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3-(Ethyl thio) butanol, also known as 3-(ethylmercapto) butanol, is an organic compound with the chemical formula C6H14OS. It is a pale yellow to colorless liquid with a high-strength, cooked, brown-roasted nutty aroma. 3-(ethyl thio) butanol is characterized by its strong, pleasant odor, which is recommended to be smelled in a 0.10% solution or less to avoid overpowering the senses.

117013-33-9

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117013-33-9 Usage

Uses

Used in Flavor and Fragrance Industry:
3-(Ethyl thio) butanol is used as a flavoring agent for its cooked, brown-roasted nutty aroma. It is particularly suitable for enhancing the taste and smell of various food products, making it a valuable addition to the flavor and fragrance industry.
Used in Perfumery:
In the perfumery industry, 3-(ethyl thio) butanol is utilized as a fragrance ingredient. Its unique, strong aroma adds depth and complexity to perfume compositions, contributing to the creation of long-lasting and memorable scents.
Used in Aromatherapy:
3-(Ethyl thio) butanol can be employed in aromatherapy as a natural, pleasant-smelling compound that may help promote relaxation and a sense of well-being. Its strong, nutty aroma can be used in aromatherapy practices to create a calming and soothing atmosphere.
Used in Chemical Research:
Due to its unique chemical properties, 3-(Ethyl thio) butanol can be used in chemical research and development. It may serve as a starting material or intermediate in the synthesis of various organic compounds, contributing to the advancement of chemical science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 117013-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117013-33:
(8*1)+(7*1)+(6*7)+(5*0)+(4*1)+(3*3)+(2*3)+(1*3)=79
79 % 10 = 9
So 117013-33-9 is a valid CAS Registry Number.

117013-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylsulfanylbutan-1-ol

1.2 Other means of identification

Product number -
Other names UNII-408AF93G1U

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:117013-33-9 SDS

117013-33-9Downstream Products

117013-33-9Relevant articles and documents

Identification of selective 8-(piperidin-4-yloxy)quinoline sulfone and sulfonamide histamine H1 receptor antagonists for use in allergic rhinitis

Procopiou, Panayiotis A.,Ford, Alison J.,Gore, Paul M.,Hancock, Ashley P.,Hodgson, Simon T.,Holmes, Duncan S.,Looker, Brian E.,Vile, Sadie,Clark, Kenneth L.,Saunders, Ken A.,Slack, Robert J.,Watts, Clarissa J.

, p. 4914 - 4919 (2017/09/29)

A series of potent, selective and long-acting quinoline-based sulfonamide human H1 histamine receptor antagonists, designed for once-daily intranasal administration for the treatment of rhinitis were developed. Sulfonamide 33b had a slightly lower affinity for the H1 receptor than azelastine, had low oral bioavailability in the rat and dog, and was turned over to five major metabolites. Furthermore, 33b had longer duration of action than azelastine in guinea pigs, lower rat brain-penetration, and did not cause time dependent inhibition of CYP2D6 or CYP3A4. The clinical dose in humans is expected to be low (approximately 0.5 mg per day) based on the clinical dose used for azelastine and a comparison of efficacy data from animal models for 33b and azelastine.

PHTHALAZINE AND PYRIDO [3,4-D] PYRIDAZ INE COMPOUNDS AS H1 RECEPTOR ANTAGONISTS

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Page/Page column 51, (2009/05/30)

The present invention relates to compounds of formula (I), and salts thereof, processes for their preparation, to compositions containing them and to their use in the treatment of various diseases, such as allergic rhinitis.

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