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13162-46-4

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13162-46-4 Usage

Description

trans,trans-2,4-Undecadienal is a chemical compound with a powerful green odor and a fatty, waxy green taste with chicken nuances at 10 ppm. It is commonly found in various food items such as chicken fat, beer, potato chips, grilled and roasted beef, boiled mutton, raw cured pork, roasted peanut, soybean, mushrooms, malt, and buckwheat.

Uses

Used in Flavor and Fragrance Industry:
trans,trans-2,4-Undecadienal is used as a flavoring agent for its characteristic fatty, waxy green taste with chicken nuances. It is added to various food products to enhance their flavor and aroma.
Used in Aromatherapy:
trans,trans-2,4-Undecadienal is used as an aromatherapy agent for its powerful green odor. It can be used in essential oils and other aromatherapy products to provide a refreshing and invigorating scent.
Used in Perfumery:
trans,trans-2,4-Undecadienal is used as a fragrance ingredient in perfumery due to its unique green odor. It can be used to create a variety of scent profiles in perfumes, colognes, and other fragranced products.
Used in Research:
trans,trans-2,4-Undecadienal is used as a research compound in various scientific studies. It can be used to investigate the chemical properties and applications of aldehydes in different industries.
Used in Food Industry:
trans,trans-2,4-Undecadienal is used as a flavor enhancer in the food industry. It can be added to various food products to improve their taste and aroma, making them more appealing to consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 13162-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13162-46:
(7*1)+(6*3)+(5*1)+(4*6)+(3*2)+(2*4)+(1*6)=74
74 % 10 = 4
So 13162-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O/c1-2-3-4-5-6-7-8-9-10-11-12/h7-11H,2-6H2,1H3/b8-7+,10-9+

13162-46-4SDS

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 trans,trans-2,4-undecadienal

1.2 Other means of identification

Product number -
Other names 1,6-Undecadiyne

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:13162-46-4 SDS

13162-46-4Downstream Products

13162-46-4Relevant articles and documents

Method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and diphosphine ligand used in method

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Paragraph 0183-0187, (2021/05/29)

The invention discloses a method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and a diphosphine ligand used in the method. According to the invention, indole-substituted phosphoramidite diphosphine ligand which is stable in air and insensitive to light is synthesized by utilizing a continuous one-pot method, and the indole-substituted phosphoramidite diphosphine ligand and a rhodium catalyst are used for jointly catalyzing to successfully achieve a hydroformylation reaction of aromatic terminal alkyne and terminal conjugated eneyne under the condition of synthesis gas for the first time, so that an olefine aldehyde structure compound can be rapidly and massively prepared, and particularly, a polyolefine aldehyde structure compound which is more difficult to synthesize in the prior art can be easily prepared and synthesized, and a novel method is provided for synthesis and modification of drug molecules, intermediates and chemical products.

A Novel and General Route to 1-Iodo-2,4(E,E)-dienes via Pentadienyl Dithiocarbamate

Hayashi, Toshio,Sasaoka, Kazuo,Oishi, Takeshi

, p. 1362 - 1363 (2007/10/02)

The title compounds were prepared from pentadienyl dithiocarbamate via S-methylathion and by use of the iodide an unsymmetric, all-trans-conjugated pentaene was synthesized.

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