DL-Pipecolic Acid - ≥98% , CAS No.535-75-1

CAS: 535-75-1 Cat. No.: S136371 Molecular Weight: 129.16 EC Number: 208-616-3
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(+/-)-Pipecolinic acid | 2-PIPERIDINECARBOXYLIC ACID | 2-piperidine-carboxylic acid | Acide pipecolique [French] | FT-0613361 | SY003075 | 2-Piperidinecarboxylic acid, (S)- | 2-piperidinic acid | DL-Pipecolic acid;H-DL-Pip-OH | DL-Pipecolinic acid | (D)-(
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
S136371-5g
1
$9.90
25g
S136371-25g
4
$10.90
100g
S136371-100g
6

$34.90

$52.90
Save $18.00 (34.03%)
500g
S136371-500g
1

$98.90

$148.90
Save $50.00 (33.58%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
(+/-)-Pipecolinic acid | 2-PIPERIDINECARBOXYLIC ACID | 2-piperidine-carboxylic acid | Acide pipecolique [French] | FT-0613361 | SY003075 | 2-Piperidinecarboxylic acid, (S)- | 2-piperidinic acid | DL-Pipecolic acid;H-DL-Pip-OH | DL-Pipecolinic acid | (D)-(
Specifications & Purity
≥98%
Storage
Room temperature
Shipped In
Normal
Action Type
INHIBITOR
Purity
≥98%
Names and Identifiers
Pubchem Sid488179560
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179560
Canonical SmilesC1CCNC(C1)C(=O)O
IUPAC Namepiperidine-2-carboxylic acid
InChIKeyHXEACLLIILLPRG-UHFFFAOYSA-N
INCHI1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)
Isomeric SMILES C1CCNC(C1)C(=O)O
WGK Germany 3
Alternate CAS 4043-87-2
Molecular Weight 129.16
Reaxy-Rn 81095
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=81095&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlpha amino acids
Alternative Parents Piperidinecarboxylic acids  Amino acids  Monocarboxylic acids and derivatives  Dialkylamines  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Alpha-amino acid - Piperidinecarboxylic acid - Piperidine - Amino acid - Azacycle - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Carboxylic acid - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic oxide - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors piperidinemonocarboxylic acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIPOX Tbio Peroxisomal sarcosine oxidase (13 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLI1 Tchem Zinc finger protein GLI1 (201 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Slc25a20 Carnitine/acylcarnitine translocase (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dapA Dihydrodipicolinate synthase (65 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeDateItem
H2019026Certificate of AnalysisJan 05, 2026 S136371
L2530015Certificate of AnalysisJan 04, 2026 S136371
E1821042Certificate of AnalysisJul 09, 2025 S136371
I2423637Certificate of AnalysisSep 28, 2024 S136371
G2429055Certificate of AnalysisApr 25, 2024 S136371
G2429138Certificate of AnalysisApr 25, 2024 S136371
K2116387Certificate of AnalysisSep 13, 2023 S136371
K2116393Certificate of AnalysisSep 13, 2023 S136371
K2116394Certificate of AnalysisSep 13, 2023 S136371
K2116400Certificate of AnalysisSep 13, 2023 S136371
Chemical and Physical Properties
SolubilitySoluble in water (50 mg/ml), and boiling alcohol.
Melt Point(°C)280°C
Molecular Weight129.160 g/mol
XLogP3-2.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass129.079 Da
Monoisotopic Mass129.079 Da
Topological Polar Surface Area49.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity114.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Chengyi Xie, Liancheng Gu, Qidi Wu, Lei Li, Chenlu Wang, Jiancheng Yu, Keqi Tang.  (2020)  Effective Chiral Discrimination of Amino Acids through Oligosaccharide Incorporation by Trapped Ion Mobility Spectrometry.  ANALYTICAL CHEMISTRY,      [PMID:33226780] [10.1021/acs.analchem.0c03461]
2. Yi Diao, Xiaolong Chang, Fan Liu, Keyi Wang, Mingda Li, Fanbao Meng.  (2025)  Graphene oxide hydrogen bonding liquid crystals using carboxylic acids as proton donors: Liquid-crystalline behavior and ferroelectric property.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2025.142134]
3. SunHongzheng , HanLongsen , GuoYueshuai , AnHuiqing , WangBing , ZhangXiangzheng , LiJiashuo , JiangYingtong , WangYue , SunGuangyi , ZhuShuai , TangShoubin , GeJuan , ChenMinjian , GuoXuejiang , WangQiang.  (2024)  The global phosphorylation landscape of mouse oocytes during meiotic maturation.  EMBO JOURNAL,      [PMID:39256562] [10.1038/s44318-024-00222-1]
4. Di Wang, Longhai Yu, Qi Lu, Meiqing Han, Baikui Wang, Xianqi Peng, Min Yue, Yan Li.  (2025)  Oral pretreatment with Escherichia coli Nissle 1917 enhances the host's defense against influenza A virus infection.  mLife,  (6): (664-680).  [PMID:41479404] [10.1002/mlf2.70050]
5. Chi Yan, Xingyu Chen, Wenqing Gao, Chunlan Tang, Liwen Du, Chengyi Xie, Feng Xu, Keqi Tang, Jiancheng Yu.  (2025)  Chiral Derivatization Enables High-Resolution Ion Mobility Spectrometry of 30 Amino Acid Enantiomers.  ANALYTICAL CHEMISTRY,      [PMID:41451537] [10.1021/acs.analchem.5c06382]
Solution Calculators
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