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66576-26-9

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66576-26-9 Usage

General Description

2,3,4-trimethylpentan-2-ol, also known as diisobutyl carbinol, is a colorless liquid compound with a slightly sweet odor. It is an organic chemical that belongs to the alcohol family and is commonly used as a solvent in various industrial applications. This chemical is also used as a reaction intermediate in the manufacturing of pharmaceuticals, pesticides, and other organic compounds. It is flammable and should be handled with caution, and exposure to this chemical can cause irritation to the eyes, skin, and respiratory system. Additionally, it may have harmful effects on aquatic life if released into water bodies. Overall, 2,3,4-trimethylpentan-2-ol is an important industrial chemical with various applications, but it should be used and handled with care.

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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