(12) Patent Application Publication (10) Pub. No.: US 2010/0212214 A1 WU Et Al

Total Page:16

File Type:pdf, Size:1020Kb

(12) Patent Application Publication (10) Pub. No.: US 2010/0212214 A1 WU Et Al US 2010O212214A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2010/0212214 A1 WU et al. (43) Pub. Date: Aug. 26, 2010 (54) CANDLE COMPOSITION (30) Foreign Application Priority Data (75) Inventors: Boneng WU, Toronto (CA); Dennis Feb. 25, 2009 (CA) ...................................... 2655367 Kwok Wai YUNG, Mississauga Publication Classification (CA) (51) Int. Cl. CIIC5/00 (2006.01) Correspondence Address: B29C 39/00 (2006.01) YER iwiREET (52) U.S. Cl. ........................................... 44/275; 264/299 MEDINA, OH 44256 (US) (57) ABSTRACT A candle composition having fatty alcohol and vegetable (73) Assignee: PREMIER CANDLE CORP, based wax. A candle composition having fatty alcohol and Mississauga (CA) vegetable-based wax, and wherein the fatty alcohol com prises 0.5% to 99.5% by mass. A process for making a candle composition is also provided, the process comprising mixing (21) Appl. No.: 12/711,350 together a fatty alcohol and a vegetable-based wax, heating the mixture to a temperature of 70-80° C., pouring into a (22) Filed: Feb. 24, 2010 container or mould, and cooling the mixture. US 2010/0212214 A1 Aug. 26, 2010 CANDLE COMPOSITION stearic acid (from soy oil or animal fat). Cetyl alcohol (49°C. melting point, 180° C. boiling point, and 160° C. open cup FIELD OF THE INVENTION flash point) and stearyl alcohol (61° C. melting point, 210°C. 0001. This invention relates to candle compositions. In boiling point and 200° C. open cup flash point) are preferred particular, this invention relates to candle compositions com fatty alcohols for the purposes of the present embodiments. prising fatty alcohol and a process for making a candle com However, any of the following fatty alcohols and mixtures of positions comprising fatty alcohol. the following fatty alcohols may also be used: BACKGROUND OF THE INVENTION 0002 Candles have been used for centuries as a source of Common Molecular light and for their aesthetic appeal. Paraffin wax has been l8le UPAC name formula traditionally used in making candles, which conventionally Capryl -octanol C-8 fatty CH(CH),OH comprises 80 to 100% paraffin wax. Paraffin wax is also a 8COO 8COO Capric -decanol C-10 fatty CH(CH2)3OH petroleum by-product and is known to produce toxins, black 8COO 8COO Soot and carcinogens. While beeswax may also be used as Lauryl -dodecanol C-12 fatty CH(CH), OH candle wax, some users may not find beeswax desirable due to 8COO 8COO its poor burn performance. Moreover, although beeswax is Myristic -tetradecanol C-14 fatty CH(CH2)3OH 8COO 8COO considered a renewable wax, it is very expensive and there Cetyl -hexadecanol C-16 fatty CH(CH2)5OH fore not profitable for large-scale candle applications. It 8COO 8COO would therefore be advantageous to eliminate or reduce the Stearyl -octadecanol C-18 fatty CH(CH2),OH paraffin wax and beeswax used in candles in favour of alter 8COO 8COO Arachidyl -eicosanol C-20 fatty CH3(CH2)9COH native Substances, such vegetable derived materials and 8COO 8COO ingredients. Behenyl -docosanol C-22 fatty CH(CH2)2OH 0003. There is currently a need for a renewable candle wax 8COO 8COO composition that is natural and environmental-friendly. In Lignoceryl -tetracosanol C-24 fatty CH3(CH2)2OH 8COO 8COO particular, it would be advantageous to have a candle wax Ceryl -hexacosanol C-26 fatty CH3(CH2)5OH composition that uses renewable ingredients and therefore is 8COO 8COO also biodegradable. Montanyl -octacosanol C-28 fatty CH(CH2)2,OH 0004 Some manufacturers in the candle industry have 8COO 8COO Myricyl -triacontanol C-30 fatty CH3(CH2)2OH started using triglycerides and fatty acids as the main ingre 8COO 8COO dients of wax for candle production. However there are sev Geddy -tetratriacontanol C-34 fatty CH3(CH2)3OH eral disadvantages of Such renewable candle compositions, 8COO 8COO Such as: undesirable blooming/frosting due to crystallization of triglycerides and fatty acids during the phase changing from liquid to solid; pits, bubbles and/or holes in the candle 0010. Different kinds of fatty alcohols may be mixed to composition; and poor burn performance and low wax con obtain an amorphous, semi-transparent candle composition Sumption. with a strong structure. A single fatty alcohol tends to crys 0005. It is therefore advantageous to have an improved tallize more than a mixture of two or more fatty alcohols, and candle composition that is more environmental-friendly than therefore mixtures of fatty alcohols are preferred to form an previous compositions, and overcomes disadvantages associ amorphous Substance with a stronger structure. ated with previous compositions. 0011 Candle compositions comprised of triglycerides and fatty acid (and without fatty alcohol) tend to crystallize very easily. This crystallization is primarily due to the simi DETAILED DESCRIPTION OF THE PREFERRED larity of molecule structure and polarity of the triglyceride EMBODIMENTS and fatty acid. Crystallization causes pits, bubbles and/or 0006. In the embodiments described below, there is pro holes in the candle composition during production processing vided a renewable candle composition that may be considered and results in a significantly longer and slower cooling pro eco-friendly. cess (to avoid blooming and cracking) in production. This 0007 According to one embodiment, there is a provided a results in the following problems during the production pro candle composition comprising fatty alcohol. According to cess: high labour cost and high energy consumption due to the another embodiment, there is provided a candle composition longer and slower production; loss of fragrance during the comprising fatty alcohol and vegetable-based wax. long, slow and hot production process; a high scrap rate; a low 0008 Fatty alcohols are natural ingredients from plant production rate; and changes in colour and/or oxidation of the based or animal-based materials and thus are used as an wax due to the high temperatures during the longer produc ingredient for all-natural, renewable wax candles. tion process. In addition, the crystallization of the fatty acid 0009 Examples of fatty alcohol include plant-based fatty and triglycerides during the congealing step in the production alcohol. Such as jojoba alcohol, which is a mixture of free process causes tension build-up within the candle. As a result, fatty alcohols of between 16 and 24 carbon atoms (derived the candle becomes brittle and unstable when exposed to low from jojoba oil), and animal-based fatty alcohol. Fatty alco temperature. hols can also be made from fatty acid by the process of 0012. The crystallization that occurs in the triglyceride catalytic hydrogenation to meet the need for large-scale and fatty acid candle also causes significant bubbling when industrial applications. Cetyl alcohol (palmitic alcohol) and the candle is burned. The bubbling causes lots of cheese-like stearyl alcohol are the most widely-used fatty alcohols due to holes on the candle surface and thereby results in a candle the industrial abundance of palmitic acid (from palm oil) and having an unfavourable appearance. In addition, the triglyc US 2010/0212214 A1 Aug. 26, 2010 eride and fatty acid renewable candles usually have a poor acids, non-hydrogenated lipids and any mixtures thereof. The burn performance and low wax consumption rate due to the triglycerides can be solid form triglycerides and/or semi-solid higher boiling point and flash point of the triglyceride and form triglycerides. fatty acid. Vegetable waxes blended with paraffin can improve 0019. Examples of suitable triglycerides include, without the overall burn quality since paraffin contains alkane por limitation, fully hydrogenated vegetable oil, partially hydro tions of