507 Part 582—Substances Generally Recognized As
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Sodium Sulfate
FT-08762A Sodium Sulfate Product Information Chemical name : Sodium Sulfate, ACS grade Syn.: Na2SO4 , sodium salt of sulfuric acid, Disodium sulfate; Bisodium sulfate; Dibasic sodium sulfate; Disodium monosulfate; (All.): disodium sulphate; Natriumsulfat; sodium sulphate CAS: 7757-82-6 EC number: 231-820-9 Cat. Number : 08762A, 500g 08762B, 1Kg 08762C, 2.5Kg 08762-B, Bulk Structure : Na2SO4 (anh.) Molecular Weight : 142.04 Properties: Form: white solid crystalline powder (hygroscopic) Density: 2.664 g/cm3 Melting point: 884°C Boiling point: 1429°C Refractive index (nD)/ 1.468 pKa: 10.329 and 6.351(carbonic acid) Solubility: readily soluble in water >4% w/v Storage: Room temperature (Z) Safety: Irritant. Non-flammable. Risk Statements: 36/37/38 Safety Statements: 36/37/39 Applications: Suitable for many biochemistry and biotechnology applications. P.1 FT-08762A Specifications Test Specifications Purity >99.0% Calcium (%) 0.01 Chloride (%) 0.001 Heavy Metals (as Pb) 0.0005 Iron (%) 0.001 Magnesium (%) 0.005% Nitrogen compounds (%) 0.0005% Phosphates (%) 0.001% Insolubles 0.001% Loss on Ignition (%) 0.5 pH (5%, water, 25°C) 0.01 + Technical information ●Chemistry Sodium sulfate is a neutral salt, which forms aqueous solutions with pH of 7. The Na+ ion weakly polarizes its water lig- ands provided there are metal ions in solution. Sodium sulfate reacts with sulfuric acid to give the acid salt sodium bisulfate, leading ot a temperatude-dependant equi- librium: Na2SO4 + H2SO4 ⇌ 2 NaHSO4 2− Sulfate ions (SO4 ) in solution can be indicated by the easy formation of insoluble sulfates when these solutions are treated with Ba2+ or Pb2+ salts: Na2SO4 + BaCl2 → 2 NaCl + BaSO4 Double salts with some other alkali metal sulfates are known, including Na2SO4·3K2SO4. -
Root Touch-Up Ingredients/Ingrédients
ROOT TOUCH-UP INGREDIENTS/INGRÉDIENTS: In every box you’ll find: Color Blend Formula (#1) and the Color Blend Activator (#2). Our Color Blend Formula is uniquely formulated to achieve your desired shade. Find yours below. COLORBLEND ACTIVATOR (2) COLORBLEND FORMULA (1) WATER, HYDROGEN PEROXIDE, CETEARYL ALCOHOL, 5A/MEDIUM ASH BROWN NOL, CARAMEL, p-PHENYLENEDIAMINE, SODIUM 7/DARK BLONDE CETEARETH-20, STEARETH-21, LAURETH-23, WATER, C12-15 PARETH-3, AMMONIUM HYDROX- SULFITE, 1-NAPHTHOL, IRON OXIDES, N,N-BIS(2-HY- WATER, C12-15 PARETH-3, AMMONIUM HYDROX- POLYQUATERNIUM-37, PROPYLENE GLYCOL IDE, OLETH-10, DILINOLEIC ACID, COCAMIDE MEA, DROXYETHYL)-p-PHENYLENEDIAMINE SULFATE, MICA, IDE, OLETH-10, DILINOLEIC ACID, COCAMIDE MEA, DICAPRYLATE/DICAPRATE, STYRENE/VP COPOLYMER, LINOLEAMIDOPROPYL DIMETHYLAMINE DIMER p-AMINOPHENOL, SODIUM METASILICATE, EDTA, LINOLEAMIDOPROPYL DIMETHYLAMINE DIMER PPG-1 TRIDECETH-6, ETIDRONIC ACID. DILINOLEATE, STEARETH-21, BEHENTRIMONIUM m-AMINOPHENOL, SARGASSUM FILIPENDULA EX- DILINOLEATE, STEARETH-21, BEHENTRIMONIUM CHLORIDE, POLYQUATERNIUM-22, SODIUM SULFATE, TRACT, HYPNEA MUSCIFORMIS EXTRACT, GELLIDIELA CHLORIDE, POLYQUATERNIUM-22, FRAGRANCE, FRAGRANCE, RESORCINOL, ERYTHORBIC ACID, ACEROSA EXTRACT, TITANIUM DIOXIDE. SODIUM SULFATE, ERYTHORBIC ACID, p-AMINOPHE- p-PHENYLENEDIAMINE, CARAMEL, p-AMINOPHENOL, NOL, RESORCINOL, p-PHENYLENEDIAMINE, MICA, m-AMINOPHENOL, IRON OXIDES, MICA, SODIUM SODIUM SULFITE, TITANIUM DIOXIDE, m-AMINOPHE- SULFITE, N,N-BIS(2-HYDROXYETHYL)-p-PHENYLENE- 5G/MEDIUM GOLDEN BROWN NOL, SODIUM METASILICATE, EDTA, SARGASSUM FILI- DIAMINE SULFATE, 1-NAPHTHOL, SODIUM METASILI- WATER, C12-15 PARETH-3, AMMONIUM HYDROX- PENDULA EXTRACT, HYPNEA MUSCIFORMIS EXTRACT, CATE, EDTA, SARGASSUM FILIPENDULA EXTRACT, HY- IDE, OLETH-10, DILINOLEIC ACID, COCAMIDE MEA, 1-NAPHTHOL, IRON OXIDES, N,N-BIS(2-HYDROXYETH- PNEA MUSCIFORMIS EXTRACT, GELLIDIELA ACEROSA LINOLEAMIDOPROPYL DIMETHYLAMINE DIMER YL)-p-PHENYLENEDIAMINE SULFATE, GELLIDIELA EXTRACT, TITANIUM DIOXIDE. -
