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Ifenprodil

Product Name
Ifenprodil
CAS No.
23210-56-2
Chemical Name
Ifenprodil
Synonyms
IFENPRODIL;2-(4-Benzylpiperidino)-1-(4-hydroxyphenyl)propanol;4-[2-(4-benzylpiperidin-1-yl)-1-hydroxypropyl]phenol;2-(4-Benzylpiperidino)-1-(4-hydroxyphenyl)-1-propanol;2-(4-Benzylpiperidino)-1-(4-hydroxyphenyl)propan-1-ol;1-(4-Hydroxyphenyl)-2-(4-benzylpiperidino)-1-propanol;4-[2-[4-(benzyl)-1-piperidyl]-1-hydroxy-propyl]phenol;4-Benzyl-α-(p-hydroxyphenyl)-β-methyl-1-piperidineethanol;4-[1-Hydroxy-2-[4-(phenylmethyl)piperidin-1-yl]propyl]phenol;2-?(4-?Benzylpiperidino)?-?1-?(1-?hydroxyphenyl)?-?1-?propanol
CBNumber
CB3427239
Molecular Formula
C21H27NO2
Formula Weight
325.45
MOL File
23210-56-2.mol
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Ifenprodil Property

Melting point:
114°
Boiling point:
463.62°C (rough estimate)
Density 
1.0825 (rough estimate)
refractive index 
1.5614 (estimate)
storage temp. 
Store at RT
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
9.99±0.26(Predicted)
color 
White to Off-White
Water Solubility 
Soluble to 15 mM in water with gentle warming
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Safety

Toxicity
LD50 oral in mouse: 320mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P330Rinse mouth.

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N-Bromosuccinimide Price

Alfa Aesar
Product number
J60932
Product name
Ifenprodil hemitartrate, 99%
Packaging
10mg
Price
$84.65
Updated
2024/03/01
Alfa Aesar
Product number
J60932
Product name
Ifenprodil hemitartrate, 99%
Packaging
50mg
Price
$312.65
Updated
2024/03/01
TRC
Product number
I258003
Product name
Ifenprodil
Packaging
100mg
Price
$410
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
INB0002060
Product name
1-METHYL-2-HYDROXY-2-(4-HYDROXYPHENYL)ETHYL-1-(4-BENZYLPIPERIDINE)
Purity
95.00%
Packaging
10MG
Price
$617.3
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
INB0002060
Product name
1-METHYL-2-HYDROXY-2-(4-HYDROXYPHENYL)ETHYL-1-(4-BENZYLPIPERIDINE)
Purity
95.00%
Packaging
50MG
Price
$842.87
Updated
2021/12/16
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Ifenprodil Chemical Properties,Usage,Production

Originator

Vadilex,Carriere,France,1972

Uses

Ifenprodil is a NMDA receptor antagonist.

Uses

vasodilator

Definition

ChEBI: 4-[1-hydroxy-2-[4-(phenylmethyl)-1-piperidinyl]propyl]phenol is a member of piperidines.

Manufacturing Process

The initial steps involve reacting benzyl chloride with 4- hydroxypropiophenone. The benzyloxypropiophene thus obtained is first brominated and then reacted with 4-benzylpiperidine to give 1-(pbenzyloxyphenyl)-2-(4-benzyl-piperidino)propan-1-one.
The neutral tartrate may be prepared directly by reduction of 1-(pbenzyloxyphenyl)-2-(4-benzyl-piperidino)propan-1-one. For the reduction, a mixture of 175 g of ketone (0.425 mol) and 32 g of tartaric acid (0.213 mol) is hydrogenated at 50°C under pressure of 50 kg/cm2 in 440 ml of methanol in the presence of 12 g of palladium on charcoal.
The catalyst is filtered off at elevated temperature, and the filtrate is concentrated by evaporation under reduced pressure to a volume of 300 ml and added in a thin stream to 2.5 liters of diethyl ether with mechanical agitation. The precipitate is separated, washed with diethyl ether and dried in vacuo at 80° to 85°C for several hours. 325 g (96% yield) of the neutral tartrate of 1-(p-hydroxyphenyl)-2-(4-benzyl-piperidino)propan-1-ol are obtained.

Therapeutic Function

Vasodilator

Biological Activity

NMDA receptor antagonist, acting at the polyamine site. Also an α -adrenergic vasodilator. σ 2 ligand displaying about 3-fold selectivity over σ 1 sites.

Ifenprodil Preparation Products And Raw materials

Raw materials

Preparation Products

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Ifenprodil Suppliers

Wuhan EnTai Technology Development Co,.Ltd
Tel
86-27-82330560
Fax
86-27-82330547
Email
2536851935@qq.com
Country
China
ProdList
347
Advantage
69
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
Country
China
ProdList
8065
Advantage
58
EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8447
Advantage
60
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Aikon International Limited
Tel
025-66028182 18112977050
Fax
(3)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
15818
Advantage
58
Chengdu Saint - Kay Biotechnology Co., Ltd.
Tel
028-85157043 15882256948
Email
676046971@qq.com
Country
China
ProdList
4391
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57412
Advantage
58

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