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U.S. EPA, Pesticide Product Label, WHITE CAP 15% PINE OIL
UNITED STATES ENVIRONMENTAL PROTECTION AGENCY /0 -c:JJ - cXJ{X).. EPA Reg. Date of Issuance: U.S . ENVIRONMENTAL PRCTECTION AGENCY Number: .,-«0 $7'.-, Office of ?esticide Programs ~. ~ ~ Antimicrob:a:s Division (7510C] 72138-E 1200 Penns:(:.vania Avenue N.W. OCT 2 1 201a {$1V:Z ~ Washir:g:on, D.C. 20460 <>.,J Term of IS~..lance: NOTICE OF PESTICIDE: Conditional _x_ Registration Reregistration --- Name of Pe~:icide Product: White (under fH'RA, as amended) Cap 15% Pine Oil Cleaner/Disinfectant Name and Address of Registrant (inc! ude lIP Code): White Cap, Inc. 625 Governor Printz Blvd. lC""'i.ngton, PA 19029 .0": Changes. in 1~1~ e~~t . :li1 silbstance from that accepted in connection witlt this registration must be _.-tted t:l'I!ondacd . -,,-~~~~~~_J..strat10n 01vbion prior to use of the label ia c01MIerce. In any correspondeQoe " : _ _ rater -to. the above EPA registration number. On the basis of information furnished by the registrant, the above named pesticide is hereby registered/reregistered under the Federal Insecticide, Fungicide and Rodenticide Act. Registration is in no way to be construed as an endorsement or recommendation of this product by the Agency. In order to protect health and the environment, the Administrator, on his motion, may at any time suspend or cancel the registration of a pesticide in accordance with the Act. The acceptance of any name in connection with the registration of a product under this Act is not to be construed as giving the registrant a right to exclusive use of the name or to its use if it has been covered by others. -
An Artifact in a Synthetic Pine Oil
RESEARCH NOTE J. Ess. Oil Res., 3, 41-42 (Jan/Feb 1991) An Artifact in a Synthetic Pine Oil Duane F. Zinkel USDA Forest Service, Forest Products Laboratory* One Gifford Pinchot Drive Madison, WI 53705-2398 ABSTRACT: The isopropyl ether of a-terpineol was identified as an artifact in the synthetic pine oil produced when isopropyl alcohol was used as the emulsifier. KEY WORD INDEX: Synthetic pine oil, a-terpineol isopropyl ether, terpinen-4-ol isopropyl ether, turpentine. INTRODUCTION: The manufacture of synthetic pine oil is the primary use for turpentine. The synthesis involves the acid-catalyzed hydration of a-pinene at the in terface ofan emulsion of pinene/mineral acid (1). Various emulsifiers have been used, one of which is isopropyl alcohol. Our gas chromatographic examination of a commercial distilled pine oil, produced using the isopropyl alcohol emulsifier, revealed the presence of 4-5% of a higher boiling component product not present originally in the turpentine. EXPERIMENTAL: NMR spectra were obtained at 310 K with a Bruker WM250 (250 MHz proton and 62.9 MHz carbon) FT spectrometer controlled by an Aspect 2000A minicomputer; DEPT spectra were obtained with a standard Bruker program. Gas chromatography was done with a Hewlett Packard 5880 gas chromatograph (FID) and fused-silica columns: a DB-1 (a methyl silicone) column from J & W Scientific (Folsom, CA), 15m x 0.25mmi.d. witha 0.1-µmfilmoperatedat60°Cand a Carbowaxcolumn,30m x 0.25mm with a 0.25-µm film temperature programmed from 60°C to 225°C at 8°C/min. isopropyl etherwas isolated by liquid chromatography. -
(12) United States Patent (10) Patent No.: US 6,239,087 B1 Mao Et Al
