Description
Supply Isopropylbenzylamine CAS 102-97-6
Supply Isopropylbenzylamine CAS 102-97-6
Sell Isopropylbenzylamine CAS 102-97-6
Sell Isopropylbenzylamine CAS 102-97-6
| Description | N-Isopropylbenzylamine (NIPBA) is an organic compound with the chemical formula C9H13N. It is a colorless, flammable liquid that is used in a variety of applications, including as a solvent, a reagent, and a catalyst. NIPBA has a wide range of uses in the pharmaceutical, agrochemical, and petrochemical industries. It is also used in the synthesis of other compounds, including pharmaceuticals, agrochemicals, and intermediates. |
| Synthesis Method | N-Isopropylbenzylamine is synthesized by a variety of methods, including the reaction of amines with alkyl halides, the reaction of an amine with an alkyl halide, and the reaction of an amine with an alkyl halide in the presence of an aqueous base. The most common method of synthesis is the reaction of an amine with an alkyl halide in the presence of an aqueous base. This method is known as the Hofmann-Löffler reaction. |
| Synthesis Method Details | Design of the Synthesis Pathway The synthesis pathway of N-Isopropylbenzylamine involves the reaction of benzylamine with isopropyl chloride in the presence of a base to form N-Isopropylbenzylamine.Starting Materials Benzylamine, Isopropyl chloride, Base (e.g. sodium hydroxide)Reaction Add benzylamine to a flask Add isopropyl chloride dropwise to the flask while stirring Add base to the flask to neutralize the hydrogen chloride formed during the reaction Heat the mixture to reflux for several hours Cool the mixture and extract the N-Isopropylbenzylamine with a suitable solvent Purify the compound by recrystallization or column chromatography |
| Scientific Research Applications | N-Isopropylbenzylamine is used in a variety of scientific research applications, including as a solvent for the synthesis of organic compounds, as a catalyst for the synthesis of organic compounds, and as a reagent for the synthesis of organic compounds. It is also used in the synthesis of chiral compounds, such as chiral alcohols and chiral amines. In addition, it is used in the synthesis of pharmaceuticals, agrochemicals, and intermediates. |
| Mechanism of Action | N-Isopropylbenzylamine acts as a nucleophile, meaning that it is attracted to positively charged molecules, such as electrophiles. This attraction allows it to react with electrophiles and form covalent bonds. N-Isopropylbenzylamine is also a strong base, meaning that it can act as a proton acceptor. This allows it to react with acids and form salts. |
| Biochemical and Physiological Effects | N-Isopropylbenzylamine has been found to have a variety of biochemical and physiological effects. In studies, it has been found to have antifungal, antibacterial, and antiviral properties. It has also been found to have anti-inflammatory, anti-allergic, and anti-tumor properties. In addition, it has been found to have anti-oxidant and anti-cancer properties. |
| Advantages and Limitations for Lab Experiments | N-Isopropylbenzylamine has a number of advantages and limitations when used in laboratory experiments. One advantage is that it is relatively non-toxic, making it safe to use in laboratory experiments. Another advantage is that it is a strong base, making it useful for the synthesis of organic compounds. A limitation is that it is highly flammable, so it must be handled with care. Additionally, it is not soluble in water, so it must be used in organic solvents. |
| Future Directions | Future directions for N-Isopropylbenzylamine include further research into its biochemical and physiological effects, as well as its potential applications in drug synthesis and pharmaceuticals. Additionally, further research could be conducted into its use as a catalyst in organic synthesis, as well as its potential use as a reagent for the synthesis of chiral compounds. Finally, further research could be conducted into its potential use as a solvent for organic compounds, as well as its potential use in agrochemical and petrochemical industries. |
| CAS RN | 102-97-6 |
| Product Name | N-Isopropylbenzylamine |
| Molecular Formula | C10H15N |
| Molecular Weight | 149.23 g/mol |
| IUPAC Name | N-benzylpropan-2-amine |
| InChI | InChI=1S/C10H15N/c1-9(2)11-8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3 |
| InChI Key | LYBKPDDZTNUNNM-UHFFFAOYSA-N |
| SMILES | CC(C)NCC1=CC=CC=C1 |
| Canonical SMILES | CC(C)NCC1=CC=CC=C1 |
| Boiling Point | 200.0 °C |
| Other CAS RN | 102-97-6 |
| Pictograms | Irritant |
| Synonyms | N-benzyl-N-isopropylamine N-benzylisopropylamine N-isopropylbenzylamineSell Isopropylbenzylamine CAS 102-97-6 |
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| CBNumber: | CB05864144 |
| Chemical Name: | High Quality 102-97-6 N-Isopropylbenzylamine crystal |
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- CAS No:102-97-6
- Other Names:N-Isopropylbenzylamine
MF:C10H15N, C10H15N
- EINECS No.:203-067-6
- Place of Origin:Shanghai ,China
- Type:Syntheses Material Intermediates
- Purity:99%min, 99%MIN
- Appearance:White crystal
- Product name:N-Isopropylbenzylamine
- CAS:102-97-6
- MW:149.23
- Apperance:White crystal
- Grade:Industrial grade
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Products DescriptionProduct NameN-BenzylisopropylamineEnglish aliasn-(1-methylethyl)-benzenemethanamine
N-BENZYLISOPROPYLAMINE
N-BENZYL-N-ISOPROPYLAMINE
N-ISOPROPYLBENZYLAMINE
Benzylamine, N-isopropyl-
Benzylisopropylamine
Isopropylbenzylamine
n-(1-methylethyl)-benzenemethanamin
N-ISOPROPYLBENZYLAMINE / N-BENZYLISOPROPYLAMINE
N-(b-Hydroxyethyl)pyrrolidine
N-Isopropylbenzenemethanamine
N-IsopropylphenylmethanamineAppearanceWhite translucent Crystal blockContent99%Quality StandardPharm gradeCAS NO.102-97-6Molecular formulaC10H15NUsageMainly use in Pharmaceutical IntermediatesPacking25 kg per barrel (box) (woven bag).StorageDry and cool place and keep away from strong lightSampleAvaiableSanderson, R.M. Identification of N-methylbenzylamine hydrochloride, N-ethylbenzylamine hydrochloride, and N-isopropylbenzylamine hydrochloride. Microgram J. 6(1-2), 36-45 (2008).
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