Adamantane-1-carboxylic acid, 99%
Adamantane-1-carboxylic acid, 99%
Adamantane-1-carboxylic acid, 99%
Adamantane-1-carboxylic acid, 99%
Thermo Scientific Chemicals

Adamantane-1-carboxylic acid, 99%

CAS: 828-51-3 | C11H16O2 | 180.247 g/mol
数量:
25 g
100 g
500 g
製品番号(カタログ番号) A12959.36
または、製品番号A12959-36
価格(JPY)
-
見積もりを依頼する
数量:
500 g
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化学物質識別子
CAS828-51-3
IUPAC Nameadamantane-1-carboxylic acid
Molecular FormulaC11H16O2
InChI KeyJIMXXGFJRDUSRO-UHFFFAOYSA-N
SMILESOC(=O)C12CC3CC(CC(C3)C1)C2
さらに表示
FormCrystals or powder or crystalline powder
Assay (Silylated GC)≥98.5%
Water Content (Karl Fischer Titration)≤0.5%
Appearance (Color)White to cream or pale yellow
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
It can be used as a stabilizer in the synthesis of monodisperse, highly crystalline CoPt3 nanoparticles1 and porous platinum nanoparticles. It is a potent and reversible CerK inhibitor.

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
It can be used as a stabilizer in the synthesis of monodisperse, highly crystalline CoPt3 nanoparticles1 and porous platinum nanoparticles. It is a potent and reversible CerK inhibitor.

Solubility
Insoluble in water. Solubility in methanol gives very faint turbidity. Soluble in ethanol, chloroform, and dichloromethane.

Notes
Store away from bases and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Elena V Shevchenko et. al. Colloidal synthesis and self-assembly of CoPt(3) nanocrystals.J Am Chem Soc.,2002,124(38), 11480-11485.
  2. Xiaowei Teng et. al. Synthesis of porous platinum nanoparticles.Small.,2006,2(2), 249-253.
  3. Reaction with alkaline permanganate gives the 3-hydroxy derivative in good yield. Further modification leads to 1,3-disubstituted adamantanes: Synth. Commun., 18, 1967 (1988):