TEA-hydroiodide
2,2',2''-nitrilotrisethanol hydroiodide

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  American International Chemical, Inc.

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  CODE130408 CODE130408
  Product(s):
  130408 TEA Hydroiodide

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  CODE130408 CODE130408
  Product(s):
  7601-53-8 Ethanol,2,2',2''-nitrilotris-, hydriodide (9CI)

Name: 2-[bis(2-hydroxyethyl)amino]ethanol;hydroiodide CAS Number: 7601-53-8 3D/inchi ECHA EINECS - REACH Pre-Reg: 231-508-2 FDA UNII: DT98IT03JK Molecular Weight: 277.10259000 Formula: C6 H16 I N O3 NMR Predictor: Predict (works with chrome, Edge or firefox) Category:buffering agents   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Boiling Point: 335.40 °C. @ 760.00 mm Hg (est) Vapor Pressure: 0.000008 mmHg @ 25.00 °C. (est) Flash Point: 365.00 °F. TCC ( 185.00 °C. ) (est) logP (o/w): -1.108 (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: CosIng: cosmetic data Cosmetic Uses: buffering agents skin conditioning   Suppliers: American International Chemical, LLC. TEA Hydroiodide BOC Sciences For experimental / research use only. Ethanol,2,2',2''-nitrilotris-, hydriodide (9CI) Vevy Europe IODOTRAT Odor: characteristic Use: Low molecular weight organic iodine (thus non proteic) for body contour treatment (cosmetic cellulitis). Does not give free iodine. Very stable and non-irritating, improves skin trophism and reduces fat deposits. Iodotrat activity on cellulitis and its mechanism of action were discovered by Vevy Europe in 1983. Several imitations of the reaction which produces iodine amine exist, overlooking that Iodotrat is not the simple result of that reaction but the end result of a specific procedure for the stabilisation of iodine and its capacity to be modified by membrane receptors (Beta-receptors of mastcells). See association with Zedomine-1, Zedomine-2, and Edesal, [Deep cosmetology of the dermis (C2 Concepts and Cosmetology 1987, Article No 1:27).   Safety Information:   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: Not determined Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: buffering agents Recommendation for TEA-hydroiodide usage levels up to:   not for fragrance use.   Recommendation for TEA-hydroiodide flavor usage levels up to:   not for flavor use.   Safety References: EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :2723762 National Institute of Allergy and Infectious Diseases:Data 2-[bis(2-hydroxyethyl)amino]ethanol;hydroiodide Chemidplus:0007601538   References:   2-[bis(2-hydroxyethyl)amino]ethanol;hydroiodide NIST Chemistry WebBook: Search Inchi Pubchem (cid): 2723762 Pubchem (sid): 135231327   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements HMDB (The Human Metabolome Database): Search ChemSpider: View   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms: 2-(bis(2- hydroxyethyl)amino)ethanol hydroiodide 2-[bis(2- hydroxyethyl)amino]ethanol;hydroiodide   iodotrat (Vevy) 2,2',2''- nitrilotrisethanol hydroiodide   triethanol amine hydroiodide   triethanolamine hydroiodide   Articles:   None found yet. Try the PubMed Search.

Notes: None found