Chemical Properties:
Tryptamine (CAS: 61-54-1) AJI97 Test Method Tryptamine, when dried, contains not less than 98.0 percent and not more than 102.0 percent of Tryptamine (C10H12N2). Solubility (H2O, g/100g): Insoluble Specifications: Loss on Drying: In vacuum, at room temperature for 3 hours. Residue on Ignition (Sulfated): AJI Test 13 Assay: Dried sample, 160mg, (1), 1ml of formic acid, 50ml of glacial acetic acid, 0.1mol/L HCLO4 1ml=16.022mg C10H12N2. Melting Point: AJI Test 36 Recommended storage limit and condition: Preseved tight containers at controlled room temperature (1/2 years). Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Tryptamine (CAS: 61-54-1) with high quality. We can provide worldwide delivery, small and bulk quantities available. If you are interested in Tryptamine, Please contact: alvin@ruifuchem.com| Hazard Codes | Xi - Irritant | RTECS | NL4020000 |
| Risk Statements | 20/21/22-36/37/38-41-37/38-22 | F | 8-23 |
| Safety Statements | 24/25-36/37/39-36-26 | Hazard Class | Irritant |
| WGK Germany | 3 | HS Code | 2933990099 |
Description:
Safety Information:
Package & Storage:
| Chemical Name | Tryptamine |
| Synonyms | 3-(2-Aminoethyl)indole; 2-(3-Indolyl)ethylamine; Indol-3-Ethylamine; 3-Indoleethylamine; 3-(2-Aminoethyl)-Indol; 3-(2-Aminoethyl)-1H-Indole; 2-(Indol-3-yl)ethylamine; 2-(1H-indol-3-yl)ethanamine; 3-Indoleethanamine; β-(3-Indolyl)ethylamine |
| Stock Status | In Stock, Production Capacity 30 Tons per Month |
| CAS Number | 61-54-1 |
| Molecular Formula | C10H12N2 |
| Molecular Weight | 160.22 |
| Melting Point | 111.0~118.0℃(lit.) |
| Boiling Point | 137℃/0.15 mmHg (lit.) |
| Flash Point | 185℃(365°F) |
| Density | 1.157 |
| Sensitive | Air Sensitive, Heat Sensitive |
| Water Solubility | Insoluble in Water |
| Solubility | Soluble in DMSO, Methanol |
| Storage Temp. | Sealed in Dry, Store at Room Temperature |
| COA & MSDS | Available |
| Brand | Ruifu Chemical |
Advantages:
How to Purchase? Please contact Dr. Alvin Huang: sales@ruifuchem.com or alvin@ruifuchem.com 15 Years Experience? We have more than 15 years of experience in the manufacture and export of a wide range of high quality pharmaceutical intermediates or fine chemicals. Main Markets? Sell to domestic market, North America, Europe, India, Korea, Japanese, Australia, etc. Advantages? Superior quality, affordable price, professional services and technical support, fast delivery. Quality Assurance? Strict quality control system. Professional equipment for analysis include NMR, LC-MS, GC, HPLC, ICP-MS, UV, IR, OR, K.F, ROI, LOD, MP, Clarity, Solubility, Microbial limit test, etc. Samples? Most products provide free samples for quality evaluation, shipping cost should be paid by customers. Factory Audit? Factory audit welcome. Please make an appointment in advance. MOQ? No MOQ. Small order is acceptable. Delivery Time? If within stock, three days delivery guaranteed. Transportation? By Express (FedEx, DHL), by Air, by Sea. Documents? After sales service: COA, MOA, ROS, MSDS, etc. can be provided. Custom Synthesis? Can provide custom synthesis services to best fit your research needs. Payment Terms? Proforma invoice will be sent first after confirmation of order, enclosed our bank information. Payment by T/T (Telex Transfer), PayPal, Western Union, etc.FAQ:
Stable Supply: Maintain reasonable stock
Professional Service: One stop purchasing service
Technical Support: Technology solution available
Custom Synthesis Service: Ranged from grams to kilos
Fast Delivery: If within stock, three days delivery guaranteed
High Quality: Established a complete quality assurance system
Sufficient Capacity: Sufficient facilities and technicians
OEM Package: Custom package and label available
Specifications:
| Items | Inspection Standards |
| Appearance | Light Yellow or Pale-White Crystalline Powder |
| Melting Point | 111.0~118.0℃ |
| Heavy Metals (Pb) | ≤20ppm |
| Loss on Drying | ≤0.50% |
| Residue on Ignition (Sulfated) | ≤0.10% |
| Purity / Analysis Method | >98.0% (HPLC) |
| Assay / Analysis Method | 98.0 to 102.0% (Titration by HClO4) |
| Infrared Spectrum | Conforms to Structure |
| Proton NMR Spectrum | Conforms to Structure |
| Solubility in MeOH | Almost Transparency |
| Conclusion | Meets with the Enterprise Standard |
Application:
Tryptamine (CAS: 61-54-1) is a monoamine alkaloid that can be synthesized by decarboxylation of the amino acid tryptophan. Tryptamine has an indole ring structure and a fused double ring that is composed of a benzene ring and a pyrrole ring, linked to an amino group by 2-carbon side chain. The indole ring is the vital nucleus of many complex natural products that have significance in drug discovery as well as some synthetic and non-synthetic drugs that are based on tryptamine skeleton. The chemical’s distinct structure is an approximation to the neurotransmitter serotonin as well-known drugs and hallucinogens. Tryptamine’s significance as psychedelic drugs, neuromodulator, and neurotransmitter is well understood due to its presence in mammalian brain in small amounts. Analogs of Tryptamine that are typically produced by its synthetic modification play a significant role in individuals due to the introduction of functionalities that are biologically active in its nucleus that may cause changes in the mental and physical status of the human brain. Substitutions on the indole ring at nitrogen and C-2 of its side chain produce numerous neuroactive compounds ranging from anti-migraine drugs to toxic substances, such as Rizatriptan, Sumatriptan, and Zolmitriptan. A small amount of Tryptamine is required due to its fatalities and intoxication for several reasons. 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. The synthesis of Ttryptamines 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. Biochem/Physiol Actions: Vasoactive; may have a neuromodulator function; biogenic amine formed from the decarboxylation of tryptophan by L-aromatic amino acid decarboxylase.61-54-1 AJI97 Test Method:
Package: Fluorinated Bottle, 25kg/bag, 25kg/Cardboard Drum, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool, dry and ventilated warehouse away from incompatible substances. Protect from light and moisture.