Shandong Huashi Import & Export Co., Ltd.
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3-Iodo-9H-carbazole
  • Brand:HS
  • Model:25kg/drum
  • Purity:99%
  • Cas:16807-13-9
  • Createtime: 2026-04-14
  • Updatetime: 2026-09-30
Product Details
useage Industrial use
deliveryInfo
appearance powder
Molecular Weight 293.10
aliasen
supplyCapacity 50000MT/Month
harbor Qingdao,China
minorder 1KG
Appearance Off-white crystalline powder

Shandong Huashang Chemical Co., Ltd. is a high-tech enterprise focused on industry of fine chemicals research and develop, produce and sale. Shandong Huashang Chemical Co., Ltd. is located in Shan Dong Ji Nan China. we have the ability to provide you high quality products. More than 90 % of our products are exported to developed countries and regions such as north America, Europe, Japan, South Korea and the Middle East.

Basic Information

Product Name: 3-Iodo-9H-carbazole
CAS Number: 16807-13-9
Alias: 3-Iodocarbazole
Chemical Full Name: 3-iodo-9H-carbazole
Molecular Formula: C12H8IN
Molecular Weight: 293.10
EINECS: Not available

Structural Information

  • Structure Type: Aromatic nitrogen-containing fused heterocyclic optoelectronic intermediate
  • Structural Features: Carbazole parent ring with iodine substitution at the 3-position; iodine group provides good reactive sites for Suzuki coupling, Buchwald amination and other C-C/C-N bond synthesis; carbazole skeleton has excellent hole transport, fluorescence and photoelectric properties
  • Characteristic: Core monomer for OLED, organic photoconductor, organic semiconductor materials

Physical & Chemical Properties

  • Appearance: Off-white to light yellow crystalline powder
  • Odor: Odorless
  • Melting Point: 198–202 °C
  • Solubility: Insoluble in water; soluble in dichloromethane, chloroform, toluene, tetrahydrofuran; slightly soluble in ethanol
  • Stability: Stable under light-proof sealed low-temperature storage; easy to deiodinate and oxidize under strong light and high temperature; iodine atom can undergo metal coupling reaction with boronic acids, amines

Synthesis & Applications

Production Method

Selective iodination of carbazole with iodine under acid catalysis, recrystallization purification to obtain target monoiodinated product.

Main Applications

  1. Optoelectronic Material Intermediate: Key raw material for synthesis of OLED hole transport materials, luminescent layers, organic photodetectors
  2. Organic Synthesis Building Block: Raw material for Suzuki, Heck, Buchwald cross-coupling reactions
  3. Functional Dye Intermediate: Precursor for carbazole-based fluorescent dyes and photosensitizers
  4. Semiconductor Research Reagent: Laboratory synthetic raw material for organic field effect transistors (OFET)

Safety & Storage Instructions

GHS Hazard Classification

Warning signal word
  • H315 Causes skin irritation
  • H319 Causes serious eye irritation
  • H335 May cause respiratory irritation from dust inhalation

Personal Protection

Dust respirator, full-face splash goggles, nitrile impermeable gloves; operate in fume hood, avoid long-term dust exposure and light contact.

Storage Condition

Hermetically sealed light-proof aluminum foil lined cardboard drum, cool dry warehouse ≤20℃; isolate oxidants, avoid sunlight to prevent deiodination discoloration.

Transportation

Fine chemical solid powder; light-proof and moisture-proof packaging, separated from food supplies.

Quality Specifications

  • Purity (HPLC): ≥99.0%
  • Loss on Drying: ≤0.3%
  • Residue on Ignition: ≤0.1%
  • Di-iodocarbazole impurity: ≤0.1%

Information Summary Table

Item Specification
CAS Number 16807-13-9
Product Name 3-Iodo-9H-carbazole
Synonym 3-Iodocarbazole
Molecular Formula C12H8IN
Molecular Weight 293.10
Appearance Off-white crystalline powder
Melting Point 198–202℃
Core Advantage Iodinated carbazole coupling monomer, core OLED optoelectronic intermediate
Storage Rule Light-proof sealed low-temperature storage, away from oxidants
Hazard Property Low acute toxicity, dust irritates skin, eyes and respiratory tract
Main Usage OLED hole transport material intermediate, organic semiconductor coupling raw material, fluorescent dye precursor