low flash point (about 100° C. lower than the flash genated vegetable oil, non-hydrogenated vegetable oil, and point of triglyceride-based fuel), however the introduction of animal fat/lipid. Examples of mono-triglycerides include, paraffin is contrary to the concept of a renewable, all-natural without limitation, glyceryl moonoleate, glyceryl monolau candle. Alternatively, triglycerides-based fuel can be chemi rate, and glyceryl monostearate. Examples of di-glycerdies cally modified to improve burn performance by the process of include, without limitation, glyceryl dioleate, glyceryl dilau transesterification, which results in a biodiesel product. How rate and glyceryl distearate. ever chemical modification consumes energy and produces 0020. The fatty acids can be lauric acid, myristic acid, wastes and thus is also contrary to the concept of a renewable, palmitic acid, Stearic acid, oleic acid, linoleic acid or any eco-friendly product. mixtures thereof. A person skilled in the art would understand 0013 Fatty alcohols are amphiphatic in nature (i.e. pos the types of vegetable-based waxes and fatty acids that could sess hydrophilic and hydrophobic properties) and thus func be used in the present embodiments. tion as non-ionic Surfactants and thereby are Suitable emulsi 0021. According to another embodiment, a candle com fiers in lipid-based environments, such as a vegetable wax. position is provided having 55-100% by mass fatty alcohol 0014 Fatty alcohol inhibits the crystallization of triglyc and the remainder non-hydrogenated vegetable lipid. For the eride and fatty acid in a candle composition and thereby purposes of the present embodiments, acceptable non-hydro prevents the sharp phase change (ie. from liquid to solid) genated vegetable lipids may include, without limitation, during the congealing process of the wax composition and Soybean oil, Sunflower oil, safflower oil, grape seed oil, corn therefore results in a lower likelihood of crystallization, a oil, palm oil, olive oil, cotton seed oil, canola oil, coconut oil, lower likelihood oftension build-up within the wax and there jojoba oil, and any mixture thereof. fore less cracking. As a result, there is less blooming and 0022. According to a further embodiment, there is pro frosting during the candle manufacturing process, and less vided a process for making a candle composition.
Recommended publications
  • ( 12 ) United States Patent ( 10 ) Patent No .: US 10,751,310 B2 Freeman Et Al
    US010751310B2 ( 12 ) United States Patent ( 10 ) Patent No .: US 10,751,310 B2 Freeman et al . ( 45 ) Date of Patent : Aug. 25 , 2020 ( 54 ) PREVENTION , TREATMENT AND ( 56 ) References Cited REVERSAL OF DISEASE USING THERAPEUTICALLY EFFECTIVE U.S. PATENT DOCUMENTS AMOUNTS OF DICARBOXYLIC ACID 3,527,789 A 9/1970 Payne COMPOUNDS 4,166,913 A 9/1979 Kesling , Jr. et al . 6,528,499 B1 * 3/2003 Kozikowski C07C 59/347 ( 71 ) Applicant: UNIVERSITY OF 514/574 8,324,277 B2 12/2012 Freeman PITTSBURGH — OF THE 8,735,449 B2 5/2014 Freeman COMMONWEALTH SYSTEM OF 9,066,902 B2 6/2015 Freeman et al . HIGHER EDUCATION , Pittsburgh , 9,186,408 B2 11/2015 Freeman et al . PA (US ) 9,700,534 B2 7/2017 Freeman et al . 9,750,725 B2 9/2017 Freeman et al . 10,213,417 B2 2/2019 Freeman et al . ( 72 ) Inventors : Bruce A. Freeman , Pittsburgh , PA 10,258,589 B2 4/2019 Freeman et al . ( US ) ; Francisco J. Schopfer , 2015/0018417 Al 1/2015 Freeman et al . Pittsburgh , PA ( US ) FOREIGN PATENT DOCUMENTS ( 73 ) Assignee : University of Pittsburgh — of the CN 103705499 4/2014 Commonwealth System of Higher DE 102011118462 5/2013 Education , Pittsburgh , PA ( US ) GB 1153464 5/1969 WO WO 2002/022627 3/2002 WO WO 2009/017802 2/2009 ( * ) Notice : Subject to any disclaimer , the term of this WO WO 2009/112455 9/2009 patent is extended or adjusted under 35 WO WO 2010/005521 1/2010 U.S.C. 154 ( b ) by 0 days . WO WO 2010/014889 2/2010 WO WO 2011/014261 2/2011 WO WO 2013/116753 8/2013 ( 21 ) Appl.