Management of Poisoning
MOH CLINICAL PRACTICE GUIDELINES December/2011 Management of Poisoning Health Ministry of Sciences Chapter of Emergency College of College of Family Manpower Authority Physicians Physicians, Physicians Academy of Medicine, Singapore Singapore Singapore Singapore Medical Pharmaceutical Society Society for Emergency Toxicology Singapore Paediatric Association of Singapore Medicine in Singapore Society (Singapore) Society Executive summary of recommendations Details of recommendations can be found in the main text at the pages indicated. Principles of management of acute poisoning – resuscitating the poisoned patient GPP In a critically poisoned patient, measures beyond standard resuscitative protocol like those listed above need to be implemented and a specialist experienced in poisoning management should be consulted (pg 55). GPP D Prolonged resuscitation should be attempted in drug-induced cardiac arrest (pg 55). Grade D, Level 3 1 C Titrated doses of naloxone, together with bag-valve-mask ventilation, should be administered for suspected opioid-induced coma, prior to intubation for respiratory insuffi ciency (pg 56). Grade C, Level 2+ D In bradycardia due to calcium channel or beta-blocker toxicity that is refractory to conventional vasopressor therapy, intravenous calcium, glucagon or insulin should be used (pg 57). Grade D, Level 3 B Patients with actual or potential life threatening cardiac arrhythmia, hyperkalaemia or rapidly progressive toxicity from digoxin poisoning should be treated with digoxin-specifi c antibodies (pg 57). Grade B, Level 2++ B Titrated doses of benzodiazepine should be given in hyperadrenergic- induced tachycardia states resulting from poisoning (pg 57). Grade B, Level 1+ D Non-selective beta-blockers, like propranolol, should be avoided in stimulant toxicity as unopposed alpha agonism may worsen accompanying hypertension (pg 57). -
United States Patent 1191 Lll] 3,983,266 Bahls [451 Sept
United States Patent 1191 lll] 3,983,266 Bahls [451 Sept. 28, 1976 [54] METHOD FOR APPLYING METALLIC 3.776.740 [2/1973 Sivcrz ct al. .......................... .. l06/l SILVER TO A SUBSTRATE OTHER PUBLICATIONS [75] Inventor: Harry Bahls, Wayne, Pa. lvanov et al., Chem. Abs. 43:2548c, I949, [73] Assignee: Peacock Laboratories, Inc., Philadelphia, Pa. Primary Examiner-Ralph S. Kendall [22] Filed: Oct. 9, I974 I 57] ABSTRACT [2!] ,Appl. No.: 513,417 High efficiency deposition of silver on the surface of a substrate is obtained by providing a solution contain [52] [1.8. CI ............................... .. 427/164; 427/165; ing reducible dissolved silver in the presence of an al 427/168; 427/424; 427/426; l06/l kali metal hydroxide and ammonia, all of which are [51] Int. CLZ. ......................................... .. C23C 3/02 applied to the substrate in the presence of an aqueous [58] Field of Search .............. .. l06/l; 427/l68. I69, solution of a moderating reducer containing :1 poly 427/165, I64, 426, 304, 125, 425 hydric alcohol of the formula CH2OH(CHOH),,C H,OH, where n is an integer from 1 to 6. Preferably [56] References Cited the polyhydric alcohol is sorbitol, and in a preferred UNITED STATES PATENTS embodiment a moderator is the form of a thio glycerol is present. 2,996,406 8/l96l Weinrich ........... ............ .. 427/168 3,772,078 ll/l973 Polichcttc ct al ................. .. l06/l X l5 Claims, No Drawings 3,983,266 1 Other objects and advantages of this invention, in METHOD FOR APPLYING METALLIC SILVER TO cluding the economy of the same, and the case with A SUBSTRATE which it may be applied to existing silver coating equip ment and apparatus, will further become apparent BRIEF SUMMARY OF THE INVENTION 5 hereinafter. -
