(S)-()-2-Butanol

98%

  • Product Code: 66785
  CAS:    4221-99-2
Molecular Weight: 74.12 g./mol Molecular Formula: C₄H₁₀O
EC Number: MDL Number: MFCD00064281
Melting Point: Boiling Point: 100°C(lit.)
Density: 0.81g/ml Storage Condition: room temperature, dry
Product Description: This chemical is widely used as a chiral building block in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in producing optically active compounds, particularly in the development of drugs where stereochemistry plays a critical role in efficacy. Additionally, it serves as a solvent in organic reactions, especially in cases where a polar, non-aqueous medium is required. It is also employed in the production of esters, which are used as flavoring agents and fragrances in the food and cosmetic industries. Its application extends to research laboratories, where it is utilized as a reagent for asymmetric synthesis and chiral resolution studies.
Product Specification:
Test Specification
Appearance Colorless to yellow clear liquid
Purity 97.5-100
Specific gravity (20°C) 0.8070-0.8100
Refractive index (n20D) 1.3960-1.3980
Specific rotation [α]20D neat +11-+14
Infrared Spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size Availability Price Quantity
1ml 10-20 days ฿4,190.00
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-
5ml 10-20 days ฿13,960.00
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-
(S)-()-2-Butanol
This chemical is widely used as a chiral building block in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in producing optically active compounds, particularly in the development of drugs where stereochemistry plays a critical role in efficacy. Additionally, it serves as a solvent in organic reactions, especially in cases where a polar, non-aqueous medium is required. It is also employed in the production of esters, which are used as flavoring agents and fragrances in the food and cosmetic industries. Its application extends to research laboratories, where it is utilized as a reagent for asymmetric synthesis and chiral resolution studies.
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