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DL-2-Aminoadipic acid

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DL-2-Aminoadipic acid manufacturers

  • 2-Aminoadipic acid
  • 2-Aminoadipic acid pictures
  • 2026-09-11
  • CAS:542-32-5
  • Min. Order: 1KG
  • Purity: 98.0%
  • Supply Ability: 5000kg/month
DL-2-Aminoadipic acid Basic information
Product Name:DL-2-Aminoadipic acid
Synonyms:(2R)-2-ammoniohexanedioate;2-aminoadipicacid;(RS)-2;(+/-)-a-Aminoadipic Acid;NSC 46994;rac a-Aminoadipic Acid;DL-2-Aminoadipic acid hydrate,97%;rac α-Aminoadipic Acid
CAS:542-32-5
MF:C6H11NO4
MW:161.16
EINECS:208-809-2
Product Categories:amino acids;Amino Acids & Derivatives
Mol File:542-32-5.mol
DL-2-Aminoadipic acid Structure
DL-2-Aminoadipic acid Chemical Properties
Melting point 196-198 °C(lit.)
Boiling point 287.44°C (rough estimate)
density 1.333
refractive index 1.4230 (estimate)
storage temp. 2-8°C
solubility Aqueous Acid (Slightly)
form Powder or Crystalline Powder
pka2.14, 4.21, 9.77(at 25℃)
color White to off-white
Water Solubility Soluble in water (2.2 mg/ml at 20°C), 1 M HCl (50 mg/ml), ethanol (slightly), ether (slightly), and 80% formic acid (25 mg/ml).
Merck 14,416
BRN 1773077
InChI1S/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)
InChIKeyOYIFNHCXNCRBQI-UHFFFAOYSA-N
SMILESNC(CCCC(O)=O)C(O)=O
CAS DataBase Reference542-32-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-43
Safety Statements 22-24/25-36-26-36/37
WGK Germany 3
RTECS MO1852000
HS Code 29224999
Storage Class11 - Combustible Solids
Hazard ClassificationsSkin Sens. 1
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
DL-2-Aminoadipic acid Usage And Synthesis
Chemical PropertiesCrystalline
UsesAn amino acid isolated from Cholera vibrio
UsesDL-2-Aminoadipic acid is a labeled amino acid which is used in chemical research and as pharmaceutical intermediate.
DefinitionChEBI: An alpha-amino acid that is adipic acid bearing a single amino substituent at position 2. An intermediate in the formation of lysine.
Biochem/physiol ActionsDL-2-Aminoadipic acid (AAA) is a six-carbon homolog of glutamate and a gliotoxic compound. It is generally used to considerably reduce the number of astroglia in cerebellar cultures that acts as a model to study the mechanisms of a-aminoadipic acid induced glial toxicity.
Purification MethodsCrystallise the acid from H2O. Alternatively purify it by precipitating the Cu salt and decomposing
DL-2-Aminoadipic acid Preparation Products And Raw materials
Raw materialsHexanedioic acid, 2-bromo-, 1,6-diethyl ester-->(2S)-2-hydroxy-hexanedioic acid-->2-Oxoadipic acid, 98-->Adipic acid
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