What is the (E)-2-Octadecenol?

(E)-2-Octadecenol is , while it's Molecular Formula is C 18 H 36 O. Used in Food Industry: (E)-2-Octadecenol is used as a flavoring agent for imparting its distinctive sweet, floral, and waxy notes to food products, enhancing their overall sensory appeal and consumer experience. Used in Cosmetic Industry: In the cosmetic sector, (E)-2-Octadecenol serves as a fragrance component, adding a pleasant and natural scent to various cosmetic products, thereby increasing their marketability and consumer acceptance. Used in Pharmaceutical Industry: (E)-2-Octadecenol finds potential applications in the pharmaceutical field, where it may be utilized for its properties or as a component in the development of new medicinal formulations. Used as a Chemical Intermediate: (E)-2-Octadecenol also functions as an intermediate in the synthesis of other chemicals, contributing to the production of a range of chemical products that serve diverse industrial needs.

What is the CAS number for (E)-2-Octadecenol?

The CAS number of (E)-2-Octadecenol is 41207-34-5.

What is (E)-2-Octadecenol (41207-34-5) used for?

(E)-2-Octadecenol, also known as (E)-2-octadecen-1-ol or 2-octadecen-1-ol, is a long-chain fatty alcohol characterized by the chemical formula C18H36O. It is a colorless to pale yellow liquid that exhibits limited solubility in water. (E)-2-Octadecenol is distinguished by its sweet, floral, and waxy odor, and is naturally present in a variety of fruits, vegetables, and essential oils. Beyond its natural occurrence, (E)-2-Octadecenol is synthesized for use in various industrial applications, particularly in the realms of flavoring, fragrances, pharmaceuticals, and as a chemical intermediate.

What is the (E)-2-Octadecenol?

(E)-2-Octadecenol is , while it's Molecular Formula is C 18 H 36 O. Used in Food Industry: (E)-2-Octadecenol is used as a flavoring agent for imparting its distinctive sweet, floral, and waxy notes to food products, enhancing their overall sensory appeal and consumer experience. Used in Cosmetic Industry: In the cosmetic sector, (E)-2-Octadecenol serves as a fragrance component, adding a pleasant and natural scent to various cosmetic products, thereby increasing their marketability and consumer acceptance. Used in Pharmaceutical Industry: (E)-2-Octadecenol finds potential applications in the pharmaceutical field, where it may be utilized for its properties or as a component in the development of new medicinal formulations. Used as a Chemical Intermediate: (E)-2-Octadecenol also functions as an intermediate in the synthesis of other chemicals, contributing to the production of a range of chemical products that serve diverse industrial needs.

What is the CAS number for (E)-2-Octadecenol?

The CAS number of (E)-2-Octadecenol is 41207-34-5.

What is (E)-2-Octadecenol (41207-34-5) used for?

(E)-2-Octadecenol, also known as (E)-2-octadecen-1-ol or 2-octadecen-1-ol, is a long-chain fatty alcohol characterized by the chemical formula C18H36O. It is a colorless to pale yellow liquid that exhibits limited solubility in water. (E)-2-Octadecenol is distinguished by its sweet, floral, and waxy odor, and is naturally present in a variety of fruits, vegetables, and essential oils. Beyond its natural occurrence, (E)-2-Octadecenol is synthesized for use in various industrial applications, particularly in the realms of flavoring, fragrances, pharmaceuticals, and as a chemical intermediate.

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(E)-2-Octadecenol

Basic Information

CAS No.: 41207-34-5
Purity: 99%

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Details

Factory supply good quality (E)-2-Octadecenol 41207-34-5 with stock

Molecular Formula: C₁₈H₃₆O
Molecular Weight: 268.483
Boiling Point: 351.1 °C at 760 mmHg
Flash Point: 154.6 °C
PSA： 20.23000
Density: 0.847 g/cm³
LogP: 6.01620

41207-34-5 Relevant articles

Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes

Huang, Jiaxin,Li, Jie,Yang, Wen,Zhang, Kezhuo,Zhao, Pei,Zhao, Wanxiang

, p. 302 - 305 (2022/01/03)

The Co-catalyzed remote hydroboration an...

Synthesis of C -glycoside analogues of α-galactosylceramide via linear allylic C-H oxidation and allyl cyanate to isocyanate rearrangement

Liu, Zheng,Bittman, Robert

supporting information; scheme or table, p. 620 - 623 (2012/03/22)

C-Glycoside analogues of α-galactosylcer...

Ring-opening hydrofluorination of 2,3- and 3,4-epoxy amines by HBF 4·OEt2: Application to the asymmetric synthesis of (S, S)-3-deoxy-3-fluorosafingol

Cresswell, Alexander J.,Davies, Stephen G.,Lee, James A.,Morris, Melloney J.,Roberts, Paul M.,Thomson, James E.

experimental part, p. 4617 - 4627 (2011/07/30)

Treatment of a range of 2,3- and 3,4-epo...

Asymmetric total syntheses of spisulosine, its diastereo- and regio-isomers

Dinda, Subal Kumar,Das, Sajal Kumar,Panda, Gautam

experimental part, p. 9304 - 9309 (2011/01/12)

Starting from palmityl alcohol, divergen...

41207-34-5 Process route

: 7390-81-0
2-hexadecyloxirane

: 4111-54-0
lithium diisopropyl amide

: 7373-13-9
octadecan-2-one

: 2831-86-9,22104-84-3,41207-34-5
trans-octadec-2-en-1-ol

: 638-66-4
n-Octadecanal

: 1-Diisopropylamino-octadecan-2-ol

Conditions

Conditions	Yield
In tetrahydrofuran; at 20 ℃; for 12h; Product distribution; var. of lithium amide, ratio;	27% 4% 2% 24%

: 94874-12-1,97975-07-0
ethyl trans-octadec-2-enoate

: 2831-86-9,22104-84-3,41207-34-5
trans-octadec-2-en-1-ol

Conditions

Conditions	Yield
ethyl trans-octadec-2-enoate; With diisobutylaluminium hydride; In toluene; at 0 - 20 ℃; for 1h; Inert atmosphere; With water; In toluene; Inert atmosphere;	95%
With diisobutylaluminium hydride; In toluene; at -78 ℃; for 1h;	94%
With diisobutylaluminium hydride; In diethyl ether; toluene; at 0 - 20 ℃; for 0.5h;	92%
With diisobutylaluminium hydride; In diethyl ether; hexane; for 0.5h; Ambient temperature;	91%
With diisobutylaluminium hydride; In diethyl ether; toluene; at 0 ℃; Inert atmosphere;	77%
With 1-bromo-butane; lithium aluminium tetrahydride; In tetrahydrofuran; Inert atmosphere;

41207-34-5 Upstream products

150989-02-9
octadec-2t -enoyl chloride
2833-97-8
octadec-2-yn-1-ol
7390-81-0
2-hexadecyloxirane
4111-54-0
lithium diisopropyl amide

41207-34-5 Downstream products

51534-37-3
(E)-octadec-2-enal
1164104-56-6
(R,E)-1-(tert-butyldiphenylsilyloxy)-3-(octadec-2-en-1-yloxy)propan-2-ol
1164104-62-4
(R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol
1354747-56-0
C₄₃H₇₄FNO₇

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