Glycerol (/ ˈ ɡ l ɪ s ə r ɒ l /; also called glycerine or glycerin; see spelling differences) is a simple polyol compound. It has a molecular weight of 92.09 g/mol and its IUPAC name is 1, 2, 3- Propanetriol or 1, 2, 3- Trihydroxypropane. It has a role as an algal metabolite and a Caenorhabditis elegans metabolite. Combustible. It has a role as a vasodilator agent, a nitric oxide donor, an explosive, a prodrug, a tocolytic agent, a muscle relaxant and a xenobiotic. [Note: The solid form melts above 64F but the liquid form freezes at a much lower temperature. 1-Stearoyl-rac-glycerol. CopyCopied, Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, Click to predict properties on the Chemicalize site, For medical information relating to Covid-19, please consult the. EC number: 200-289-5 | CAS number: 56-81-5. Stars This entity has been manually annotated by … The glycerol backbone is found in those lipids known as glycerides. Aldo MSD. Stearic acid 1-monoglyceride. ], Skin: No recommendation Eyes: No recommendation Wash skin: No recommendation Remove: No recommendation Change: No recommendation, NIOSH REL : See Appendix D OSHA PEL ? Display Name: Glycerol EC Number: 200-289-5 EC Name: Glycerol CAS Number: 56-81-5 Molecular formula: C3H8O3 IUPAC Name: propane-1,2,3-triol Please upgrade your Internet Explorer to a newer version. By standard biochemical convention, the ending ‘-ate’ 1-Glyceryl stearate. Glycerol is a simple polyol compound. ; Ruiz-Rodriguez A.; Pernin K.; Cayot N., Influence of eggs on the aroma composition of a sponge cake and on the aroma release in model studies on flavored sponge cakes, J. Agric. Owing to the presence of three hydroxyl groups, glyc… Information on Registered Substances comes from registration dossiers which have been assigned a registration number. ; Reichenbacher, M.; Danzer, K.; Hurlbeck, C.; Bartzsch, C.; Feller, K.-H., Investigations on wine bouquet components by solid-phase microextraction-capillary gas chromatography (SPME-CGC) using different fibers, J. Hi. Glycerol monopalmitate. Glycerin 1-monostearate. C(C(CO)O)O It is also widely used as a sweetener in the food industry and as a humectant in pharmaceutical formulations. MG(16:0) monopalmitin-1-glyceride. Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice. Widely used in sample buffer preparation. Due to having antimicrobial and antiviral properties it is widely used in FDA approved wound and burn treatments. 1-MONOSTEARIN. This site is not fully supported in Internet Explorer 7 (and earlier versions). IPR-RAT LD50 8700 mg kg-1 , ORL-RAT LD50 12600 mg kg-1, SCU-RAT LD50 100 mg kg-1, ORL-MUS LD50 8700 mg kg-1, Organic Compound; Food Toxin; Metabolite; Household Toxin; Animal Toxin; Natural Compound, Eye: Irrigate immediately Skin: Water wash Breathing: Fresh air, Irritation eyes, skin, respiratory system; headache, nausea, vomiting; kidney injury, Strong oxidizers (e.g., chromium trioxide, potassium chlorate, potassium permanganate) [Note: Hygroscopic (i.e., absorbs moisture from the air). It is a colorless, odorless, viscous liquid that is sweet-tasting and non-toxic. Fatty acids are numbered with the carbon atom of the carboxyl group as C-1. Display Name: Glycerol monomyristate EC Number: 248-329-0 EC Name: Glycerol monomyristate CAS Number: 27214-38-6 Molecular formula: C17H34O4 IUPAC Name: