(S)-(−)-α-Methylbenzylamine

>99.0%(GC)

Reagent Code: #71651
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Alias (S)-(-)-α-Methylbenzylamine ;S-1-Phenylethylamine, S(-)-α-Phenylethylamine, Methylbenzylamine
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CAS Number 2627-86-3
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Properties Reminder: The product can only be used for scientific research purposes

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 121.18 g/mol
Formula C₈H₁₁N
badge Registry Numbers
EC Number 220-098-0
MDL Number MFCD00064406
thermostat Physical Properties
Melting Point -10 °C
Boiling Point 187 °C(lit.)
inventory_2 Storage & Handling
Density 0.94 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

(S)-(−)-α-Methylbenzylamine is widely used as a chiral resolving agent in organic synthesis. It is particularly valuable for separating racemic mixtures of carboxylic acids and other chiral compounds through the formation of diastereomeric salts. This process allows for the isolation of enantiomerically pure substances, which is crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. Additionally, it serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or ligand in catalytic reactions, enhancing enantioselectivity. This compound is also utilized in research and development for studying stereochemical effects and developing new chiral catalysts.

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Test Parameter Specification
Appearance Colorless liquid
Specific Rotation (α20D, neat) -41
Purity 99

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1ml
10-20 days Ft2,865.20
inventory 2.5L
10-20 days Ft124,636.15
inventory 5ml
10-20 days Ft3,069.86
inventory 25ml
10-20 days Ft3,683.83
inventory 100ml
10-20 days Ft11,256.14
inventory 500ml
10-20 days Ft30,186.92
(S)-(−)-α-Methylbenzylamine
(S)-(−)-α-Methylbenzylamine is widely used as a chiral resolving agent in organic synthesis. It is particularly valuable for separating racemic mixtures of carboxylic acids and other chiral compounds through the formation of diastereomeric salts. This process allows for the isolation of enantiomerically pure substances, which is crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. Additionally, it serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or ligand in catalytic reactions, enhancing enantioselectivity. This compound is also utilized in research and development for studying stereochemical effects and developing new chiral catalysts.
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