isoaminile
- Product Name
- isoaminile
- CAS No.
- 77-51-0
- Chemical Name
- isoaminile
- Synonyms
- TAT-1;MCT10;Dimyril;Aprecon;SLC16A10;Nullatuss;Isoaminilo;isoaminile;Brn 2849321;Einecs 201-033-5
- CBNumber
- CB3875690
- Molecular Formula
- C16H24N2
- Formula Weight
- 244.38
- MOL File
- 77-51-0.mol
isoaminile Property
- Boiling point:
- bp3 138-146°
- Density
- 1.0080 (rough estimate)
- refractive index
- 1.5519 (estimate)
- storage temp.
- -196°C
- pka
- 9.02±0.50(Predicted)
- form
- buffered aqueous solution
- biological source
- rabbit
N-Bromosuccinimide Price
- Product number
- CB_00020911
- Product name
- TAT-1
- Purity
- NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose -1VL or VIAL for cells, or -DNA-5UG for DNA.
- Packaging
- 1 unit
- Price
- $402
- Updated
- 2025/07/31
- Product number
- CB_00020911
- Product name
- TAT-1
- Purity
- NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose
- Packaging
- 1 unit
- Price
- $402
- Updated
- 2025/07/31
- Product number
- SAB1303352
- Product name
- ANTI-SLC16A10 (C-TERM) antibody produced in rabbit
- Purity
- IgG fraction of antiserum, buffered aqueous solution
- Packaging
- 400 μL
- Price
- $496
- Updated
- 2025/07/31
- Product number
- CB_00020911
- Product name
- TAT-1
- Purity
- Reactivity: Anti-α-Tubulin, 00020911
- Packaging
- 1VIAL
- Price
- $981
- Updated
- 2025/07/31
- Product number
- CB_00020911
- Product name
- TAT-1
- Purity
- Reactivity: Anti-α-Tubulin, 00020911
- Packaging
- 00020911-DNA-5UG
- Price
- $390
- Updated
- 2024/03/01
isoaminile Chemical Properties,Usage,Production
Originator
Peracon,Toyo Jozo,Japan,1969
Uses
Treatment of rheumatoid arthritis.
Definition
ChEBI: Isoaminile is an alkylbenzene.
Manufacturing Process
140 cc of benzene and 24 g of α-isopropyl phenyl acetonitrile are added to 7.5
g of sodium amide. The mixture is stirred and refluxed for one hour. After
cooling, 25 g of 2-dimethylamino-1-chloropropane, dissolved in 20 cc of
benzene, are added and stirring and refluxing of the mixture is continued for
4 hours. After the reaction is completed, water is added to the reaction
mixture. The benzene layer is separated from the aqueous layer and is
extracted by means of 4N hydrochloric acid. The acid solution is rendered
alkaline.
The separated oil is taken up in ether. After drying the ethereal solution over
sodium sulfate and distilling off the ether, the resulting crude α-isopropyl-α- (β'-dimethylamino propyl) phenyl acetonitrile is purified by distillation in a
vacuum. The compound boils at 138° to 146°C/3 mm, according to US Patent
2,934,557.
Therapeutic Function
Antitussive
isoaminile Preparation Products And Raw materials
Raw materials
Preparation Products
isoaminile Suppliers
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- Country
- United States
- ProdList
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- Advantage
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- United States
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