USOO6239087B1 (12) United States Patent (10) Patent No.: US 6,239,087 B1 Mao et al. (45) Date of Patent: May 29, 2001 (54) DETERGENT COMPOSITIONS (56) References Cited CONTAINING FRAGRANCE PRECURSORS U.S. PATENT DOCUMENTS AND THE FRAGRANCE PRECURSORS THEMSELVES 2,448,660 9/1948 Croxall et al. ....................... 568/600 2,490,337 12/1949 Croxall et al. ....................... 568/594 (75) Inventors: Hsiang Kuen Mao, Kobe (JP); Joseph 5,288,423 * 2/1994 Behan et al...... ... 252/174.11 Paul Morelli; Henry Cheng Na, both 5,447,644 9/1995 Guenin et al. ........................ 252/8.6 5,500,138 3/1996 Bacon et al. ......................... 510/102 of Cincinnati, OH (US); Robert Ya-Lin 5,500,154 3/1996 Bacon et al. ......................... 510/102 Pan, Kobe (JP); Mark Robert Sivik, 5,656,584 * 8/1997 Angell et al. ........................ 510/441 Fairfield, OH (US) 5,668,862 9/1997 Price et al. ........................... 568/594 (73) Assignee: The Procter & Gamble Company, 5,731,282 3/1998 Duquesne ............................. 510/423 Cincinnati, OH (US) OTHER PUBLICATIONS Rothman et al., “Enol Esters XVI: Enol Ethers in Synthe Notice: Subject to any disclaimer, the term of this sis”: Eastern Regional Research Laboratory, Philadelphia, patent is extended or adjusted under 35 Pennsyvania, pp. 376-377, (Jun. 1972). U.S.C. 154(b) by 0 days. Dejarlais et al., “Preparation of Some Ethyl Higher-Alkyl Appl. No.: 09/155,140 Acetals and Their Conversion to Vinyl Ethers': Northern (21) Regional Research Laboratory, Peoria, Illinois, pp. 241-243, (22) PCT Fed: Mar. 22, 1996 (May 1961). (86) PCT No.: PCT/US96/04060 * cited by examiner S371 Date: Sep. -
Effect of Curcumin, Mixture of Curcumin and Piperine and Curcum (Turmeric) on Lipid Profile of Normal and Hyperlipidemic Rats
The Egyptian Journal of Hospital Medicine Vol., 21: 145 – 161 December 2005 I.S.S.N: 12084 2002–1687 Effect of Curcumin, Mixture of Curcumin and Piperine and Curcum (Turmeric) on Lipid Profile of Normal and Hyperlipidemic Rats GHADA, Z. A. Soliman Lecturer of Biochemistry, Biochemistry Department, National Nutrition Institute, Cairo Abstract Curcumin is a polyphenolic, yellow pigment obtained from rhizomes of Curcuma longa (curcum), used as a spice and food colouring. The extracts have several pharmacological effects. We evaluated the effect of curcum, curcumin, and mixture of curcumin and piperine on plasma lipids in normal and hypercholesterolemic rats. A total of 270 rats, divided into 27 groups, were used. G1, G11: control, G2-G11: normal rats fed control diet supplemented with different levels of curcumin and curcum (G2-G6: 0.1%, 0.25%, 0.5%, 1.0%, 2.0% respectively, G7-G11: 1.67%, 4.167%, 8.34%, 16.67%, and 33.34). G12-G26: at first fed control diet supplemented with 2% cholesterol then G13-17, 21-25 fed a control diet supplemented with different levels of curcumin, and curcum [the same levels as G2-G11; G18-20 fed control diet supplemented with mixture of curcumin (0.1, 0.25, 0.5%) and piperine (20 mg/kg BW)], G12 was sacrificed before addition of studied materials, G26 were fed control diet. Lipid profile, triacylglycerol and phospholipids of plasma and organs as liver and heart were measured. Serum cholesterol (total, LDL-C, VLDL-C), triacylglycerol and phospholipids contents were elevated in cholesterol-fed rats, while HDL-C were decreased. -
Mechanistic Study of Physicochemical and Biochemical Processes
