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CAS 27607-33-6

cis-Cyclooctane-1,2-diol TCI C4056

cis-Cyclooctane-1,2-diol TCI C4056

Chemical Identity

Other names
cis-1,2-Cyclooctanediol · cis-1,2-Dihydroxycyclooctane · meso-1,2-Cyclooctanediol
CAS No.
27607-33-6
PubChem
CID 10888034
Formula
C8H16O2
Molecular weight
144.21 g/mol
Purity
>95.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
cis-(1S,2R)-cyclooctane-1,2-diol
SMILES
C1CCCC(C(CC1)O)O
InChIKey
HUSOFJYAGDTKSK-OCAPTIKFSA-N
MDL
MDL00134226
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TCI C4056 27607-33-6 cis-Cyclooctane-1,2-diol is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a diol, it provides two hydroxyl groups that serve as reactive sites for various chemical transformations. This compound plays a crucial role in organic chemistry by acting as a building block for the creation of more intricate molecular structures. Its versatility makes it an essential tool for researchers working in synthetic chemistry and molecular design.

The compound's cyclic structure contributes to its stability and controlled reactivity, making it ideal for applications requiring precision. Its polar nature allows it to interact effectively with both polar and non-polar solvents, expanding its utility in different reaction conditions. This property is particularly valuable in reactions involving esterification, hydrolysis, and oxidation processes. The combination of stability and reactivity ensures that cis-Cyclooctane-1,2-diol is a reliable choice for a wide range of chemical applications.

In Indonesian laboratories, this compound is commonly used in organic synthesis research, especially in the development of cyclic structures. Its controlled reactivity and molecular stability make it a preferred choice for studies requiring precise chemical reactions. Researchers in Indonesia rely on this compound for its consistent performance and adaptability in various experimental setups. Its presence in laboratory workflows supports the advancement of chemical research and innovation in the region.

  • Organic synthesis of cyclic compounds due to its stable cyclic structure and reactive hydroxyl groups.
  • Esterification reactions where hydroxyl groups can be converted into ester functionalities.
  • Hydrolysis processes for breaking down complex molecules using its polar nature and reactivity.
  • Oxidation reactions where the hydroxyl groups can be modified under controlled conditions.
  • Molecular design applications requiring controlled reactivity and structural versatility.

Brand TCI
CAS number 27607-33-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes —
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its polar nature, it is advisable to use glass or polyethylene containers that are chemically inert. Avoid storing near incompatible substances such as strong oxidizers or acids. Always ensure proper ventilation when handling to minimize inhalation risks. Regular inspection of storage conditions is essential to maintain the compound's effectiveness and safety in laboratory settings.

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