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106399

1-Adamantanecarboxylic acid

Name: 1-Adamantanecarboxylic acid
Brand: ALDRICH

99%

Synonym(s):

Adamantane carboxylic acid

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₆O₂

CAS Number:

828-51-3

Molecular Weight:

180.24

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24846732

EC Number:

212-584-6

Beilstein/REAXYS Number:

1910637

MDL number:

MFCD00074720

Assay:

99%

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Properties

Quality Level

200

assay

99%

mp

172-174 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)C12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C11H16O2/c12-10(13)11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H,12,13)/t7-,8+,9-,11-

InChI key

JIMXXGFJRDUSRO-KJZNFTALSA-N

Description

Application

1-Adamantanecarboxylic acid can be used as:

A stabilizer in the synthesis of monodisperse, highly crystalline CoPt₃ nanoparticles and porous platinum nanoparticles.
An additive in polycondensation reactions to yield conjugated polymers as possible optoelectronic materials.
An additive in the allylic substitution reaction, which is catalyzed by palladium in an aqueous medium.

Biochem/physiol Actions

1-Adamantanecarboxylic acid undergoes complexation reactions with cyclohexaamylose. It is an inhibitor of phenyl ester hydrolysis of cycloheptaamylose.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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1H NMR studies on the hydrogen-bonding network in mono-altro-beta-cyclodextrin and its complex with adamantane-1-carboxylic acid.

Birgit Hakkarainen et al.

Carbohydrate research, 340(8), 1539-1545 (2005-05-12)

The hydrogen-bond network in mono-altro-beta-cyclodextrin and in its inclusion complex with adamantane-1-carboxylic acid were investigated by (1)H NMR spectroscopy using the chemical shifts, temperature coefficients and vicinal coupling constants of the exchangeable hydroxy protons. The chemical shifts of the 3-OH

Peak shape modeling by Haarhoff-Van der Linde function for the determination of correct migration times: a new insight into affinity capillary electrophoresis.

Thomas Le Saux et al.

Electrophoresis, 26(16), 3094-3104 (2005-07-26)

Among the different experimental strategies available in capillary electrophoresis (CE) to determine binding parameters, affinity capillary electrophoresis (ACE) has been the most widely embraced due to its easiness of implementation and of data handling. Ligand-substrate binding constants are thus directly

Detailed optimization of polycondensation reaction via direct C-H arylation of ethylenedioxythiophene

Yamazaki K, et al.

Macromolecular Rapid Communications, 34(1), 69-73 (2013)

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Global Trade Item Number

SKU	GTIN
106399-25G	04061838673947
106399-100G	04061838673930