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5-BUTYLNONANE, also known as nonylbutane, is a hydrocarbon compound belonging to the alkane family with the chemical formula C12H26. It features a straight-chain alkane structure with a butyl group attached at the 5th carbon atom. This colorless, odorless liquid is recognized for its relatively low toxicity and is considered non-hazardous to human health and the environment when managed with proper handling and storage procedures.

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  • 17312-63-9 Structure
  • Basic information

    1. Product Name: 5-BUTYLNONANE
    2. Synonyms: 5-BUTYLNONANE
    3. CAS NO:17312-63-9
    4. Molecular Formula: C13H28
    5. Molecular Weight: 184.36142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17312-63-9.mol
  • Chemical Properties

    1. Melting Point: -28.13°C (estimate)
    2. Boiling Point: 217.5°C
    3. Flash Point: 64.9 °C
    4. Appearance: /
    5. Density: 0.7635
    6. Vapor Pressure: 0.204mmHg at 25°C
    7. Refractive Index: 1.4273
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-BUTYLNONANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-BUTYLNONANE(17312-63-9)
    12. EPA Substance Registry System: 5-BUTYLNONANE(17312-63-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 17312-63-9(Hazardous Substances Data)

17312-63-9 Usage

Uses

Used in Chemical Industry:
5-BUTYLNONANE is used as a solvent for various industrial applications, including the manufacturing of plastics, resins, and adhesives. Its properties as a solvent make it suitable for dissolving and processing a wide range of substances in the chemical industry.
Used in Fuel and Lubricant Industry:
5-BUTYLNONANE is utilized as a component in fuel and lubricants, where it contributes to the performance and quality of these products. Its inclusion in fuel formulations can enhance combustion efficiency, while in lubricants, it can improve the fluidity and reduce friction in mechanical systems.
Used in Research and Laboratory Settings:
Due to its chemical stability and low reactivity, 5-BUTYLNONANE is also employed in research and laboratory settings for various experiments and as a reference material in chemical analyses. Its predictable behavior under controlled conditions makes it a valuable tool for scientific investigations.

Check Digit Verification of cas no

The CAS Registry Mumber 17312-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,1 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17312-63:
(7*1)+(6*7)+(5*3)+(4*1)+(3*2)+(2*6)+(1*3)=89
89 % 10 = 9
So 17312-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H28/c1-4-7-10-13(11-8-5-2)12-9-6-3/h13H,4-12H2,1-3H3

17312-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BUTYLNONANE

1.2 Other means of identification

Product number -
Other names tributylmethane

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:17312-63-9 SDS

17312-63-9Downstream Products

17312-63-9Relevant articles and documents

Cross coupling reactions of multiple CCl bonds of polychlorinated solvents with Grignard reagent using a pincer nickel complex

Gartia, Yashraj,Nasini, Udaya Bhasker,Ghosh, Anindya,Biswas, Abhijit,Stadler, Matthew

, p. 322 - 327,6 (2020/07/30)

The nickel(II) complex of a bulky pincer-type ligand, N,N′-bis(2,6- diisopropylphenyl)-2,6-pyridinedicarboxamido, was examined for sp 3-sp3 coupling of Grignard reagents with polychlorinated solvents. The nickel(II) complex catalyzed CC coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents. The effective activation of multiple CCl bonds proceeded under ambient reaction conditions and within a short time (20 min). This catalyst displays the highest activity yet reported for this reaction type, with catalyst loading as low as 0.4 mol% and turnover frequency (TOF) as high as 724 h-1. The catalyst is capable of replacing all chlorine atoms with CC bond formations for all of the polychlorinated solvents under investigation. The catalytic process could prove to be an efficient method of remediation of toxic polychlorinated solvents while generating synthetically and commercially important chemicals.

A novel iron complex for cross-coupling reactions of multiple C-Cl bonds in polychlorinated solvents with grignard reagents

Gartia, Yashraj,Pulla, Sharon,Ramidi, Punnamchandar,Farris, Carolina Costa,Nima, Zeid,Jones, Darin E.,Biris, Alexandru S.,Ghosh, Anindya

, p. 1397 - 1404 (2013/01/15)

A novel iron(III) complex (2) of a pincer ligand [1, N2,N6-bis(2,6- diisopropylphenyl)pyridine-2,6-dicarboxamide] was developed and used for remediation of polychlorinated solvents via sp3-sp3 coupling of Grignard reagents with C-Cl bonds. The use of an iron catalyst for such coupling reactions is highly desirable due to its greener and more economical nature. Complex 2 was characterized using various spectroscopic techniques: electrospray ionization mass spectrometer (ESI-MS, m/z 575.1), cyclic voltammetry (E 1/2, 0.03 V and ΔE, 0.97 V), and ultraviolet visible (UV/Vis) spectroscopic techniques. The iron(III) complex showed efficient activation of multiple C-Cl bonds and catalyzing C-C coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents under ambient reaction conditions. Complex 2 showed exceptional activity with reactions approaching near completion in about 5 min. With the required catalyst loading as low as 0.2 mol%, considerably high turnover numbers (TON = 483) and turnover frequency (TOF = 5,800 h-1) were obtained. None of the products detected during the reaction contained any chlorine, indicating an efficient dechlorination method while synthesizing products of synthetic and commercial interest. Interestingly, the catalyst was capable of replacing all chlorine atoms in each polychlorinated solvent under the investigations with high conversion. Springer Science+Business Media, LLC 2012.

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