Mechanistic study of physicochemical and biochemical processes affecting intestinal absorption of the sesquiterpene lactone nobilin from multi-component systems in the Caco-2 model. Inauguraldissertation zur Erlangung der Würde eines Doktors der Philosophie vorgelegt der Philosophisch-Naturwissenschaftlichen Fakultät der Universität Basel von URSULA STEPHANIE THORMANN aus Bern (BE) Basel, 2015 Originaldokument gespeichert auf dem Dokumentenserver der Universität Basel edoc.unibas.ch Dieses Werk ist unter dem Vertrag „Creative Commons Namensnennung-Keine kommerzielle Nutzung-Keine Bearbeitung 3.0 Schweiz“ (CC BY-NC-ND 3.0 CH) lizenziert. Die vollständige Lizenz kann unter creativecommons.org/licenses/by-nc-nd/3.0/ch/eingesehen werden. Genehmigt von der Philosophisch-Naturwissenschaftlichen Fakultät auf Antrag von Prof. Dr. G. Imanidis und Prof. Dr. H. E. U. Meyer zu Schwabedissen Basel, den 18. Februar 2014 Prof. Dr. J. Schibler Namensnennung-Keine kommerzielle Nutzung-Keine Bearbeitung 3.0 Schweiz (CC BY-NC-ND 3.0 CH) Sie dürfen: Teilen — den Inhalt kopieren, verbreiten und zugänglich machen Unter den folgenden Bedingungen: Namensnennung — Sie müssen den Namen des Autors/Rechteinhabers in der von ihm festgelegten Weise nennen. Keine kommerzielle Nutzung — Sie dürfen diesen Inhalt nicht für kommerzielle Zwecke nutzen. Keine Bearbeitung erlaubt — Sie dürfen diesen Inhalt nicht bearbeiten, abwandeln oder in anderer Weise verändern. Wobei gilt: Verzichtserklärung — Jede der vorgenannten Bedingungen kann aufgehoben werden, sofern Sie die -
Pine DC Plus™ Disinfectant Cleaner a One-Step Disinfectant Cleaner That Is Effective in the Reduction of Cross-Contamination
Pine DC Plus™ Disinfectant Cleaner A one-step disinfectant cleaner that is effective in the reduction of cross-contamination. Units Item # Description Size Per Case BPR460001-A Pine DC Plus™ Gallon 4 Features • Formulated as a one-step cleaner/disinfectant • Kills Trichophyton Mentagrophytes (Athlete’s foot fungus) • Neutral pH does not dull floor finishes when diluted correctly • Hospital grade to meet strict requirements • Quat formula has broad spectrum efficacy • Contains no phosphates to reduce pollution of waterways • Effective against the HIV-1 (AIDS Virus) when used on previously • EPA-registered formula confirms efficacy compliance cleaned surfaces • Pleasant pine oil fragrance • Powerful cleaning, deodorizing and disinfecting performance Order today at Order.StaplesAdvantage.com, EWay.comTM, CoastwideLabs.com, or your online ordering system. Pine DC Plus™ One-Step Germicidal Detergent A one-step disinfectant cleaner that is effective against a broad spectrum of bacteria and viruses and inhibits the growth of mold and mildew. When used as directed, Pine DC Plus will deodorize surfaces in toilet areas, behind and under sinks and counter, garbage cans and garbage storage areas, and other places where bacterial growth can cause malodors. Recommended for use in hospitals, public restrooms, athletic facilities, restaurants and bars, airports, hotels and motels. Contains no phosphorous. Pine DC Plus is a no-rinse neutral pH disinfectant cleaner that disinfects, cleans and deodorizes in one labor-saving step. Provides effective cleaning strength that will not dull most metal-interlock floor finishes, and does not require a rinse prior to recoat. Pine DC Plus is recommended for nonscratch cleaning of showers and tubs, shower doors and curtains, fixtures and toilet bowls. -
Impact of Lipid Sources on Quality Traits of Medical Cannabis-Based Oil Preparations
