Tryptamine
- CAS No.
- 61-54-1
- Chemical Name:
- Tryptamine
- Synonyms
- L-TRYPTAMINE;1H-INDOLE-3-ETHANAMINE;TRYPTAMINE CAS 61-54-1;2-(1H-INDOL-3-YL)ETHANAMINE;2-(1H-indol-3-yl)ethan-1-aMine hydrochloride;TRIPTAMINE;3-(2-AMINOETHYL)INDOLE;b mk-2;Tryptamin;ryptamine
- CBNumber:
- CB8192006
- Molecular Formula:
- C10H12N2
- Molecular Weight:
- 160.22
- MOL File:
- 61-54-1.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/8/2 20:38:39
Melting point | 113-116 °C (lit.) |
---|---|
Boiling point | 137 °C/0.15 mmHg (lit.) |
Density | 0.9787 (rough estimate) |
refractive index | 1.6210 (estimate) |
Flash point | 185 °C |
storage temp. | 2-8°C |
solubility | water: soluble1g/L at 20°C |
pka | 10.2(at 25℃) |
form | crystalline |
color | white |
PH | 11.07 (10g/l, H2O, 24.7℃) |
Water Solubility | negligible |
Sensitive | Air Sensitive |
Merck | 14,9796 |
BRN | 125513 |
CAS DataBase Reference | 61-54-1(CAS DataBase Reference) |
NIST Chemistry Reference | 1H-Indole-3-ethanamine(61-54-1) |
EPA Substance Registry System | Tryptamine (61-54-1) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS05,GHS07 |
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Signal word | Danger | |||||||||
Hazard statements | H302-H317-H318 | |||||||||
Precautionary statements | P261-P264-P280-P301+P312-P302+P352-P305+P351+P338 | |||||||||
Hazard Codes | Xi | |||||||||
Risk Statements | 20/21/22-36/37/38-41-37/38-22 | |||||||||
Safety Statements | 24/25-36/37/39-36-26 | |||||||||
WGK Germany | 3 | |||||||||
RTECS | NL4020000 | |||||||||
F | 8-23 | |||||||||
HazardClass | IRRITANT | |||||||||
HS Code | 28259080 | |||||||||
HS Code | 29339990 | |||||||||
NFPA 704 |
|
Tryptamine price More Price(5)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich(India) | 193747 | Tryptamine ≥97% | 61-54-1 | 10G | ₹2392.33 | 2022-06-14 | Buy |
Sigma-Aldrich(India) | 76706 | Tryptamine analytical standard | 61-54-1 | 100MG | ₹5780.55 | 2022-06-14 | Buy |
Sigma-Aldrich(India) | 193747 | Tryptamine ≥97% | 61-54-1 | 50G | ₹8724.95 | 2022-06-14 | Buy |
TCI Chemicals (India) | T0890 | Tryptamine | 61-54-1 | 25G | ₹5400 | 2022-05-26 | Buy |
ottokemi | T 2456 | Tryptamine, 99% | 61-54-1 | 250mg | ₹1404 | 2022-05-26 | Buy |
Tryptamine Chemical Properties,Uses,Production
Description
Tryptamine is an indole alkaloid and intermediate in the biosynthesis of serotonin and the phytohormone melatonin in plants. It increases the levels of the terpenoid indole alkaloids ajmalicine, strictosidine, and catharanthine in cultures of C. roseus. Tryptamine is also a product of tryptophan metabolism in mammals. Tryptamine derivatives have been synthetically produced as hallucinogenic drugs of abuse that act on the serotonergic system.
Chemical Properties
Tryptamine is a biogenic imine derived from the decarboxylation of tryptophan. It is a white to orange crystalline Powder, melting point 118°C (decomposition at 145-146°C). Soluble in ethanol and acetone, almost insoluble in ether, benzene, chloroform and water.
Uses
Tryptamine is a monoamine alkaloid found in plants. Tryptamine is commonly used in the preparation of biologically active compounds such as neurotransmitters and psychedelics.
Definition
ChEBI: Tryptamine is an aminoalkylindole consisting of indole having a 2-aminoethyl group at the 3-position. It has a role as a human metabolite, a plant metabolite and a mouse metabolite. It is an aminoalkylindole, an indole alkaloid, an aralkylamino compound and a member of tryptamines. It is a conjugate base of a tryptaminium.
Preparation
Tryptamine, a monoamine alkaloid containing an indole ring structure is derived by the decarboxylation of amino acid tryptophan.
The synthesis of tryptamines is typically conducted following a classic route starting with a Mannich reaction of an indole heterocycle, followed by quaternization of the amine, nucleophilic substitution with highly toxic cyanide and final reduction.
General Description
Tryptamines which are usually found in plants, fungi, animals, etc. are categorized under the monoamine alkaloids class of compounds.
Purification Methods
Crystallise tryptamine from *benzene, Et2O (m 114o) or pet ether (m 118o). It has UV: 222n 276, 282 and 291nm (EtOH) and max 226, 275, 281 and 290nm (HCl). [Beilstein 22 II 346, 22 III/IV 4319, 22/10 V 45.]
Tryptamine Preparation Products And Raw materials
Raw materials
Preparation Products
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GLR Innovations | +91 9891111994 | New Delhi, India | 4542 | 58 | Inquiry |
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CLEARSYNTH LABS LTD. | +91-22-45045900 | Hyderabad, India | 6351 | 58 | Inquiry |
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Triveni chemicals | 08048762458 | New Delhi, India | 6093 | 58 | Inquiry |
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Pharma Affiliates | 172-5066494 | Haryana, India | 6761 | 58 | Inquiry |
Supplier | Advantage |
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GLR Innovations | 58 |
JSK Chemicals | 58 |
CLEARSYNTH LABS LTD. | 58 |
A.J Chemicals | 58 |
Pharmaffiliates Analytics and Synthetics P. Ltd | 58 |
Triveni chemicals | 58 |
Otto Chemie Pvt. Ltd. | 58 |
ASM Organics | 58 |
Chiral Chemicals | 58 |
Pharma Affiliates | 58 |
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