Indazole-Cl
Indazole-Cl (CAS: 848142-62-1), with the molecular formula C13H9ClN2O2 and a molecular weight of 260.68 g/mol, is a chemical compound supplied by Tech Serve Solutions. This white to brown powder is primarily utilised in cell biology research, focusing on cell signalling, neuroscience, and studies involving cytokines, growth factors, and hormones, particularly within the realm of steroid hormones like estrogen. Its assay is typically ≥98% (HPLC).
- IUPAC
- 3-Chloro-2-(4-hydroxyphenyl)-2H-indazol-5-ol

Cell Biology Research
Indazole-Cl is employed in advanced cell biology studies, particularly those investigating cellular signalling pathways. It serves as a valuable tool for researchers examining the intricate mechanisms within cells.
Neuroscience Investigations
This compound finds application in neuroscience research, aiding scientists in understanding neuronal functions and signalling. It can be instrumental in exploring neurological processes at a molecular level.
Hormone and Cytokine Studies
Indazole-Cl is utilised in research concerning cytokines, growth factors, and hormones, including steroid hormones such as estrogen. It helps scientists elucidate the roles of these biological molecules.
| Molecular weight | 260.68 |
|---|---|
| Empirical formula | C13H9ClN2O2 |
| Assay | ≥98% (HPLC) |
| Form | powder |
| Colour | white to brown |
| Solubility | DMSO: >5 mg/mL |
| Storage temperature | 2-8°C |

Hazard statements
- H302Harmful if swallowed
| Water hazard class (WGK, DE) | 3 |
|---|---|
| Hazard codes (EU) | Xn |
| Risk statements (R) | 22 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Indazole-Cl used for?
+
Indazole-Cl is used in cell biology research, particularly in studies of cell signalling, neuroscience, and investigations involving cytokines, growth factors, hormones, and steroid hormones such as estrogen.
What is the CAS number and chemical formula for Indazole-Cl?
+
The CAS number for Indazole-Cl is 848142-62-1, and its chemical formula is C13H9ClN2O2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Indazole-Cl with a purity of ≥98% (HPLC). This product is a technical/research grade chemical and is not represented as USP, BP, or EP.
How should Indazole-Cl be handled and stored?
+
Indazole-Cl is classified as harmful if swallowed (H302). It should be handled with appropriate personal protective equipment in a well-ventilated area. Recommended storage is at 2-8°C.
How is Indazole-Cl packed, shipped, and exported?
+
Indazole-Cl is carefully packed for safe transit and is available for global export by Tech Serve Solutions, adhering to all relevant shipping regulations for chemical compounds.
How can I request a sample or quote for Indazole-Cl?
+
To request a sample or quote for Indazole-Cl, please contact our sales team through the TSS website or by calling our customer service line.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis