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18229-78-2

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18229-78-2 Usage

General Description

2-Hexynal diethyl acetal is a chemical compound commonly used as a flavoring agent and fragrance ingredient. It is a colorless liquid with a fruity, green, and waxy odor, and is often added to cosmetic, personal care, and food products for its pleasant scent. 2-HEXYNAL DIETHYL ACETAL has also been identified as a potential insect repellent, with studies showing its effectiveness in repelling and deterring various types of insects. Additionally, 2-hexynal diethyl acetal has been investigated for its potential pharmacological applications, including its antimicrobial and antifungal properties. Overall, this chemical is widely utilized for its appealing aroma and potential practical uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 18229-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,2 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18229-78:
(7*1)+(6*8)+(5*2)+(4*2)+(3*9)+(2*7)+(1*8)=122
122 % 10 = 2
So 18229-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-4-7-8-9-10(11-5-2)12-6-3/h10H,4-7H2,1-3H3

18229-78-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L06098)  2-Hexynal diethyl acetal, 98%   

  • 18229-78-2

  • 5g

  • 370.0CNY

  • Detail
  • Alfa Aesar

  • (L06098)  2-Hexynal diethyl acetal, 98%   

  • 18229-78-2

  • 25g

  • 1453.0CNY

  • Detail

18229-78-2SDS

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 1,1-diethoxyhex-2-yne

1.2 Other means of identification

Product number -
Other names 2-HEXYNAL DIETHYL ACETAL

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:18229-78-2 SDS

18229-78-2Relevant articles and documents

Neighbouring-group influence on the ring opening of some 2-alkyl-1,1,2-tribromocyclopropanes under phase-transfer conditions

Sydnes, Leiv K.,Alnes, Karl F. S.,Erdogan, Natalia

, p. 1737 - 1749 (2007/10/03)

Several 2-alkyl-1,1,2-tribromocyclopropanes were treated with sodium hydroxide and ethanol under phase-transfer conditions. Ring opening gave mixtures of the corresponding acetylenic diethyl ketals and acetals. When the steric bulk of the alkyl substituent was increased acetal formation dominated, and in the case of 1,1,2-tribromo-2-(tert-butyl)cyclopropane, the acetal was formed as the only product. Springer-Verlag 2005.

NATURAL ACETYLENES. PART 56. BIOSYNTHETIC EXPERIMENTS WITH THE FUNGUS LEPISTA DIEMII (SINGER). ORIGIN OF THE NITRILE GROUP OF THE C8 ACETYLENIC CYANO-ACID, DIATRETYNE 2

Jones, Ewart R. H.,Macrides, Theodore A.,Thaller, Viktor

, p. 2017 - 2030 (2007/10/02)

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