Didodecylamine - ≥97% , CAS No.3007-31-6

CAS: 3007-31-6 Cat. No.: D154719 Molecular Weight: 353.68 Beilstein Registry Number: 1777050 EC Number: 221-114-9

GRADE & PURITY ≥97%

Synonyms

AKOS015915202 | Propanedioic acid, 2-amino-, 1,3-diethyl ester | AS-37823 | BP-31196 | Di-n-dodecylamine | N-dodecyl-1-dodecanamine | N-dodecyldodecan-1-amine | UNII-5KR2ML6H0C | dilauryl amine | Dilaurylamine | SY053355 | N,N-Didodecylamine

Storage

Argon charged,Room temperature

Shipped In

Normal

Application

228,229

Overview

Didodecylamine is a secondary amine. It is reported as standard amine enhancer and its dermal enhancement properties has been studied using in vitro diffusion cell techniques. Solidification point of dodecylamine has been reported to be 26.2°C.

Application：

Didodecylamine may be used:

to promote the crystal growth of 2D nanosheets of GdOCl with approximately square cross sections；

to investigate the effect of alkyl chain length of amine on phase transfer of aqueous synthesized gold nanoparticles (AuNPs) from water to toluene；

in the preparation of novel class of liquid crystalline complexes, by the interaction of copper nitrate；

Specifications

Synonyms

AKOS015915202 | Propanedioic acid, 2-amino-, 1, 3-diethyl ester | AS-37823 | BP-31196 | Di-n-dodecylamine | N-dodecyl-1-dodecanamine | N-dodecyldodecan-1-amine | UNII-5KR2ML6H0C | dilauryl amine | Dilaurylamine | SY053355 | N, N-Didodecylamine

Specifications & Purity

≥97%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488182440
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182440
• Canonical Smiles: CCCCCCCCCCCCNCCCCCCCCCCCC
• IUPAC Name: N-dodecyldodecan-1-amine
• InChIKey: MJCJUDJQDGGKOX-UHFFFAOYSA-N
• INCHI: 1S/C24H51N/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h25H,3-24H2,1-2H3
• Isomeric SMILES: CCCCCCCCCCCCNCCCCCCCCCCCC
• WGK Germany: 3
• Molecular Weight: 353.68
• Beilstein: 1777050
• Reaxy-Rn: 1777050
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1777050&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen.
• 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

Chemical and Physical Properties

• Sensitivity: Air Sensitive；Moisture sensitive
• Boil Point(°C): 265 °C/27 mmHg
• Melt Point(°C): 51 °C
• Molecular Weight: 353.700 g/mol
• XLogP3: 11.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 22
• Exact Mass: 353.402 Da
• Monoisotopic Mass: 353.402 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 192.000
• 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

References

1. Liu Yaoyang, Liu Zhibin, Zhao Chuang, Jiao Caishan, Zhang Meng, Zhou Yu, Gao Yang, Li Huibo, He Hui.  (2022)  Comparative study on the extraction performance of Nd(III) by isomeric unsymmetrical diglycoamides.  JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY,  331  (4): (1759-1767).  [PMID:] [10.1007/s10967-022-08244-x]

2. Jing Liang, Lei Yu, Xue Li, Jiejing Zhang, Guang Chen, Jianfeng Zhang.  (2019)  Self-assembled quantum dot microstructure guided by a microemulsion approach for immunoassays.  RSC Advances,  9  (46): (26838-26842).  [PMID:35528605] [10.1039/C9RA05719F]

3. Jing Liang, Lei Yu, Ziying Lin, Keji Song, Jiejing Zhang, Jianfeng Zhang.  (2019)  Self-organized nanocrystal rings formed by microemulsion for selective recognition of proteins and immunoassays.  RSC Advances,  9  (2): (699-703).  [PMID:35517599] [10.1039/C8RA09662G]

4. Pengbo Ding, Pui Kei Ko, Pai Geng, Dezhang Chen, Zengshan Xing, Hoi Lam Tammy Tsang, Kam Sing Wong, Liang Guo, Jonathan E. Halpert.  (2024)  Strongly Confined and Spectrally Tunable CsPbBr3 Quantum Dots for Deep Blue QD-LEDs.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202302477]

5. Jianfeng Zhang, Shuxin Gong, Jiahang Zhu, Jiejing Zhang, Jing Liang.  (2020)  Mono-Dispersed Microspheres Locally Assembled on Porous Substrates Formed through a Microemulsion Approach.  Polymers,  12  (4): (964).  [PMID:32326253] [10.3390/polym12040964]