Amberlite® IRA-900 , CAS No.9050-97-9

CAS: 9050-97-9 Cat. No.: A108090

Synonyms

AKOS015833138 | BCP24457 | EINECS 200-880-8 | SCHEMBL35736 | USAF AN-8 | AI3-19012 | Amberlite(R) IRA-900 chloride form, chloride form, strongly basic, 20-50 mesh | EN300-219151 | AMBERLITE IRA-900 | HSDB 7987 | FT-0659748 | STR05669 | CAS-75-57-0 | DTXCI

Storage

Room temperature

Shipped In

Normal

Overview

Amberlite® IRA-900 chloride form is a macroporous, polystyrenic type 1 resin. This resin was found to catalyze the photodecomposition of carbon tetrachloride in ethanol.
Amberlite® IRA-900 modified with metallophthalocyanines was used to remove 4-nitorphenol.

Specifications

Synonyms

AKOS015833138 | BCP24457 | EINECS 200-880-8 | SCHEMBL35736 | USAF AN-8 | AI3-19012 | Amberlite(R) IRA-900 chloride form, chloride form, strongly basic, 20-50 mesh | EN300-219151 | AMBERLITE IRA-900 | HSDB 7987 | FT-0659748 | STR05669 | CAS-75-57-0 | DTXCI

Legal Information

Amberlite is a trademark of DuPont de Nemours, Inc.

Storage

Room temperature

Shipped In

Normal

Names and Identifiers

• Pubchem Sid: 488180059
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180059
• Canonical Smiles: C[N+](C)(C)C.[Cl-]
• IUPAC Name: tetramethylazanium;chloride
• InChIKey: OKIZCWYLBDKLSU-UHFFFAOYSA-M
• INCHI: 1S/C4H12N.ClH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
• Isomeric SMILES: C[N+](C)(C)C.[Cl-]
• WGK Germany: 3
• Reaxy-Rn: 3911201
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3911201&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Amine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
• External Descriptors: organic molecular entity

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

Associated Targets(Human)

SLC22A1 Tchem Solute carrier family 22 member 1 (646 Activities)

Discover Target: SLC22A1

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

SLC22A2 Tchem Solute carrier family 22 member 2 (261 Activities)

Discover Target: SLC22A2

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

Associated Targets(non-human)

Slc5a7 Choline transporter (45 Activities)

Discover Target: Slc5a7

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

Slc22a5 Solute carrier family 22 member 5 (44 Activities)

Discover Target: Slc22a5

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

Mechanisms of Action

Chemical and Physical Properties

• Molecular Weight: 109.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 109.066 Da
• Monoisotopic Mass: 109.066 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 19.100
• 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: 2

XLogP3

References

1. Youan Ji, Yucui Hou, Shuhang Ren, Muge Niu, Congfei Yao, Weize Wu.  (2017)  Efficient extraction of indole from wash oil by quaternary ammonium salts via forming deep eutectic solvents.  FUEL,      [PMID:] [10.1016/j.fuel.2017.10.057]

2. Youan Ji, Yucui Hou, Shuhang Ren, Congfei Yao, Weize Wu.  (2016)  Phase equilibria of high pressure CO2 and deep eutectic solvents formed by quaternary ammonium salts and phenol.  FLUID PHASE EQUILIBRIA,      [PMID:] [10.1016/j.fluid.2016.08.020]

3. Ting Tao, Yuyu Cao, Liping Zhang, Dayi Xu, Kaiyuan Pang, Yanli Li, Xiaobao Wei, Zengxian Sun.  (2024)  Preparation of thiol-free amino acid plasma matrix for quantification of thiol amino acids and their oxidized forms in human plasma by UPLC-MS/MS.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38432109] [10.1016/j.chroma.2024.464776]

4. Ji Wu, Qimeng Li, Xuan Huang, Liu Yang, Nan Shen, Wentao Li, Zhenkun Ma, Chen Xie, Ziwu Fan, Guoxiang Wang.  (2025)  Synergistic ozonation–ion exchange strategy for nutrient recovery from algal filtrate.  Water Research X,      [PMID:] [10.1016/j.wroa.2025.100407]

5. Wu Zijun, Tang Yun, Huang Manna, Wan Yiqian.  (2025)  A green one pot approach for extracting free fatty acids from microalgae.  Scientific Reports,  15  (1): (1-9).  [PMID:40341704] [10.1038/s41598-025-00235-8]

6. Jian Song, Hai-Long Qian, Shu-Ting Xu, Cheng Yang, Xiu-Ping Yan.  (2025)  Room-Temperature Synthesis of a Multifunctional Covalent Organic Framework for Highly Efficient Extraction of Anionic Per- and Polyfluoroalkyl Substances.  ANALYTICAL CHEMISTRY,      [PMID:41348093] [10.1021/acs.analchem.5c05349]