    [Show full text]
  • Organic Synthesis Using Clay and Clay-Supported Catalysts.Pdf
    Applied Clay Science 53 (2011) 106–138 Contents lists available at ScienceDirect Applied Clay Science journal homepage: www.elsevier.com/locate/clay Review Article Organic synthesis using clay and clay-supported catalysts Gopalpur Nagendrappa ⁎,1 Department of Chemistry, Bangalore University, Bangalore 560 001, India article info abstract Article history: Clays and modified clays are used to catalyze various types of organic reactions such as addition, Michael Received 20 May 2010 addition, carbene addition and insertion, hydrogenation, allylation, alkylation, acylation, pericyclic reactions, Received in revised form 17 October 2010 condensation reactions, aldol formation, imine synthesis, diazotization reactions, synthesis of heterocycles, Accepted 19 October 2010 esterification reactions, rearrangement/isomerization reactions, cyclization reactions, oxidation of alcohols, Available online 6 October 2010 dehydrogenation, epoxidation and several more. Clays function as Brønsted and/or Lewis acids, or as bases. Clays with combined acidic and basic properties have been developed by simple procedures of modification. Keywords: Clay mineral Such clays are employed to catalyze a sequence of acid and base-catalyzed reactions in one pot. Good Activated bentonite enantioselectivity and stereoselectivity are achieved using chiral organic compounds and chiral complexes Montmorillonite intercalated between clay layers. Examples from recent literature are described here. Saponite © 2010 Elsevier B.V. All rights reserved. Organic synthesis Heterogeneous catalyst 1. Introduction compatibility and cheapness, much effort is expended in discovering newer methods of using clays in their native and modified forms as Clays are widespread, easily available and low-cost chemical catalysts for diverse organic reactions. substances. Both in their native state and in numerous modified Clays have a long history of use as catalysts and as supports in organic forms, clays are versatile materials that catalyze a variety of chemical reactions (Vogels et al., 2005).
    [Show full text]
  • Literature Digest, March 2018
    Joseph Samec Research Group Digest Digest March 2018 Joseph Samec Research Group Digest Silver(I)‐Catalyzed Widely Applicable Aerobic 1,2‐Diol Oxidative Cleavage Dr. Zhong‐zhen Zhou Dr. Mingxin Liu Dr. Leiyang Lv Prof. Dr. Chao‐Jun Li Angew. Chem. Int. Ed. 2018, 57(10), 2616-2620 Abstract The oxidative cleavage of 1,2‐diols is a fundamental organic transformation. The stoichiometric oxidants that are still predominantly used for such oxidative cleavage, such as H5IO6 , Pb(OAc)4 , and KMnO4 , generate stoichiometric hazardous waste. Herein, we describe a widely applicable and highly selective silver(I)‐catalyzed oxidative cleavage of 1,2‐diols that consumes atmospheric oxygen as the sole oxidant, thus serving as a potentially greener alternative to the classical transformations. Solvent‐Free Enzyme Activity: Quick, High‐Yielding Mechanoenzymatic Hydrolysis of Cellulose into Glucose Dr. Fabien Hammerer Dr. Leigh Loots Jean‐Louis Do J. P. Daniel Therien Christopher W. Nickels Prof. Tomislav Friščić Prof. Dr. Karine Auclair Angew. Chem. Int. Ed. 2018, 57(10), 2621-2624 Abstract Mechanochemistry enables enzymatic cleavage of cellulose into glucose without bulk solvents, acids, other aggressive reagents, or substrate pre‐treatment. This clean mechanoenzymatic process (coined RAging) is also directly applicable to biomass, avoids many limitations associated with the use of cellulases, and produces glucose concentrations greater than three times that obtained by conventional methods. Joseph Samec Research Group Digest Synergistic N‐Heterocyclic Carbene/Palladium‐Catalyzed Reactions of Aldehyde Acyl Anions with either Diarylmethyl or Allylic Carbonates Dr. Shigeo Yasuda Takuya Ishii Shunsuke Takemoto Hiroki Haruki Prof. Dr. Hirohisa Ohmiya Angew. Chem. Int. Ed.
