DOCSLIB.ORG

CLA TG Powder 60% WDP (Low Odour)

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
CLA TG Powder 60% WDP (Low Odour) CLA TG Powder 60% WDP (Low Odour) Cambridge Commodities Chemwatch Hazard Alert Code: 2 Part Number: P10615 Issue Date: 11/01/2021 Version No: 1.1.23.11 Print Date: 24/09/2021 Safety data sheet according to REACH Regulation (EC) No 1907/2006, as amended by UK REACH Regulations SI 2019/758 S.REACH.GB.EN SECTION 1 Identification of the substance / mixture and of the company / undertaking 1.1. Product Identifier Product name CLA TG Powder 60% WDP (Low Odour) Chemical Name Not Applicable Synonyms Not Available Chemical formula Not Applicable Other means of P10615 identification 1.2. Relevant identified uses of the substance or mixture and uses advised against Polyunsaturated fatty acid (PUFA) or its derivative or contains significant amounts of its derivatives. Fatty acid viscosity (thickness) and melting temperature increases with decreasing number of double bonds; therefore, monounsaturated fatty acids (MUFAs) have a higher melting point than polyunsaturated fatty acids (more double bonds) and a lower melting point than saturated fatty acids (no double bonds). Polyunsaturated fatty acids are generally liquids at room temperature. Vegetable oils (triglycerides) can be divided into three groups; non-drying, semi-drying, and drying oils, depending on their fatty acid pattern. Drying-oils are highly unsaturated oils that oxidise in air to produce a tack-free film with time. A drying-oil is traditionally defined as an oil with an average number of greater than 2.2 diallylic (unsaturated) groups per molecule. Linseed and tung oil (PUFAs) are commonly used drying-oils. Omega-6 fatty acids (also referred to as omega-6 fatty acids or n-6 fatty acids) are a family of pro-inflammatory and anti-inflammatory polyunsaturated fatty acids that have in common a final carbon-carbon double bond in the n-6 position, that is, Relevant identified uses the sixth bond, counting from the methyl end The biological effects of the omega-6 fatty acids are largely produced during and after physical activity for the purpose of promoting growth and during the inflammatory cascade to halt cell damage and promote cell repair by their conversion to omega-6 eicosanoids that bind to diverse receptors found in every tissue of the body. The conversion of cell membrane arachidonic acid (20:4n-6) to omega-6 prostaglandin and omega-6 leukotriene eicosanoids during the inflammatory cascade provides many targets for pharmaceutical drugs to impede the inflammatory process in atherosclerosis, asthma, arthritis, vascular disease, thrombosis, immune-inflammatory processes, and tumour proliferation. Competitive interactions with the omega-3 fatty acids affect the relative storage, mobilisation, conversion and action of the omega-3 and omega-6 eicosanoid precursor. Drying oils are characterized by high levels of fatty acids One common measure of the siccative (drying) property of oils is iodine number. Oils with an iodine number greater than 130 are considered drying, those with an iodine number of 115-130 are semi-drying oils and those with an iodine number of less than 115 are non-drying oils Product code: P10615 Version No: 1.1.23.2 Page 1 of 34 S.REACH.GB.EN Lancaster Way Business Park Safety Data Sheet (Conforms to Regulation (EU) No 2020/878) Ely, Cambridgeshire, CB6 3NX, UK. Chemwatch: 9-799394 +44 (0) 1353 667258 Issue Date: 11/01/2021 [email protected] Print Date: 24/09/2021 www.c-c-l.com The "drying"," hardening", or, more properly, "curing" of oils is the result of an exothermic reaction in the form of autoxidation Oxygen attacks the hydrocarbon chain, touching off a series of addition reactions. As a result, the oil, forms long, chain-like a vast polymer network molecules, resulting in a vast polymer network. Over time, this