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1-Nonadecene is a chemical compound that belongs to the class of organic compounds known as alkenes. It is essentially a hydrocarbon with 19 carbon atoms, making it a relatively long-chain compound. These substances are distinguished by the presence of one or more carbon-carbon double bonds. Its molecular formula is C19H38, and it is often used in manufacturing, particularly in the production of detergents and other cleaning products. Its structure gives it hydrophobic properties, making it excellent for uses associated with repelling water. It is also used within the perfume and flavoring industry for its ability to lock in and maintain fragrance smells.

18435-45-5

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18435-45-5 Usage

Uses

Used in Detergent and Cleaning Products Industry:
1-Nonadecene is used as a raw material for the production of detergents and other cleaning products due to its hydrophobic properties, which help in the formulation of effective cleaning agents.
Used in Perfume and Flavoring Industry:
1-Nonadecene is used as a fixative agent for fragrances in the perfume and flavoring industry. Its ability to lock in and maintain fragrance smells makes it a valuable component in creating long-lasting scents.

Check Digit Verification of cas no

The CAS Registry Mumber 18435-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,3 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18435-45:
(7*1)+(6*8)+(5*4)+(4*3)+(3*5)+(2*4)+(1*5)=115
115 % 10 = 5
So 18435-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H38/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h3H,1,4-19H2,2H3

18435-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name nonadec-1-ene

1.2 Other means of identification

Product number -
Other names 1-NONADECENE

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:18435-45-5 SDS

18435-45-5Relevant articles and documents

An Engineered Self-Sufficient Biocatalyst Enables Scalable Production of Linear α-Olefins from Carboxylic Acids

Lu, Chen,Shen, Fenglin,Wang, Shuaibo,Wang, Yuyang,Liu, Juan,Bai, Wen-Ju,Wang, Xiqing

, p. 5794 - 5798 (2018/06/01)

Fusing the decarboxylase OleTJE and the reductase domain of P450BM3 creates a self-sufficient protein, OleT-BM3R, which is able to efficiently catalyze oxidative decarboxylation of carboxylic acids into linear α-olefins (LAOs) under mild aqueous conditions using O2 as the oxidant and NADPH as the electron donor. The compatible electron transfer system installed in the fusion protein not only eliminates the need for auxiliary redox partners, but also results in boosted decarboxylation reactivity and broad substrate scope. Coupled with the phosphite dehydrogenase-based NADPH regeneration system, this enzymatic reaction proceeds with improved product titers of up to 2.51 g L-1 and volumetric productivities of up to 209.2 mg L-1 h-1 at low catalyst loadings (~0.02 mol%). With its stability and scalability, this self-sufficient biocatalyst offers a nature-friendly approach to deliver LAOs.

Photobiocatalytic decarboxylation for olefin synthesis

Zachos, Ioannis,Ga?meyer, Sarah Katharina,Bauer, Daniel,Sieber, Volker,Hollmann, Frank,Kourist, Robert

supporting information, p. 1918 - 1921 (2015/02/05)

Here, we describe the combination of OleTJE with a light-driven in situ H2O2-generation system for the selective and quantitative conversion of fatty acids into terminal alkenes. The photobiocatalytic system shows clear advantages regarding enzyme activity and yield, resulting in a simple and efficient system for fatty acid decarboxylation.

Iron-catalyzed decarbonylation reaction of aliphatic carboxylic acids leading to α-olefins

Maetani, Shinji,Fukuyama, Takahide,Suzuki, Nobuyoshi,Ishihara, Daisuke,Ryu, Ilhyong

scheme or table, p. 2552 - 2554 (2012/03/26)

The catalytic decarbonylation reaction of aliphatic carboxylic acids can be carried out in the presence of an iron complex, and it proceeds smoothly to give α-olefins with high selectivity. The Royal Society of Chemistry 2012.

Cobalt-catalyzed reductive allylation of alkyl halides with allylic acetates or carbonates

Qian, Xin,Auffrant, Audrey,Felouat, Abdellah,Gosmini, Corinne

supporting information; experimental part, p. 10402 - 10405 (2011/12/03)

An efficient method for the direct allylation of alkyl halides catalyzed by simple cobalt(II) bromide has been developed. This reaction, using a variety of substituted allylic acetates or carbonates, provides the linear product as the major product. It displays broad substrate scope and good functional group tolerance. Copyright

Efficient iridium-catalyzed decarbonylation reaction of aliphatic carboxylic acids leading to internal or terminal alkenes

Maetani, Shinji,Fukuyama, Takahide,Suzuki, Nobuyoshi,Ishihara, Daisuke,Ryu, Ilhyong

experimental part, p. 1389 - 1394 (2011/04/25)

Vaska's complex, IrCl(CO)(PPh3)2, when combined with KI as an additive, served as an excellent catalyst for the decarbonylation of long-chain aliphatic carboxylic acids to give internal alkenes with high selectivity. On combination with KI and Ac2O as additives under controlled temperatures, decarbonylation proceeded to give terminal alkenes with high selectivity.

Semivolatile and volatile compounds in combustion of polyethylene

Font, Rafael,Aracil, Ignacio,Fullana, Andrés,Conesa, Juan A.

, p. 615 - 627 (2007/10/03)

The evolution of semivolatile and volatile compounds in the combustion of polyethylene (PE) was studied at different operating conditions in a horizontal quartz reactor. Four combustion runs at 500 and 850°C with two different sample mass/air flow ratios and two pyrolytic runs at the same temperatures were carried out. Thermal behavior of different compounds was analyzed and the data obtained were compared with those of literature. It was observed that α,ω-olefins, α-olefins and n-paraffins were formed from the pyrolytic decomposition at low temperatures. On the other hand, oxygenated compounds such as aldehydes were also formed in the presence of oxygen. High yields were obtained of carbon oxides and light hydrocarbons, too. At high temperatures, the formation of polycyclic aromatic hydrocarbons (PAHs) took place. These compounds are harmful and their presence in the combustion processes is related with the evolution of pyrolytic puffs inside the combustion chamber with a poor mixture of semivolatile compounds evolved with oxygen. Altogether, the yields of more than 200 compounds were determined. The collection of the semivolatile compounds was carried out with XAD-2 adsorbent and were analyzed by GC-MS, whereas volatile compounds and gases were collected in a Tedlar bag and analyzed by GC with thermal conductivity and flame ionization detectors.

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