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2,5-Octadien-1-ol, (Z,Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67548-44-1

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67548-44-1 Usage

Physical state

Colorless liquid

Odor

Floral, fruity

Common uses

Flavor and fragrance ingredient in perfumes, soaps, and other cosmetic products

Natural occurrence

Found in certain fruits and flowers

Stereochemistry

(Z,Z) configuration of the double bonds

Affects

Chemical reactivity and biological activity

Potential uses

Flavoring agent in the food industry and for the synthesis of other compounds in the pharmaceutical industry

Hazards

Potential toxicity, should be handled and used with care.

Check Digit Verification of cas no

The CAS Registry Mumber 67548-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,4 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67548-44:
(7*6)+(6*7)+(5*5)+(4*4)+(3*8)+(2*4)+(1*4)=161
161 % 10 = 1
So 67548-44-1 is a valid CAS Registry Number.

67548-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z,5Z)-2,5-octadien-1-ol

1.2 Other means of identification

Product number -
Other names (2Z,5Z)-2,5-octadienol

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:67548-44-1 SDS

67548-44-1Relevant academic research and scientific papers

Pheromone synthesis. Part 257: Synthesis of methyl (2E,4Z,7Z)-2,4,7-decatrienoate and methyl (E)-2,4,5-tetradecatrienoate, the pheromone components of the male dried bean beetle, Acanthoscelides obtectus (Say)

Mori, Kenji

, p. 5589 - 5596 (2015)

Tandem Dess-Martin oxidation/Wittig reaction of (2Z,5Z)-2,5-octadien-1-ol yielded methyl (2E,4Z,7Z)-2,4,7-decatrienoate, a newly discovered pheromone component of the male dried bean beetle, while that of (±)-2,3-dodecadien-1-ol gave (±)-methyl (E)-2,4,5-tetradecatrienoate, the racemate of the known and major pheromone component. Methyl (2E,4E,7Z)-2,4,7-decatrienoate was also synthesized, which is the methyl ester of an acid metabolite of a green alga. Reduction of 2,5-octadiyn-1-ol with Zn-Cu/EtOH cleanly gave (2Z,5Z)-2,5-octadien-1-ol.

A Systematic Study of Unsaturation in Lipid Nanoparticles Leads to Improved mRNA Transfection In Vivo

Lee, Sang M.,Cheng, Qiang,Yu, Xueliang,Liu, Shuai,Johnson, Lindsay T.,Siegwart, Daniel J.

supporting information, p. 5848 - 5853 (2021/02/05)

Lipid nanoparticles (LNPs) represent the leading concept for mRNA delivery. Unsaturated lipids play important roles in nature with potential for mRNA therapeutics, but are difficult to access through chemical synthesis. To systematically study the role of unsaturation, modular reactions were utilized to access a library of 91 amino lipids, enabled by the synthesis of unsaturated thiols. An ionizable lipid series (4A3) emerged from in vitro and in vivo screening, where the 4A3 core with a citronellol-based (Cit) periphery emerged as best. We studied the interaction between LNPs and a model endosomal membrane where 4A3-Cit demonstrated superior lipid fusion over saturated lipids, suggesting its unsaturated tail promotes endosomal escape. Furthermore, 4A3-Cit significantly improved mRNA delivery efficacy in vivo through Selective ORgan Targeting (SORT), resulting in 18-fold increased protein expression over parent LNPs. These findings provide insight into how lipid unsaturation promotes mRNA delivery and demonstrate how lipid mixing can enhance efficacy.

Pheromone Bouquet of the Dried Bean Beetle, Acanthoscelides obtectus (Col.: Chrysomelidae), Now Complete

Vuts, J?zsef,Francke, Wittko,Mori, Kenji,Zarbin, Paulo H. G.,Hooper, Antony M.,Millar, Jocelyn G.,Pickett, John A.,T?th, Mikl?s,Chamberlain, Keith,Caulfield, John C.,Woodcock, Christine M.,Tr?ger, Armin G.,Csonka, éva Bálintné,Birkett, Michael A.

, p. 4843 - 4846 (2015/08/03)

Male-specific volatile components, released by the dried bean beetle, Acanthoscelides obtectus, were identified as methyl (E,R)-2,4,5-tetradecatrienoate, methyl (2E,4Z,7Z)-2,4,7-decatrienoate, methyl (2E,4Z)-2,4-decadienoate, octadecanal and the sesquiterpenes (3Z,6E)- and (3E,6E)-α-farnesene. In olfactometer bioassays, pure methyl (E,R)-2,4,5-tetradecatrienoate was only weakly attractive to unmated females. However, a blend of the six identified compounds released in physiologically relevant ratios and doses proved to be as active as headspace odours collected from live males.

A Quick Procedure for the Partial Reduction of Triple Bonds

Aerssens, M.H.P.J.,Heiden, R. van der,Heus, M.,Brandsma, L.

, p. 3421 - 3425 (2007/10/02)

Regio- as well as stereospecific cis-reductions of a wide variety of acetylenic derivatives can be carried out in absolute ethanol with zinc powder activated with 1,2-dibromoethane and with zinc power treated successively with dibromoethane and lithium bromocuprate, the first reagent being less powerful and more selective than the second one.

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