2,2',2''-nitrilotrisethanol hydroiodide
None found
  • American International Chemical, LLC.
    • American International Chemical, Inc.
      Consistent sources
      North American supplier for globally sourced ingredients.
      AIC is a Framingham, MA based ISO Certified sales and marketing company serving the food, pharmaceutical, nutritional, personal care, biotech, and industrial markets of North America since 1972. Our success is a result of a company culture built on customer needs, along with partnerships with global manufacturers committed to the rigors and demands of the North American market. Our team of 30 Sales Representatives, along with our 19 strategically located warehouses are ready to supply product when and where you need it.
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      130408 TEA Hydroiodide
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2-[bis(2-hydroxyethyl)amino]ethanol;hydroiodide (Click)
CAS Number: 7601-53-8Picture of molecule
ECHA EINECS - REACH Pre-Reg: 231-508-2
Molecular Weight: 277.10259000
Formula: C6 H16 I N O3
NMR Predictor: Predict (works with chrome or firefox)
Category: buffering agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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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 mm/Hg @ 25.00 °C. (est)
Flash Point: 365.00 °F. TCC ( 185.00 °C. ) (est)
logP (o/w): -1.108 (est)
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Organoleptic Properties:
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: buffering agents
skin conditioning
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American International Chemical, LLC.
TEA Hydroiodide
BOC Sciences
For experimental / research use only.
Ethanol,2,2',2''-nitrilotris-, hydriodide (9CI)
Vevy Europe
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).
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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
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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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.
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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
Chemidplus: 0007601538
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NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 2723762
Pubchem (sid): 135231327
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (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
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Potential Blenders and core components note
None Found
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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2-(bis(2-hydroxyethyl)amino)ethanol hydroiodide
 iodotrat (Vevy)
2,2',2''-nitrilotrisethanol hydroiodide
 triethanol amine hydroiodide
 triethanolamine hydroiodide
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