network may undergo further change. Certain functional groups in the networks become ionised and the network transitions from a system held together by nonpolar covalent bonds to one governed by the ionic forces between these functional groups and the metal ions present in the paint pigment. In oil autoxidation, oxygen attacks a hydrocarbon chain, often at the site of an allylic hydrogen (a hydrogen on a carbon atom adjacent to a double bond). This produces, a free radical a substance with an unpaired electron which makes it highly reactive. A series of addition reactions ensues. Each step produces additional free radicals, which then engage in further polymerization. The process finally terminates when free radicals collide, combining their unpaired electrons to form a new bond. The polymerisation stage occurs over a period of days to weeks, and renders the film dry to the touch. Uses advised against Not Applicable 1.3. Details of the supplier of the safety data sheet Registered company name Cambridge Commodities Address Lancaster Way Business Park, Ely, Cambridgeshire Cambridgeshire CB6 3NX United Kingdom Telephone +44 1353 667258 Fax Not Available Website Not Available Email [email protected] 1.4. Emergency telephone number Association / Organisation Not Available Emergency telephone Not Available numbers Other emergency Not Available telephone numbers SECTION 2 Hazards identification 2.1. Classification of the substance or mixture Classified according to GB-CLP Regulation, UK SI H335 - Specific Target Organ Toxicity - Single Exposure (Respiratory Tract Irritation) Category 3, H315 - Skin Corrosion/Irritation 2019/720 and UK SI Category 2, H319 - Serious Eye Damage/Eye Irritation Category 2 2020/1567 [1] Legend: 1. Classified by Chemwatch; 2. Classification drawn from GB-CLP Regulation, UK SI 2019/720 and UK SI 2020/1567 2.2. Label elements Product code: P10615 Version No: 1.1.23.2 Page 2 of 34 S.REACH.GB.EN Lancaster Way Business Park Safety Data Sheet (Conforms to Regulation (EU) No 2020/878) Ely, Cambridgeshire, CB6 3NX, UK. Chemwatch: 9-799394 +44 (0) 1353 667258 Issue Date: 11/01/2021 [email protected] Print Date: 24/09/2021 www.c-c-l.com Hazard pictogram(s) Signal word Warning Hazard statement(s) H335 May cause respiratory irritation. H315 Causes skin irritation. H319 Causes serious eye irritation. Supplementary statement(s) EUH019 May form explosive peroxides. EUH001 Explosive when dry. Precautionary statement(s) Prevention P271 Use only outdoors or in a well-ventilated area. P261 Avoid breathing dust/fumes. P280 Wear protective gloves, protective clothing, eye protection and face protection. P264 Wash all exposed external body areas thoroughly after handling. Precautionary statement(s) Response P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P312 Call a POISON CENTER/doctor/physician/first aider/if you feel unwell. P337+P313 If eye irritation persists: Get medical advice/attention. P302+P352 IF ON SKIN: Wash with plenty of water and soap. P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing. P332+P313 If skin irritation occurs: Get medical advice/attention. P362+P364 Take off contaminated clothing and wash it before reuse. Precautionary statement(s) Storage P405 Store locked up. P403+P233 Store in a well-ventilated place. Keep container tightly closed. Precautionary statement(s) Disposal P501 Dispose of contents/container to authorised hazardous or special waste collection point in accordance with any local regulation. 