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(+/-)-Methamphetamine, also known as "Meth," is a potent central nervous system stimulant that is chemically similar to amphetamine. It is a synthetic drug that comes in various forms, including white, odorless, bitter-tasting crystalline powder, which is often snorted, injected, or smoked. Methamphetamine has a high potential for abuse and addiction due to its intense euphoric effects and its ability to increase alertness, concentration, and energy levels. It is classified as a Schedule II controlled substance in the United States due to its medical use as a treatment for attention deficit hyperactivity disorder (ADHD) and obesity, despite its high potential for abuse. However, non-medical use of methamphetamine can lead to severe health issues, including addiction, cardiovascular problems, and neurological damage.

4846-07-5

4846-07-5 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

4846-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4846-07-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4846-07:
(6*4)+(5*8)+(4*4)+(3*6)+(2*0)+(1*7)=105
105 % 10 = 5
So 4846-07-5 is a valid CAS Registry Number.

4846-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methamphetamine

1.2 Other means of identification

Product number -
Other names DL-METHAMPHETAMINE

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:4846-07-5 SDS

4846-07-5Upstream product

4846-07-5Downstream Products

4846-07-5Relevant academic research and scientific papers

Enantiomer separation via diastereoisomeric salt formation and liquid-liquid phase transition

Acs, Maria,Kozma, David,Fogassy, Elemer

, p. 475 - 478 (2007/10/02)

On reacting racemic amine bases with half equivalent amount of sodium-hydrogen-tartrate in a water-benzene solvent system, the mixed-neutral tartrate accumulates in the aqueous phase, while the free base concentrates in the organic phase, resulting in enantiomer separation without crystallization.