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(5E)-tetradec-5-enoic acid, also known as 5E-tetradecenoic acid, is a long-chain unsaturated fatty acid characterized by a 14-carbon chain and a double bond at the 5th carbon in the E configuration. This naturally occurring compound is derived from various plant and animal sources, such as fish oils, vegetable oils, and certain types of algae. It is integral to biological processes, acting as a precursor for the synthesis of essential lipid molecules like phospholipids, triglycerides, and cholesterol esters. Studies have highlighted its potential health benefits, which include anti-inflammatory and anti-microbial properties, and it is utilized as a dietary supplement in some formulations. The chemical structure and functional attributes of (5E)-tetradec-5-enoic acid render it a valuable component across different industries, including the food, pharmaceutical, and cosmetic sectors.

5684-69-5

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5684-69-5 Usage

Uses

Used in the Food Industry:
(5E)-tetradec-5-enoic acid is used as a natural additive for enhancing the nutritional value and health benefits of various food products. Its presence contributes to the overall fatty acid profile, which is essential for human health and well-being.
Used in the Pharmaceutical Industry:
(5E)-tetradec-5-enoic acid is utilized as an active ingredient in the development of drugs targeting inflammation and microbial infections. Its anti-inflammatory and anti-microbial properties make it a promising candidate for pharmaceutical applications.
Used in the Cosmetic Industry:
(5E)-tetradec-5-enoic acid is employed as a key component in the formulation of cosmetic products, where it serves to improve skin health and provide moisturizing and nourishing benefits due to its lipid-enriching properties.
Used as a Dietary Supplement:
(5E)-tetradec-5-enoic acid is used as a dietary supplement to support general health and well-being. Its inclusion in supplement formulations aims to provide the body with essential fatty acids that contribute to various biological processes and offer potential health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 5684-69-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5684-69:
(6*5)+(5*6)+(4*8)+(3*4)+(2*6)+(1*9)=125
125 % 10 = 5
So 5684-69-5 is a valid CAS Registry Number.

5684-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans 5-tetradecenoic acid

1.2 Other means of identification

Product number -
Other names -

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:5684-69-5 SDS

5684-69-5Relevant academic research and scientific papers

Formation of COOH-Ylides, and Their Reactivities and Selectivities in Wittig Reactions

Suganuma, Yuta,Kobayashi, Yuichi

supporting information, p. 333 - 337 (2019/02/12)

Whereas two equivalents of base are typically required to prepare carboxylate (CO 2-) ylides [Ph 3 P + C - (H)-alk-CO 2- ] (alk = alkanediyl) from carboxy (CO 2 H) pho

1H-Nuclear magnetic resonance spectroscopic studies of saturated, acetylenic and ethylenic triacylglycerols

Lie Ken Jie, Marcel S.F.,Lam

, p. 155 - 171 (2007/10/03)

The 1H-NMR spectroscopic properties of 15 synthetic homologous saturated triacylglycerols of type AAA and 16 mixed saturated triacylglycerols of type ABA and AAB have been studied. Triacylglycerols containing short-chain fatty acids (2:0-6:0) are readily identified. Triacylglycerols containing medium- and long-chain fatty acid components are not differentiated. From the analysis of 19 acetylenic triacylglycerols of type AAA, ABA and AAB (containing positional isomers of acetylenic fatty acids), it is only possible to characterize triacylglycerols with acyl groups containing the acetylenic bond at the Δ2-Δ5 position. 1H-NMR analysis could not confirm the positions (α- or β-acyl) of the acetylenic acids in mixed triacylglycerols. In the study of 22 ethylenic triacylglycerols of type AAA containing positional isomers of (Z)- or (E)-ethylenic acids, molecules containing an ethylenic bond in the Δ2 position of the acyl chains were readily characterized, as the ethylenic protons in the α- and β-acyl chains were fully resolved. Triacylglycerols containing an unsaturated center at the position were characterized by the shifts of the 2-H protons. The spectra of the remaining triacylglycerol molecules were very similar and the position of the ethylenic system could not be determined by this technique.

SYNTHESIS OF DODEC-5E-EN-1-OL - THE PHEROMONE OF TRICIMBA CINCTA - AND TETRADEC-5E-1-YL ACETATE - AN IMITATOR OF THE PHEROMONE OF RHYNCHOPACHA SP.

Verba, G. G.,Bukulova, L. M.,Abduvakhabov, A. A.,Kamaev, F. G.

, p. 113 - 116 (2007/10/02)

On the basis of a modified Knoevenagel reaction starting from octanal and decanal, the stereodirected synthesis has been effected of dodec-5E-en-ol (the pheromone of the grass fly Tricimba cincta - and tetradec-5E-en-yl acetate) an imitator of the pheromone of the moth Rhynchopacha sp.

TRANS STEREOSELECTIVITY IN THE REACTION OF (4-CARBOXYBUTYLIDENE)TRIPHENYLPHOSPHORANE WITH AROMATIC ALDEHYDES

Maryanoff, Bruce E.,Duhl-Emswiler, Barbara A.

, p. 4185 - 4188 (2007/10/02)

Aromatic aldehydes react with 1 to give predominantly trans 6-aryl-5-hexenoic acids, under special conditions.A systematic study of the reaction of 1 with aldehydes, in a preliminary attempt to define the cause and scope of the trans stereoselectivity, is reported.

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