2.3. Other hazards Cumulative effects may result following exposure*. Product code: P10615 Version No: 1.1.23.2 Page 3 of 34 S.REACH.GB.EN Lancaster Way Business Park Safety Data Sheet (Conforms to Regulation (EU) No 2020/878) Ely, Cambridgeshire, CB6 3NX, UK. Chemwatch: 9-799394 +44 (0) 1353 667258 Issue Date: 11/01/2021 [email protected] Print Date: 24/09/2021 www.c-c-l.com Limited evidence of a carcinogenic effect*. Possible respiratory and skin sensitizer*. REACh - Art.57-59: The mixture does not contain Substances of Very High Concern (SVHC) at the SDS print date. SECTION 3 Composition / information on ingredients 3.1.Substances See 'Composition on ingredients' in Section 3.2 3.2.Mixtures 1.CAS No 2.EC No Classified according to GB-CLP Regulation, UK SI 2019/720 and Nanoform Particle %[weight] Name 3.Index No UK SI 2020/1567 Characteristics 4.REACH No 1.121250-47-3 Skin Corrosion/Irritation Category 2, Serious Eye Damage/Eye 2.200-470-9 Irritation Category 2, Specific Target Organ Toxicity - Single 70 linoleic acid Not Available 3.Not Available Exposure (Respiratory Tract Irritation) Category 3; H315, H319, 4.Not Available H335, EUH001, EUH019 [1] 1.68131-37-3 2.268-616-4 corn syrup, 10-25 Not Applicable Not Available 3.Not Available dehydrated 4.Not Available 1.9005-46-3 2.Not Available 2-8 casein sodium Not Applicable Not Available 3.Not Available 4.Not Available 1.7631-86-9 2.231-545-4 silica 0.2-2 Not Applicable Not Available 3.Not Available amorphous 4.Not Available 1.7758-11-4 potassium 2.231-834-5 Serious Eye Damage/Eye Irritation Category 2, Hazardous to the 0.1-2 phosphate, Not Available 3.Not Available Aquatic Environment Long-Term Hazard Category 4; H319, H413 [1] dibasic 4.Not Available 1.137-66-6 2.205-305-4 ascorbyl 0.01-0.2 Not Applicable Not Available 3.Not Available palmitate 4.Not Available Legend: 1. Classified by Chemwatch; 2. Classification drawn from GB-CLP Regulation, UK SI 2019/720 and UK SI 2020/1567; 3. Classification drawn from C&L; * EU IOELVs available; [e] Substance identified as having endocrine disrupting properties SECTION 4 First aid measures 4.1. Description of first aid measures If this product comes in contact with the eyes: Wash out immediately with fresh running water. Eye Contact Ensure complete irrigation of the eye by keeping eyelids apart and away from eye and moving the eyelids by occasionally lifting the upper and lower lids.
Load more

Recommended publications
  • Enhanced Fatty Acid Methyl Esters Recovery Through a Simple And
    www.nature.com/scientificreports OPEN Enhanced fatty acid methyl esters recovery through a simple and rapid direct transesterifcation of freshly harvested biomass of Chlorella vulgaris and Messastrum gracile Saw Hong Loh1,2*, Mee Kee Chen1,2, Nur Syazana Fauzi2,3, Ahmad Aziz1,2 & Thye San Cha1,2* Conventional microalgae oil extraction applies physicochemical destruction of dry cell biomass prior to transesterifcation process to produce fatty acid methyl esters (FAMEs). This report presents a simple and rapid direct transesterifcation (DT) method for FAMEs production and fatty acid profling of microalgae using freshly harvested biomass. Results revealed that the FAMEs recovered from Chlorella vulgaris were 50.1 and 68.3 mg with conventional oil-extraction-transesterifcation (OET) and DT method, respectively. While for Messastrum gracile, the FAMEs recovered, were 49.9 and 76.3 mg, respectively with OET and DT methods. This demonstrated that the DT method increased FAMEs recovery by 36.4% and 53.0% from C. vulgaris and M. gracile, respectively, as compared to OET method. Additionally, the DT method recovered a signifcantly higher amount of palmitic (C16:0) and stearic (C18:0) acids from both species, which indicated the important role of these fatty acids in the membranes of cells and organelles. The DT method performed very well using a small volume (5 mL) of fresh biomass coupled with a shorter reaction time (~ 15 min), thus making real-time monitoring of FAMEs and fatty acid accumulation in microalgae culture feasible. Te key processes involved in the fatty acid profling of microalgae are cultivation, biomass harvesting and drying, oil extraction and transesterifcation to produce fatty acid methyl esters (FAMEs).
    [Show full text]
  • Oilseeds As Crop Biofactories for Industrial Raw Materials
    AOF Forum, 2004 Grain & chemical industry drivers Oilseeds as crop ! Global competition increasing biofactories for ! Downward pressure on price and market share industrial raw ! Need to diversify away from commodities ! Need to capture maximum value materials Allan Green ! Desirable to replace petroleum with renewable CSIRO Plant Industry sources of industrial raw materials ! Need for increased biodegradability of C O C O C O industrial products C C C C C C O C O C O C Opportunities for industrial use Seed oils are triglycerides ! Current Australian non-food use of vegetable oils ! Seed oils are comprised almost entirely of is about 12,000 tonnes (~3% of total oil usage) triglycerides composed of fatty acids ! Long-term opportunities exist for:- ! Oils are deposited in the seed in oilbodies - direct use in lubricants and inks - bio-diesel fuels (e.g. rapeseed ME) - specialty oleochemicals - pure fatty acids (e.g. oleic acid) - fatty acid derivatives (e.g. erucamide) - alkyl units for polymers (e.g. nylon) - biodegradable plastics - pharmaceutical proteins Fatty acids are like petrochemicals Oil composition can be changed ! Fatty acids are simply hydrocarbon chains ! Seed oils are needed only for energy of various lengths with a carboxyl group storage and release during germination (~COOH) at one end (i.e. no structural role) ! Fatty acids can have bond types or functional groups that allow them to be ! Fatty acid composition can therefore be cleaved or derivatised by chemical dramatically modified, provided that new processing fatty
    [Show full text]
  • Role of Epoxide Hydrolases in Lipid Metabolism
    Biochimie 95 (2013) 91e95 Contents lists available at SciVerse ScienceDirect Biochimie journal homepage: www.elsevier.com/locate/biochi Mini-review Role of epoxide hydrolases in lipid metabolism Christophe Morisseau* Department of Entomology and U.C.D. Comprehensive Cancer Center, One Shields Avenue, University of California, Davis, CA 95616, USA article info abstract Article history: Epoxide hydrolases (EH), enzymes present in all living organisms, transform epoxide-containing lipids to Received 29 March 2012 1,2-diols by the addition of a molecule of water. Many of these oxygenated lipid substrates have potent Accepted 8 June 2012 biological activities: host defense, control of development, regulation of blood pressure, inflammation, Available online 18 June 2012 and pain. In general, the bioactivity of these natural epoxides is significantly reduced upon metabolism to diols. Thus, through the regulation of the titer of lipid epoxides, EHs have important and diverse bio- Keywords: logical roles with profound effects on the physiological state of the host organism. This review will Epoxide hydrolase discuss the biological activity of key lipid epoxides in mammals. In addition, the use of EH specific Epoxy-fatty acids Cholesterol epoxide inhibitors will be highlighted as possible therapeutic disease interventions. Ó Juvenile hormone 2012 Elsevier Masson SAS. All rights reserved. 1. Introduction hydrolyzed by a water molecule [8]. Based on this mechanism, transition-state inhibitors of EHs have been designed (Fig. 1B). Epoxides are three atom cyclic ethers formed by the oxidation of These ureas and amides are tight-binding competitive inhibitors olefins. Because of their highly polarized oxygen-carbon bonds and with low nanomolar dissociation constants (KI) [9] [10].
    [Show full text]
  • Utrecht Art Supplies What Not to Use As Varnish
    Utrecht Art Supplies What Not to Use as Varnish • Removable with light solvents and gentle manipulation (should not require strong solvents or hard scrubbing) • Should not fuse with, soften or dissolve completely dry paint • Resin content should be documented to aid in later cleaning and care Alkyd Alkyd-based painting mediums are great for improving paint flow, imparting gloss, increasing transparency, and promoting a tough, flexible Ask the Expert: "Lately I've been finishing my paint film, but as a top-coat, they aren't oil paintings with a coat of alkyd medium to give reversible with even very harsh solvents. A coat a shiny finish. My friend says this might not be a of alkyd is permanent, for better or worse. Also, good idea. If I can coat an acrylic painting with some alkyd mediums impart harsh glare, making gloss medium, what's the problem with using it difficult to install and light the finished work. alkyd medium on oils?" Wax A: Artists sometimes make the mistake of top- coating a painting with a medium or other Wax is sometimes used as a top-coat over material which gives a good appearance in the paintings, but it has some significant short term, but which causes problems later. shortcomings for this application. Wax remains Alkyd-based painting mediums are great for their soft indefinitely, so it doesn't impart protection intended purpose, but alkyds don't meet the against mechanical damage from handling and requirements of a picture varnish. casual contact. Wax also tends to attract and hold dust. Cold wax medium has an attractive A picture varnish should satisfy these appearance when first applied, especially when functions: buffed to a shine, but can later become • Permanently neutral in color and lackluster.
