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2,4-Dimethylpentan-3-amine hydrochloride, also known as 2,4-Dimethyl-3-pentanamine hydrochloride, is a chemical compound with the molecular formula C7H17ClN. It is a derivative of amphetamine and exhibits psychoactive properties with stimulant effects. 2,4-Dimethylpentan-3-amine hydrochloride acts as a norepinephrine-dopamine releasing agent, increasing the levels of these neurotransmitters in the brain, which contributes to its central nervous system stimulant properties.

4083-58-3

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4083-58-3 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Dimethylpentan-3-amine hydrochloride is used as a central nervous system stimulant for its ability to increase the levels of norepinephrine and dopamine in the brain. This property makes it potentially useful in the treatment of certain medical conditions that may benefit from enhanced neurotransmitter activity.
Used in Recreational Drug Use:
Despite its potential medical applications, 2,4-Dimethylpentan-3-amine hydrochloride is often used as a recreational drug due to its psychoactive and stimulant effects. It is commonly consumed orally, intranasally, or by injection, and its use in this context carries a risk of abuse and addiction.

Check Digit Verification of cas no

The CAS Registry Mumber 4083-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4083-58:
(6*4)+(5*0)+(4*8)+(3*3)+(2*5)+(1*8)=83
83 % 10 = 3
So 4083-58-3 is a valid CAS Registry Number.

4083-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isopropyl-2-methyl-propylamine, hydrochloride

1.2 Other means of identification

Product number -
Other names 1-isopropyl-2-methyl-propylamine, hydrochloride

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:4083-58-3 SDS

4083-58-3Upstream product

4083-58-3Downstream Products

4083-58-3Relevant academic research and scientific papers

Cerium-Catalyzed C-H Functionalizations of Alkanes Utilizing Alcohols as Hydrogen Atom Transfer Agents

An, Qing,Chen, Yuegang,Liu, Weimin,Pan, Hui,Wang, Xin,Wang, Ziyu,Zhang, Kaining,Zuo, Zhiwei

supporting information, p. 6216 - 6226 (2020/04/27)

Modern photoredox catalysis has traditionally relied upon metal-to-ligand charge-transfer (MLCT) excitation of metal polypyridyl complexes for the utilization of light energy for the activation of organic substrates. Here, we demonstrate the catalytic application of ligand-to-metal charge-transfer (LMCT) excitation of cerium alkoxide complexes for the facile activation of alkanes utilizing abundant and inexpensive cerium trichloride as the catalyst. As demonstrated by cerium-catalyzed C-H amination and the alkylation of hydrocarbons, this reaction manifold has enabled the facile use of abundant alcohols as practical and selective hydrogen atom transfer (HAT) agents via the direct access of energetically challenging alkoxy radicals. Furthermore, the LMCT excitation event has been investigated through a series of spectroscopic experiments, revealing a rapid bond homolysis process and an effective production of alkoxy radicals, collectively ruling out the LMCT/homolysis event as the rate-determining step of this C-H functionalization.

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