(2R,3R)-(-)-2,3-Butanediol

97 %

Reagent Code: #230049
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CAS Number 24347-58-8

science Other reagents with same CAS 24347-58-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 90.12 g/mol
Formula C₄H₁₀O₂
badge Registry Numbers
MDL Number MFCD00064267
thermostat Physical Properties
Boiling Point 77.3-77.4°C 10mm Hg (Lit.)
inventory_2 Storage & Handling
Density 0.9870 g/cm3
Storage Room temperature, dry

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for producing enantiomerically pure compounds. Serves as a precursor in the synthesis of antibiotics, antifungals, and other bioactive molecules. Also utilized in the preparation of specialty polymers and as a solvent or intermediate in organic reactions requiring low toxicity and high stereochemical control.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to light yellow liquid
Purity (%) 96.5-100%
Refractive Index (N20/D) 1.432-1.434
Infrared Spectrum Conforms to Structure
Specific gravity (20/20°C) 0.992-0.995
Specific rotation [a]20/D (neat) -12 to -14 Degree Celsius
Enantiomeric Excess 98-100%

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿450.00
1g
10-20 days ฿580.00
5g
10-20 days ฿2,610.00
25g
10-20 days ฿11,320.00
100g
10-20 days ฿34,750.00
(2R,3R)-(-)-2,3-Butanediol
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Used as a chiral building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for producing enantiomerically pure compounds. Serves as a precursor in the synthesis of antibiotics, antifungals, and other bioactive molecules. Also utilized in the preparation of specialty polymers and as a solvent or intermediate in organic reactions requiring low toxicity and high stereochemical control.

Used as a chiral building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for producing enantiomerically pure compounds. Serves as a precursor in the synthesis of antibiotics, antifungals, and other bioactive molecules. Also utilized in the preparation of specialty polymers and as a solvent or intermediate in organic reactions requiring low toxicity and high stereochemical control.

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