Brij™ S10 - average Mn ~711 , CAS No.9005-00-9

CAS: 9005-00-9 Cat. No.: B129086 Fórmula: C₁₈H₃₇(OCH₂CH₂)nOH, n~20 Número CE: 500-017-8

GRADE & PURITY average Mn ~711

Synonyms

Volpo S10 | A4605 | BB 0256761 | 2-(octadecyloxy) ethanol | PD160410 | 2-Octadecyloxyethanol | D08975 | FT-0682442 | F20467 | (S)-Methyl 2-amino-3-(3,4-dihydroxyphenyl)propanoate | F77844 | CAS-9005-00-9 | Ethanol,2-(octadecyloxy)- | 8K0ZV6FAIZ | DSSTox_G

Storage

Argon charged,Room temperature

Shipped In

Normal

Visão geral

Brij S10 is an ethoxylated (10) natural fatty alcohol, based on stearyl alcohol. This naturally derived surfactant offers a number of functional benefits including wetting and high foaming to a variety of applications. Chemical group Nonionic Surfactants - Ethoxylated Fatty Alcohols Manufacturer：Croda

Specifications

Sinónimos

Volpo S10 | A4605 | BB 0256761 | 2-(octadecyloxy) ethanol | PD160410 | 2-Octadecyloxyethanol | D08975 | FT-0682442 | F20467 | (S)-Methyl 2-amino-3-(3,4-dihydroxyphenyl)propanoate | F77844 | CAS-9005-00-9 | Ethanol,2-(octadecyloxy)- | 8K0ZV6FAIZ | DSSTox_G

Especificações e pureza

average Mn ~711

Informações legais

Brij is a registered trademark of Croda International PLC

Condições de armazenamento de armazenamento

Argon charged,Room temperature

Enviado em

Normal

Nomes e identificadores

• Pubchem Sid: 508810363
• Sorrisos canónicos: CCCCCCCCCCCCCCCCCCOCCO
• IUPAC Name: 2-octadecoxyethanol
• InChIKey: ICIDSZQHPUZUHC-UHFFFAOYSA-N
• INCHI: 1S/C20H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-20-18-21/h21H,2-20H2,1H3
• SMILES isoméricas: CCCCCCCCCCCCCCCCCCOCCO
• WGK Alemanha: 2
• Reaxy-Rn: 1770489
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1770489&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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

Propriedades químicas e físicas

• Ponto de fusão (°C): 44-45 °C (lit.)
• Peso molecular: 314.500 g/mol
• XLogP3: 8.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 19
• Exact Mass: 314.318 Da
• Monoisotopic Mass: 314.318 Da
• Topological Polar Surface Area: 29.500 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 183.000
• 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

Referências

1. Mengyuan Tian, Fuhua Xin, Yanjing Gao, Jun Nie, Fang Sun.  (2021)  Design of a near-infrared-triggered photo/thermal dual-responsive composite carrier with excellent biocompatibility for controllable drug release.  JOURNAL OF APPLIED POLYMER SCIENCE,  139  (17): (52029).  [PMID:] [10.1002/app.52029]

2. Sirui Chen, Guoyuan Xiong, Shuangling Cui, Shufang Zhao, Jilong Lai, Xuening Zhang, Guangyong Zeng, Ying Zeng, Hao Shi.  (2024)  Selective isolation of rubidium with mesoporous silica loaded with ammonium phosphomolybdate via an in-pore crystallization reaction.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.128364]