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L-Arginine monohydrochloride - Ultrapure BioReagent, ≥99.5% (AT), high purity , CAS No.1119-34-2

  • BioReagent
  • Ultra pure
  • UltraBio™
  • ≥99.5%(AT)
Item Number
L431483
Grouped product items
SKUSizeAvailabilityPrice Qty
L431483-100g
100g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$314.90
L431483-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,083.90
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Basic Description

SynonymsL-Arginine hydrochloride|1119-34-2|Arginine Hydrochloride|L-Arginine monohydrochloride|L-ARGININE HCL|H-Arg-OH.HCl|15595-35-4|Arginine HCl|Argamine|Argivene|Detoxargin|Levargin|Minophagen A|R-Gene|Arginine monohydrochloride|Tivortin|R-gene 10|L-(+)-Argini
Specifications & PurityUltraBio™, Ultra pure, BioReagent, ≥99.5%(AT)
Biochemical and Physiological MechanismsL-Arginine is considered as a semi essential amino acid. In most mammals including humans, L-Arginine synthesis occurs through intestinal-renal axis, from glutamine, glutamate and proline. Abnormal levels of L-Arginine is associated with the development o
GradeBioReagent, Ultra pure, UltraBio™
Product Description

Application

L-Arginine monohydrochloride has been used to study the reversal of the inhibitory effect of L-N G 0-nitroarginine on non-cholinergic relaxations. It has also been used as a dietary supplement to study its effect on endothelium-dependent vasodilation.

Associated Targets

DRD1 Tclin D(1A) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ESR1 Tclin Estrogen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HRH3 Tclin Histamine H3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A2 Tclin Sodium-dependent noradrenaline transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PGR Tclin Progesterone receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE3A Tclin cGMP-inhibited 3',5'-cyclic phosphodiesterase A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE4A Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD3 Tclin D(3) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDR Tclin Vascular endothelial growth factor receptor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM2 Tclin Muscarinic acetylcholine receptor M2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA3 Tchem Adenosine receptor A3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TBXA2R Tclin Thromboxane A2 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

F2 Tclin Prothrombin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRM1 Tclin Mu-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (2S)-2-amino-5-(diaminomethylideneamino)pentanoic acid;hydrochloride
INCHI InChI=1S/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
InChi Key KWTQSFXGGICVPE-WCCKRBBISA-N
Canonical SMILES Cl[H].N[C@@H](CCCNC(N)=N)C(O)=O
Isomeric SMILES C(C[C@@H](C(=O)O)N)CN=C(N)N.Cl
WGK Germany 1
Alternate CAS 15595-35-4
PubChem CID 66250
Molecular Weight 210.66
Beilstein 6099937

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

SolubilityH2O: 1M at20°C, clear, colorless
Specific Rotation[α]23 ° (C=8, HCl(1+1))
Melt Point(°C)226-230°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P264:Wash hands [and …] thoroughly after handling.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

WGK Germany 1
Merck Index 780

Related Documents

 SDS

 Specification Sheet

References

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9. Yumiko Mizukoshi,Koh Takeuchi,Misa Arutaki,Takeshi Takizawa,Hiroyuki Hanzawa,Hideo Takahashi,Ichio Shimada.  (2015-03-12)  Suppression of problematic compound oligomerization by cosolubilization of nondetergent sulfobetaines..  ChemMedChem,  10  ((4)): (736-741).  [PMID:25760302]
10. Jenna Gallie,Eric Libby,Frederic Bertels,Philippe Remigi,Christian B Jendresen,Gayle C Ferguson,Nicolas Desprat,Marieke F Buffing,Uwe Sauer,Hubertus J E Beaumont,Jan Martinussen,Mogens Kilstrup,Paul B Rainey.  (2015-03-13)  Bistability in a metabolic network underpins the de novo evolution of colony switching in Pseudomonas fluorescens..  PLoS biology,  13  ((3)): (e1002109-e1002109).  [PMID:25763575]
11. L Rascón-Valenzuela,C Velázquez,A Garibay-Escobar,L A Medina-Juárez,W Vilegas,R E Robles-Zepeda.  (2015-06-13)  Antiproliferative activity of cardenolide glycosides from Asclepias subulata..  Journal of ethnopharmacology,  171  (280-286).  [PMID:26068432]
12. Jun Yeul Lim,Nam Ah Kim,Dae Gon Lim,Ki Hyun Kim,Shavron Hada,Seong Hoon Jeong.  (2015-07-19)  Evaluation of etanercept degradation under oxidative stress and potential protective effects of various amino acids..  International journal of pharmaceutics,  492  ((1-2)): (127-136).  [PMID:26187168]
13. Caroline Nava,Johanna Rupp,Jean-Paul Boissel,Cyril Mignot,Agnès Rastetter,Claire Amiet,Aurélia Jacquette,Céline Dupuits,Delphine Bouteiller,Boris Keren,Merle Ruberg,Anne Faudet,Diane Doummar,Anne Philippe,Didier Périsse,Claudine Laurent,Nicolas Lebrun,Vincent Guillemot,Jamel Chelly,David Cohen,Delphine Héron,Alexis Brice,Ellen I Closs,Christel Depienne.  (2015-07-29)  Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders..  Amino acids,  47  ((12)): (2647-2658).  [PMID:26215737]
14. N E Paul,R Lösel,K Hemmrich,D Goy,N Pallua,D Klee.  (2015-09-26)  L-arginine and arginine ethyl ester enhance proliferation of endothelial cells and preadipocytes - how an arginine ethyl ester-releasing biomaterial could support endothelial cell growth in tissue engineering..  Bio-medical materials and engineering,  25  ((3)): (289-297).  [PMID:26407115]
15. Enrique Niza,Matěj Božik,Iván Bravo,Pilar Clemente-Casares,Agustín Lara-Sanchez,Alberto Juan,Pavel Klouček,Carlos Alonso-Moreno.  (2020-06-03)  PEI-coated PLA nanoparticles to enhance the antimicrobial activity of carvacrol..  Food chemistry,  328  (127131-127131).  [PMID:32485586]
16. Joseph J Dalluge,Jennifer L McCurtain,Adam J Gilbertsen,Kyle A Kalstabakken,Bryan J Williams.  (2015-05-11)  Determination of agmatine using isotope dilution UPLC-tandem mass spectrometry: application to the characterization of the arginine decarboxylase pathway in Pseudomonas aeruginosa..  Analytical and bioanalytical chemistry,  407  ((18)): (5513-5519).  [PMID:25957842]

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