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CAS RN: 196597-26-9 | Product Number: R0216

Ramelteon


Purity: >98.0%(GC)
Synonyms:
  • (S)-N-[2-(2,6,7,8-Tetrahydro-1H-indeno[5,4-b]furan-8-yl)ethyl]propionamide
Product Documents:
100MG
€68.00
1   ≥60 
1G
€438.00
2   17  

*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Product Number R0216
Purity / Analysis Method >98.0%(GC)
Molecular Formula / Molecular Weight C__1__6H__2__1NO__2 = 259.35 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Packaging and Container 100MG-Glass Bottle with Plastic Insert (View image)
CAS RN 196597-26-9
Reaxys Registry Number 9277585
PubChem Substance ID 468592788
Merck Index (14) 8101
MDL Number

MFCD08067736

Specifications
Appearance White to Almost white powder to crystal
Purity(GC) min. 98.0 %
Melting point 114.0 to 118.0 °C
Specific rotation [a]20/D -55.0 to -60.0 deg(C=1, CHCL3)
Properties (reference)
Melting Point 116 °C
Specific Rotation -57° (C=1,CHCl3)
Solubility in water Insoluble
Degree of solubility in water 11 mg/l   25 °C
Solubility (soluble in) Ethanol
GHS
Pictogram Pictogram Pictogram
Signal Word Warning
Hazard Statements H302 : Harmful if swallowed.
H361 : Suspected of damaging fertility or the unborn child.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P202 : Do not handle until all safety precautions have been read and understood.
P201 : Obtain special instructions before use.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P308 + P313 : IF exposed or concerned: Get medical advice/ attention.
Related Laws:
RTECS# TX1498230
Transport Information:
HS Number 2932990090
Application
Ramelteon: A Selective Melatonin MT1 and MT2 Receptors Agonist

Ramelteon (TAK-375) is a melatonin [M1105] receptor agonist with both high affinity for melatonin MT1 and MT2 receptors, and high selectivity for MT1 and MT2 receptors compared to the MT3 receptor. In addition, ramelteon showed no measurable affinity for a large number of ligand binding sites, including benzodiazepine receptors, dopamine receptors, opiate receptors, ion channels, and transporters. Ramelteon also does not interfere with the activity of a number of enzymes. The agonist activity at the MT1 and MT2 receptors has been reported to contribute to its sleep-promoting properties. And then, ramelteon currently is approved in the United States and Japan for the treatment of insomnia. (The product is for research purpose only.)

References


TCIMAIL
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