    [Show full text]
  • UNITED STATES PATENT OFFICE 2,509,174 PROCESS of WATERPROOF NG TEXT LE Fabrics Milton J
    Patented May 23, 1950 2,509,174 UNITED STATES PATENT OFFICE 2,509,174 PROCESS OF WATERPROOF NG TEXT LE FABRICs Milton J. Scott and Stuart H. Rider, Springfield, Mass, assignors to Monsanto Chemical Com pany, St. Louis, Mo., a corporation of Dela No Drawing. Application May 22, 1947, Serial No. 49,880 10 Claims. (C. 117-161) This invention relates to waterproofing con melamine containing about 2 mols of stearyl al positions and to materials treated therewith. cohol per mol of hexamethylol melamine. More particularly, the invention relates to cer tain aminotriazine-aldehyde-alcohol reaction Ecample I products and to cellulosic and proteinaceous ma 314 parts of spray dried crystalline hexa terials treated therewith. methylol melamine of Example I were mixed An object of this invention is to prepare water with 320 parts (10 mols) of anhydrous methanol proofing compositions. and 0.5 part of ethyl phosphoric acid. The mix A further object is to prepare aqueous emul ture was refluxed for 30 minutes at atmospheric sions of aminotriazine-aldehyde-alcohol reaction O pressure and then 404 (1.5 mols) parts of stearyl products. alcohol were added and refluxing continued for Another object is to provide waterproof coat 30 minutes. The solution was concentrated by S. vacuum distillation at about 25 inches of mercury Still another object is to provide Waterproof until the temperature rose to about 130 C. The textiles. S resulting material was a methyl stearyl ether of These and other objects are attained by pre hexamethylol melamine containing about 1.5 paring a liquid reaction product of an amino mols of stearyl alcohol per mol of hexamethylol triazine, an aldehyde, and two alcohols one of melamine.
    [Show full text]
  • Synthesis of Guerbet Alcohols by Self and Cross Condensation Reactions of a Variety of Fatty Alcohols and Terpenes Over Ni/Cu Hydrotalcite-Derived Mixed Oxides W.Y
    Synthesis of Guerbet alcohols by self and cross condensation reactions of a variety of fatty alcohols and terpenes over Ni/Cu hydrotalcite-derived mixed oxides W.Y. Hernández a, K. De Vlieger b, P. Van Der Voort a, A. Verberckmoes b ([email protected]) aCenter for Ordered Materials, Organometallics & Catalysis (COMOC), Ghent University, Krijgslaan 281-S3, 9000 Ghent, Belgium. bIndustrial Catalysis and Adsorption Technology (INCAT), Ghent University, Valentin Vaerwyckweg 1, 9000 Ghent, Belgium. Introduction • Due to the growing importance of renewable feedstocks and use of heterogeneous catalysts the interest in hydrotalcite-derived mixed oxides to perform the Guerbet reaction increased. • The Compound Annual Growth Rate (CAGR) of Guerbet alcohols in 2016-2024 is 5.6%. • Ni/Cu hydrotalcite derived mixed oxides are employed as highly selective, stable and active catalysts in combination with KOH. • The Ni/Cu catalysts are tested in the self and cross condensation on a broad variety of starting alcohols. Hydrotalcite-derived mixed oxides Schematic representation Hydrotalcite-like Mixed Oxides Guerbet Reaction material CalcinationCalcination:: T = 500500°°°°CCCC 1. Dehydrogenation NiNiNi 0,80,80,8-0,8 ---xxxxCuCuCu xxxMgMgMg 5,25,25,2 AlAlAl 222OOO999 444.4. Hydrogenation - 2- e.g. Ni 0,72 Cu 0,08 Mg 5,2 Al 2(OH )16 [CO 3 xH 2O] Ni 0,72 Cu 0,08 Mg 5,2 Al 2O9 2+3. Aldol condensation Hydroxide layer Interlayer (Ni9Cu1HT) (+ dehydration) Materials Characterization Influence of composition Self condensation of 1-Octanol a) XRD patterns obtained for: (((b(bbb) H2-TPR profiles obtained for: Calcined mixed oxides Calcined mixed oxides Full lines: C16 Guerbet alcohol Cu(10) (A); Ni(2.5)Cu(7.5) (B); Ni(5.0)Cu(5.0) (C); Ni(7.5)Cu(2.5) (D); Ni(10) (E) Dashed lines: C16 other products Combining Cu & Ni leads to: Ni/Cu ratio plays significant role in reactivity and selectivity.
    [Show full text]
  • Basic Surface-Active Properties in the Homologous Series of Β-Alkyl (C 12H25/C18H37) Polyethyleneoxy (N = 0-20) Propionamides
    Riviş et al. Chemistry Central Journal 2013, 7:31 http://journal.chemistrycentral.com/content/7/1/31 RESEARCH ARTICLE Open Access Basic surface-active properties in the homologous series of β-alkyl (C12H25/C18H37) polyethyleneoxy (n = 0-20) propionamides Adrian Riviş, Gabriel Bujanca and Teodor Traşcă* Abstract Background: Heterogeneous β-Alkyl (C12H25/C18H37) polyethyleneoxy (n = 0-20) propionamides [R(EO)nPD] represent new “hybrid” nonionic-ionic colloidal structures in the field of surface-active products (technical products). These “niche” compounds have three structural and compositional characteristics that also define their basic colloidal properties: mixture of R and PEO chain homologues; specific conformations due to the PEO chains; and the presence of side products from the addition of higher alcohols, polyethyleneglycols and traces of water to acrylamide. The proposed major objective of this paper is the basic informative colloidal characterization (functional classification, HLB balance, surface tension, critical micelle concentration) in direct correlation with the structural changes in the homologous series of LM(EO)nPD and CS(EO)nPD. The structures were obtained either indirectly by cyanoethylation followed by partial acid hydrolysis of the corresponding β-propionitriles, or directly by the nucleophilic addition under alkaline catalysis of linear higher alcohols C12H25/C14H29 (7/3) (LM) and C16H33/C18H37 (CS) as such and heterogeneous polyethoxylated (n = 3-20) to acrylamide monomer, through an adapted classic reaction scheme.
    [Show full text]
  • Us 6372918 B1 Us. Patent Documents 1
    US006372918B1 (12) United States Patent (10) Patent No.: US 6,372,918 B1 Feustel et al. (45) Date of Patent: Apr. 16, 2002 (54) COMPOUND FOR INHIBITING CORROSION (74) Attorney, Agent, or Firm—Richard P. Silverman (75) Inventors: Michael Feustel, Kongernheim; Peter (57) ABSTRACT Klug, Grossostheim, both of (DE) (73) Assigneez Clariant GmbH, Frankfurt (DE) The invention relates to compounds of the formula 1 ( * ) Notice: Subject to any disclaimer, the term of this R1—O—(A—O)X—(CH2)y—R2 (1) patent is extended or adjusted under 35 U.S.C. 154(b) by 34 days. in which (21) App1_ No; 09/607,819 R1 is branched or straight-chain C4—C30-alkyl, C4—C3O (22) Filed: Jun_ 30’ 2000 alkenyl or C4—C3O-alkylaryl, (30) Foreign Application Priority Data A Is C2_C4'a1ky1ene’ Jul 2 1999 (DE) 199 30 683 X is an integer from 1 to 100, (51) Int. c1.7 .................. .. C07D 233/14; C07D 233/22; Y 15 1’ 2’ 3 or 4 and C07C 233/05; C09K 3/00; C23F 11/00 R2 is a radical selected from structures of the formulae 2 (52) US. Cl. .................. .. 548/349.1; 252/387; 252/390; and 3 252/392; 252/394; 548/350.1; 564/201 (58) Field of Search .................... .. 548/349.1; 564/201; _CO_NR3R4 (2) 502/387, 390, 392, 394 (56) References Cited (3) US. PATENT DOCUMENTS N 1 2,211,001 A * 8/1940 ChWala ................. .. 548/3501 N 2,267,965 A * 12/1941 ...... .. 548/3501 I RE23,227 E * 5/1950 Blair et al.