Potassium-Magnesium Citrate Is an Effective Prophylaxis Against Recurrent Calcium Oxalate Nephrolithiasis
0022-5347/97/1586-2069$03.00/0 JOURNAL OF UROLOGY Vol. 158,2069-2073, December 1997 Copyright Q 1997 by AMERICANUROLOGICAL ASS~CIATION, INC. Printed in U.S.A. POTASSIUM-MAGNESIUM CITRATE IS AN EFFECTIVE PROPHYLAXIS AGAINST RECURRENT CALCIUM OXALATE NEPHROLITHIASIS BRUCE ETTINGER,* CHARLES Y. C. PAK, JOHN T. CITRON, CARL THOMAS, BEVERLEY ADAMS-HIJET AND ARLINE VANGESSEL From the Diuision of Research, Kaiser Permanente Medical Care Program, Oakland, California, the Department of Mineral Metabolism, Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, Department of Medicine, Kaiser Permanente Medical Center, Walnut Creek, California, Department of Urology, Kaiser Permanente Medical Center, San Francisco, California, and Kaiser Foundation Research Institute, Kaiser Foundation Hospitals, Oakland, California ABSTRACT Purpose: We examined the efficacy of potassium-magnesium citrate in preventing recurrent calcium oxalate kidney calculi. Materials and Methods: We conducted a prospective double-blind study of 64 patients who were randomly assigned to receive placebo or potassium-magnesium citrate (42 mEq. potassium, 21 mEq. magnesium, and 63 mEq. citrate) daily for up to 3 years. Results. New calculi formed in 63.6%of subjects receiving placebo and in 12.9%of subjects receiving potassium-magnesiumcitrate. When compared with placebo, the relative risk of treat- ment failure for potassium-magnesium citrate was 0.16 (95%confidence interval 0.05 to 0.46). potassium-magnesium citrate had a statistically significant effect (relative risk 0.10,95%confi- dence interval 0.03 to 0.36) even after adjustment for possible confounders, including age, pretreatment calculous event rate and urinary biochemical abnormalities. -
Electro-Activation of Potassium Acetate, Potassium Citrate and Calcium
Liato et al. SpringerPlus (2016) 5:1760 DOI 10.1186/s40064-016-3453-1 RESEARCH Open Access Electro‑activation of potassium acetate, potassium citrate and calcium lactate: impact on solution acidity, Redox potential, vibrational properties of Raman spectra and antibacterial activity on E. coli O157:H7 at ambient temperature Viacheslav Liato1,2, Steve Labrie1,3 and Mohammed Aïder1,2,4* *Correspondence: [email protected] Abstract 1 Institute of Nutrition and Functional Foods (INAF), Aims: To study the electro-activation of potassium acetate, potassium citrate and Université Laval, Quebec, QC calcium lactate aqueous solutions and to evaluate their antimicrobial effect against E. G1V 0A6, Canada coli O157:H7 at ambient temperature. Full list of author information is available at the end of the Methods and results: Potassium acetate, potassium citrate and calcium lactate aque- article ous solutions were electrically excited in the anodic compartment of a four sectional electro-activation reactor. Different properties of the electro-activated solutions were measured such as: solutions acidity (pH and titratable), Redox potential and vibrational properties by Raman spectroscopy. Moreover, the antimicrobial activity of these solu- tions was evaluated against E. coli O157:H7. The results showed a pH decrease from 7.07 0.08, 7.53 0.12 and 6.18 0.1 down to 2.82 0.1, 2.13 0.09 and 2.26 0.15, after ±180 min of electro-activation± ± of potassium acetate,± potassium± citrate and calcium± lactate solution, respectively. These solutions were characterized by high oxidative ORP of 1076 12, 958 11 and 820 14 mV, respectively. -
