutical production, suitable for cell culture

L-arginine is an amino acid naturally found in red meat, poultry, fish, and dairy.
L-arginine is necessary for making proteins and is commonly used for circulation.
L-arginine is converted in the body into a chemical called nitric oxide.

Nitric oxide causes blood vessels to open wider for improved blood flow.
L-arginine also stimulates the release of growth hormone, insulin, and other substances in the body.

L-arginine can be made in a lab and used in supplements.
People use L-arginine for chest pain and various blow flow issues, erectile dysfunction, high blood pressure during pregnancy, and a serious disease in premature infants called necrotizing enterocolitis (NEC).

L-arginine's also used for many other conditions, but there is no good scientific evidence to support these other uses.
L-arginine is an amino acid that helps the body make proteins.

L-arginine can be obtained naturally in the diet and is also found in dietary supplement form.
Foods rich in L-arginine include plant and animal proteins, such as dairy products, meat, poultry, fish, and nuts.

In addition to building protein, L-arginine releases nitric oxide in the blood.
Nitric oxide acts to widen blood vessels in the blood stream, which may help aid certain circulatory conditions.

A person’s body naturally produces L-arginine under normal circumstances.
People also get additional L-arginine as part of their regular diet.
Red meats, fish, dairy, and eggs all contain low amounts of L-arginine that help the body to replenish L-arginines necessary resources.

Arginine, also known as l-arginine (symbol Arg or R), is an α-amino acid that is used in the biosynthesis of proteins.
L-arginine contains an α-amino group, an α-carboxylic acid group, and a side chain consisting of a 3-carbon aliphatic straight chain ending in a guanidino group.

At physiological pH, the carboxylic acid is deprotonated (−COO−), the amino group is protonated (−NH3+), and the guanidino group is also protonated to give the guanidinium form (-C-(NH2)2+), making arginine a charged, aliphatic amino acid.
L-arginine is the precursor for the biosynthesis of nitric oxide.

L-arginine is encoded by the codons CGU, CGC, CGA, CGG, AGA, and AGG.
Arginine is classified as a semiessential or conditionally essential amino acid, depending on the developmental stage and health status of the individual.

Preterm infants are unable to synthesize or create arginine internally, making the amino acid nutritionally essential for them.
Most healthy people do not need to supplement with arginine because L-arginine is a component of all protein-containing foods and can be synthesized in the body from glutamine via citrulline.

Occasionally, a person’s need for L-arginine may exceed the body’s ability to produce or consume L-arginine naturally.
This is often true for older adults or people with certain medical conditions.

In these cases, people may be prescribed artificial L-arginine in the form of oral medication, injections, or creams.
Several potential health conditions may benefit from an increased intake of L-arginine.

L-arginine is an amino acid.
Amino acids are the building blocks of proteins and divided into essential and nonessential categories.

Nonessential amino acids are made in the body, but essential amino acids are not.
As such, they must be provided through dietary intake.

L-arginine is considered semi-essential or conditionally essential, meaning that L-arginine becomes essential under certain circumstances and conditions, including pregnancy, infancy, critical illness, and trauma.
L-arginine’s necessary for the production of nitric oxide, a signaling molecule that’s needed for a variety of bodily processes and functions, including blood flow regulation, mitochondrial function, and cellular communication.

Additionally, L-arginine acts as a precursor to other amino acids, including glutamate, proline, and creatine, and is essential for the health and functioning of your immune system.
Arginine is necessary for the development of T-cells, which are white blood cells that play central roles in immune response.

Because L-arginine has so many critical roles in your body, a deficiency in this amino acid can disrupt cellular and organ function and lead to serious adverse health outcomes.
L-arginine is produced in several ways.
L-arginine can be synthesized from the amino acid citrulline through the breakdown of body proteins, or L-arginine can be obtained through dietary protein intake.

L-arginine’s concentrated in certain protein-rich foods, including meat, poultry, dairy, nuts, soy products, and fish.
The average daily intake of L-arginine from foods is reported to be 4–6 grams.

For reference, research shows that a typical Western diet provides between 25–30% of total arginine present in the body.
Additionally, L-arginine can be obtained by taking supplements.

L-arginine supplements are widely available and can be found in powder, liquid, capsule, and tablet form at grocery stores, supplement stores, and online.
This article mainly focuses on the benefits and uses of L-arginine supplements.

L-arginine is an amino acid that helps make proteins.
L-arginine also becomes the gas nitric oxide (NO) in the body.

NO is important for erectile function because L-arginine helps blood vessels relax, so more oxygen-rich blood can circulate through your arteries.
Healthy blood flow to the arteries of the penis is essential for normal erectile function.

L-Arginine is an amino acid critical to the production of nitric oxide (NO) in the body.
NO helps regulate and improve blood circulation.

L-Arginine cannot be made in the body, but must obtained through food or supplementation.
Kyowa Quality L-Arginine is an pure, allergen-free ingredient that has been manufactured to the highest quality standards.

Eggs, meats, milk, soy proteins, peanuts, and walnuts are all sources of arginine.
The physiologically active form, L-arginine, is obtained by breaking down proteins.

Arginine also may be synthesized in the laboratory.
Because L-arginine may be synthesized in the body, L-arginine is classified as a nonessential amino acid in adults.
However, in children and in people with certain conditions (eg, infection, trauma), L-arginine synthesis may become compromised and then may be considered semi-essential.

Natural ways to get enough L-arginine:
A major benefit of obtaining L-arginine through diet is that L-arginine is difficult to get too much.
Therefore, some of the side effects of consuming too much L-arginine can be avoided.

On the other hand, food consumption alone may not provide enough L-arginine to meet a person’s needs.
A person should discuss their options with their doctor prior to changing their diet.

The best natural source for L-arginine is food high in protein.
For some people, animal proteins, such as red meat (beef), chicken and turkey breast, pork loin, and dairy products, may be the primary source of L-arginine.

For people who do not eat meat, plant-based proteins that contain L-arginine include lentils, chickpeas, peanuts, pumpkin seeds, and soybeans.
People who find they have a deficient amount of L-arginine to meet their needs may want to modify their diet to include foods rich in protein.
A dietician or doctor may be able to make meal plan suggestions to boost natural intake of L-arginine prior to taking supplements.

Uses of L-arginine:
L-arginine supplements are taken by many populations, including athletes and those who have certain medical conditions like high blood pressure, for a variety of reasons.
They’re also used in the clinical setting to treat critically ill people or those with wounds.

Research has shown that L-arginine may offer a variety of potential benefits when used as a supplement.
However, results are mixed, and L-arginine may not be as effective for some conditions as many supplement companies claim.

Athletic performance enhancement:
Limited evidence suggests that L-arginine supplements may enhance exercise performance by increasing nitric oxide in the body, which improves blood flow and oxygenation to muscles.
For example, a 2017 randomized study in 56 male soccer players found that treatment with 2 grams of L-arginine daily for 45 days significantly increased sport performance, compared with a placebo group.

Another small study in 9 men demonstrated that those who drank a beverage containing 6 grams of L-arginine 1 hour before intense exercise had significantly increased blood levels of nitric oxide and were able to exercise longer, compared with a placebo group.
However, most studies investigating this relationship have found that L-arginine is not beneficial for improving athletic performance.
L-citrulline, a precursor to L-arginine that’s discussed later in this article, may be a better choice for boosting athletic performance.

Blood pressure regulation:
L-arginine supplements may benefit those with high blood pressure.
Studies have shown that taking L-arginine supplements may help lower both your systolic (the top number) and diastolic (the bottom number) blood pressure readings.

L-arginine is needed for the production of nitric oxide, which is necessary for the relaxation of the cells that make up blood vessels, as well as blood pressure regulation.
A 2016 review of 7 studies found that supplementing with L-arginine by both oral and intravenous (IV) administration significantly reduced systolic and diastolic blood pressure in adults with high blood pressure by up to 5.4 mm/Hg and 3.1 mm/Hg, respectively.

