Basic information Safety Supplier Related

3,3',5-TRIIODOTHYROACETIC ACID

Basic information Safety Supplier Related

3,3',5-TRIIODOTHYROACETIC ACID Basic information

Product Name:
3,3',5-TRIIODOTHYROACETIC ACID
Synonyms:
  • TIRATRICOL
  • TRIAC
  • 3,3',5-TRIIODOTHYROACETIC ACID
  • 4-[4-HYDROXY-3-IODOPHENOXY]-3,5-DIIODOPHENYLACETIC ACID
  • 4'-HYDROXY-3,5,3'-TRIIODOPHENOXY-4-PHENYLACETIC ACID
  • 2-[4-(4-hydroxy-3-iodo-phenoxy)-3,5-diiodo-phenyl]acetic acid
  • 3,3,5-triiodothyroacetic acid,*free acid
  • TRIIODOTHYROACETICACID
CAS:
51-24-1
MF:
C14H9I3O4
MW:
621.93
EINECS:
200-086-1
Product Categories:
  • API
  • Bioactive Small Molecules
  • Building Blocks
  • C13 to C42+
  • Carbonyl Compounds
  • Carboxylic Acids
  • Aromatics
  • Drug Analogues
  • Cell Biology
  • Chemical Synthesis
  • Organic Building Blocks
  • T
  • Aromatics, Drug Analogues, Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
  • TRIAC
  • Aromatic Phenylacetic Acids and Derivatives
  • Impurities
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
51-24-1.mol
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3,3',5-TRIIODOTHYROACETIC ACID Chemical Properties

Melting point:
65°; mp 180-183°
Boiling point:
531.6±50.0 °C(Predicted)
Density 
2.466±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated)
form 
Solid
pka
4.02±0.10(Predicted)
color 
White to Pale Beige
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22
Safety Statements 
36
WGK Germany 
3
HS Code 
2916.39.7900

MSDS

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3,3',5-TRIIODOTHYROACETIC ACID Usage And Synthesis

Chemical Properties

White to Off-White Solid

Originator

Triacana,Ana,Italy,1972

Uses

thyroid agent

Uses

3,3'',5-Triiodo Thyroacetic Acid (T3-Acetic Acid (USP)) is a thyroid hormone analogue. A potent Thyroxine impurity. Levothyroxine EP Impurity C.

Manufacturing Process

Preparation of 3:5-diiodo-4-(4'-hydroxyphenoxy)phenylacetic acid (diacid): A solution of ethyl 3:5-diiodo-4-(4'-methoxyphenoxy)phenyl acetate (9.5 g) in acetic acid (60 ml) was heated under reflux with hydroiodic acid (SG 1.7, 50 ml) and red phosphorus (0.5 g) for 1 hour. The hot solution was filtered and the filtrate concentrated at 50°C and 15 mm of mercury to above 20 ml. The residue was treated with water (70 ml) containing a little sodium thiosulfate to decolorize the product. The solid was collected by filtration and purified by the method of Harington and Pitt-Rivers [Biochem. J. (1952), Vol. 50, page 438]. Yield 8.36 g (95%). After crystallization from 70% (v/v) acetic acid it melted at 219°C.
A solution of 438 mg of diac in methanol (20 ml) and ammonia solution (SG 0.88; 20 ml) was iodinated at 0°C with 1.8 ml 1 N iodine solution. The product was isolated in almost theoretical yield in a manner similar to that described for tetrac. After crystallization from 50% (v/v) methanol, triac was obtained as colorless needles which melted over the range 65°C to 90°C according to the rate of heating. The molten form resolidified at about 110°C and finally melted at 180°C to 181°C without decomposition. The compound, dried at 25°C/3 mm over silica gel, contains methanol of crystallization.

Therapeutic Function

Thyroid hormone

3,3',5-TRIIODOTHYROACETIC ACIDSupplier

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