Product Information Sheet
September 17, 2015 productISOVACTIN information AA PLUS Nutrients 8.5 fl oz (250mL) per 100mL SKU 37002 Calories 186 74 Calories From Fat 57 23 NET WEIGHT 2 GAL (7.5 L) Protein Equivalent, g 20 8 Free Amino Acids, g 22 9 SERVING SIZE 8.5 fl oz (250mL) Carbohydrates, g 13 5 Sugar, g 5 2 SERVINGS PER PACKAGE 30 Sugar Alcohols, g 0 0 Dietary Fiber, g 2.8 1 Fat, g 6 2.4 24359-0702-03 REIMBURSEMENT CODE Saturated Fat, g 0.5 0.2 (for USA only) Trans Fat, g 0.0 0.0 DHA, mg 150.0 60.0 Cholesterol, mg 0.4 0 MEDICAL FOOD PRODUCT Vitamin A, IU 1100.0 440.0 For the dietary management of Isovaleric Acidemia. Dispensed by prescription. Vitamin C, mg 40.0 16.0 Isovactin AA Plus is a ready-to-drink metabolic formula product for Isovaleric Acidemia Vitamin D, IU 620.0 248.0 patients, over 1 year of age. Isovactin contains an advanced fortification blend. Product Vitamin E, IU 10.0 4.0 Vitamin K1, mcg 20.0 8.0 comes in a 250 mL carton. Vitamin K2 (MK-7), mcg 20.0 8.0 Thiamin (B1), mg 0.5 0.2 Riboflavin (B2), mg 0.5 0.2 Niacin (B3), mg 6.6 2.6 PRECAUTIONS For the dietary management of Isovaleric Acidemia (IVA) and Vitamin B6, mg 0.5 0.2 other disorders of leucine metabolism. Use as directed by physician. Must be Folic acid, mcg 186.0 74.4 administered under medical supervision only. -
GHS Calcium Lactate Gluconate MSDS.Pdf
Safety Data Sheet (Calcium Lactate Gluconate) DATE PREPARED: 7/9/2015 Section 1. Product and Company Identification Product Name Calcium Lactate Gluconate CAS Number 11116-97-5 Parchem - fine & specialty chemicals EMERGENCY RESPONSE NUMBER 415 Huguenot Street CHEMTEL New Rochelle, NY 10801 Toll Free US & Canada: 1 (800) 255-3924 (914) 654-6800 (914) 654-6899 All other Origins: 1 (813) 248-0585 parchem.com [email protected] Collect Calls Accepted Section 2. Hazards Identification Classification of the substance or mixture Classification according to Directive 67/548/EEC or 1999/45/EC as amended: This preparation does not meet the criteria for classification according to Directive 1999/45/EC as amended. Classification according to Regulation (EC) No 1272/2008 as amended: This mixture does not meet the criteria for classification according to Regulation (EC) 1272/2008 as amended. Hazard and precautionary statements Hazard statements: The substance does not meet the criteria for classification. Precautionary statements: Not available. Appearance & Odor: White powder with no odor. Fire & Explosion Hazards Potential for dust explosion may exist. This product is not defined as flammable or combustible. However, the product may decompose under fire conditions to produce toxic oxides of carbon. Depending upon conditions, dusts may be sensitive to static discharge. Avoid possibility of dry powder and friction causing static electricity in presence of flammables (See NFPA-77, Chpt. 6) Primary Route of Exposure: Skin and eye contact are the primary routes of exposure to this product. Inhalation Acute Exposure: Inhalation of dust may cause mild irritation. Skin Contact - Acute: Skin contact is not expected to cause irritation. -
Brochure-Product-Range.Pdf
