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10522-26-6

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10522-26-6 Usage

General Description

2-Methyl-1-undecanol, also known as isoundecanol, is a clear, colorless liquid with a slightly sweet, floral odor. It is classified as a fragrance ingredient and is commonly used in the production of perfumes, colognes, and other scented products. This chemical is a long-chain primary alcohol, and its structure includes a 2-methyl branching at the 1-position of the undecanol chain. It is known for its ability to impart a fresh, floral scent and is often used as a blending agent to enhance the overall fragrance profile of a product. Additionally, 2-methyl-1-undecanol can also be used as a solvent, emollient, and surfactant in personal care products and various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10522-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10522-26:
(7*1)+(6*0)+(5*5)+(4*2)+(3*2)+(2*2)+(1*6)=56
56 % 10 = 6
So 10522-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H26O/c1-3-4-5-6-7-8-9-10-12(2)11-13/h12-13H,3-11H2,1-2H3

10522-26-6SDS

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-methylundecan-1-ol

1.2 Other means of identification

Product number -
Other names 2-methyl-undecan-1-ol

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:10522-26-6 SDS

10522-26-6Relevant articles and documents

Organoboranr-Catalyzed anti-Markownikoff Hydration of Olefins

Maruoka, Keiji,Sano, Hiromi,Shinoda, Kiyotaka,Yamamoto, Hisashi

, p. 73 - 76 (1987)

A new, catalytic procedure for the anti-Markownikoff hydration of olefins in the presence of organoborane catalyst and dichloroaluminum hydride under dry air has been described.

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van Tamelen,E.E.,Gladysz,J.A.

, p. 5290 - 5291 (1974)

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Organoborane-Catalyzed Hydroalumination of Olefins

Maruoka, Keiji,Sano, Hiromi,Shinoda, Kiyotaka,Nakai, Shuichi,Yamamoto, Hisashi

, p. 6036 - 6038 (1986)

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POLYOL ETHERS AND PROCESS FOR MAKING THEM

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Paragraph 0080, (2011/05/14)

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

Compounds having protected hydroxy groups

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, (2008/06/13)

The present invention relates to compounds with protected hydroxy groups of formula (I) These compounds are precursors for organoleptic agents, such as fragrances, and masking agents and for antimicrobial agents. When activated, the compounds of formula (I) are cleaved and form one or more organoleptic and/or antimicrobial compounds.

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