Article Impact of Lipid Sources on Quality Traits of Medical Cannabis-Based Oil Preparations Alberto Ramella 1, Gabriella Roda 2, Radmila Pavlovic 3,*, Michele Dei Cas 4, Eleonora Casagni 2, Giacomo Mosconi 3, Francisco Cecati 5, Paola Minghetti 2 and Carlo Grizzetti 6 1 Farmacia Dott.ri Giuliana e Alberto Ramella–SAS, Via A. Diaz 1, 21021 Angera (VA), Italy; [email protected] 2 Department of Pharmaceutical Sciences, Università degli Studi di Milano, Via L. Mangiagalli 25, 20133 Milan, Italy; [email protected] (G.R.); [email protected] (E.C.); [email protected] (P.M.) 3 Department of Health, Animal Science and Food Safety, University of Milan, 20133 Milan, Italy; [email protected] 4 Department of Health Sciences, Università degli Studi di Milano, Via A.di Rudinì 8, 20142 Milan, Italy; [email protected] 5 INTEQUI-CONICET, Faculty of Chemistry, Biochemistry and Pharmacy, National University of San Luis, Almirante Brown 1455, CP 5700 San Luis, Argentina; [email protected] 6 S.S.D. Cure Palliative e Terapia del Dolore, Ospedale di Circolo–Fondazione Macchi, ASST Sette Laghi, Viale L. Borri 57, 21100 Varese, Italy; [email protected] * Correspondence: [email protected] Academic Editor: Maria Carla Marcotullio Received: 2 June 2020; Accepted: 29 June 2020; Published: 30 June 2020 Abstract: The feasibility of the use of two lipid sources and their impact on the cannabinoid profile, terpene fingerprint, and degradation products in medical cannabis oil preparations during 3 months of refrigerated storage time were investigated. LCHRMS-Orbitrap® and HS-SPME coupled to GC- MS for the investigation of targeted and untargeted cannabinoids, terpenes, and lipid degradation products in Bedrocan® and Bediol® macerated oils were used as analytical approaches. -
Phospholipid Metabolism in Stimulated Human Platelets: CHANGES in PHOSPHATIDYLINOSITOL, PHOSPHATIDIC ACID, and LYSOPHOSPHOLIPIDS
Phospholipid Metabolism in Stimulated Human Platelets: CHANGES IN PHOSPHATIDYLINOSITOL, PHOSPHATIDIC ACID, AND LYSOPHOSPHOLIPIDS M. Johan Broekman, … , Jean W. Ward, Aaron J. Marcus J Clin Invest. 1980;66(2):275-283. https://doi.org/10.1172/JCI109854. Endogenous phospholipid metabolism in stimulated human platelets was studied by phosphorus assay of major and minor components following separation by two-dimensional thin-layer chromatography. This procedure obviated the use of radioactive labels. Extensive changes were found in quantities of phosphatidylinositol (PI) and phosphatidic acid (PA) as a consequence of thrombin or collagen stimulation. Thrombin addition was followed by rapid alterations in the amount of endogenous PI and PA. The decrease in PI was not precisely reciprocated by an increase in PA when thrombin was the stimulus. This apparent discrepancy could be explained by removal of a transient intermediate in PI metabolism, such as diglyceride, formed by PI-specific phospholipase C (Rittenhouse-Simmons, S., J. Clin. Invest.63: 580-587, 1979). Diglyceride would be unavailable for PA formation by diglyceride kinase, if hydrolyzed by diglyceride lipase (Bell, R. L., D. A. Kennerly, N. Stanford, and P. W. Majerus. Proc. Natl. Acad. Sci. U. S. A.76: 3238-3241, 1979) to yield arachidonate for prostaglandin endoperoxide formation. Thrombin-treated platelets also accumulated lysophospho-glycerides. Specifically, lysophosphatidyl ethanolamines accumulated within 15s following thrombin addition. Fatty acid and aldehyde analysis indicated phospholipase A2 activity, with an apparent preference for diacyl ethanolamine phosphoglycerides. In the case of collagen, these changes occurred concomitantly with aggregation and consumption of oxygen for prostaglandin endoperoxide formation. These studies of endogenous phospholipid metabolism provide information supporting the existence of […] Find the latest version: https://jci.me/109854/pdf Phospholipid Metabolism in Stimulated Human Platelets CHANGES IN PHOSPHATIDYLINOSITOL, PHOSPHATIDIC ACID, AND LYSOPHOSPHOLIPIDS NI. -