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 7417,165 B2
    USOO7417165B2 (12) UnitedO States Patent (10) Patent No.: US 7417,165 B2 Aronhime et al. (45) Date of Patent: Aug. 26, 2008 (54) CRYSTALLINE FORMS OF PREGABALIN WO WO 2006,136087 12/2006 WO WO 2008/004044 1, 2008 (75) Inventors: Judith Aronhime, Rehovot (IL); Sigalit WO WO 2008/OO7145 1, 2008 Levi, Modi'in (IL); Lilach Hedvati, WO WO 2008/OO9897 1, 2008 Doar Na Hefer (IL) (73) Assignee: Teva Pharmaceutical Industries Ltd., OTHER PUBLICATIONS Petah Tiqva (IL) Andruszkiewicz and Silverman, "A Convenient Synthesis of 3-Alkyl-4-Aminobutanoic Acids.” Synthesis, 953-955 (1989). (*) Notice: Subject to any disclaimer, the term of this Barnes et al., “Development of a Catalytic Enantioselective Conju patent is extended or adjusted under 35 gate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes for the U.S.C. 154(b) by 0 days. Synthesis of Endothelin-A Antagonist ABT-546. Scope, Mechanism, and Further Application to the Synthesis of the Antidepressant (21) Appl. No.: 11/400,484 Rolipram.” J. Am. Chem. Soc., 124(44): 13097-13105 (2002). Berneretal. “Asymmetric Michael Additions to Nitroalkenes.” Euro (22) Filed: Apr. 6, 2006 pean Journal of Organic Chemistry, 1877-1894 (2002). Cason et al., “Branched-Chain Fatty Acids. XXVII. Further Study of O O the Dependence of Rate of Amide Hvdrolvsis on Substitution near the (65) Prior Publication Data EFGroup. Relative Rates of E. of Nitrile to Amide and US 2006/0276543 A1 Dec. 7, 2006 Amide to Acid.” J. Org. Chem., 18(9): 1129-1136 (1953). Chen et al., “Synthesis of Pregabalin.” Zhongguo Yi Yao Gongye Related U.S.
    [Show full text]
  • Branched Poly(Gamma-Stearyl-L-Glutamate). Drew Scott Op Che Louisiana State University and Agricultural & Mechanical College
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1990 Synthesis and Characterization of Linear and Star - Branched Poly(gamma-Stearyl-L-Glutamate). Drew Scott oP che Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Poche, Drew Scott, "Synthesis and Characterization of Linear and Star -Branched Poly(gamma-Stearyl-L-Glutamate)." (1990). LSU Historical Dissertations and Theses. 5017. https://digitalcommons.lsu.edu/gradschool_disstheses/5017 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. INFORMATION TO USERS The most advanced technology has been used to photograph and reproduce this manuscript from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overlaps.
    [Show full text]
  • Functionality and Role of Different Fatty Alcohols in Topical O/W Cream Formulation
    University of Mississippi eGrove Electronic Theses and Dissertations Graduate School 2018 Functionality And Role Of Different Fatty Alcohols In Topical O/W Cream Formulation Supriya Bhide University of Mississippi Follow this and additional works at: https://egrove.olemiss.edu/etd Part of the Pharmacy and Pharmaceutical Sciences Commons Recommended Citation Bhide, Supriya, "Functionality And Role Of Different Fatty Alcohols In Topical O/W Cream Formulation" (2018). Electronic Theses and Dissertations. 725. https://egrove.olemiss.edu/etd/725 This Thesis is brought to you for free and open access by the Graduate School at eGrove. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of eGrove. For more information, please contact [email protected]. FUNCTIONALITY AND ROLE OF DIFFERENT FATTY ALCOHOLS IN TOPICAL O/W CREAM FORMULATION A thesis presented in partial fulfillment of requirements for the degree of Master of Science in the Department of Pharmaceutics and Drug Delivery The University of Mississippi by SUPRIYA S.BHIDE May 2018 Copyright Supriya S. Bhide 2018 ALL RIGHTS RESERVED ABSTRACT Fatty alcohols are excipients that are abundantly used in various pharmaceutical formulations. The objective of the present study was to evaluate the impact of incorporating different fatty alcohols on microstructural and formulation characteristics of topical o/w clotrimazole cream formulation. The formulations containing different fatty alcohols as Kolliwax® CSA 50 (CSA 50), Kolliwax® CSA 70 (CSA 70), Kolliwax® MA (MA), Kolliwax® CA (CA), Kolliwax® SA (SA) were prepared by selecting suitable RPM and homogenization time. The M.P. of API and fatty alcohols were determined using DSC technique.