    [Show full text]
  • Prohibited Materials for Organic Crop Production
    United States Department of Agriculture 1400 Independence Avenue SW. NOP 5034-2 Agricultural Marketing Service Room 2646-South Building Effective Date: December 2, 2016 National Organic Program Washington, DC 20250 Page 1 of 2 Guidance Appendix of Prohibited Materials for Organic Crop Production This list is provided for reference purposes and is not intended to be comprehensive. In addition to the materials identified below, any synthetic material that is not included at section 205.601 of the National List is prohibited for crop production. The materials listed below have been specifically prohibited on the National List at section 205.602, have been petitioned and reviewed by National Organic Standards Board and not recommended for addition to the National list, have expired from the National List, and/or have been reviewed by a Federal agency and determined to be prohibited for organic crop production. 1,4-Dimethylnaphthalene Manganous Oxide, except as provided on 3-Decen-2-one § 205.601(j) 6-Benzyladenine Methyl Bromide Acetylated Lanolin Alcohol Methyl Laurate Acrylic Acid Methyl Ester, Polymer with Monocalcium Phosphate Acrylonitrile and 1,3-Butadiene Nickel Salts, Synthetic Ammonium Nonanoate, except as provided Niter on § 205.601 Pelargonic Acid Arsenic Pentaerythritol Monostearate Ash from Manure Burning Pentaerythritol Tetrastearate Avermectin Piperonyl Butoxide Basic Slag, agricultural slag Propylene glycol monolaurate (PGML) Biosolids Polyoxin D Zinc Salt Calcium Carbide Potassium Sulfate (synthetic form) Calcium Oxide, fertilizer
    [Show full text]
  • Vinyl Toluene Modified Alkyd Resins
    VINYL TOLUENE MODIFIED ALKYD RESINS VT can be used to prepare a wide variety of alkyd coating resins. In general, the base alkyd is formulated to use low cost VT to reduce the oil length of the vehicle. For example using VT with a very long-oil soya alkyd produces improved drying time and hardness. These improvements are realized without reducing the good naphtha solubility of the vehicle. OIL AND BASE ALKYD SELECTION The type of oil used in the copolymer reaction is an important variable. Variations in the chemical structure such as degree of unsaturation, type of unsaturation and degree of polymerization have an effect on the product. Copolymers prepared from heavy-bodied oils have higher viscosities, faster drying rates and greater utility for protective coatings than those based on lower viscosity oils. Conjugated oils react readily with VT to form compatible products without use of a catalyst. VT reactivity with unconjugated oils is less active and appears to be a function of the Iodine value of the oil. Use of a small amount of suitable catalyst allows production of products with good homogeneity from any of the convential drying and semi-drying oils. Copolymers of maximum hardness, toughness and flexibility can be prepared by using one of the highly reactive oils such as dehydrated castor oil. VT modified alkyd properties depend upon the base alkyd resin used. Close attention must be given to the choice of polyhydric alcohols and the average functionality of the acids in addition to the type and amount of drying oil used. Viscosity buildup, dry time and film integrity are influenced by the functionality of both the polyhydric alcohol and acid constituents.
    [Show full text]
  • Influence of the Fatty Acid Pattern on the Drying of Linseed Oils
    Influence of the fatty acid pattern on the drying of linseed oils Cecilia Stenberg AKADEMISK AVHANDLING Som med tillstånd av Kungliga Tekniska Högskolan i Stockholm framlägges till offentlig granskning för avläggande av teknisk licentiatexamen tisdagen den 15 juni 2004, kl.10.00 i sal K1, Teknikringen 56, KTH, Stockholm. LIST OF PAPERS This thesis is a summary of the following papers: 1 “A study of the drying of linseed oils with different fatty acid patterns using RTIR-spectroscopy and Chemiluminescence (CL)” Accepted in Industrial Crops and Products (2004) 2 “Drying of linseed oil wood coatings using reactive diluents” To be submitted to Surface Coatings International Part B: Coatings Transactions (2004) ABSTRACT The interest in renewable resources due to environmental factors has increased the interest to use new VOC-free linseed oil qualities together with reactive diluents for coating applications. The drying of two linseed oils, Oil A with a high content (74,2 %) of linoleic acid (C18:2) and oil B, a more traditional linseed oil with a high amount (55,2-60,4 %) of linolenic acid (C18:3), was followed in order to reveal how the structural variations of the oils fatty acid pattern and the addition of the fatty acid methyl ester of oil A as a reactive diluent (0, 20 40 wt%) can change the drying performances of the oils and their final film properties. The influence of the drying temperature and the influence of driers was investigated. The drying performance of the different oil formulations applied on pinewood substrates was briefly investigated. Two different analytical techniques, chemiluminescence (CL), and real-time infrared spectroscopy, (RTIR), were shown to be versatile tools for the analysis of the drying process.