Positive Allosteric Modulators (Pams) in Mouse Models of Overt Cannabimimetic Activity, Subjective Drug Effects, and Neuropathic Pain
Virginia Commonwealth University VCU Scholars Compass Theses and Dissertations Graduate School 2021 Investigating Cannabinoid Type-1 Receptor (CB1R) Positive Allosteric Modulators (PAMs) in Mouse Models of Overt Cannabimimetic Activity, Subjective Drug Effects, and Neuropathic Pain Jayden Elmer Virginia Commonwealth University Follow this and additional works at: https://scholarscompass.vcu.edu/etd Part of the Behavioral Neurobiology Commons, Behavior and Behavior Mechanisms Commons, Medicinal and Pharmaceutical Chemistry Commons, Nervous System Diseases Commons, and the Pharmacology Commons © The Author Downloaded from https://scholarscompass.vcu.edu/etd/6777 This Thesis is brought to you for free and open access by the Graduate School at VCU Scholars Compass. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of VCU Scholars Compass. For more information, please contact [email protected]. 2021 Investigating Cannabinoid Type-1 Receptor (CB1R) Positive Allosteric Modulators (PAMs) in Mouse Models of Overt Cannabimimetic Activity, Subjective Drug Effects and Neuropathic Pain Jayden A. Elmer Investigating Cannabinoid Type-1 Receptor (CB1R) Positive Allosteric Modulators (PAMs) in Mouse Models of Overt Cannabimimetic Activity, Subjective Drug Effects and Neuropathic Pain A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science at Virginia Commonwealth University By Jayden Aric Elmer Bachelor of Science, University of Virginia, 2018 Director: Dr. Aron Lichtman, Professor, Department of Pharmacology & Toxicology; Associate Dean of Research and Graduate Studies, School of Pharmacy Virginia Commonwealth University Richmond, Virginia July 2021 Acknowledgements I would first like to extend my gratitude towards the CERT program at VCU. The CERT program opened the doors for me to get involved in graduate research. -
Complementary Analytical Platforms of NMR Spectroscopy and LCMS Analysis in the Metabolite Profiling of Isochrysis Galbana
marine drugs Article Complementary Analytical Platforms of NMR Spectroscopy and LCMS Analysis in the Metabolite Profiling of Isochrysis galbana Muhammad Safwan Ahamad Bustamam 1, Hamza Ahmed Pantami 2 , Awanis Azizan 1 , Khozirah Shaari 1,2, Chong Chou Min 3, Faridah Abas 1 , Norio Nagao 3, Maulidiani Maulidiani 4, Sanjoy Banerjee 1, Fadzil Sulaiman 1 and Intan Safinar Ismail 1,2,* 1 Natural Medicine and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia; [email protected] (M.S.A.B.); [email protected] (A.A.); [email protected] (K.S.); [email protected] (F.A.); [email protected] (S.B.); [email protected] (F.S.) 2 Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia; [email protected] 3 Department of Aquaculture, Faculty of Agriculture, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia; [email protected] (C.C.M.); [email protected] (N.N.) 4 Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Kuala Nerus 21030, Terengganu, Malaysia; [email protected] * Correspondence: safi[email protected]; Tel.: +60-3-9769-7492 Abstract: This study was designed to profile the metabolites of Isochrysis galbana, an indigenous and Citation: Bustamam, M.S.A.; less explored microalgae species. 1H Nuclear Magnetic Resonance (NMR) spectroscopy and Liquid Pantami, H.A.; Azizan, A.; Shaari, K.; Chromatography-Mass Spectrometry (LCMS) were used to establish the metabolite profiles of five Min, C.C.; Abas, F.; Nagao, N.; different extracts of this microalga, which are hexane (Hex), ethyl acetate (EtOAc), absolute ethanol Maulidiani, M.; Banerjee, S.; (EtOH), EtOH:water 1:1 (AqE), and 100% water (Aq). -