Management of critical illness:
Arginine becomes essential when your body is compromised due to conditions like infection and trauma, and your arginine needs significantly increase due to physiologic demands.
Under these circumstances, your body can no longer fulfill your arginine needs, which must be met through external sources.

Arginine depletion during critical illness or after surgery leads to serious adverse effects, including impaired immune function and blood flow.
To avoid these potential complications, arginine supplements are used frequently in the clinical setting to treat a variety of conditions.
For example, oral or IV arginine is commonly used to treat serious infections like necrotizing enterocolitis in infants, cases of sepsis, burns, chronic disease, and wounds, as well as in pre- and post-surgical and trauma patients.

Blood sugar regulation:
Research shows that L-arginine may benefit those with diabetes by improving glucose metabolism and insulin sensitivity.
L-arginine is needed for the production of nitric oxide.

Nitric oxide plays important roles in cellular function and how your body responds to insulin, a hormone that shuttles blood sugar from your blood into cells, where L-arginine’s used for energy.
Therefore, increasing nitric oxide availability may help enhance the function of cells that secrete insulin and help your body use blood sugar more efficiently.

Some research has shown that long-term treatment with L-arginine supplements may prevent diabetes in at-risk populations.
A study in 144 people with impaired blood sugar regulation found that treatment with 6.4 grams of L-arginine per day for 18 months reduced the chances of diabetes development over a 90-month period, compared with a placebo group.

Traditional/Ethnobotanical uses of L-arginine:
L-arginine is a nonessential amino acid that may play an important role in the treatment of heart disease due to L-arginines block arterial plaque buildup, blood clots, platelet clumping, and to increase blood flow through the coronary artery.
L-arginine is commonly sold as a health supplement claiming to improve vascular health and treat erectile dysfunction in men.

L-arginine, which is promoted as a human growth stimulant, has also been used in bodybuilding.
In the 1800s, L-arginine was first isolated from animal horn.

Use in specific populations of L-arginine:
The safety of L-arginine has been demonstrated in many populations, including pregnant women and older adults.
However, some people, including those with conditions that affect the liver or kidneys, should avoid L-arginine.

L-arginine supplements are sometimes used in children in the clinical setting and deemed safe when prescribed in appropriate doses.
Yet, arginine supplementation in children should always be monitored by a healthcare provider.

L-arginine’s not recommended to give your child L-arginine unless L-arginine’s medically necessary and was suggested by a healthcare provider.
This advice is extremely important to follow, as giving a child too high a dose of L-arginine may result in serious side effects and can even be fata.

Alternatives of L-arginine:
After consumption, your gut and liver rapidly metabolize L-arginine before L-arginine has the chance to reach systemic circulation.
For this reason, some argue that L-citrulline, a precursor to L-arginine, may be a better choice for increasing arginine levels.

L-citrulline is an amino acid that may be used as an alternative to L-arginine when taken as a supplement.
L-citrulline is a nonessential amino acid that’s a precursor to L-arginine.

L-citrulline is converted into L-arginine through a series of enzymatic reactions that take place primarily in your kidneys.
Research shows that L-citrulline supplements can raise body levels of L-arginine.

In fact, some studies show that L-citrulline is more effective at increasing arginine levels than L-arginine supplements.
Research has likewise shown that L-citrulline supplements may offer benefits similar to those of L-arginine supplements.

For example, similarly to L-arginine, L-citrulline has been shown to help reduce blood pressure and improve erectile dysfunction in some studies.
Additionally, studies show that when L-citrulline used on L-arginines own or in combination with L-arginine, L-arginine may improve athletic performance and enhance muscle recovery in athletes.

Furthermore, some of these studies found that citrulline supplements may be more effective than L-arginine supplements at enhancing athletic performance.
Therefore, athletes may benefit more from L-citrulline or a combination of L-arginine and L-citrulline over L-arginine alone.

Benefits of L-arginine:
L-arginine has two effects: L-arginine turns into nitric oxide and helps the body build protein.
These effects give L-arginine an array of potential benefits that range from heart health and chest pain to helping to build muscles, repair wounds, and improve male fertility.
Although there are many claims about the benefits of L-Arginine, not all of them are supported by scientific research studies.

