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3892-00-0

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3892-00-0 Usage

General Description

2,6,10-Trimethylpentadecane is a long-chain hydrocarbon with the molecular formula C18H38. It is a member of the alkane family, characterized by straight-chain or branched carbon chains with single bonds. This chemical is commonly found in crude oils, petroleum products, and natural gas. It has a high boiling point and is used as a fuel additive, lubricant, and in the production of specialty chemicals. Its properties make it valuable in industrial processes for its high stability and resistance to oxidation and corrosion. Additionally, it is used as a component in the production of various consumer products, such as cosmetics and personal care items.

Check Digit Verification of cas no

The CAS Registry Mumber 3892-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3892-00:
(6*3)+(5*8)+(4*9)+(3*2)+(2*0)+(1*0)=100
100 % 10 = 0
So 3892-00-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H38/c1-6-7-8-12-17(4)14-10-15-18(5)13-9-11-16(2)3/h16-18H,6-15H2,1-5H3

3892-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,10-TRIMETHYLPENTADECANE

1.2 Other means of identification

Product number -
Other names 2.6.10-Trimethyl-pentadecan

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:3892-00-0 SDS

3892-00-0Downstream Products

3892-00-0Relevant articles and documents

The formation features of C10–C20 regular petroleum isoprenanes

Gordadze,Giruts,Poshibaeva,Koshelev

, p. 672 - 676 (2016/10/04)

To model the formation processes of C10–C20 petroleum isoprenanes, thermolysis of regular and irregular C20–C40 isoprenanes (phytane, crocetane, squalane, and lycopane) and the suggested precursors of regular pe

Microbial Oxidation of Isoprenoid Alkanes, Phytane, Norpristane and Farnesane

Nakajima, Kenji,Sato, Akio,Takahara, Yoshimasa,Iida, Takeo

, p. 1993 - 2002 (2007/10/02)

Rhodococcus sp.BPM 1613, a pristane oxidizing microorganism, grows on isoprenoid hydrocarbons such as phytane (2,6,10,14-tetramethylhexadecane), norpristane (2,6,10-trimethyl-pentadecane) and farnesane (2,6,10-trimethyldodecane) as the sole carbon source, resulting in accumulation of oxidation products in the culture broth.The oxidation products of phytane, norpristane and farnesane in the respective culture broth were isolated and purified by the use of silica gel column chromatography.Their chemical structures were determined by instrumental analyses such as IR, NMR and mass spectrometry.The oxidation products of phytane were identified as 2,6,10,14-tetramethyl-1-hexadecanol and 2,6,10,14-tetramethylhexadecanoic acid, the product of norpristane as 2,6,10-trimethyl-1-pentadecanol, and that of farnesane as 2,6,10-trimethyl-1-dodecanol.All these oxidation products were either monoalcohols or monocarboxylic acids derived through oxidation of the isopropyl terminus of each alkane.In addition, the relationship between the terminal structure of isoprenoid hydrocarbons and microbial oxidation was explored on the basis of these results.

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