(S)-(-)-2-METHYLBUTYLAMINE

95%

Reagent Code: #235909
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CAS Number 34985-37-0

science Other reagents with same CAS 34985-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 87.16 g/mol
Formula C₅H₁₃N
badge Registry Numbers
MDL Number MFCD00064430
inventory_2 Storage & Handling
Density 0.756 g/mL at 20 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its asymmetric center makes it valuable in the development of active pharmaceutical ingredients where stereochemistry influences biological activity. Also employed as a resolving agent for racemic mixtures and as an intermediate in the synthesis of agrochemicals and fine chemicals. Its amine functionality allows for easy derivatization, enabling its use in ligands for asymmetric catalysis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿18,880.00
(S)-(-)-2-METHYLBUTYLAMINE
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Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its asymmetric center makes it valuable in the development of active pharmaceutical ingredients where stereochemistry influences biological activity. Also employed as a resolving agent for racemic mixtures and as an intermediate in the synthesis of agrochemicals and fine chemicals. Its amine functionality allows for easy derivatization, enabling its use in
Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its asymmetric center makes it valuable in the development of active pharmaceutical ingredients where stereochemistry influences biological activity. Also employed as a resolving agent for racemic mixtures and as an intermediate in the synthesis of agrochemicals and fine chemicals. Its amine functionality allows for easy derivatization, enabling its use in ligands for asymmetric catalysis.
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