Glycidyl Lauryl Ether - ≥95%(GC) , CAS No.2461-18-9

CAS: 2461-18-9 Cat. No.: G156844 Peso molecular: 242.40 Número EC: 219-554-1

GRADE & PURITY ≥95%(GC)

Synonyms

Oxirane, 2-[(dodecyloxy)methyl]- | T72150 | MFCD00022344 | 84653J97E3 | Glycidyl Lauryl Ether | CCRIS 2635 | DSSTox_CID_5494 | G0448 | 6-AMINO-2-METHYL-2-HEPTANOLHYDROCHLORIDE | DODECYL ALCOHOL GLYCIDYL ETHER | Tox21_200787 | C12Ge cpd | NCGC00258341-01 |

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Oxirane, 2-[(dodecyloxy)methyl]- | T72150 | MFCD00022344 | 84653J97E3 | Glycidyl Lauryl Ether | CCRIS 2635 | DSSTox_CID_5494 | G0448 | 6-AMINO-2-METHYL-2-HEPTANOLHYDROCHLORIDE | DODECYL ALCOHOL GLYCIDYL ETHER | Tox21_200787 | C12Ge cpd | NCGC00258341-01 |

Especificaciones y pureza

≥95%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%(GC)

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCCCCCCOCC1CO1
• IUPAC Name: 2-(dodecoxymethyl)oxirane
• InChIKey: VMSIYTPWZLSMOH-UHFFFAOYSA-N
• INCHI: 1S/C15H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-16-13-15-14-17-15/h15H,2-14H2,1H3
• Isómeros SMILES: CCCCCCCCCCCCOCC1CO1
• Peso molecular: 242.40
• Reaxy-Rn: 113355
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=113355&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Epoxides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Epoxides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Epoxides
• Alternative Parents: Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
• 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

Objetivos asociados (humanos)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

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

Objetivos asociados (no humanos)

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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

Mecanismos de acción

Propiedades químicas y físicas

• Índice de refracción: 1.44
• Punto de inflamación (°C): 145 °C
• Punto de ebullición (°C): 324°C(lit.)
• Peso molecular: 242.400 g/mol
• XLogP3: 5.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 13
• Exact Mass: 242.225 Da
• Monoisotopic Mass: 242.225 Da
• Topological Polar Surface Area: 21.800 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 159.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Yu Ding, Guosheng Ai, Jinliang Du, Guangming Yu, Lu Lai, Xuemin Yan, Weichu Yu, Yuanzhu Mi.  (2023)  Synthesis and demulsification performance of a Gemini ionic liquid with dual cationic active centers.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125242]

2. Liwei Shen, Shi Liu, Ji'an He, Qian Qu, Yuqi Tang, Zejun Zhang, Dong Xiang, Xuemin Yan, Yuanzhu Mi.  (2023)  Synthesis of a low temperature ionic liquid demulsifier and its demulsification mechanism.  FUEL,      [PMID:] [10.1016/j.fuel.2022.127343]

3. Xiangdong Wang, Jiaxing He, Lanhua Ma, Bin Yan, Lingying Shi, Rong Ran.  (2020)  Self-assembling graphene oxide/modified amphipathic hydroxyethyl cellulose hybrid stabilized Pickering emulsion polymerization for functional hydrogel.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2020.125742]

4. Yu Ding, Xuebin Jiang, Hanjun Liu, Huanyu Liu, Guoyun Liu, Wentao Ma, Zhoucheng Li, Baiyun Jin, Yuanzhu Mi, Xuemin Yan.  (2024)  Hydrophobically modified hyperbranched polymer and its demulsification performance in W/O emulsion.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.131272]

5. Xinpeng Zhang, Hongli Bian, Xiangze Meng, Jing Yuan, Jianping Ding, Wanli Li, Jun Xu, Baohua Guo.  (2025)  Synthesis of Poly(butylene adipate-co-terephthalate) with Branched Monomer for Biodegradable Copolyesters with Enhanced Processability and Rheological Properties.  ACS Omega,      [PMID:40256559] [10.1021/acsomega.5c00277]