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2,3,4-trimethylpentan-2-ol, also known as diisobutyl carbinol, is a colorless liquid organic chemical belonging to the alcohol family. It has a slightly sweet odor and is commonly used as a solvent in various industrial applications. This versatile compound also serves as a reaction intermediate in the manufacturing of pharmaceuticals, pesticides, and other organic compounds. Due to its flammable nature, it requires careful handling to prevent irritation to the eyes, skin, and respiratory system, as well as potential harm to aquatic life if released into water bodies.

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  • 66576-26-9 Structure
  • Basic information

    1. Product Name: 2,3,4-trimethylpentan-2-ol
    2. Synonyms: 2,3,4-trimethylpentan-2-ol
    3. CAS NO:66576-26-9
    4. Molecular Formula: C8H18O
    5. Molecular Weight: 130.2279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66576-26-9.mol
  • Chemical Properties

    1. Melting Point: -61.15°C (estimate)
    2. Boiling Point: 170.96°C (estimate)
    3. Flash Point: 50 °C
    4. Appearance: /
    5. Density: 0.8040
    6. Refractive Index: 1.4350
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,3,4-trimethylpentan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4-trimethylpentan-2-ol(66576-26-9)
    11. EPA Substance Registry System: 2,3,4-trimethylpentan-2-ol(66576-26-9)
  • 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: 66576-26-9(Hazardous Substances Data)

66576-26-9 Usage

Uses

Used in Chemical Industry:
2,3,4-trimethylpentan-2-ol is used as a solvent for various industrial applications, including the production of paints, coatings, and adhesives. Its solubility properties make it suitable for dissolving a wide range of substances, facilitating processes in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,3,4-trimethylpentan-2-ol is utilized as a reaction intermediate. It plays a crucial role in the synthesis of various drugs, contributing to the development of new medications and improving the efficacy of existing ones.
Used in Pesticide Industry:
2,3,4-trimethylpentan-2-ol is employed as a reaction intermediate in the manufacturing of pesticides. Its involvement in the production process helps create effective pest control agents, ensuring agricultural productivity and crop protection.
Used in Other Organic Compounds Production:
This chemical is also used in the synthesis of other organic compounds, expanding its applications across various industries. Its versatility as a building block allows for the creation of a diverse range of products, highlighting its importance in the chemical market.

Check Digit Verification of cas no

The CAS Registry Mumber 66576-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66576-26:
(7*6)+(6*6)+(5*5)+(4*7)+(3*6)+(2*2)+(1*6)=159
159 % 10 = 9
So 66576-26-9 is a valid CAS Registry Number.

66576-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4-trimethylpentan-2-ol

1.2 Other means of identification

Product number -
Other names 2,3,4-TRIMETHYL-2-PENTANOL

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:66576-26-9 SDS

66576-26-9Relevant articles and documents

Structure-activity relationship observations for the bagworm moth pheromone

Warthen,Klun,DeVilbiss

, p. 1315 - 1324 (2007/10/03)

Structure-activity relationship (SAR) observations were made for the bagworm moth pheromone. (R)-2-pentyl decanoate, and a series of analogs with modifications in the alcohol portion of the molecule. Observed attractiveness of these analogs was related to molecular structure and their physical attributes using computational chemistry. Electrostatic potential and Van der Waals (VdW) electrostatic coded surface three-dimensional (3D) maps of the molecular mechanics (MM) minimized lowest energy conformation of the pheromone show that size, shape, charge distribution, and chirality of the molecule are related to attractiveness.

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