4-Methyl-2-hexanamine hydrochloride Property

Melting point:

128.0 to 132.0 °C

Flash point:

9℃

storage temp. 

room temp

solubility 

H2O: soluble5mg/mL (clear solution)

form 

powder

color 

white to beige

InChI

InChI=1S/C7H17N.ClH/c1-4-6(2)5-7(3)8;/h6-7H,4-5,8H2,1-3H3;1H

InChIKey

ZKKBPHUAHARETG-UHFFFAOYSA-N

SMILES

C(C)(CC)CC(N)C.Cl

CAS DataBase Reference

13803-74-2(CAS DataBase Reference)

Safety

Hazard Codes 

Xn,T,F

Risk Statements 

22-36/37/38-39/23/24/25-23/24/25-11

Safety Statements 

26-45-36/37-16-7

RIDADR 

UN1230 - class 3 - PG 2 - Methanol, solution

WGK Germany 

3

HS Code 

2921199990

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

4-Methyl-2-hexanamine hydrochloride Chemical Properties,Usage,Production

Description

1,3-Dimethylpentylamine is a pseudo-adrenergic drug introduced by Lilly Company in the United States in the mid-1940s under the trade name Forthane. 1,3-dimethylpentylamine and its hydrochloride have obvious curative effects in the treatment of nasal congestion and gingival hyperplasia, and are much less stimulating to the mind than pseudoephedrine and amphetamine, and their unique pharmacological advantages cause attached great importance to the experts.

Chemical Properties

White Solid

Uses

Methylhexanamine (hydrochloride) is a simple aliphatic amine that was once marketed as a nasal decongestant (Forthane) but is now sold as a bodybuilding supplement (Floradrene, Geranamine). It is also sold as a mild stimulant in the form of party pills and has been reported to cause cerebral hemorrhage in a case report. While little is known about its mode of action, methylhexanamine interferes in immunoassays for amphetamines, presumably because of the common ethylamine structure. This compound is intended for forensic or research purposes.[Cayman Chemical]

Uses

1,3-Dimethylpentylamine is useful in composition in treating hypertrophied and hyperplastic gums which showed a significant reduction in swelling.

General Description

4-Methyl-2-hexanamine hydrochloride is a psychoactive substance and has been found to be an inhibitor of serotonin uptake, which may be related to its ability to inhibit the function of the serotonin transporter. The amount of 4-methyl-2-hexanamine hydrochloride absorbed by the body varies depending on how it is taken. When taken orally, 4-methyl-2-hexanamine hydrochloride enters through the digestive tract and reaches high levels in the blood stream. When taken intravenously, it enters the bloodstream directly and can reach higher concentrations in the blood. When inhaled, 4-methyl-2-hexanamine hydrochloride can enter into the lungs at high concentrations and then is absorbed into the bloodstream. 4-Methyl-2-hexanamine hydrochloride also degrades quickly in natural environments due to its biodegradable properties.

Biochem/physiol Actions

Methylhexanamine is a naturally substance isolated from Pelargonium graveolen. It is a component of geranium oil. Methylhexanamine is a sympathomimentic that increase levels of norepinephrine in the synaptic cleft.

Synthesis

At room temperature, 800 mL absolute ethanol was added into a 2 L three neck flask, stirred, and 35.38 g (1.538 mol) of metal sodium was added in batches to obtain a colorless transparent liquid. Cool slightly, add 200g (1.537 rnol) of ethyl acetoacetate, continue heating slowly, and add 232g (1.693 mol) of 2-bromobutane drop under weak reflux. Continue heating and react for 8 h at 80~84 ??. Stop heating, cool naturally to room temperature, leave it still, filter by suction, and concentrate the yellow green filtrate under reduced pressure to obtain 241.4 g of 1,3-Dimethylpentanamine Hydrochloride with light yellow viscous solid in 84.3% yield.