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1H-indole-3-propylamine

CAS No.
6245-89-2
Chemical Name:
1H-indole-3-propylamine
Synonyms
Einecs 228-361-1;1H-indole-3-propylamine;1H-Indole-3-propanamine;N-propyl-1H-indol-3-amine;1H-Indole-3-propan-1-amine;(1H-Indol-3-yl)-1-propanamine
CBNumber:
CB5927122
Molecular Formula:
C11H14N2
Molecular Weight:
174.24
MDL Number:
MFCD00130194
MOL File:
6245-89-2.mol
Last updated:2023-05-04 15:14:06

1H-indole-3-propylamine Properties

Melting point 64 °C
Boiling point 353.7±25.0 °C(Predicted)
Density 1.125±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 17.29±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H315-H335-H302
Precautionary statements  P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Risk Statements  20/21/22-37/38-48
Safety Statements  22-26-7/8-36/37/39-45
HS Code  29339900

1H-indole-3-propylamine price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC I633913 3-(Indol-3-yl)propanamine 6245-89-2 50mg $95 2021-12-16 Buy
TRC I633913 3-(Indol-3-yl)propanamine 6245-89-2 250mg $250 2021-12-16 Buy
AK Scientific J55003 (1H-Indol-3-yl)-1-propanamine 6245-89-2 1g $135 2021-12-16 Buy
Matrix Scientific 072031 (1H-Indol-3-yl)-1-propanamine 95+% 6245-89-2 1g $440 2021-12-16 Buy
American Custom Chemicals Corporation CHM0074502 3-(1H-INDOL-3-YL)-1-PROPANAMINE 95.00% 6245-89-2 1G $925.31 2021-12-16 Buy
Product number Packaging Price Buy
I633913 50mg $95 Buy
I633913 250mg $250 Buy
J55003 1g $135 Buy
072031 1g $440 Buy
CHM0074502 1G $925.31 Buy

1H-indole-3-propylamine Chemical Properties,Uses,Production

Synthesis

A solution of LAH (1.0 M in ether, 36.5 mL, 36.5 mmol) was cooled to 0 °C, and  a solution of the cyanoethyl indole (2.78 g, 16.3 mmol) was added slowly. Then, the solution was heated at reflflux for 3 h. It was cooled to 0 °C and quenched by dropwise addition of water (20 mL) followed by 1 N sodium hydroxide (40 mL). The phases were separated, and the aqueous phase was extracted with ether. The combined organic phases were washed with brine and then dried (potassium hydroxide). Evaporation of the solvent gave 2.6 g (92%) of homotryptamine as a yellow oil, which solidifified on standing. The hydrochloride was prepared by dissolving the amine in a minimum of ethanol and then a saturated solution of hydrogen chloride in ether was added until no additional salt formation was observed. The hydrochloride was recrystallized from ethanol.
synthesis of 1H-indole-3-propylamine
Reference: Kuehne, M. E.; Cowen, S. D.; Xu, F.; Borman, L. S. J. Org. Chem. 2001, 66, 5303–5316.

Chemical Properties

Light yellow powder

1H-indole-3-propylamine Preparation Products And Raw materials

Raw materials

Preparation Products

1H-indole-3-propylamine Suppliers

Global( 59)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
ShanghaiFineBiotechCoLtd
+8618717800556 18717800556 sales@finebioetch.com CHINA 318 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503259 +86-19930503259 cherry@crovellbio.com China 18451 58
Changzhou AniKare Pharmatech Co., Ltd.
+86-0519-8359-8696 +8618018249389 sales@anikare.com China 8469 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33350 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Shanghai Anya Pharmaceutical Technology Co., LTD 19106202509 3626423147@qq.com China 998 58
1H-indole-3-propylamine 1H-Indole-3-propan-1-amine (1H-Indol-3-yl)-1-propanamine Einecs 228-361-1 N-propyl-1H-indol-3-amine 1H-Indole-3-propanamine 6245-89-2