(S)-(-)-α,4-Dimethylbenzylamine

95%

Reagent Code: #71679
label
Alias (S)-1-(4-methylphenyl)ethylamine; (S)-(-)-1-p-methylphenylethylamine
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CAS Number 27298-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.21 g/mol
Formula C₉H₁₃N
badge Registry Numbers
MDL Number MFCD00145246
thermostat Physical Properties
Boiling Point 205 °C(lit.)
inventory_2 Storage & Handling
Density 0.919 g/mL at 25 °C(lit.)
Storage room temperature, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature allows for the creation of compounds with high stereochemical purity, enhancing drug efficacy and reducing side effects. Additionally, it is employed in asymmetric synthesis and catalysis, contributing to the development of advanced chemical processes in organic chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 94.5-100
Refractive Index N20D 1.52-1.522
Specific Gravity (2020) 0.935-0.937
Optical Purity (EE) 99 (GLC)
Specific rotation (α20D neat) -38 to -34

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿440.00
inventory 1g
10-20 days ฿1,180.00
inventory 5g
10-20 days ฿4,150.00
(S)-(-)-α,4-Dimethylbenzylamine
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature allows for the creation of compounds with high stereochemical purity, enhancing drug efficacy and reducing side effects. Additionally, it is employed in asymmetric synthesis and catalysis, contributing to the development of advanced chemical processes in organic chemistry.
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