L-Arginine hydrochloride - PharmPure™, USP, JP, Ph.Eur., for cell culture, ≥98.5% , CAS No.1119-34-2

CAS: 1119-34-2 Cat. No.: A103485 Peso molecular: 210.66 Beilstein Registry Number: 6099937 Número EC: 214-275-1
Disponible para pedir
GRADE & PURITY PharmPure™ ? PharmPure™ — Aladdin's line of biopharmaceutical raw and starting materials. Use for pharma manufacturing inputs needing high purity and documentation. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance. JP ? Japanese Pharmacopoeia grade — conforms to JP monograph standards. Use for pharmaceutical products subject to Japanese regulatory requirements. Ph.Eur. ? European Pharmacopoeia grade — conforms to Ph.Eur. monographs across EU member states. Use for pharmaceutical work needing European compendial compliance. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥98.5%
Synonyms
(S)-2-Amino-5-guanidinopentanoic acid hydrochloride | L-ARGININE HCL | L-Arginine monohydrochloride, BioUltra, >=99.5% (AT) | NSC-203450 | ARGININE HYDROCHLORIDE [ORANGE BOOK] | ARGININE HYDROCHLORIDE [USAN] | L-ARGININE HYDROCHLORIDE [JAN] | H-Arg-OH.HCl
Storage
Protected from light,Room temperature,Argon charged,Desiccated,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100g
A103485-100g
10
24,90US$
500g
A103485-500g
3
81,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

PharmPure™, USP, JP, Ph.Eur., for cell culture, ≥98.5% for Cell culture,JP,Ph.Eur.,PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Argon charged,Desiccated,Cool 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
(S)-2-Amino-5-guanidinopentanoic acid hydrochloride | L-ARGININE HCL | L-Arginine monohydrochloride, BioUltra, >=99.5% (AT) | NSC-203450 | ARGININE HYDROCHLORIDE [ORANGE BOOK] | ARGININE HYDROCHLORIDE [USAN] | L-ARGININE HYDROCHLORIDE [JAN] | H-Arg-OH.HCl
Especificaciones y pureza
PharmPure™, USP, JP, Ph.Eur., for cell culture, ≥98.5%
Mecanismos bioquímicos y fisiológicos
Substrate of nitric oxide synthase (NOS), which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.
Condiciones de almacenamiento de almacenamiento
Protected from light, Room temperature, Argon charged, Desiccated, Cool
Enviado en
Normal
Grado
for Cell culture, JP, Ph.Eur., PharmPure™, USP
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98.5%
Nombres e identificadores
Sonrisas canónicasCl[H].N[C@@H](CCCNC(N)=N)C(O)=O
IUPAC Name(2S)-2-amino-5-(diaminomethylideneamino)pentanoic acid;hydrochloride
InChIKeyKWTQSFXGGICVPE-WCCKRBBISA-N
INCHI1S/C6H14N4O2.ClH/c7-4(5(11)12)2-1-3-10-6(8)9;/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);1H/t4-;/m0./s1
Isómeros SMILES C(C[C@@H](C(=O)O)N)CN=C(N)N.Cl
WGK Alemania 1
CAS alternativo 15595-35-4
Peso molecular 210.66
Beilstein 6099937
Reaxy-Rn 3631658
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3631658&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
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Fatty acids and conjugates  Guanidines  Amino acids  Propargyl-type 1,3-dipolar organic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Carboximidamides  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Fatty acid - Guanidine - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Amine - Hydrochloride - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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
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
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
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
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.

23 results found

Lot NumberCertificate TypeFechaArticulo
C2625727Certificate of AnalysisMar 13, 2026 A103485
C2625728Certificate of AnalysisMar 13, 2026 A103485
L2518626Certificate of AnalysisDec 06, 2025 A103485
L2518625Certificate of AnalysisDec 06, 2025 A103485
K2510595Certificate of AnalysisOct 20, 2025 A103485
K2510594Certificate of AnalysisOct 20, 2025 A103485
H2528126Certificate of AnalysisAug 13, 2025 A103485
F2512132Certificate of AnalysisMay 20, 2025 A103485
F2512112Certificate of AnalysisMay 20, 2025 A103485
C2511058Certificate of AnalysisFeb 26, 2025 A103485
C2521874Certificate of AnalysisFeb 26, 2025 A103485
K2413159Certificate of AnalysisOct 30, 2024 A103485
I2429083Certificate of AnalysisSep 19, 2024 A103485
H2415076Certificate of AnalysisJul 27, 2024 A103485
E2428031Certificate of AnalysisMay 11, 2024 A103485
E2428030Certificate of AnalysisMay 11, 2024 A103485
E2428029Certificate of AnalysisMay 11, 2024 A103485
L2311150Certificate of AnalysisDec 12, 2023 A103485
D23061236Certificate of AnalysisApr 08, 2023 A103485
K2204216Certificate of AnalysisOct 12, 2022 A103485
K2204217Certificate of AnalysisOct 12, 2022 A103485
B2301186Certificate of AnalysisOct 12, 2022 A103485
G1429035Certificate of AnalysisMay 06, 2022 A103485

