Naphthalene - Standard for GC, ≥99.5%(GC) , CAS No.91-20-3

CAS: 91-20-3 Cat. No.: N110801 Formule: C₁₀H₈ Poids moléculaire: 128.17 Beilstein Registry Number: 1421310 Numéro CE: 202-049-5

GRADE & PURITY Standard for GC, ≥99.5%(GC)

Synonyms

Mighty RD1 | MLS001055498 | NSC37565 | NSC-37565 | UN2304 | Mighty 150 | naftaleno | Tox21_202004 | WLN: L66J | Moth balls | NAPHTHALENE [IARC] | naphtalene | NAPHTHALINUM [HPUS] | NCGC00090793-02 | NCGC00090793-05 | DTXSID8020913 | N0004 | Naphthalene 10

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications

Synonymes

Mighty RD1 | MLS001055498 | NSC37565 | NSC-37565 | UN2304 | Mighty 150 | naftaleno | Tox21_202004 | WLN: L66J | Moth balls | NAPHTHALENE [IARC] | naphtalene | NAPHTHALINUM [HPUS] | NCGC00090793-02 | NCGC00090793-05 | DTXSID8020913 | N0004 | Naphthalene 10

Spécifications et pureté

Standard for GC, ≥99.5%(GC)

Conditions de stockage de stockage

Room temperature

Expédié en

FedEx DG Service

Grade

Standard for GC

Pureté

≥99.5%(GC)

Noms et identifiants

Pubchem Sid

508816501

Sourires canoniques

C1=CC=C2C=CC=CC2=C1

IUPAC Name

naphthalene

InChIKey

UFWIBTONFRDIAS-UHFFFAOYSA-N

INCHI

1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H

Isomères SMILES

C1=CC=C2C=CC=CC2=C1

WGK Allemagne

3

RTECS

QJ0525000

Numéro ONU

1334,2304(molten)

Groupe d'emballage

III

Poids moléculaire

128.17

Beilstein

1421310

Reaxy-Rn

1421310

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1421310&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• External Descriptors: an aromatic compound

Data sources

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

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PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

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CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

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Eysarcoris (24 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive.
• Indice de réfraction: 1.5898
• Point d'éclair (°F): 173.3 °F - closed cup
• Point d'éclair (°C): 78.5 °C - closed cup
• Point d'ébullition (°C): 218°C
• Point de fusion (°C): 80.29°C
• Poids moléculaire: 128.169 g/mol
• XLogP3: 3.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 128.063 Da
• Monoisotopic Mass: 128.063 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 80.600
• 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