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2051-32-3

3-ethyloctan-3-ol, also known as 3-ethyl-3-octanol, is a colorless liquid chemical compound with the molecular formula C10H22O. It has a faint, sweet odor and is commonly used in various industries due to its unique properties.
Used in Food and Beverage Industry:
3-ethyloctan-3-ol is used as a flavoring agent for enhancing the taste and aroma of food and beverage products. Its sweet scent makes it suitable for adding a pleasant flavor to a variety of consumables.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 3-ethyloctan-3-ol is used as a fragrance ingredient. Its mild and sweet smell contributes to the overall scent profile of products such as perfumes, lotions, and other personal care items.
Used in Biofuel Industry:
3-ethyloctan-3-ol is considered a potential biofuel additive due to its favorable properties as a fuel component. Its use in this industry is aimed at improving the efficiency and performance of biofuels, making them more viable as an alternative to traditional fossil fuels.
Production Method:
3-ethyloctan-3-ol is primarily produced through chemical synthesis, which allows for a controlled and efficient manufacturing process. This method ensures a consistent supply of the compound for various applications across different industries.

2051-32-3

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2051-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2051-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2051-32:
(6*2)+(5*0)+(4*5)+(3*1)+(2*3)+(1*2)=43
43 % 10 = 3
So 2051-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O/c1-4-7-8-9-10(11,5-2)6-3/h11H,4-9H2,1-3H3

2051-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyloctan-3-ol

1.2 Other means of identification

Product number -
Other names 3-Octanol, 3-ethyl-

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:2051-32-3 SDS

2051-32-3Relevant articles and documents

Chemical and Spectroscopic Observations on the Properties and Composition of Higher Order, Mixed Organocuprates, R2Cu(CN)Li2

Lipshutz, Bruce H.,Kozlowski, Joseph A.,Wilhelm, Robert S.

, p. 3943 - 3949 (1984)

The nature of organocuprates of general formula R2Cu(CN)Li2, derived from CuCN and 2RLi, is described in terms of their structural integrity in solution.A combination of chemical and spectroscopic tests conclusively demonstrates facile dissociation-reassociation of alkyl groups on copper.Data derived from both IR and variable temperature NMR spectra suggest that different aggregation states between Et2O and THF based solutions of these reagents exist.

REACTION OF ETHYLMAGNESIUM BROMIDE WITH CARBOXYLIC ESTERS IN THE PRESENCE OF TRIBUTYL VANADATE

Kulinkovich, O. G.,Sorokin, V. L.,Kel'in, A. V.

, p. 55 - 57 (2007/10/02)

The reaction of the butyl esters of carboxylic acids with an excess of ethylmagnesium bromide in the presence of catalytic amounts of tributyl vanadate leads to 1-substituted 1-cyclopropanols with yields of 41-83percent.

Substitution Reactions of Secondary Halides and Epoxides with Higher Order, Mixed Organocuprates, R2Cu(CN)Li2: Synthetic, Stereochemical, and Mechanistic Aspects

Lipshutz, Bruce H.,Wilhelm, Robert S.,Kozlowski, Joseph A.,Parker, David

, p. 3928 - 3938 (2007/10/02)

Higher order cuprates, represented by the general formula R2Cu(CN)Li2, are readily prepared from copper cyanide and 2 equiv of an organolithium.These novel reagents react readily and efficiently with secondary unactivated iodides and bromides affording products of substitution.Likewise, mono-, di-, and trisubstituted epoxides undergo ring opening leading to the corresponding alcohols in excellent yields.The effects of solvent, temperature, gegenion, and variations in ligands are discussed.Replacement of the second equivalent of RLi by CH3Li strongly encouragestransfer of R over CH3 in R(CH3)Cu(CN)Li2 with halides.Use of PhLi as RRLi in place of one RTLi (i.e.RT(Ph)Cu(CN)Li2) is suggested for oxirane cleavage.The stereochemical implications associated with both couplings are also addressed.

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