93-30-1

Basic information

• Product Name: 2-METHOXYPHENAMINE HCL
• Synonyms: 2-METHOXYPHENAMINE HCL;1-(2-Methoxyphenyl)-N-methyl-2-propanamine;1-(o-Methoxyphenyl)-2-methylaminopropane;2-Methoxy-N,alpha-dimethylbenzeneethanamine;2-Methoxy-N-methylamphetamine;alpha-(2-Methoxyphenyl)-beta-methylaminopropane;Benzeneethanamine, 2-methoxy-N,alpha-dimethyl-;beta-(o-Methoxyphenyl)isopropylmethylamine
• CAS NO: 93-30-1
• Molecular Formula: C₁₁H₁₇NO
• Molecular Weight: 179.25878
• EINECS: 202-237-7
• Mol File: 93-30-1.mol
• Article Data: 1

Chemical Properties

• Melting Point: 271℃
• Boiling Point: 252℃
• Flash Point: 103℃
• Appearance: /
• Density: 0.951
• CAS DataBase Reference: 2-METHOXYPHENAMINE HCL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXYPHENAMINE HCL(93-30-1)
• EPA Substance Registry System: 2-METHOXYPHENAMINE HCL(93-30-1)

Safety Data

• Hazardous Substances Data: 93-30-1(Hazardous Substances Data)

Usage

General Description

2-Methoxyphenamine HCL is a chemical compound that belongs to the class of organic compounds known as anisoles. It is a hydrochloride salt form of 2-methoxyphenamine, which is an aromatic ether with a methoxy group at the 2-position. 2-METHOXYPHENAMINE HCL is commonly used as a decongestant and antihistamine to treat symptoms of common colds, hay fever, and allergies. It works by narrowing blood vessels in the nasal passages, reducing swelling and congestion. Additionally, 2-methoxyphenamine HCL may also have mild sedative effects, making it useful for treating insomnia and other sleep disorders. However, it is important to note that this chemical should be used under the guidance of a healthcare professional due to its potential side effects and interactions with other medications.

InChI:InChI=1/C11H17NO/c1-9(12-2)8-10-6-4-5-7-11(10)13-3/h4-7,9,12H,8H2,1-3H3

Upstream product

• 75-52-5 nitromethane 
• 5211-62-1 1-(2-methoxyphenyl)propan-2-one 
• 7035-03-2 2-methoxy-benzeneacetonitrile 
• 28033-63-8 2-(2-methoxyphenyl)acetyl chloride 
• 15402-84-3 (d,l)-2-methoxyamphetamine 
• 135-02-4 ortho-anisaldehyde 
• 101430-42-6 [(2-methoxy-phenyl)-acetyl]-malonic acid diethyl ester 
• 100137-54-0 1-acetoxy-1-(2-methoxy-phenyl)-2-nitro-propane 
• 70751-30-3 2-(2-methoxyphenyl)-3-oxobutanenitrile 
• 58645-50-4 2-methoxy-β-methyl-β-nitrostyrene 
• 10577-44-3 2-(1-propenyl)anisole 
• 74-89-5 methylamine 
• 75-87-6 chloral 
• 74-88-4 methyl iodide 

Downstream Products

• 582-43-4 O-desmethylmethoxyphenamine 
• 93-30-1 (+)-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-methyl-amine 
• 93-30-1 (-)-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-methyl-amine 
• 5588-10-3 (+-)-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-methyl-amine; hydrochloride 
• 3505-03-1 benzyl-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-methyl-amine 

Relevant articles and documents

Method for synthesizing methoxyphenamine hydrochloride

The invention relates to the technical field of synthesis of medicinal raw materials and chemical intermediates, in particular to a method for synthesizing methoxyphenamine hydrochloride. The method comprises the following steps: adding o-methoxyl phenylacetone and a methylamine ethanol solution into a reaction kettle, performing a reaction to obtain Schiff base, and further adding a metal reducing agent into the Schiff base obtained through the reaction to reduce the Schiff base. The method for synthesizing the methoxyphenamine hydrochloride is low in cost, high in product content and easy to industrialize, and the mole yield is greater than 82%.