L-Proline - ≥99% , CAS No.147-85-3

CAS: 147-85-3 Cat. No.: P108709 Fórmula: C5H9NO2 Peso molecular: 115.13 Beilstein Registry Number: 80810 Número EC: 205-702-2 PubChem CID: 145742
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
(-)-2-Pyrrolidinecarboxylic acid | (2S)-pyrrolidine-2-carboxylic acid | (S)-Pyrrolidine-2-carboxylic acid | 2-pyrrolidinecarboxylic acid | L-proline | (S)-2-Pyrrolidinecarboxylic acid | proline | (-)-(S)-Proline | H-Pro-OH | L-(-)-Proline | Prolinum | (-)
Storage
Protected from light,Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
100g
P108709-100g
5 Disponible
9 Disponible
11,19€
500g
P108709-500g
4 Disponible
2 Disponible
34,62€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,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 460 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
(-)-2-Pyrrolidinecarboxylic acid | (2S)-pyrrolidine-2-carboxylic acid | (S)-Pyrrolidine-2-carboxylic acid | 2-pyrrolidinecarboxylic acid | L-proline | (S)-2-Pyrrolidinecarboxylic acid | proline | (-)-(S)-Proline | H-Pro-OH | L-(-)-Proline | Prolinum | (-)
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Protected from light,Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508810670
IUPAC Name
(2S)-pyrrolidine-2-carboxylic acid
InChIKey
ONIBWKKTOPOVIA-BYPYZUCNSA-N
INCHI
1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1
Isómeros SMILES
C1C[C@H](NC1)C(=O)O
WGK Alemania
1
RTECS
TW3584000
PubChem CID
145742
Peso molecular
115.13
Beilstein
80810
Reaxy-Rn
80810

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

Objetivos asociados (humanos)
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EPHX1 Tchem Epoxide hydrolase 1 (644 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC1A4 Tbio Neutral amino acid transporter A (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (16955 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC1A5 Tchem Neutral amino acid transporter B(0) (65 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Slc25a20 Carnitine/acylcarnitine translocase (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hyaloperonospora parasitica (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brassica oleracea (32 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAP1 General amino-acid permease GAP1 (481 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a5 Amino acid transporter (271 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc7a10 Asc-type amino acid transporter 1 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

