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300-42-5

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300-42-5 Usage

Description

N,alpha-dimethylphenethylamine hydrochloride, also known as N,alpha-dimethylphenethylamine hydrochloride, is an odorless white crystalline compound with a bitter taste. It is a controlled substance classified as a stimulant and is used in various applications due to its stimulant properties. Its aqueous solutions have a pH of approximately 6.

Uses

Used in Pharmaceutical Industry:
N,alpha-dimethylphenethylamine hydrochloride is used as a central nervous system (CNS) stimulant for treating attention deficit disorder with hyperactivity. It helps improve focus, attention, and impulse control in individuals with this condition.
Used in Weight Loss Applications:
N,alpha-dimethylphenethylamine hydrochloride is used as an anorexic agent, which helps suppress appetite and promote weight loss. It is particularly useful for individuals struggling with obesity or those who need assistance in managing their food intake.
Used as a Controlled Substance:
Due to its stimulant properties, N,alpha-dimethylphenethylamine hydrochloride is classified as a controlled substance. This classification helps regulate its distribution, use, and potential abuse, ensuring that it is used responsibly and for approved medical purposes only.

Air & Water Reactions

Water soluble.

Reactivity Profile

An acidic salt of the amine, therefore behaves as a weak acid.

Fire Hazard

Flash point data for N,alpha-dimethylphenethylamine hydrochloride are not available; however, N,alpha-dimethylphenethylamine hydrochloride is probably combustible.

Safety Profile

Poison by ingestion, intravenous, intraperitoneal, subcutaneous, and intramuscular routes. Human systemic effects by ingestion: altered sleep patterns, anorexia, and change in heart rate. Experimental reproductive effects. An eye irritant, A powerful central nervous system stimulant. When heated to decomposition it emits very toxic fumes of NOx and HCl. See also BENZEDRINE.

Check Digit Verification of cas no

The CAS Registry Mumber 300-42-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 300-42:
(5*3)+(4*0)+(3*0)+(2*4)+(1*2)=25
25 % 10 = 5
So 300-42-5 is a valid CAS Registry Number.

300-42-5SDS

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 rac Methamphetamine Hydrochloride

1.2 Other means of identification

Product number -
Other names Benzeneethanamine, N,α-dimethyl-, 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:300-42-5 SDS

300-42-5Downstream Products

300-42-5Relevant articles and documents

Significant determinants of isotope composition during HI/Pred synthesis of methamphetamine

David, Gabrielle E.,Hibbert, D. Brynn,Frew, Russell D.,Hayman, Alan R.

, p. 22 - 29 (2010)

Methamphetamine HCl was synthesized using three variations of the hydriodic acid/red phosphorus (HI/Pred) synthetic route. A Plackett-Burman experimental design was used to determine how reaction parameters affected the isotopic composition of the product. Isotope ratio mass spectrometry results showed only the source of precursor 13C was significant in determining product δ13C; the manufacturer, reaction temperature, time, scale, and source of HI were not significant. The precursor was also the main determinant of product δ2H, with smaller contributions from the HI source for one method. From precursor to product, large δ2H depletion occurred for most samples. Deuterium nuclear magnetic resonance spectroscopy (2H NMR) was used to investigate the specific site of this. Significant fraction of deuterium was observed only at the benzylic position, the site of hydrogen addition during synthesis. Methamphetamine synthesized from ephedrine was shown to be depleted in this position.