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Nonane - analytical standard, ≥99.8%(GC) , CAS No.111-84-2

Nonane - analytical standard, ≥99.8%(GC) , CAS No.111-84-2

Name: Nonane - analytical standard, ≥99.8%(GC) , CAS No.111-84-2
SKU: N103393
Availability: InStock

CAS: 111-84-2 Cat. No.: N103393 Fórmula: C₉H₂₀ Peso molecular: 128.26 Beilstein Registry Number: 1(4)447 Número EC: 203-913-4

43 Citations COA

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Nonane - analytical standard, ≥99.8%(GC) CAS No(111-84-2) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY Analytical standard ? ≥99.8%(GC)

Synonyms

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Citations of This Product Calculadoras de soluciones Reseñas

🧪

Why this grade

analytical standard, ≥99.8%(GC) Patrón analítico for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 43 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos

Especificaciones y pureza

analytical standard, ≥99.8%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

FedEx DG Service

Grado

Patrón analítico

Pureza

≥99.8%(GC)

Nombres e identificadores

Pubchem Sid

528772319

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528772319

Sonrisas canónicas

CCCCCCCCC

IUPAC Name

nonane

InChIKey

BKIMMITUMNQMOS-UHFFFAOYSA-N

INCHI

1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3

Isómeros SMILES

CCCCCCCCC

RTECS

RA6115000

Número ONU

1920

Grupo de embalaje

III

Peso molecular

128.26

Beilstein

1(4)447

Reaxy-Rn

1696917

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1696917&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Hydrocarbons
  - Clase Saturated hydrocarbons
    - Subclass Alkanes

Kingdom	Organic compounds
Superclass	Hydrocarbons
Clase	Saturated hydrocarbons
Subclass	Alkanes
Intermediate Tree Nodes	Not available
Direct Parent	Alkanes
Alternative Parents	Not available
Molecular Framework	Aliphatic acyclic compounds
Substituents	Acyclic alkane - Alkane - Aliphatic acyclic compound
Descripción	This compound belongs to the class of organic compounds known as alkanes. These are acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estructura 3D

Objetivos asociados (humanos)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Lymphoblastoid cell (5959 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number	Certificate Type	Fecha	Articulo
G2628406	Certificate of Analysis	Jul 16, 2026	N103393
D1713208	Certificate of Analysis	Jun 15, 2024	N103393

Propiedades químicas y físicas

Solubilidad	Insoluble in water, soluble in ethanol and ether, miscible in benzene, acetone and chloroform.
Índice de refracción	1.4
Punto de inflamación (°F)	87.8 °F
Punto de inflamación (°C)	31°C(lit.)
Punto de ebullición (°C)	151°C
Punto de fusión (°C)	-53°C
Peso molecular	128.250 g/mol
XLogP3	4.500
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	6
Exact Mass	128.157 Da
Monoisotopic Mass	128.157 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	33.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

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Reseñas

📚 Citations by Application

Chromatography (HPLC / GC / TLC)12

Extraction & workup solvent14

Organic synthesis — reaction medium23

Other applications14

Industrial & non-pharma application9

Cross-coupling reactions2

Controlled-release & nanoparticle carrier2

Drug / compound screening2

Crystallization & recrystallization1

Electrochemistry & battery electrolyte1

Nanoparticle / material biocompatibility1

Cancer cell line characterization1

Polymer synthesis & polymerization2

Spectroscopy sample preparation1

View all 43 citations →

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