42 results found

Lot NumberCertificate TypeFechaArticulo
C2627682Certificate of AnalysisMar 12, 2026 P108709
C2627570Certificate of AnalysisMar 12, 2026 P108709
C2627569Certificate of AnalysisMar 12, 2026 P108709
K2513533Certificate of AnalysisNov 05, 2025 P108709
K2513529Certificate of AnalysisNov 05, 2025 P108709
K2513528Certificate of AnalysisNov 05, 2025 P108709
H2527352Certificate of AnalysisAug 06, 2025 P108709
H2527363Certificate of AnalysisAug 06, 2025 P108709
H2527480Certificate of AnalysisAug 06, 2025 P108709
G2531418Certificate of AnalysisJul 11, 2025 P108709
G2531417Certificate of AnalysisJul 11, 2025 P108709
D2514388Certificate of AnalysisMar 19, 2025 P108709
D2514436Certificate of AnalysisMar 19, 2025 P108709
D2514492Certificate of AnalysisMar 19, 2025 P108709
A2513433Certificate of AnalysisDec 14, 2024 P108709
A2513431Certificate of AnalysisDec 14, 2024 P108709
A2513432Certificate of AnalysisDec 14, 2024 P108709
J2428587Certificate of AnalysisOct 10, 2024 P108709
J2428631Certificate of AnalysisOct 10, 2024 P108709
J2428633Certificate of AnalysisOct 10, 2024 P108709
I2424006Certificate of AnalysisJul 05, 2024 P108709
I2404105Certificate of AnalysisJul 05, 2024 P108709
K2408316Certificate of AnalysisJul 05, 2024 P108709
G2418659Certificate of AnalysisJul 05, 2024 P108709
G2418660Certificate of AnalysisJul 05, 2024 P108709
G2418661Certificate of AnalysisJul 05, 2024 P108709
E2411302Certificate of AnalysisApr 29, 2024 P108709
E2411301Certificate of AnalysisApr 29, 2024 P108709
E2411300Certificate of AnalysisApr 29, 2024 P108709
E2411299Certificate of AnalysisApr 29, 2024 P108709
E2411298Certificate of AnalysisApr 29, 2024 P108709
C2421626Certificate of AnalysisMar 12, 2024 P108709
L2321363Certificate of AnalysisDec 25, 2023 P108709
B2311046Certificate of AnalysisJan 11, 2023 P108709
B2311033Certificate of AnalysisJan 11, 2023 P108709
B2310806Certificate of AnalysisJan 11, 2023 P108709
I2202709Certificate of AnalysisAug 04, 2022 P108709
I2202710Certificate of AnalysisAug 04, 2022 P108709
B2302360Certificate of AnalysisAug 04, 2022 P108709
B2222098Certificate of AnalysisJan 07, 2022 P108709
B2222095Certificate of AnalysisJan 07, 2022 P108709
B2222091Certificate of AnalysisJan 07, 2022 P108709
Propiedades químicas y físicas
SolubilidadSoluble in water and ethanol. Insoluble in ether, butanol and isopropanol.
SensibilidadLight sensitive,moisture sensitive
Rotación específica [α]-85 ° (C=4, H2O)
Punto de fusión (°C)228°C
Peso molecular115.130 g/mol
XLogP3-2.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass115.063 Da
Monoisotopic Mass115.063 Da
Topological Polar Surface Area49.300 Ų
Heavy Atom Count8
Formal Charge0
Complexity103.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Macrophage Activation
Asymmetric Organocatalysts
Proline-type Organocatalysts
N-Fluorobenzenesulfonimide (NFSI)
Peptide Basics
Buffer Additives to Prevent Protein Precipitation
Common Protectants and Formulations for Protein Storage
Structure, Function, and Applications of Glutamate Dehydrogenase
Chiral Amines in Asymmetric Synthesis: Role Map (A–F), a Minimal Evidence Chain, and a Research Selection Guide (with Tables 1–3)
Pyrrolidine and Its Derivative Systems: How a Five-Membered N-Heterocycle Tunes Properties and Use Cases via “Charge State–Conformation–Functional-Group Switching” (with Tables 1–4 for Selection Navigation)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
Technical Comparison and Method Selection for Hydroxyproline Determination
Chiral Catalyst and Ligand Selection Guide: From Reaction Task to Catalytic System Screening
Why Small Molecules Can Also Serve as Catalysts: Judging Organocatalytic Systems from Reaction Objectives and Activatable Structural Sites
Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
How Do Collagen Peptides Act on the Skin? From Surface Hydration and Percutaneous Delivery to Fibroblasts and Collagen Homeostasis
Anti-Photoaging Potential of Artemia Extract: UV-Induced Damage Cascades, HSP70-Related Stress Protection, and GP4G Metabolic Insights
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis
What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling
Mechanisms of Retinol Action in the Skin: From Metabolic Activation and RAR/RXR-Mediated Transcriptional Regulation to Epidermal Renewal and Collagen Homeostasis
What Is “Plant Collagen”? Distinguishing Ingredient Types, Structural Differences, Production Methods, and Skincare Effects
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
Differences Between Animal-Derived Collagen and Recombinant Collagen in Skincare: Sequence and Structure, Safety, Skin Effects, and Evidence Evaluation
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Conformational Control by Proline Derivatives and Their Medicinal Chemistry Effects: Ring Puckering, Amide Cis–Trans Isomerization, and Drug Properties
Citations of This Product
Calculadoras de soluciones
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