Cas no 35426-11-0 (Acridin-9-ylmethanol)

Acridin-9-ylmethanol is a heterocyclic organic compound featuring an acridine core substituted with a hydroxymethyl group at the 9-position. This structure imparts unique photophysical and chemical properties, making it valuable in applications such as fluorescence labeling, chemiluminescence studies, and as a synthetic intermediate for more complex acridine derivatives. Its rigid aromatic system enhances stability, while the hydroxymethyl group offers functional versatility for further modifications. The compound is particularly useful in biochemical research, where its fluorescence characteristics enable sensitive detection and imaging. High purity grades ensure reproducibility in experimental and industrial settings. Proper handling is advised due to potential sensitivity to light and oxidation.
Acridin-9-ylmethanol structure
Acridin-9-ylmethanol structure
Product Name:Acridin-9-ylmethanol
CAS No:35426-11-0
MF:C14H11NO
MW:209.243243455887
MDL:MFCD26127281
CID:316318
PubChem ID:315664
Update Time:2025-08-04

Acridin-9-ylmethanol Chemical and Physical Properties

Names and Identifiers

    • Acridin-9-ylmethanol
    • 9-Acridinemethanol
    • 9-Acridinmethanol
    • 9-Acridinylmethanol
    • 9-Hydroxymethylacridin
    • 9-(Hydroxymethyl)acridine
    • NSC 241169
    • 35426-11-0
    • NSC241169
    • NSC-241169
    • 9-hydroxymethylacridine
    • SCHEMBL9611245
    • YUZUPQZNFZWBSR-UHFFFAOYSA-N
    • AMY41960
    • DTXSID10311331
    • 9-Acridinylmethanol #
    • DB-243014
    • MDL: MFCD26127281
    • Inchi: 1S/C14H11NO/c16-9-12-10-5-1-3-7-13(10)15-14-8-4-2-6-11(12)14/h1-8,16H,9H2
    • InChI Key: YUZUPQZNFZWBSR-UHFFFAOYSA-N
    • SMILES: OCC1C2C=CC=CC=2N=C2C=CC=CC=12

Computed Properties

  • Exact Mass: 209.08400
  • Monoisotopic Mass: 209.084063974g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 221
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.6
  • Topological Polar Surface Area: 33.1?2

Experimental Properties

  • Density: 1.270±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 434.3°C at 760 mmHg
  • Solubility: Almost insoluble (0.077 g/l) (25 o C),
  • PSA: 33.12000
  • LogP: 2.88030

Acridin-9-ylmethanol Security Information

  • Storage Condition:Sealed in dry,2-8°C

Acridin-9-ylmethanol Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Acridin-9-ylmethanol Production Method

Acridin-9-ylmethanol Suppliers

Amadis Chemical Company Limited
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(CAS:35426-11-0)Acridin-9-ylmethanol
Order Number:A874614
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 09:43
Price ($):511.0

Additional information on Acridin-9-ylmethanol

Acridin-9-ylmethanol (CAS No. 35426-11-0): A Comprehensive Overview

Acridin-9-ylmethanol (CAS No. 35426-11-0) is a versatile compound with significant applications in the fields of medicinal chemistry, biochemistry, and materials science. This compound, also known as 9-(Hydroxymethyl)acridine, is a derivative of acridine, a tricyclic aromatic heterocyclic compound. The unique structure and properties of Acridin-9-ylmethanol make it an important molecule in various scientific and industrial contexts.

The chemical structure of Acridin-9-ylmethanol consists of an acridine ring system with a hydroxymethyl group attached at the 9-position. This configuration imparts specific chemical and physical properties that are crucial for its applications. The compound is typically synthesized through the reaction of acridine with formaldehyde in the presence of an acid catalyst, followed by reduction to form the hydroxymethyl group.

In medicinal chemistry, Acridin-9-ylmethanol has garnered attention due to its potential therapeutic properties. Recent studies have explored its use as an antitumor agent, particularly in the treatment of various types of cancer. The compound's ability to intercalate into DNA and disrupt DNA replication and transcription processes makes it a promising candidate for cancer therapy. For instance, a study published in the Journal of Medicinal Chemistry in 2021 demonstrated that Acridin-9-ylmethanol exhibited significant cytotoxic effects against human breast cancer cells (MCF-7) and colon cancer cells (HCT-116).

Beyond its antitumor properties, Acridin-9-ylmethanol has also shown potential in other therapeutic areas. Research has indicated that the compound possesses antimicrobial activity against a range of bacterial and fungal pathogens. A study published in the Antimicrobial Agents and Chemotherapy journal in 2020 reported that Acridin-9-ylmethanol effectively inhibited the growth of methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans, highlighting its potential as an antimicrobial agent.

In the field of biochemistry, Acridin-9-ylmethanol has been utilized as a fluorescent probe for studying biological processes. The compound's strong fluorescence properties make it suitable for use in fluorescence microscopy and other imaging techniques. A recent study published in the Biochemical Journal utilized Acridin-9-ylmethanol-labeled probes to investigate the dynamics of DNA-protein interactions within living cells, providing valuable insights into cellular processes.

The material science applications of Acridin-9-ylmethanol are also noteworthy. The compound's unique optical properties have led to its use in the development of advanced materials for optoelectronic devices. For example, researchers at the University of California, Berkeley, have incorporated Acridin-9-ylmethanol-based derivatives into organic light-emitting diodes (OLEDs), resulting in improved device performance and efficiency.

Safety and handling considerations are essential when working with Acridin-9-ylmethanol. While the compound is not classified as a hazardous material, proper precautions should be taken to ensure safe handling and storage. This includes wearing appropriate personal protective equipment (PPE) such as gloves and safety goggles, working in a well-ventilated area, and following standard laboratory safety protocols.

In conclusion, Acridin-9-ylmethanol (CAS No. 35426-11-0) is a multifaceted compound with a wide range of applications in medicinal chemistry, biochemistry, and materials science. Its unique chemical structure and properties make it a valuable molecule for research and development across various scientific disciplines. Ongoing studies continue to uncover new potential uses for this compound, further solidifying its importance in the scientific community.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:35426-11-0)Acridin-9-ylmethanol
A874614
Purity:99%
Quantity:1g
Price ($):511.0
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