5-Hydroxyindole-3-acetaldehyde

Base Information

Chemical Name:5-Hydroxyindole-3-acetaldehyde
CAS No.:1892-21-3
Molecular Formula:C10H9NO2
Molecular Weight:175.18
Hs Code.:2933990090
UNII:DAE26MT2UK
DSSTox Substance ID:DTXSID60172318
Nikkaji Number:J139.626I
Wikidata:Q27073985
Metabolomics Workbench ID:38455
Mol file:1892-21-3.mol

Synonyms:1H-indole-3-acetaldehyde, 5-hydroxy-;5-HIAL;5-hydroxyindole-3-acetaldehyde;hydroxyindoleacetaldehyde

Suppliers and Price of 5-Hydroxyindole-3-acetaldehyde

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Medical Isotopes, Inc.
5-Hydroxyindole-3-acetaldehyde
250 mg
$ 2200.00

Medical Isotopes, Inc.
5-Hydroxyindole-3-acetaldehyde
25 mg
$ 650.00

AccelPharmtech
5-hydroxy-1H-Indole-3-acetaldehyde 97.00%
25G
$ 12500.00

AccelPharmtech
5-hydroxy-1H-Indole-3-acetaldehyde 97.00%
5G
$ 4980.00

AccelPharmtech
5-hydroxy-1H-Indole-3-acetaldehyde 97.00%
1G
$ 3800.00

Total 37 raw suppliers

Chemical Property of 5-Hydroxyindole-3-acetaldehyde

Chemical Property:

Vapor Pressure:4.54E-08mmHg at 25°C
Refractive Index:1.695
Boiling Point:431.998 °C at 760 mmHg
PKA:9.93±0.40(Predicted)
Flash Point:215.065 °C
PSA：53.09000
Density:1.343 g/cm³
LogP:1.61490
XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:175.063328530
Heavy Atom Count:13
Complexity:195

Purity/Quality:

99%, ^*data from raw suppliers

5-Hydroxyindole-3-acetaldehyde ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1O)C(=CN2)CC=O
Uses 5-Hydroxyindole-3-acetaldehyde is a metabolite of Nω-methylserotonin, a constituent of black cohosh root.

Technology Process of 5-Hydroxyindole-3-acetaldehyde

There total 2 articles about 5-Hydroxyindole-3-acetaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 50-67-9
3-(2-aminoethyl)-1H-indol-5-ol

: 1892-21-3
Hydroxyindoleacetaldehyde

Guidance literature:: With Lathyrus cicera copper amine oxidase; at 25 ℃; pH=7.2; Concentration; pH-value; Kinetics; aq. phosphate buffer;
DOI:10.1016/j.jinorgbio.2012.01.002

Reference yield:

: 153-98-0,21591-86-6
serotonin hydrochloride

: 1892-21-3
Hydroxyindoleacetaldehyde

Guidance literature:: With potassium hydroxide; sodium disulfite; sodium pyrophosphate buffer; potassium chloride; sodium succinate; Multistep reaction; rat brain synaptosomal protein, 1.) 37 deg C, 4 h;
DOI:10.1021/jm00092a018