Welcome to LookChem.com Sign In|Join Free
  • or
2-(1H-Indol-2-yl)ethan-1-ol, commonly known as tryptophol, is a chemical compound with the molecular formula C10H11NO. It is a derivative of indole and is classified as an alcohol. Tryptophol is found in trace amounts in certain alcoholic beverages, foods like cheese and cocoa, and is known for its sedative and hypnotic effects. It also serves as a precursor to psychoactive tryptamine alkaloids, making it a compound with diverse potential applications in the pharmaceutical and food industries.

52098-05-2

Post Buying Request

52098-05-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

52098-05-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(1H-Indol-2-yl)ethan-1-ol is used as a therapeutic agent for its sedative and hypnotic properties, particularly for the treatment of sleep disorders and anxiety. Its calming effects make it a promising candidate for pharmaceutical formulations aimed at improving sleep quality and reducing anxiety levels.
Used in Food Industry:
In the food industry, 2-(1H-Indol-2-yl)ethan-1-ol is used as a flavoring agent and a precursor to psychoactive tryptamine alkaloids. Its presence in certain foods like cheese and cocoa contributes to their unique taste and aroma profiles. Additionally, its role as a precursor allows for the development of novel food products with potential psychoactive effects, enhancing the sensory experience of consumers.
Used in Sleep Aid Formulations:
2-(1H-Indol-2-yl)ethan-1-ol is used as an active ingredient in sleep aid formulations for its sedative and hypnotic effects. It helps in promoting relaxation and improving sleep quality by modulating the sleep-wake cycle and reducing sleep disturbances.
Used in Anxiety Management:
2-(1H-Indol-2-yl)ethan-1-ol is used as an anxiolytic agent in the development of medications and supplements for managing anxiety disorders. Its calming properties help in reducing anxiety levels and promoting a sense of well-being.
Used in Psychoactive Compound Research:
In the field of psychopharmacology, 2-(1H-Indol-2-yl)ethan-1-ol is used as a precursor to psychoactive tryptamine alkaloids. Its role in the synthesis of these compounds allows for the exploration of their potential therapeutic applications and the development of novel psychoactive substances with unique effects.

Check Digit Verification of cas no

The CAS Registry Mumber 52098-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52098-05:
(7*5)+(6*2)+(5*0)+(4*9)+(3*8)+(2*0)+(1*5)=112
112 % 10 = 2
So 52098-05-2 is a valid CAS Registry Number.

52098-05-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-indol-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names 1H-Indole-2-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52098-05-2 SDS

52098-05-2Upstream product

52098-05-2Relevant academic research and scientific papers

6,7,14,15-Tetrahydro-15aH-azocino[1,2-a:6,5-b′]diindole. Synthesis of a novel pentacyclic ring system

Sripha, Kittisak,Zlotos, Darius P.,Buller, Stefan,Mohr, Klaus

, p. 7183 - 7186 (2007/10/03)

In search of new lead structures for potent allosteric enhancers of antagonist binding to muscarinic M2 receptors, a novel heterocyclic ring system, 6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-b′]diindole, has been synthesized. The new ring skeleton was obtained from indol-2-yl-acetic acid in three steps.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 52098-05-2