    [Show full text]
  • Nonanoic Acid Product-Type 2 (Disinfectants and Algaecides Not Intended for Direct Application to Humans Or Animals) September 2013 Austria
    Regulation (EU) n°528/2012 concerning the making available on the market and use of biocidal products Evaluation of active substances Assessment Report Modification of the conditions of approval Nonanoic acid Product-type 2 (Disinfectants and algaecides not intended for direct application to humans or animals) September 2013 Austria Nonanoic acid Product-type 10 2013 Nonanoic acid (PT 2) Assessment report Finalised in the Standing Committee on Biocidal Products at its meeting on 27 September 2013 CONTENTS 1. STATEMENT OF SUBJECT MATTER AND PURPOSE ....................................... 4 1.1. Principle of evaluation ...................................................................................... 4 1.2. Purpose of the assessment ................................................................................. 4 1.3. Procedure followed ........................................................................................... 5 2. OVERALL SUMMARY AND CONCLUSIONS ...................................................... 7 2.1. Presentation of the Active Substance ................................................................ 7 2.1.1. Identity, Physico-Chemical Properties & Methods of Analysis ........ 7 2.1.2. Intended Uses and Efficacy ................................................................. 8 2.1.3. Classification and Labelling of the active substance Nonanoic acid .. 9 2.1.4. Classification and labelling of the biocidal product NEU 1170 H.... 12 2.2. Summary of the Risk Assessment ..................................................................
    [Show full text]
  • ANTICORROSION UV CURABLE ALKYDS a Thesis Presented to The
    ANTICORROSION UV CURABLE ALKYDS A Thesis Presented to The Graduate Faculty of The University of Akron In Partial Fulfillment of the Requirements for the Degree Master of Science Rongcheng Xu December, 2017 ANTICORROSION UV CURABLE ALKYDS Rongcheng Xu Thesis Approved: Accepted: ______________________________ _____________________________ Advisor Department Chair Dr. Mark Soucek Dr. Sadhan Jana ______________________________ ______________________________ Faculty Reader Dean of the College Dr. Xiong Gong Dr. Eric Amis ______________________________ ______________________________ Faculty Reader Executive Dean of Graduate School Dr. Younjin Min Dr. Chand Midha ______________________________ _____________________________ Date:_________________________ ii ACKNOWLEDGEMENTS I would like to sincerely thank the amazing people who have helped and supported me throughout my graduate research. I would like to sincerely thank Professor Mark Soucek, for his guidance, support, training, and advice during my time at the University of Akron. I had the pleasure of being trained by excellent mentors and group members, especially Dr. Qianhe Wang, Dr. Lei Meng, and Dr. Ryan Salata. I’d also like to thank Anisa Cobaj, Brittany Pellegrene, and Dr. Sayyed Abed for their experimental support. Especially, I want to thank my classmates Cheng Zhang and Haoran Wang for their precious help and encouragement. Most importantly, I want to thank my parents for their unconditional love and everything they have done for me. In addition, I want to thank my girlfriend Yidan Zhang for her support all the way and hope her a happy PhD life in Cornell University. iii ABSTRACT Alkyds are essentially oil modified polyesters derived from oils, dibasic acids and polyols. Being bio-renewable, versatile and low-cost made alkyds one of the most consumed coating material in the world.
    [Show full text]
  • Fatty Acids As Essential Adjuvants to Treat Various Ailments and Their Role in Drug Delivery: a Review
    Nutrition 65 (2019) 138À157 Contents lists available at ScienceDirect Nutrition journal homepage: www.nutritionjrnl.com Review article Fatty acids as essential adjuvants to treat various ailments and their role in drug delivery: A review Aakash Katdare B. Pharm, MS. Pharm, Shreya Thakkar B. Pharm, M. Pharm, Shivshankar Dhepale B. Pharm, MS. Pharm, Dignesh Khunt B. Pharm, M. Pharm, Manju Misra B. Pharm, M. Pharm, Ph.D. * Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Ahmedabad, India ARTICLE INFO ABSTRACT Article History: Since the discovery of fatty acids, a niche has been carved for their vital role as adjuvants in drug delivery and Received 23 May 2018 as treatment for various diseases. The literature has repeatedly described the essential role of various fatty Received in revised form 1 February 2019 acids in treating a wide range of diseases and disorders, from central nervous system diseases to wound heal- Accepted 20 March 2019 ing. The use of fatty acids has expanded to many horizons and in recent decades they have gained impor- tance as drug delivery adjuvants in addition to their auxiliary benefits in treating various diseases. Although Keywords: fatty acids aid in solving both formulation-based and therapeutic challenges to our knowledge, they have Polyunsaturated FA never been viewed as dual agents in modern scientific literature. The aim of this review was to provide this FA Lipids perspective and combine the very discreet literature about fatty acids, which includes their role as therapeu- Oils tic adjuvants and drug delivery agents. It gives insights on the use of fatty acids in treating the diseases of the Penetration enhancers eye, skin, central nervous system, viral diseases, and so on.
