Span® 80 - tensioattivo non ionico , CAS No.1338-43-8

CAS: 1338-43-8 Cat. No.: S110839 Formula: C₂₄H₄₄O₆ Peso molecolare: 428.61 Beilstein Registry Number: 8172514 Numero EC: 215-665-4

GRADE & PURITY nonionic surfactant

Synonyms

Oleate de sorbitan [INN-French] | MO 33F | n-BUTYL HYDRAZINE OXALATE | Sorbitan mono-oletae | Kosteran O 1 | S0060 | Anhydrosorbitol monooleate | Sorbitani oleas [INN-Latin] | Armotan MO | Dianhydromannitol monooleate | Sorbon S 80 | Span(R) 80, viscosity

Storage

Room temperature

Shipped In

Normale

Panoramica

Lo Span 80 è un tensioattivo biodegradabile basato su un acido grasso naturale (acido oleico) e sull'alcol zuccherino sorbitolo. Questo estere di sorbitano è molto efficace nella formazione di emulsioni O/W, in particolare se utilizzato in combinazione con il suo derivato polietossilato, Tween 80. Gruppo chimico: Tensioattivi non ionici - Esteri di sorbitano ed esteri di sorbitano etossilati Composizione in acidi grassi: Acido oleico (C18:1) ≤ 60%; saldo principalmente acido linoleico (C18:2), linolenico (C18:3) e palmitico (C16:0). Produttore: Croda
Span® 80 è stato utilizzato in uno studio per valutare i trasferimenti come sistema di somministrazione transdermica della sertralina. È stato inoltre utilizzato in uno studio per indagare i fattori dominanti che influenzano la stabilità delle nanoemulsioni attraverso l'uso di reti neurali artificiali (RNA).

Specifications

Sinonimi

Oleate de sorbitan [INN-French] | MO 33F | n-BUTYL HYDRAZINE OXALATE | Sorbitan mono-oletae | Kosteran O 1 | S0060 | Anhydrosorbitol monooleate | Sorbitani oleas [INN-Latin] | Armotan MO | Dianhydromannitol monooleate | Sorbon S 80 | Span(R) 80, viscosity

Specifiche e purezza

tensioattivo non ionico

Informazioni legali

Span è un marchio registrato di Croda International PLC

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normale

Nomi e identificatori

Pubchem Sid

488196427

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488196427

Sorrisi canonici

CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O

IUPAC Name

[(2R)-2-[(2R,3R,4S)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (Z)-octadec-9-enoate

InChIKey

NWGKJDSIEKMTRX-AAZCQSIUSA-N

INCHI

1S/C24H44O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22(27)29-19-21(26)24-23(28)20(25)18-30-24/h9-10,20-21,23-26,28H,2-8,11-19H2,1H3/b10-9-/t20-,21+,23+,24+/m0/s1

Isomeri SMILES

CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H]([C@@H]1[C@@H]([C@H](CO1)O)O)O

WGK Germania

1

RTECS

WG2932400

Peso molecolare

428.61

Beilstein

8172514

Reaxy-Rn

6346073

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acid esters
• Alternative Parents: Tetrahydrofurans Secondary alcohols Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Fatty acid ester - Tetrahydrofuran - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Carbonyl group - Organic oxide - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.
• External Descriptors: Not available

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

Obiettivi associati (umani)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

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

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in ethanol at 50mg/mlMiscible with water, ethanol, isopropanol and ether. Insoluble in acetone.
• Sensibilità: Moisture sensitive.
• Indice di rifrazione: 1.48
• Punto di infiammabilità (°F): >230℉
• Punto di infiammabilità (°C): >110℃
• Peso molecolare: 428.600 g/mol
• XLogP3: 6.000
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 19
• Exact Mass: 428.314 Da
• Monoisotopic Mass: 428.314 Da
• Topological Polar Surface Area: 96.200 Ų
• Heavy Atom Count: 30
• Formal Charge: 0
• Complexity: 453.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Domande frequenti

How should this product be stored?

Store at room temperature.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 1338-43-8, the molecular formula is C24H44O6, and the molecular weight is 428.61 g/mol. InChIKey NWGKJDSIEKMTRX-AAZCQSIUSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.