(S)-2-Amino-3-methylbutan-1-ol hydrochloride

95%

Reagent Code: #38283
fingerprint
CAS Number 17016-89-6

science Other reagents with same CAS 17016-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.6300 g/mol
Formula C₅H₁₄ClNO
badge Registry Numbers
MDL Number MFCD00050559
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral nature makes it valuable in the development of active pharmaceutical ingredients (APIs) that require high stereochemical specificity. Additionally, it is employed in organic synthesis for constructing complex molecules, especially in asymmetric synthesis, where it acts as a building block or chiral auxiliary. Its hydrochloride form enhances solubility and stability, making it suitable for various chemical reactions and formulations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,540.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-Amino-3-methylbutan-1-ol hydrochloride
No image available

This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral nature makes it valuable in the development of active pharmaceutical ingredients (APIs) that require high stereochemical specificity. Additionally, it is employed in organic synthesis for constructing complex molecules, especially in asymmetric synthesis, where it acts as a building block or chira

This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral nature makes it valuable in the development of active pharmaceutical ingredients (APIs) that require high stereochemical specificity. Additionally, it is employed in organic synthesis for constructing complex molecules, especially in asymmetric synthesis, where it acts as a building block or chiral auxiliary. Its hydrochloride form enhances solubility and stability, making it suitable for various chemical reactions and formulations.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...