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629-96-9

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629-96-9 Usage

General Description

1-Eicosanol, also known as arachidyl alcohol, is a long-chain fatty alcohol with the molecular formula C20H42O. It is a white, waxy solid at room temperature and is insoluble in water. 1-Eicosanol is commonly used as an emollient in skin care products due to its moisturizing properties. It is also used as an intermediate in the production of fatty amine derivatives, lubricant additives, and surfactants. Additionally, 1-Eicosanol has been studied for its potential anti-inflammatory and insecticidal properties, making it a versatile chemical with a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 629-96-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 629-96:
(5*6)+(4*2)+(3*9)+(2*9)+(1*6)=89
89 % 10 = 9
So 629-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H42O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21/h21H,2-20H2,1H3

629-96-9 Well-known Company Product Price

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  • USP

  • (1042270)  Arachidylalcohol  United States Pharmacopeia (USP) Reference Standard

  • 629-96-9

  • 1042270-125MG

  • 4,647.24CNY

  • Detail
  • Aldrich

  • (234494)  1-Eicosanol  98%

  • 629-96-9

  • 234494-5G

  • 532.35CNY

  • Detail
  • Sigma-Aldrich

  • (44861)  1-Eicosanol  technical, ≥90% (GC)

  • 629-96-9

  • 44861-100G

  • 1,297.53CNY

  • Detail

629-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name icosan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Eicosanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Lubricants and lubricant additives,Processing aids, not otherwise listed,Processing aids, specific to petroleum production,Surface active agents
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:629-96-9 SDS

629-96-9Relevant articles and documents

MOF-derived hcp-Co nanoparticles encapsulated in ultrathin graphene for carboxylic acids hydrogenation to alcohols

Dong, Mei,Fan, Weibin,Gao, Xiaoqing,Zhu, Shanhui

, p. 201 - 211 (2021/06/03)

Highly efficient conversion of carboxylic acids to valuable alcohols is a great challenge for easily corroded non-noble metal catalysts. Here, a series of few-layer graphene encapsulated metastable hexagonal closed-packed (hcp) Co nanoparticles were fabricated by reductive pyrolysis of metal-organic framework precursor. The sample pyrolyzed at 400 °C (hcp-Co@G400) presented outstanding performance and stability for converting a variety of functional carboxylic acids and its turnover frequency was one magnitude higher than that of conventional facc-centered cubic (fcc) Co catalysts. In situ DRIFTS spectroscopy of model reaction acetic acid hydrogenation and DFT calculation results confirm that carboxylic acid initially undergoes dehydroxylation to RCH2CO* followed by consecutive hydrogenation to RCH2CH2OH through RCH2COH*. Acetic acid prefers to vertically adsorb at hcp-Co (0 0 2) facet with a much lower adsorption energy than parallel adsorption at fcc-Co (1 1 1) surface, which plays a key role in decreasing the activation barrier of the rate-determining step of acetic acid dehydroxylation.

Enantiomeric synthesis of natural alkylglycerols and their antibacterial and antibiofilm activities

Fernández Montoya, Deicy J.,Contreras Jordan, Luis A.,Moreno-Murillo, Bárbara,Silva-Gómez, Edelberto,Mayorga-Wandurraga, Humberto

supporting information, p. 2544 - 2550 (2019/11/13)

Alkylglycerols (AKGs) are bioactive natural compounds that vary by alkyl chain length and degree of unsaturation, and their absolute configuration is 2S. Three AKGs (5l–5n) were synthesised in enantiomerically pure form, and were characterised for the first time together with 12 other known and naturally occurring AKGs (5a–5k, 5o). Their structures were established using 1H and 13C APT NMR with 2D-NMR, ESI-MS or HRESI-MS and optical rotation data, and they were tested for their antibacterial and antibiofilm activities. AKGs 5a–5m and 5o showed activity against five clinical isolates and P. aeruginosa ATCC 15442, with MIC values in the range of 15–125 μg/mL. In addition, at half of the MIC, most of the AKGs reduced S. aureus biofilm formation in the range of 23%–99% and P. aeruginosa ATCC 15442 biofilm formation in the range of 14%–64%. The antibiofilm activity of the AKGs assessed in this work had not previously been studied.

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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