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1-Amino-1-cyclopropanecarboxylic acid, 98%
A NMDA glutamate receptor agonist at glycine site | CAS: 22059-21-8 | C4H7NO2 | 101.11 g/mol
$162.77 - $321.29
Chemical Identifiers
| CAS | 22059-21-8 |
|---|---|
| Molecular Formula | C4H7NO2 |
| Molecular Weight (g/mol) | 101.11 |
| MDL Number | MFCD00009944 |
| InChI Key | PAJPWUMXBYXFCZ-UHFFFAOYSA-N |
| Synonym | 1-aminocyclopropanecarboxylic acid, 1-amino-1-cyclopropanecarboxylic acid, cyclopropanecarboxylic acid, 1-amino, carboxycyclopropylamine, acc, alpha-aminocyclopropanecarboxylic acid, alpha-aminocyclopropane carboxylic acid, 1-amino-cyclopropanecarboxylic acid, h-acpc-oh, aminocyclopropanecarboxylic acid |
| PubChem CID | 535 |
| ChEBI | CHEBI:18053 |
| IUPAC Name | 1-aminocyclopropane-1-carboxylic acid |
| SMILES | NC1(CC1)C(O)=O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAJ65118MD
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Thermo Scientific Chemicals
J65118MD |
250 mg |
N/A
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AAJ6511803
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Thermo Scientific Chemicals
J6511803 |
1 g |
N/A
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Description
1-Aminocyclopropane-1-carboxylic Acid is an intermediate in the conversion of methionine to ethylene during the ripening in apples. It also plays an important role in the biosynthesis of the plant hormone ethylene.1-Aminocyclopropane-1-carboxylic Acid is shown to block convulsions and death produced by NMDA exposure, significantly reducing seizure induction and cell death of NMDA-treated hippocampal neurons. 1-Aminocyclopropane-1-carboxylic Acid is produced endogenously in the tomato and other higher plants as a product of the action of 1-aminocyclopropane-1-carboxylic acid synthase in the biosynthesis of ethylene.
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.
Applications1-Aminocyclopropane-1-carboxylic Acid is an intermediate in the conversion of methionine to ethylene during the ripening in apples. It also plays an important role in the biosynthesis of the plant hormone ethylene.1-Aminocyclopropane-1-carboxylic Acid is shown to block convulsions and death produced by NMDA exposure, significantly reducing seizure induction and cell death of NMDA-treated hippocampal neurons. 1-Aminocyclopropane-1-carboxylic Acid is produced endogenously in the tomato and other higher plants as a product of the action of 1-aminocyclopropane-1-carboxylic acid synthase in the biosynthesis of ethylene.
Solubility
Soluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
Chemical Identifiers
| 22059-21-8 | |
| 101.11 | |
| PAJPWUMXBYXFCZ-UHFFFAOYSA-N | |
| 535 | |
| 1-aminocyclopropane-1-carboxylic acid |
| C4H7NO2 | |
| MFCD00009944 | |
| 1-aminocyclopropanecarboxylic acid, 1-amino-1-cyclopropanecarboxylic acid, cyclopropanecarboxylic acid, 1-amino, carboxycyclopropylamine, acc, alpha-aminocyclopropanecarboxylic acid, alpha-aminocyclopropane carboxylic acid, 1-amino-cyclopropanecarboxylic acid, h-acpc-oh, aminocyclopropanecarboxylic acid | |
| CHEBI:18053 | |
| NC1(CC1)C(O)=O |
Specifications
| 22059-21-8 | |
| White | |
| MFCD00009944 | |
| 2076413 | |
| Soluble in water. | |
| NC1(CC1)C(O)=O | |
| 101.11 | |
| CHEBI:18053 | |
| 98% | |
| 1-Amino-1-cyclopropanecarboxylic acid |
| 229°C to 231°C | |
| C4H7NO2 | |
| 250 mg | |
| 1-aminocyclopropanecarboxylic acid, 1-amino-1-cyclopropanecarboxylic acid, cyclopropanecarboxylic acid, 1-amino, carboxycyclopropylamine, acc, alpha-aminocyclopropanecarboxylic acid, alpha-aminocyclopropane carboxylic acid, 1-amino-cyclopropanecarboxylic acid, h-acpc-oh, aminocyclopropanecarboxylic acid | |
| PAJPWUMXBYXFCZ-UHFFFAOYSA-N | |
| 1-aminocyclopropane-1-carboxylic acid | |
| 535 | |
| 101.11 | |
| Crystalline Powder |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
RTECSNumber : GZ1110000
TSCA : No
Recommended Storage : Keep cold
RUO – Research Use Only