Welcome to LookChem.com Sign In|Join Free
  • or
2-(R)-isobutyl-oxirane, also known as (R)-2-(1-methylethyl)oxirane, is a colorless, volatile liquid with a slightly sweet odor and the molecular formula C6H12O. It is classified as an epoxide, an organic chemical with a three-membered ring structure containing one oxygen atom. 2-(R)-isobutyl-oxirane is commonly used as a solvent in various industries, including pharmaceuticals and cosmetics, due to its unique properties.

60856-89-5

Post Buying Request

60856-89-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

60856-89-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(R)-isobutyl-oxirane is used as a solvent for the synthesis of various pharmaceutical compounds. Its ability to dissolve a wide range of substances makes it a valuable component in the production of medications.
Used in Cosmetics Industry:
In the cosmetics industry, 2-(R)-isobutyl-oxirane is utilized as a solvent for formulating cosmetic products. Its volatility and sweet odor contribute to the texture and scent of the final product.
Safety Precautions:
As a flammable substance, 2-(R)-isobutyl-oxirane may cause irritation to the skin, eyes, and respiratory system upon prolonged exposure. It is crucial to handle this chemical with caution and follow proper safety precautions when using it in industrial processes to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 60856-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60856-89:
(7*6)+(6*0)+(5*8)+(4*5)+(3*6)+(2*8)+(1*9)=145
145 % 10 = 5
So 60856-89-5 is a valid CAS Registry Number.

60856-89-5Relevant academic research and scientific papers

Pheromone synthesis, CLXXVII: Synthesis of the enantiomers of 2-methyl-4-heptanol and 2-methyl-4-octanol, the pheromone components of the West Indian sugarcane borer

Takenaka, Motonobu,Takikawa, Hirosato,Mori, Kenji

, p. 1963 - 1964 (1996)

Both the enantiomers of 2-methyl-4-heptanol (1) and 2-methyl-4-octanol (2), the components of the male-produced aggregation pheromone of the West Indian sugarcane borer (Metamasius hemipterus), were synthesized by starting from the enantiomers of leucine. VCH Verlagsgesellschaft mbH, 1996.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 60856-89-5