2010 National Ambulatory Medical Care Survey Public Use Data File
2010 NAMCS MICRO-DATA FILE DOCUMENTATION PAGE 1 ABSTRACT This material provides documentation for users of the 2010 National Ambulatory Medical Care Survey (NAMCS) public use micro-data file. NAMCS is a national probability sample survey of visits to office-based physicians conducted by the National Center for Health Statistics, Centers for Disease Control and Prevention. It is a component of the National Health Care Surveys which measure health care utilization across a variety of health care providers. Section I, "Description of the National Ambulatory Medical Care Survey," includes information on the scope of the survey, the sample, field activities, data collection procedures, medical coding procedures, population estimates, and sampling errors. Section II provides technical information, including a detailed description of the contents of each data record by location, and a list of physician specialties represented in the survey. Section III contains marginal data and estimates for selected items on the data record. The appendixes contain sampling errors, instructions and definitions for completing the Patient Record form, and lists of codes used in the survey. PAGE 2 2010 NAMCS MICRO-DATA FILE DOCUMENTATION SUMMARY OF CHANGES FOR 2010 The 2010 NAMCS public use micro-data file is, for the most part, similar to the 2009 file, but there are some important changes. These are described in more detail below and reflect changes to the survey instruments, the Patient Record form and the Physician Induction Interview form. There are also new injury-related items on the public use file, but these are simply recoded data from existing items on the Patient Record form and are described in a separate section below. -
Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008
Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008 Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008 William A. Rutala, Ph.D., M.P.H.1,2, David J. Weber, M.D., M.P.H.1,2, and the Healthcare Infection Control Practices Advisory Committee (HICPAC)3 1Hospital Epidemiology University of North Carolina Health Care System Chapel Hill, NC 27514 2Division of Infectious Diseases University of North Carolina School of Medicine Chapel Hill, NC 27599-7030 1 Guideline for Disinfection and Sterilization in Healthcare Facilities, 2008 3HICPAC Members Robert A. Weinstein, MD (Chair) Cook County Hospital Chicago, IL Jane D. Siegel, MD (Co-Chair) University of Texas Southwestern Medical Center Dallas, TX Michele L. Pearson, MD (Executive Secretary) Centers for Disease Control and Prevention Atlanta, GA Raymond Y.W. Chinn, MD Sharp Memorial Hospital San Diego, CA Alfred DeMaria, Jr, MD Massachusetts Department of Public Health Jamaica Plain, MA James T. Lee, MD, PhD University of Minnesota Minneapolis, MN William A. Rutala, PhD, MPH University of North Carolina Health Care System Chapel Hill, NC William E. Scheckler, MD University of Wisconsin Madison, WI Beth H. Stover, RN Kosair Children’s Hospital Louisville, KY Marjorie A. Underwood, RN, BSN CIC Mt. Diablo Medical Center Concord, CA This guideline discusses use of products by healthcare personnel in healthcare settings such as hospitals, ambulatory care and home care; the recommendations are not intended for consumer use of the products discussed. 2