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56862-62-5

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56862-62-5 Usage

Classification

Alkane

Subgroup

Nonadecanes

Structural feature

Methyl substituent at the tenth carbon position

Physical state

Colorless, odorless liquid at room temperature

Solubility

Insoluble in water, soluble in organic solvents

Industrial applications

Raw material for lubricants, waxes, and other chemical compounds

Automotive use

Component in the formulation of automotive fuels

Industrial processes

Utilized as a solvent

Additional applications

Potential use in pharmaceutical and cosmetic industries

Check Digit Verification of cas no

The CAS Registry Mumber 56862-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,6 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56862-62:
(7*5)+(6*6)+(5*8)+(4*6)+(3*2)+(2*6)+(1*2)=155
155 % 10 = 5
So 56862-62-5 is a valid CAS Registry Number.

56862-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-METHYLNONADECANE

1.2 Other means of identification

Product number -
Other names 10-Methylnonadecan

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:56862-62-5 SDS

56862-62-5Downstream Products

56862-62-5Relevant academic research and scientific papers

FURAN BASED COMPOSITIONS AND METHODS OF MAKING THEREOF

-

Paragraph 0356, (2021/02/12)

Disclosed herein are processes for the preparation of compounds of formula (I) from one or more bio-derived reactants, and their use as base oils: [in-line-formulae](R1-A)b-(CHx)a(CHR2)m—(C(R4R5))n—(CHR3)o—(CHy)c-(A-R1′)d??(I)[/in-line-formulae] wherein a and c are independently 0 or 1, b and d are independently 1 or 2, x and y are independently 1 or 2, dependent upon the values of a-d, m and o are independently 0 or 1, n is an integer of 0-6, and each A is independently an unsaturated furan ring, a partially saturated furan ring, a saturated furan ring, or —(CH2)4—. Also, R1, R1′, R2, R3, R4 and R5 are independently selected from the group consisting of H and alkyl groups having 1 to 18 carbon atoms, with a proviso that at least one of R2, R3, R4, and R5 is not hydrogen, and the total carbon content of the compound of formula (I) is in the range of 20-62.

Molybdenum Oxide-Modified Iridium Catalysts for Selective Production of Renewable Oils for Jet and Diesel Fuels and Lubricants

Liu, Sibao,Zheng, Weiqing,Fu, Jiayi,Alexopoulos, Konstantinos,Saha, Basudeb,Vlachos, Dionisios G.

, p. 7679 - 7689 (2019/08/20)

Supported inverse metal-metal oxide catalysts have received significant research interest owing to their effective hydrodeoxygenation (HDO) activity toward biomass substrates, but the high cost of the reported catalysts poses a challenge for commercialization. We present the synthesis of a series of metal-metal oxide catalysts, Ir-MOx/SiO2 (M = Re, Mo, W, V, or Nb) and M′-MoOx/SiO2 (M = Rh, Ru, Pt, or Pd) and their HDO performance on multifuran (high carbon) substrates to produce renewable jet and diesel fuels and lubricant base oils. A MoOx-modified Ir/SiO2 catalyst with a Mo/Ir ratio of 0.13 (Ir-MoOx/SiO2) exhibits the highest product yield (78-96%) under mild reaction conditions. Controlled experiments using probe substrates reveal that furan ring hydrogenation and C-O hydrogenolysis of saturated and unsaturated furan rings occur in a sequential manner. The carbon atom adjacent to the furan or saturated furan ring of substrates or intermediate compounds undergoes slow C-C bond scission, resulting in a small fraction of lighter alkanes. Catalyst characterization suggests that Ir is reduced to a fully metallic state to dissociate hydrogen for hydrogenation. Intact MoOx, partly covering the Ir metal surface, promotes ring opening, hydrogenolysis of etheric and alcoholic C-O bonds, and hydrogenation of Ca? O bonds. This study highlights the potential of low-cost metal-metal oxide catalysts with low loading of oxophilic metals to enable cost-competitive production of bioproducts and demonstrates applicability of these catalysts on other substrates, including fatty acids, fatty esters, and lipids.

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