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(S,S)-(+)-1,2-Cyclododecanediol, also known as Dodecanediol, is a chemical compound with the molecular formula C12H24O2. It is a white, waxy solid with a melting point of 58-60°C. This chiral molecule possesses unique chemical properties due to its specific stereochemistry, making it a valuable compound for various applications.

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  • 118101-31-8 Structure
  • Basic information

    1. Product Name: (S,S)-(+)-1,2-CYCLODODECANEDIOL
    2. Synonyms: (S,S)-(+)-1,2-CYCLODODECANEDIOL
    3. CAS NO:118101-31-8
    4. Molecular Formula: C12H24O2
    5. Molecular Weight: 200.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118101-31-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S,S)-(+)-1,2-CYCLODODECANEDIOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,S)-(+)-1,2-CYCLODODECANEDIOL(118101-31-8)
    11. EPA Substance Registry System: (S,S)-(+)-1,2-CYCLODODECANEDIOL(118101-31-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 118101-31-8(Hazardous Substances Data)

118101-31-8 Usage

Uses

Used in Polymer Industry:
(S,S)-(+)-1,2-Cyclododecanediol is used as a monomer in the production of thermoplastic polyurethane elastomers. Its unique structure contributes to the formation of polymers with desirable properties, such as flexibility and durability.
Used in Coatings Industry:
(S,S)-(+)-1,2-Cyclododecanediol is used as a crosslinking agent in the preparation of epoxy resins. Its ability to form crosslinks enhances the mechanical properties and chemical resistance of the resulting coatings.
Used in Pharmaceutical Industry:
Due to its unique chemical structure and properties, (S,S)-(+)-1,2-Cyclododecanediol has potential applications in the pharmaceutical industry. It can be utilized as an intermediate in the synthesis of various pharmaceutical compounds.
Used in Agrochemical Industry:
(S,S)-(+)-1,2-Cyclododecanediol also has potential applications in the agrochemical industry, where it can be used as an intermediate in the synthesis of agrochemical products.
Used in Fragrance Industry:
(S,S)-(+)-1,2-Cyclododecanediol has potential applications as a fragrance ingredient due to its unique chemical structure and properties. Its ability to impart specific scents can be utilized in the development of various fragrances for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 118101-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,1,0 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118101-31:
(8*1)+(7*1)+(6*8)+(5*1)+(4*0)+(3*1)+(2*3)+(1*1)=78
78 % 10 = 8
So 118101-31-8 is a valid CAS Registry Number.

118101-31-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S,S)-(+)-1,2-CYCLODODECANEDIOL

1.2 Other means of identification

Product number -
Other names trans-Cyclododecan-1,2-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:118101-31-8 SDS

118101-31-8Relevant articles and documents

Formation of persulphate from sodium sulphite and molecular oxygen catalysed by H5PV2Mo10O40-aerobic epoxidation and hydrolysis

Rubinstein, Amir,Carmeli, Raanan,Neumann, Ronny

, p. 13247 - 13249 (2015/05/20)

The H5PV2Mo10O40 polyoxometalate catalysed the electron transfer oxidation of sulphite to yield a sulphite radical, SO3- that upon addition of O2 yielded a peroxosulphate species efficient for the H5PV2Mo10O40 catalysed epoxidation of alkenes. The acidic polyoxometalate further catalysed hydrolysis of the epoxide to give vicinal diols in high yields. This journal is

SYNTHESIS OF 1,2-CYCLOALKANEDIOLS BY INTRAMOLECULAR TITANIUM-INDUCED PINACOL COUPLING

McMurry, John E.,Rico, Joseph G.

, p. 1169 - 1172 (2007/10/02)

Seven representative 1,2-cycloalkanediols of ring size 6-14 were prepared in high yield by titanium-induced pinacol coupling of dialdehydes.Cis stereochemistry predominated in six- and eight-membered rings, but trans products were formed in ring sizes ten and above.

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