    [Show full text]
  • TC-90 High Gamma Mixed Tocopherols
    TC-90 High Gamma Mixed Tocopherols Cambridge Commodities Chemwatch Hazard Alert Code: 2 Part Number: P28128 Issue Date: 24/07/2019 Version No: 2.5.22.11 Print Date: 23/09/2021 Safety data sheet according to REACH Regulation (EC) No 1907/2006, as amended by UK REACH Regulations SI 2019/758 S.REACH.GB.EN SECTION 1 Identification of the substance / mixture and of the company / undertaking 1.1. Product Identifier Product name TC-90 High Gamma Mixed Tocopherols Chemical Name Not Applicable Synonyms Not Available ENVIRONMENTALLY HAZARDOUS SUBSTANCE, LIQUID, N.O.S. (contains gamma-tocopherol, beta-tocotrienol, delta- Proper shipping name tocopherol, sunflower oil and alpha-tocopherol) Chemical formula Not Applicable Other means of P28128 identification 1.2. Relevant identified uses of the substance or mixture and uses advised against Relevant identified uses Use according to manufacturer's directions. Uses advised against Not Applicable 1.3. Details of the supplier of the safety data sheet Registered company name Cambridge Commodities Address Lancaster Way Business Park, Ely, Cambridgeshire Cambridgeshire CB6 3NX United Kingdom Telephone +44 1353 667258 Fax Not Available Website Not Available Email [email protected] 1.4. Emergency telephone number Association / Organisation Not Available Emergency telephone Not Available numbers Other emergency Not Available telephone numbers Product code: P28128 Version No: 2.5.22.2 Page 1 of 25 S.REACH.GB.EN Lancaster Way Business Park Safety Data Sheet (Conforms to Regulation (EU) No 2020/878) Ely, Cambridgeshire, CB6 3NX, UK. Chemwatch: 9-596035 +44 (0) 1353 667258 Issue Date: 24/07/2019 [email protected] Print Date: 23/09/2021 www.c-c-l.com SECTION 2 Hazards identification 2.1.
    [Show full text]
  • CLH Report for Nonanoic Acid
    CLH Report For Nonanoic Acid CLH report Proposal for Harmonised Classification and Labelling Based on Regulation (EC) No 1272/2008 (CLP Regulation), Annex VI, Part 2 Substance Name: Nonanoic Acid EC Number: 203-931-2 CAS Number: 112-05-0 Index Number: 607-197-00-8 Contact details for dossier submitter: Umweltbundesamt GMbH on behalf of AT Competent Authority Federal Ministry of Agriculture, Forestry, Environment and Water Management Version number: 2 Date: 22.Dec. 2011 1 CLH Report For Nonanoic Acid 2 CLH Report For Nonanoic Acid CONTENTS Part A. 1 PROPOSAL FOR HARMONISED CLASSIFICATION AND LABELLING ................................................ 6 1.1 SUBSTANCE .................................................................................................................................................... 6 1.2 HARMONISED CLASSIFICATION AND LABELLING PROPOSAL ............................................................................... 6 1.3 PROPOSED HARMONISED CLASSIFICATION AND LABELLING BASED ON CLP REGULATION AND/OR DSD CRITERIA 7 2 BACKGROUND TO THE CLH PROPOSAL ............................................................................................... 11 2.1 HISTORY OF THE PREVIOUS CLASSIFICATION AND LABELLING ......................................................................... 11 2.2 SHORT SUMMARY OF THE SCIENTIFIC JUSTIFICATION FOR THE CLH PROPOSAL ................................................ 12 2.3 CURRENT HARMONISED CLASSIFICATION AND LABELLING .............................................................................
    [Show full text]