PRODUCT RANGE 2015 edition ANSI Standard 60 NSF® CERTIFIED HALAL M ISLAMIC FOOD AND NUTRITION ® COUNCIL OF AMERICA Rue Joseph Wauters, 144 ISO 9001:2008 (Quality) / OHSAS 18001:2007 (Health/ B-4480 Engis Safety) / ISO 14001:2004 (Environment) / ISO 22000:2005 www.globulebleu.com (Food Safety) / FSSC 22000:2013 (Food Safety). Tel. +32 (0) 4 273 93 58 Our food grade phosphates are allergen free, GMO free, Fax. +32 (0) 4 275 68 36 BSE/TSE free. www.prayon.com mail. [email protected] Design by www.prayon.com PRODUCT RANGE | 11 TABLE OF CONTENTS HORTICULTURE APPLICATIONS HORTIPRAY® RANGE FOR HORTICULTURE* FOOD AND INDUSTRIAL APPLICATIONS PRODUCT NAME Bulk density P O pH N-NH Made 2 5 4 MONOAMMONIUM PHOSPHATE - NH4H2PO4 in 3 3 % 1% % Sodium orthophosphates ................................................................................... 03 g/cm lbs/ft indicative indicative indicative Water-soluble fertilisers. Sodium pyrophosphates .................................................................................... 04 HORTIPRAY® MAP Horticultural Grade 0.9 56 61 4.5 12 Sodium tripolyphosphates ................................................................................. 05 HORTIPRAY® MAP 12.60 Horticultural Grade 0.9 56 60 5 12.1 Water-soluble fertilisers; Sodium polyphosphates ..................................................................................... 06 HORTIPRAY® MAP anticalc Horticultural Grade 0.9 56 61 4.5 12 preventive action against clogging. Potassium orthophosphates ............................................................................. -
Ionic Liquid + Biomolecule
Sónia Isabel Pereira Branco Licenciatura em Ciências da Engenharia Química e Bioquímica Aqueous Biphasic System based on Cholinium Ionic Liquids: Extraction of Biologically Active Phenolic Acids Dissertação para obtenção do Grau de Mestre em Engenharia Química e Bioquímica Orientador: Doutora Isabel Maria Delgado Jana Marrucho Ferreira, Investigadora Coordenadora, Laboratório de Termodinâmica Molecular, ITQB-UNL Presidente: Doutora Susana Filipe Barreiros Arguente: Doutor Alexandre Babo de Almeida Paiva Vogal: Doutora Isabel Maria Delgado Jana Marrucho Ferreira Setembro 2014 II UNIVERSIDADE NOVA DE LISBOA Faculdade de Ciências e Tecnologia Departamento de Química Aqueous Biphasic System based on Cholinium Ionic Liquids: Extraction of Biologically Active Phenolic Acids Sónia Isabel Pereira Branco Dissertação apresentada na Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa para obtenção do grau Mestre em Engenharia Química e Bioquímica Orientadores: Doutora Isabel Maria Delgado Jana Marrucho Ferreira 2014 III IV Aqueous Biphasic Systems based on Cholinium Ionic Liquids: Extraction of Biologically Active Phenolic Acids COPYRIGHT Sónia Isabel Pereira Branco Faculdade de Ciências e Tecnologia Universidade Nova de Lisboa A Faculdade de Ciências e Tecnologia e a Universidade Nova de Lisboa têm o direito, perpétuo e sem limites geográficos, de arquivar e publicar esta dissertação através de exemplares impressos reproduzidos em papel ou de forma digital, ou por qualquer outro meio conhecido ou que venha a ser inventado, e de a divulgar através de repositórios científicos e de admitir a sua cópia e distribuição com objectivos educacionais ou de investigação, não comerciais, desde que seja dado crédito ao autor e editor. V VI Agradecimentos Durante a realização desta tese, contei com o apoio de várias pessoas sem as quais não teria concluído esta etapa. -
Using Sodium and Potassium Bicarbonates in the Prevention and Treatment of All Sickness and Disease
International Journal of Complementary & Alternative Medicine Using Sodium and Potassium Bicarbonates in the Prevention and Treatment of all Sickness and Disease Abstract Mini Review This article suggests that the use sodium and potassium bicarbonates are non- Volume 9 Issue 6 - 2017 toxic primary alkalizing agents in the prevention and treatment of all cancers, kidney disease, liver disease, Type I & Type II diabetes, Lupus, heart disease, Pharmacological toxicosis, vascular surgery operation, tonsillar herniation due Universal Medical Imaging Group, USA to cerebral edema, lactic acid toxicosis, and hyponatremia or low salt or loss of salts due to excessive or over-exercise! *Corresponding author: Robert O Young, Universal Medical Imaging Group, 16390 Dia Del Sol Valley Center, California Keywords: Cancer; Diabetes; Lupus; Heart disease; Vascular surgery; 92082, USA, Tel: 760 751 8321; Herniation; Cerebral edema; Lactic acid toxicosis; Liver disease; Kidney disease; Email: Hyponatremia; Pharmacological toxicosis Received: January 10, 2016 | Published: December 08, 2017 Introduction Sodium and potassium bicarbonate increases the hydroxyl ions or electron levels through increased alkalinity to the cells Sodium and potassium bicarbonate are excellent agents for buffering the metabolic acids that can cause cancer [20]. It is a natural alkaline approach in the treatment for all sickness and also one of the most basic medicines in allopathic and alternative disease, including cancer. Sodium bicarbonate is the universal medicine we have for the treatment of kidney disease. Research by mainstream treatment of acidosis. It is used every day by British scientists at the Royal London Hospital shows that sodium oncologists to neutralize the heavy acidic nature of their chemical bicarbonate can dramatically slow the progress of chronic kidney and chemotherapeutic agents which are often quite toxic. -
Food and Drug Administration, HHS § 184.1639
Food and Drug Administration, HHS § 184.1639 (2) The ingredient is used in food at Academy Press, 2101 Constitution Ave. levels not to exceed current good man- NW., Washington, DC 20418, or may be ufacturing practice. examined at the National Archives and (d) Prior sanctions for this ingredient Records Administration (NARA). For different from the uses established in information on the availability of this this section do not exist or have been material at NARA, call 202–741–6030, or waived. go to: http://www.archives.gov/ federallregister/ [48 FR 52444, Nov. 18, 1983] codeloflfederallregulations/ § 184.1634 Potassium iodide. ibrllocations.html. (c) The ingredient is used as a dough (a) Potassium iodide (KI, CAS Reg. strengthener as defined in § 170.3(o)(6) No. 7681–11–0) is the potassium salt of of this chapter. hydriodic acid. It occurs naturally in (d) The ingredient is used in the man- sea water and in salt deposits, but can ufacture of bread in accordance with be prepared by reacting hydriodic acid § 184.1(b)(2) of this chapter in an (HI) with potassium bicarbonate amount not to exceed 0.0075 percent (KHCO ). 3 based on the weight of the flour. (b) The ingredient meets the speci- (e) Prior sanctions for this ingredient fications of the ‘‘Food Chemicals different from the uses established in Codex,’’ 3d Ed. (1981), pp. 246–247, which this section do not exist or have been is incorporated by reference. Copies waived. may be obtained from the National Academy Press, 2101 Constitution Ave. [43 FR 11699, Mar. 21, 1978, as amended at 49 NW., Washington, DC 20418, or may be FR 5613, Feb.