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Sell Isopropylbenzylamine CAS 102-97-6
Home / Uncategorized / Hot Selling / Sell Isopropylbenzylamine CAS 102-97-6
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Sell Isopropylbenzylamine CAS 102-97-6

Product Name: CAS:102-97-6 Benzylisopropylamine
CAS NO.: CAS:102-97-6 Benzylisopropylamine
Purity:
Specification:
MOQ: 1.00 KG
Origin: China
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Sell Isopropylbenzylamine CAS 102-97-6

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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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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
Products Description
Product Name
N-Benzylisopropylamine
English alias
n-(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-Isopropylphenylmethanamine
Appearance
White translucent Crystal block
Content
99%
Quality Standard
Pharm grade
CAS NO.
102-97-6
Molecular formula
C10H15N
Usage
Mainly use in Pharmaceutical Intermediates
Packing
25 kg per barrel (box) (woven bag).
Storage
Dry and cool place and keep away from strong light
Sample
Avaiable

Sanderson, 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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    WebProduct Description. PRODUCT. N-Isopropylbenzylamine. CAS #. 102-97-6. SYNONYM. NIPBA; Benzenemethanamine, N- (1-methylethyl)-. FORMULA. C10H15N.

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    WebCAS RN: 102-97-6: Reaxys Registry Number: 2638437: PubChem Substance ID: 87564152: SDBS (AIST Spectral DB) 13356: MDL Number: MFCD00008863

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    • Physical State (20 deg.C): Liquid
    • Molecular Formula / Molecular Weight: C10H15N = 149.24
    • Product Number: B1216
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