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2084-19-7

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2084-19-7 Usage

Description

2-Pentanethiol is an organic compound characterized by its unpleasant odor, which is sulfuraceous and gassy. It is known for its distinctive taste and aroma, with a taste threshold value that imparts a sulfurous coffee and bacon flavor with roasted savory and tropical pulpy pineapple-like notes. Additionally, it has an aroma threshold value that describes it as sulfurous, ripe fruity, pineapple, and tropical fruit-like with a sautéed and roasted savory nuance. 2-Pentanethiol is also reported to be found in guava and yellow passion fruit.

Uses

Used in Flavor and Fragrance Industry:
2-Pentanethiol is used as a flavoring agent for its unique taste and aroma characteristics. Its ability to impart sulfurous coffee and bacon flavors, as well as roasted savory and tropical pulpy pineapple-like notes, makes it a valuable addition to the flavor industry. It is particularly useful in creating complex and nuanced flavor profiles in various food and beverage products.
Used in Aromatherapy and Perfumery:
In the aromatherapy and perfumery industries, 2-Pentanethiol is used as a fragrance ingredient due to its distinctive sulfurous, ripe fruity, pineapple, and tropical fruit-like aroma with a sautéed and roasted savory nuance. Its unique scent can be used to create captivating and long-lasting fragrances for various applications, such as perfumes, colognes, and scented products.
Used in Chemical Research and Development:
2-Pentanethiol's chemical properties, including its sulfuraceous and gassy nature, make it a valuable compound for research and development in the chemical industry. It can be used as a starting material or intermediate in the synthesis of various chemicals and materials, contributing to the advancement of new products and technologies.
Used in Analytical Chemistry:
Due to its distinct taste and aroma characteristics, 2-Pentanethiol can be employed in analytical chemistry as a reference compound for the development and calibration of analytical instruments and methods. Its unique properties can help improve the accuracy and sensitivity of these instruments, leading to better detection and quantification of target compounds in various samples.

Check Digit Verification of cas no

The CAS Registry Mumber 2084-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2084-19:
(6*2)+(5*0)+(4*8)+(3*4)+(2*1)+(1*9)=67
67 % 10 = 7
So 2084-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H12S/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3

2084-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name pentane-2-thiol

1.2 Other means of identification

Product number -
Other names Pentyl-mercaptan-(2)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:2084-19-7 SDS

2084-19-7Relevant articles and documents

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Miron,Richter

, p. 453 (1949)

-

Method of making 2-thiols

-

Page/Page column 5, (2008/06/13)

A process for selectively making 2-thiols from alpha olefins is described. The process includes contacting a linear or branched alpha olefin having with H2S in the presence of a catalyst and recovering the 2-thiol from a product mixture. The catalyst includes a support and at least one metal selected from Group IIIA-VIIIA and the branched olefin is branched at the 3-position or higher with respect to the olefin double bond. Compositions wherein the 2-thiols are substantially free of 1 -thiol and 3-thiol isomers are also described.

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