ChemicalBook > CAS DataBase List > METHOXAMINE HYDROCHLORIDE

METHOXAMINE HYDROCHLORIDE

Product Name
METHOXAMINE HYDROCHLORIDE
CAS No.
61-16-5
Chemical Name
METHOXAMINE HYDROCHLORIDE
Synonyms
vasoxyl;Mexan;Vasylox;vasoxine;METHOXAMINE HCL;vasoxylhydrochloride;Naproxen Impurity 47;vasoxinehydrochloride;pressominhydrochloride;Methoxamine hydrochlorid
CBNumber
CB1380846
Molecular Formula
C11H18ClNO3
Formula Weight
247.72
MOL File
61-16-5.mol
More
Less

METHOXAMINE HYDROCHLORIDE Property

Melting point:
215℃
refractive index 
1.5204
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
9.2(at 25℃)
form 
Solid
color 
White to off-white
CAS DataBase Reference
61-16-5(CAS DataBase Reference)
More
Less

Safety

WGK Germany 
3
RTECS 
DN4025000
Hazardous Substances Data
61-16-5(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
M6524
Product name
Methoxamine hydrochloride
Packaging
500mg
Price
$187
Updated
2024/03/01
Sigma-Aldrich
Product number
M6524
Product name
Methoxamine hydrochloride
Packaging
1g
Price
$336
Updated
2024/03/01
TRC
Product number
M260740
Product name
MethoxamineHydrochloride(MixtureofDiastereomers)
Packaging
250mg
Price
$160
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003335
Product name
METHOXAMINE HYDROCHLORIDE
Purity
95.00%
Packaging
0.5G
Price
$538
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
41303
Product name
MethoxamineHCl(MixtureofDiastereomers)
Packaging
250mg
Price
$650
Updated
2021/12/16
More
Less

METHOXAMINE HYDROCHLORIDE Chemical Properties,Usage,Production

Originator

Vasoxyl ,Burroughs-Wellcome,US,1949

Uses

Antihypotensive;Alpha adrenergic agonist

Uses

Methoxamine is an α1-adrenergic receptor agonist. It induces vasoconstriction of skin and splanchnic blood vessels, thereby increasing peripheral vascular resistance and raising mean arterial blood pressure.

Uses

anti-fungal

Definition

ChEBI: Methoxamine hydrochloride is a dimethoxybenzene.

Manufacturing Process

2,5-Dimethoxypropiophenone is treated in absolute ether with methyl nitrite and hydrogen chloride. The hydrochloride of 2,5-dimethoxy-αisonitrosopropiophenone crystallizes out of the solution. It is removed, the base is liberated and crystallized from benzene-heptane forming yellow leaflets that melt at about 97° to 98°C. This isonitrosoketone is dissolved in absolute alcohol containing an excess of hydrogen chloride and is hydrogenated with palladized charcoal, yielding β-(2,5-dimethoxyphenyl)-βketoisopropylamine hydrochloride, a salt that melts at about 176°C with decomposition.
12.3 g (1/20 mol) of β-(2,5-dimethoxyphenyl)-β-ketoisopropylamine hydrochloride (MP 176°C) is dissolved in 50 cc of water and hydrogenated with platinum oxide platinum black in the customary Adams-Burgess Parr apparatus. About 1/20 mol of hydrogen is absorbed, after which the solution is filtered off from the catalyst, evaporated to dryness in vacuo and recrystallized from absolute alcohol, absolute ether being added to decrease solubility. The hydrochloride is thus obtained in substantially theoretical yield. It crystallizes in plates and melts at 215°C.

Therapeutic Function

Hypertensive

Biochem/physiol Actions

α1-adrenoceptor agonist.

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Experimental reproductive effects. An FDA proprietary drug. When heated to decomposition it emits very toxic fumes of HCl and NOx.

METHOXAMINE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

METHOXAMINE HYDROCHLORIDE Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aceschem Inc.
Tel
+1-817863-6948 +1-(817)863-6948
Email
sales@aceschem.com
Country
United States
ProdList
19632
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
CarboMer, Inc.
Tel
--
Fax
--
Email
sales@carbomer.com
Country
United States
ProdList
4026
Advantage
67
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
ASDI Incorporated
Tel
--
Fax
--
Email
customerservice@asdi.net
Country
United States
ProdList
6922
Advantage
67
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
More
Less

View Lastest Price from METHOXAMINE HYDROCHLORIDE manufacturers

Career Henan Chemical Co
Product
METHOXAMINE HYDROCHLORIDE 61-16-5
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kg
Release date
2019-08-04

61-16-5, METHOXAMINE HYDROCHLORIDERelated Search:


  • vasoxyl
  • vasoxylhydrochloride
  • Methoxamine Hydrochloride (200 mg)
  • 2-aMino-1-(2,5-diMethoxyphenyl)propan-1-ol hydrochloride
  • MethoxaMine Hydrochloride (Mixture of DiastereoMers)
  • BenzeneMethanol,a-(1-aMinoethyl)-2,5-diMethoxy-,hydrochloride (1:1)
  • α-[1-Aminoethyl]-2,5-dimethoxybenzenemethanol hydrochloride
  • α-(1-aminoethyl)-2,5-dimethoxybenzyl alcohol hydrochloride
  • 2-Amino-1-hydroxy-1-(2,5-dimethoxyphenyl)propane hydrochloride
  • a-(a-Aminoethyl)-2,5-dimethoxybenzyl alcohol hydrochloride
  • Benzenemethanol, a-(1-aminoethyl)-2,5-dimethoxy-, hydrochloride (9CI)
  • Benzyl alcohol, a-(1-aminoethyl)-2,5-dimethoxy-, hydrochloride (8CI)
  • Beta-hydroxy-beta-(2,5-dimethoxyphenol)-isopropylamine hydrochloride
  • b-Hydroxy-b-(2,5-dimethoxyphenyl)isopropylamine hydrochloride
  • Vasylox
  • Mexan
  • ALPHA-[1-AMINOETHYL]-2,5-DIMETHOXYBENZYL ALCOHOL HYDROCHLORIDE
  • 1-(2,5-dimethoxyphenyl)-2-aminopropanol
  • 2-amino-1-(2,5-dimethoxyphenyl)-1-propanolhydrochloride
  • alpha-(1-aminoethyl)-2,5-dimethoxy-benzenemethanohydrochloride
  • alpha-(1-aminoethyl)-2,5-dimethoxybenzenemethanolhydrochloride
  • alpha-(1-aminoethyl)-2,5-dimethoxy-benzylalcohohydrochloride
  • Methoxamine hydrochlorid
  • alpha-(alpha-aminoethyl)-2,5-dimethoxybenzylalcoholhydrochloride
  • beta-(2,5-dimethoxyphenyl)-beta-hydroxyisopropylaminehydrochloride
  • beta-hydroxy-beta-(2,5-dimethoxyphenyl)isopropylaminehydrochloride
  • beta-hydroxy-beta-(2,5-dimethoxyphenyl)-isopropylaminehydrochloride
  • pressominhydrochloride
  • vasoxine
  • vasoxinehydrochloride
  • METHOXAMINE HCL
  • METHOXAMINE HYDROCHLORIDE
  • Benzenemethanol,α-(1-aminoethyl)-2,5-dimethoxy-,hydrochloride(1:1)
  • METHOXAMINE HYDROCHLORIDE USP/EP/BP
  • Methoxamine hydrochloride salt
  • Naproxen Impurity 47
  • 61-16-5
  • C11H19Cl2NO3
  • alpha1-adrenoceptor agonist.
  • A type adrenergic receptor stimulants