Show more ⌵

Propiedades químicas y físicas
SolubilidadSoluble in water. Slightly soluble in hot alcohol.
SensibilidadLight & Moisture Sensitive.
Rotación específica [α]23 ° (C=8, HCl(1+1))
Punto de fusión (°C)226-230°C
Peso molecular210.660 g/mol
XLogP3
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass210.088 Da
Monoisotopic Mass210.088 Da
Topological Polar Surface Area128.000 Ų
Heavy Atom Count13
Formal Charge0
Complexity176.000
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 Count2
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Qiang Zheng, Shuai He, Song-Lin Xu, Meng-Die Ma, Min Fan, Jin-Fang Ge.  (2023)  Pharmacokinetics and tissue distribution of vigabatrin enantiomers in rats.  SAUDI PHARMACEUTICAL JOURNAL,      [PMID:38223203] [10.1016/j.jsps.2023.101934]
2. Yanbo Wang, Yongzheng Wang, Jian Chen, Shigenobu Koseki, Qing Yang, Hejun Yu, Linglin Fu.  (2021)  Screening and preservation application of quorum sensing inhibitors of Pseudomonas fluorescens and Shewanella baltica in seafood products.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2021.111749]
3. Yalin Ye, Xingli Huo, Zongning Yin.  (2021)  Protein-protein interactions at high concentrations: Effects of ArgHCl and NaCl on the stability, viscosity and aggregation mechanisms of protein solution.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:33811966] [10.1016/j.ijpharm.2021.120535]
4. Jie Zhu, Hua Han, Faxue Li, Xueli Wang, Jianyong Yu, Chih-Chang Chu, Dequn Wu.  (2018)  Self-assembly of amino acid-based random copolymers for antibacterial application and infection treatment as nanocarriers.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:30690388] [10.1016/j.jcis.2018.12.091]
5. Qiang Zheng, Song-Lin Xu, Xin-Lin Guo, Chuan-Yu Wang, Meng-Die Ma, Jin-Fang Ge.  (2025)  Effects of melatonin on the pharmacokinetics and amino acid metabolism profile of vigabatrin in rats.  TOXICOLOGY AND APPLIED PHARMACOLOGY,      [PMID:39884559] [10.1016/j.taap.2025.117247]
6. Wang Jiteng, Zhang Jingyi, Li Xinyu, Xu Hanying Y., Yang Yeshun, Zhang Jiankun, Feng Wenping, Chen Qiang, Dong Fen, Han Tao.  (2025)  Metabolism of arginine in juvenile largemouth bass (Micropterus salmoides) after oral or intraperitoneal administration of arginine or its substrates.  AMINO ACIDS,  57  (1): (1-15).  [PMID:39945913] [10.1007/s00726-024-03436-z]
7. Shuangshuang Wan, Wurui Liu, Qian Wu, Kepeng Wang, Yaocheng Li, Peihong Huang, Yu Wu, Yunfei Mu, Yulin Fan, Jun Tao, Jia Yao, Fei Peng, Yu Zou, Lianhui Wang, Zhiyao Yuan, Xianguang Ding.  (2024)  Nanobiohybrid Extracellular Vesicle Nanoreactor with Improving Metabolical Activity for Biocatalytic Therapy.  ACS Nano,      [PMID:39536071] [10.1021/acsnano.4c12458]
8. Yingjie Sun, Changheng Li, Xiaofei Deng, Wenjie Li, Xiaoyi Deng, Weiqi Ge, Miaoyuan Shi, Ying Guo, Yanxun V Yu, Hai-bing Zhou, Youngnam N Jin.  (2024)  Target protein identification in live cells and organisms with a non-diffusive proximity tagging system.  eLife,      [PMID:39728918] [10.7554/eLife.102667]
9. Cheng Cao, Qi Yang, Liming Chen, Xiuqiang Li, Jiazhuo Gong, Lei Liang, Chaojie Yu, Bingyan Guo, Xueyu Wang, Zhongming Zhao, Yuwei Qiu, Fanglian Yao, Junjie Li, Hong Zhang.  (2025)  Self-Gelling Hemostatic Powders Driven by Hydrogen Bonding and Electrostatic Interactions with Antibacterial and Antioxidant Properties.  Journal of Materials Chemistry B,      [PMID:40590133] [10.1039/D5TB00032G]
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.