    [Show full text]
  • 1-Octadecanol (S5751)
    1-Octadecanol Product Number S 5751 Store at Room Temperature Product Description Precautions and Disclaimer Molecular Formula: C18H38O For Laboratory Use Only. Not for drug, household or Molecular Weight: 270.5 other uses. CAS Number: 112-92-5 Melting Point: 56-60 °C (general product); Preparation Instructions 59.4-59.8 °C (pure 1-Octadecanol)1 This product is soluble in ethanol (100 mg/ml), with Synonyms: stearyl alcohol, stenol, octadecyl alcohol, heat as needed, yielding a clear, colorless solution. It 1 stearol, n-octadecanol1 is also soluble in ether, benzene, and acetone. 1-Octadecanol is a long chain primary alcohol that is References used in the production of emulsions, textile oils, 1. The Merck Index, 12th ed., Entry# 8960. antifoam agents, and lubricants. Other large scale 2. Nishihara, M., et al., Straight-chain fatty alcohols applications include the manufacture of alkyl amines, in the hyperthermophilic archaeon Pyrococcus tertiary amines, ethoxylates, halides/mercaptans, and furiosus. Extremophiles, 4(5), 275-277 (2000). polymerization stabilizers. It generally occurs as a 3. Ueda, I., and Suzuki, A., Is there a specific mixture of solid alcohols whose primary constituent is receptor for anesthetics? Contrary effects of 1-octadecanol.1 It occurs naturally in sperm whale oil alcohols and fatty acids on phase transition and and has been isolated from the hyperthermophilic bioluminescence of firefly luciferase. Biophys. J., bacterium Pyrococcus furiosus.1,2 75(2), 1052-1057 (1998). 4. Carreto, L., et al., Thermotropic mesomorphism of A study on the effects of various long chain alcohols, a model system for the plant epicuticular wax including 1-octadecanol, on the activity of firefly layer.
    [Show full text]
  • EE365: Stearyl Alcohol Patient Information Your Patch Test Result Indicates That You Have a Contact Allergy to Stearyl Alcohol
    the art and science of smart patch testingTM EE365: Stearyl alcohol Patient Information Your patch test result indicates that you have a contact allergy to stearyl alcohol. This contact allergy may cause your skin to react when it is exposed to this substance although it may take several days for the symptoms to appear. Typical symptoms include redness, swelling, itching, and fluid-filled blisters. Where is stearyl alcohol found? Stearyl alcohol is found in lubricants, resins, perfumes, cosmetics, shampoos, and conditioners. How can you avoid contact with stearyl alcohol? Avoid products that list any of the following names in the ingredients: 1-0ctadecanol Fatty alcohol(C18) 1-Hydroxyoctadecane HSDB 1082 4-01-00-01888 (Beilstein Handbook Lanol S Reference) Lorol 28 AI3-01330 NSC 5379 Adol 68 Octadecanol Alcohol stearylicus Octadecyl alcohol Alcohol(C18) Octadecylalkohol Aldol 62 Polaax Alfol 18 Sipol S Atalco S Siponol S BRN 1362907 Siponol SC C18 alcohol Stearic alcohol CCRIS 3960 Stearol CO-1895 Stearyl alcohol CO-1897 Stenol Cachalot S-43 Steraffine Crodacol-S USP XIII stearyl alcohol Decyl octyl alcohol n-1-Octadecanol Dytol E-46 n-Octadecanol Dytol e-46 n-Octadecyl alcohol EINECS 204-017-6 What are some products that may contain stearyl alcohol? Household Products: StoneTech Shining Powder Zinsser B I N Primer Sealer Stain Killer *For additional information about products that might contain stearyl alcohol, go to the Household Product Database online (http:/householdproducts.nlm.nih.gov) at the United States National Library of Medicine. These lists are brief and provide just a few examples. They are not comprehensive.
    [Show full text]