The following are some examples of researched benefits and uses of L-arginine:
Growth hormone reserve test,
Reducing high blood pressure,
Correcting inborn errors of urea synthesis,
Treating heart disease,
Treating erectile dysfunction (ED),
Easing inflammation of the digestive tract in premature infants,
Controlling blood sugar in people with diabetes.

Additionally, L-arginine may have the potential to help with many other issues.

However, more research needs to be done to evaluate further L-arginine’s potential to do the following:
Improve blood flow,
Heal wounds faster,
Alleviate anxiety,
Treat burns,
Improve kidney function for people with congestive heart failure,
Enhance exercise performance.

L-arginine also helps rid the body of ammonia (a waste product) and stimulates the release of insulin.
In addition, your body uses arginine to make nitric oxide (a compound that relaxes the blood vessels).
Although some studies suggest that L-arginine may benefit certain health conditions, other research shows that L-arginine may have harmful effects on some individuals.

Health Benefits of L-arginine:
By improving blood flow in the body, some proponents claim that L-arginine may help heart conditions, such as chest pain (angina), high blood pressure, leg cramping and weakness due to obstructed arteries (a condition known as intermittent claudication), and erectile dysfunction (ED).
Some people use L-arginine to boost the immune system, improve athletic performance, shorten recovery time after surgery, and promote weight loss.
L-arginine is also used for bodybuilding.

There are several additional areas that researchers are interested in exploring regarding L-arginine and L-arginines effects on the human body.
L-arginine is essential for anyone interested in taking L-arginine as a supplement to talk to their doctor about the potential benefits and risks before starting to use L-arginine.
Also, people should fully understand and examine the claims a manufacturer is making about their product before using L-arginine.

Other potential benefits of L-arginine:
In addition to the potential benefits listed above, some research suggests that L-arginine supplements may be helpful when used in the following ways:
Treatment of erectile dysfunction.
A 2019 review of 10 studies found that taking arginine supplements in doses ranging from 1.5–5 grams daily significantly improved erectile dysfunction, compared with a placebo or no treatment.
Improving blood flow.

Some evidence suggests L-arginine supplements may improve blood vessel function and blood flow in specific populations.
However, study results are conflicting, and many have found that L-arginine has no benefit.

Treating and preventing preeclampsia.
Studies have demonstrated that treatment with L-arginine during pregnancy may help prevent and treat preeclampsia, a dangerous condition characterized by high blood pressure and protein in the urine.
This list is not exhaustive, and L-arginine has been studied for L-arginines potential beneficial effects on various conditions, including obesity, heart disease, cancer, polycystic ovary syndrome (PCOS), infertility, and anxiety, either used on L-arginines own or in combination with other supplements.

However, research on the effects of L-arginine in people with these and many other conditions is limited and inconclusive, highlighting the need for future studies.
In addition to the potential benefits and uses above, many people take L-arginine supplements for a variety of other reasons, including reducing the risk of the common cold and boosting weight loss.
Yet, many of these purported benefits aren’t backed by scientific research.

Some people take L-arginine as a supplement.
As with any supplement, a person should use L-arginine with caution.

Although L-arginine is considered safe in moderate doses, too much L-arginine can have severe side effects, including death.
L-arginine is important to understand how the supplement may interact with the body and with additional medications before taking L-arginine.

Overdose of L-arginine:
As mentioned above, arginine is generally considered safe, even when used in high doses.
However, L-arginine’s possible to take too much arginine, which is especially dangerous for children.

Pregnancy and breastfeeding of L-arginine:
L-arginine is used in pregnancy under certain circumstances, including preeclampsia.
L-arginine supplementation during pregnancy is typically prescribed and monitored by a healthcare provider for a specific reason, such as preeclampsia or the risk of preeclampsia and intrauterine growth restriction (IUGR).

There’s some evidence that L-arginine supplements may improve pregnancy outcomes, as well as fetal and maternal health in women from both high- and low-resource areas.
This is because during pregnancy, the body’s need for L-arginine grows due to fetal development and placental growth.

