| Identification | More | [Name]
DL-2-AMINOADIPIC ACID | [CAS]
542-32-5 | [Synonyms]
2-AMINO-HEXANEDIOIC ACID
DL-2-AMINOADIPIC ACID
DL-2-AMINOHEXANEDIOIC ACID
DL-ALPHA-AMINOADIPIC ACID
H-DL-2-AAD-OH
H-DL-AAD-OH
H-DL-HOMOGLU-OH
(RS)-2-AMINOHEXANEDIOIC ACID
TIMTEC-BB SBB000133
2-aminoadipate
2-aminoadipicacid
2-amino-hexanedioicaci
alpha-aminoadipicacid
DL-a-Aminoadipic acid
DL-2-aminoadipic acid monohydrate
H-DL-2-Aad-OH~(+/-)-2-Aminohexanedioic acid
DL-A-AMINOADIPIC ACID FREE ACID
DL-2-Aminoadipicacid,98%
(n)-2-aminohexanedioic acid
Aminoadipic acid | [EINECS(EC#)]
208-809-2 | [Molecular Formula]
C6H11NO4 | [MDL Number]
MFCD00063119 | [Molecular Weight]
161.16 | [MOL File]
542-32-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Crystalline | [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
| [form ]
Powder or Crystalline Powder | [pka]
2.14, 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). | [Usage]
An amino acid isolated from Cholera vibrio | [Merck ]
14,416 | [BRN ]
1773077 | [CAS DataBase Reference]
542-32-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
MO1852000
| [HS Code ]
29224999 |
| Hazard Information | Back Directory | [Chemical Properties]
Crystalline | [Uses]
An amino acid isolated from Cholera vibrio | [Uses]
DL-2-Aminoadipic acid is a labeled amino acid which is used in chemical research and as pharmaceutical intermediate. | [Definition]
ChEBI: 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 Actions]
DL-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 Methods]
Crystallise the acid from H2O. Alternatively purify it by precipitating the Cu salt and decomposing |
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