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MIDODRINE

Product Name
MIDODRINE
CAS No.
42794-76-3
Chemical Name
MIDODRINE
Synonyms
MIDODRINE;MIDODRINE USP/EP/BP;Midodrine (metoclopramide);2-Amino-N-(2,5-dimethoxy-β-hydroxyphenethyl)acetamide;Acetamide, 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]-;Acetamide, 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]- (9CI)
CBNumber
CB4297224
Molecular Formula
C12H18N2O4
Formula Weight
254.28
MOL File
42794-76-3.mol
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MIDODRINE Property

Boiling point:
529.9±50.0 °C(Predicted)
Density 
1.204±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
form 
Solid
pka
13.47±0.20(Predicted)
color 
White to off-white
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Safety

Hazardous Substances Data
42794-76-3(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Crysdot
Product number
CD31001926
Product name
Midodrine
Purity
98+%
Packaging
5mg
Price
$56
Updated
2021/12/16
Crysdot
Product number
CD31001926
Product name
Midodrine
Purity
98+%
Packaging
10mg
Price
$77
Updated
2021/12/16
Crysdot
Product number
CD31001926
Product name
Midodrine
Purity
98+%
Packaging
50mg
Price
$315
Updated
2021/12/16
DC Chemicals
Product number
DC24075
Product name
Midodrine
Purity
>98%
Packaging
50mg
Price
$318
Updated
2021/12/16
DC Chemicals
Product number
DC24075
Product name
Midodrine
Purity
>98%
Packaging
100mg
Price
$528
Updated
2021/12/16
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MIDODRINE Chemical Properties,Usage,Production

Originator

Gutron,Hormonchemie,W. Germany,1977

Uses

Antihypotensive.

Definition

ChEBI: An aromatic ether that is 1,4-dimethoxybenzene which is substituted at position 2 by a 2-(glycylamino)-1-hydroxyethyl group. A direct-acting sympathomimetic with selective alpha-adrenergic agonist activity, it is used (generally as its hydro hloride salt) as a peripheral vasoconstrictor in the treatment of certain hypotensive states. The main active moiety is its major metabolite, deglymidodrine.

Manufacturing Process

19.5 parts of carbobenzoxyglycine, 7.1 parts of triethylamine and 162 parts ofdry toluene are mixed with 11.2 parts of isovaleric acid chloride at 0°C toform the mixed anhydride and the mixture is agitated for two hours at 0°C.32.4 parts of 1-(2',5'-dimethoxyphenyl)-2-aminoethanol-(1) are then added,the mixture is agitated for four hours at a temperature between 0°C and+10°C and then left to stand overnight at that temperature. A thick crystalpaste forms. The reaction product is dissolved in 450 parts of ethyl acetateand 200 parts of water. The ethyl acetate solution is separated, washed withhydrochloric acid, sodium bicarbonate solution and water, dried over sodiumsulfate and inspissated. The inspissation residue is digested with 342 parts ofxylene, the required product crystallizing out. 34.9 parts of 1-(2',5'-dimethoxyphenyl)-2-(N-carbobenzoxyglycineamido)-ethanol-(1) are obtained.66.2 parts of 1-(2',5'-dimethoxyphenyl)-2-(N-carbobenzoxyglycineamido)-ethanol-(1) are hydrogenated in the presence of 6.6 parts of palladium carbon(10%) in 2,000 parts of glacial acetic acid. When no more hydrogen isabsorbed (3 mols of hydrogen are used), hydrogenation stops. The catalyst isremoved by suction and the equivalent quantity of hydrochloric acid in ethanolis added to the filtrate with agitation. During further agitation at roomtemperature 28.6 parts of crude 1-(2',5'-dimethoxyphenyl)-2-glycineamidoethanol-(1)hydrochloride crystallize, and are isolated andrecrystallized from water-methanol for purification. 22.1 parts of pure productare obtained with a melting point of 192°C to 193°C.
An alternative synthesis route is described by Kleeman and Engel.

brand name

Orvaten (UpsherSmith); Proamatine (Shire).

Therapeutic Function

Peripheral vasotonic, Antihypotensive

MIDODRINE Preparation Products And Raw materials

Raw materials

Preparation Products

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MIDODRINE Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Hubei Jusheng Technology Co.,Ltd
Tel
027-59599241 18871490274
Fax
027-59599241
Email
1400878000@qq.com
Country
China
ProdList
9958
Advantage
58
Raw material medicin reagent co.,Ltd
Tel
Email
sales@njromanme.com
Country
China
ProdList
4529
Advantage
58
Beijing Solarbio Science & Tecnology Co., Ltd.
Tel
010-50973130 4009686088
Email
3193328036@qq.com
Country
China
ProdList
29785
Advantage
68
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9353
Advantage
58
Chengdu Saint - Kay Biotechnology Co., Ltd.
Tel
028-85157043 15882256948
Email
676046971@qq.com
Country
China
ProdList
4397
Advantage
58
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View Lastest Price from MIDODRINE manufacturers

Chengdu Aupone Pharmaceutical Co.Ltd.
Product
Midodrine 42794-76-3
Price
US $0.00/gram
Min. Order
10gram
Purity
99.99
Supply Ability
10Tons
Release date
2024-03-18
Hebei Mojin Biotechnology Co., Ltd
Product
MIDODRINE 42794-76-3
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1 ton
Release date
2023-06-02

42794-76-3, MIDODRINERelated Search:


  • MIDODRINE
  • Acetamide, 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]- (9CI)
  • 2-Amino-N-(2,5-dimethoxy-β-hydroxyphenethyl)acetamide
  • Acetamide, 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]-
  • MIDODRINE USP/EP/BP
  • Midodrine (metoclopramide)
  • 42794-76-3
  • 42794-76-3