Indoline, 99%
Indoline, 99%
Indoline, 99%
Thermo Scientific Chemicals

Indoline, 99%

CAS: 496-15-1 | C8H9N | 119.167 g/mol
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產品號碼 A11000.30
亦稱為 A11000-30
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Quantity:
250 g
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化學識別
CAS496-15-1
IUPAC Name2,3-dihydro-1H-indole
Molecular FormulaC8H9N
InChI KeyLPAGFVYQRIESJQ-UHFFFAOYSA-N
SMILESC1CC2=CC=CC=C2N1
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規格Specification Sheet規格表
Appearance (Color)Clear pale yellow to orange
Refractive Index1.5915-1.5945 @ 20?C
Assay (GC)≥98.5%
FormLiquid
Indole is used in perfumery and in preparing tryptophan, one of the 20 amino acids commonly found in animal proteins. It has important application in the industry of plant growth. It is used to prepare indoleacetic acid (auxin) and other plant growth substances which help the development of roots in plant. Indole and its derivatives are widely used in making perfumes, dyes, agrochemicals and medicines.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Indole is used in perfumery and in preparing tryptophan, one of the 20 amino acids commonly found in animal proteins. It has important application in the industry of plant growth. It is used to prepare indoleacetic acid (auxin) and other plant growth substances which help the development of roots in plant. Indole and its derivatives are widely used in making perfumes, dyes, agrochemicals and medicines.

Solubility
Fully misicible in water at 5 g/L (20°C).

Notes
Light Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agents, acids, acid chlorides, acid anhydrides.
RUO – Research Use Only

General References:

  1. Tamotsu Horiuchi.; Hidetoshi Miura.; Kouichi Sumioka.; Satoshi Uchida. High Efficiency of Dye-Sensitized Solar Cells Based on Metal-Free Indoline Dyes. J. Am. Chem. Soc. 2004, 126, (39), 12218-12219.
  2. Abdel-Rahmana, A.H.; Keshka, E.M.; Hannab, M.A.; Sh.M. El-Bady. Synthesis and evaluation of some new spiro indoline-based heterocycles as potentially active antimicrobial agents. Bioorganic & Medicinal Chemistry. 2004, 12, (9), 2483-2488.
  3. 2-Lithiation can be effected in a one-pot sequence via the Li carbamate: J. Chem. Soc., Perkin 1, 17, (1989); cf Indole, A14427.