| Identification | More | [Name]
DL-Pipecolinic acid | [CAS]
4043-87-2 | [Synonyms]
(+/-)-2-PIPERIDINECARBOXYLIC ACID
2-PIPERIDINECARBOXYLIC ACID
DL-2-PIPERIDINECARBOXYLIC ACID
DL-HOMOPROLINE
DL-PIPECOLIC ACID
DL-PIPECOLINIC ACID
DL-PIPECOLONIC ACID
DL-PIPERCOLINIC ACID
H-DL-HOMOPRO-OH
H-DL-HOPRO-OH
H-DL-PIC(2)-OH
LABOTEST-BB LT00847911
PIPECOLIC ACID
PIPECOLINIC ACID
(+/-)-PIPERIDINE-2-CARBOXYLIC ACID
PIPERIDINE-2-CARBOXYLIC ACID
RAC PIPERIDINE-2-CARBOXYLIC ACID
RARECHEM AH CK 0177
DL-piperidine-2-carboxylic acid
Dl-PipecolinicAcid98% | [EINECS(EC#)]
223-737-1 | [Molecular Formula]
C6H11NO2 | [MDL Number]
MFCD00064347 | [Molecular Weight]
129.16 | [MOL File]
4043-87-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant |
| Hazard Information | Back Directory | [Uses]
Pipecolic acid is involved in synaptic transmission in the central nervous system. | [Definition]
ChEBI: Pipecolic acid is a piperidinemonocarboxylic acid in which the carboxy group is located at position C-2. It is a conjugate acid of a pipecolate. | [Purification Methods]
It crystallises from water. The (±)-picrate has m 158-159o (from EtOH or C6H6). [Beilstein 22 H 7, 22 III/IV 97, 22/1 V 220.] The R(+)-enantiomer [1723-00-8] has m 277o(dec) and [] D 20 +27o (c 4, H2O), and the S(-)-enantiomer [3105-95-1] has m 277o(dec) and [] D 20 -26o (c 4, H2O).[cf p 603, Beilstein 22 III/IV 96, 22/1 V 220.] |
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