This increased need may not be met through diet, especially in women living in low-resource settings without access to protein-rich foods.
Additionally, although the increased demand for arginine during pregnancy can be provided through diet, protein or individual amino acid supplements may be necessary under certain circumstances.

This may include women who follow restrictive diets or are experiencing severe nausea and vomiting during pregnancy, rendering them unable to meet demands through dietary intake.
However, supplements during pregnancy should always be approved and monitored by a healthcare provider.

If you are pregnant and interested in taking supplemental L-arginine, consult your healthcare provider for advice.
L-arginine supplements have not been researched in breastfeeding women.
For this reason, L-arginine’s important to ask your healthcare provider whether taking L-arginine supplements is safe and necessary for your individual needs during breastfeeding.

History of L-arginine:
Arginine was first isolated in 1886 from yellow lupin seedlings by the German chemist Ernst Schulze and his assistant Ernst Steiger.
He named L-arginine from the Greek árgyros (ἄργυρος) meaning "silver" due to the silver-white appearance of arginine nitrate crystals.

In 1897, Schulze and Ernst Winterstein (1865–1949) determined the structure of arginine.
Schulze and Winterstein synthesized arginine from ornithine and cyanamide in 1899, but some doubts about arginine's structure lingered until Sørensen's synthesis of 1910.

Properties of L-arginine:
Chemical formula: C6H14N4O2
Molar mass: 174.204 g·mol−1
Appearance: White crystals
Odor: Odourless
Melting point: 260 °C; 500 °F; 533 K
Boiling point: 368 °C (694 °F; 641 K)
Solubility in water: 14.87 g/100 mL (20 °C)
Solubility: slightly soluble in ethanol
insoluble in ethyl ether
log P: −1.652
Acidity (pKa): 2.18 (carboxyl), 9.09 (amino), 13.2 (guanidino)
LAROFLEX MP 45
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.
L-Aspartic Acid
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
LAURAMIDE DEA
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
LAURAMIDOPROPYL BETAINE
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
LAURAMIDOPROPYLAMINE OXIDE ( LAUROYLAMINOPROPYLDIMETHYLAMINE OXIDE)
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
LAURAMINE OXIDE ( Lauryldimethylamine oxide ) Oxyde de lauryldiméthylamine
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
Lauramide
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
Lauramine oxide
SYNONYMS n-Dodecylamine; 1-Dodecanamine; Lauramine; 1-Aminododecane; Laurinamine;CAS NO. 124-22-1
LAURDIMONIUM HYDROXYPROPYL HYDROLYZED WHEAT
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
LAURETH-1 ( Éther de lauryl poly(oxyéthylène))
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
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-10 CARBOXYLIC ACID
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
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




LAURETH-11 CARBOXYLIC ACID
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-12
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-15
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
LAURETH-16
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
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
LAURETH-2 BENZOATE
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-2 PHOSPHATE
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-20
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-21
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
LAURETH-23
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, 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-3
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-30
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
LAURETH-4
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-5
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-50
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-6
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
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
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
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



LAURETH-7 CITRATE
Poly(oxy-1,2-ethanediyl), .alpha.-hydro-.omega.-dodecyloxy-, dihydrogen citrate cas no: 161756-30-5
LAURETH-8
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
LAURETH-9
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
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)



LAURIC ACID %98
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;
LAURIC ACID ( C12 Acide Laurique)
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)
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 (DODECANOIC ACID)

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 (EDENOR C1299)
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%
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
LAURIC ACID METHYLESTER 98%
cas no 111-82-0 dodecanoic acid, methyl ester; Methyl dodecanoate; Methyl laurate; NSC 5027; Methyl dodecanoate; Methyl dodecylate;
LAURIK ASIT 
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
Lauric acid (Acide laurique)
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)
LAUROSTEARIC ACID
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
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


Lauroyl lactylate de sodium
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
LAUROYL SARCOSINE ( Lauroylsarcosinate de sodium )
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
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
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%
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)
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 aldehyde
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
LAURYL AMINE OXIDE
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
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 AMINOPROPYLGLYCINE
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
LAURYL BETAINE
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