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W419001

Sigma-Aldrich

L-Ornithine hydrochloride

99%

Sinonimo/i:

(S)-(+)-2,5-Diaminopentanoic acid hydrochloride, (S)-2,5-Diaminopentanoic acid monohydrochloride, L-Ornithine monohydrochloride

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About This Item

Formula condensata:
NH2(CH2)3CH(CO2H)(NH2) · HCl
Numero CAS:
3184-13-2
Peso molecolare:
168.62
Numero FEMA:
4190
Beilstein:
3625847
Numero CE:
221-678-6
Numero MDL:
MFCD00064562
Codice UNSPSC:
12164502
ID PubChem:
329830679
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

400

Saggio

99%

Punto di fusione

245 °C (dec.) (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

green

Stringa SMILE

Cl.NCCC[C@H](N)C(O)=O

InChI

1S/C5H12N2O2.ClH/c6-3-1-2-4(7)5(8)9;/h4H,1-3,6-7H2,(H,8,9);1H/t4-;/m0./s1
GGTYBZJRPHEQDG-WCCKRBBISA-N

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Applicazioni


  • Subchronic tolerance trials of graded oral supplementation with ornithine hydrochloride or citrulline in healthy adults.: This research examines the safety and tolerance of varying doses of L-ornithine hydrochloride in healthy adults. The findings indicate that L-ornithine hydrochloride is well-tolerated at different dosage levels, making it a viable supplement for various applications (Miura et al., 2023).

Esclusione di responsabilità

For R&D or non-EU Food use. Not for retail sale.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
SHBL2009
MKBZ9586V
MKBS6938V
MKBP1798V
MKBL4801V

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Universal Proteomics Standard Set Protein Mass Spectrometry Calibration Standard

Sigma-Aldrich

UPS1

Universal Proteomics Standard Set

L-Citrulline ≥98% (TLC)

Sigma-Aldrich

C7629

L-Citrulline

Citocromo c ≥95% (SDS-PAGE)

Sigma-Aldrich

C2506

Citocromo c

L-arginina from non-animal source, meets EP, USP testing specifications, suitable for cell culture, 98.5-101.0%

Sigma-Aldrich

A8094

L-arginina

Tom Rimaux et al.
Research in microbiology, 164(3), 216-225 (2012-11-28)
Arginine conversion through the arginine deiminase (ADI) pathway is a common metabolic trait of Lactobacillus sakei which is ascribed to an arc operon and which inquisitively involves citrulline excretion and re-uptake. The aim of this study was to verify whether
Sherry Dadsetan et al.
Biochemical pharmacology, 85(1), 115-123 (2012-10-30)
Combined administration of ornithine and phenylacetate (OP) is proposed as a novel treatment of hyperammonemia and hepatic encephalopathy. Ornithine is believed to increase ammonia fixation into glutamine in muscle tissue and glutamine is subsequently thought to react with phenylacetate forming
Nicole Berthold et al.
Antimicrobial agents and chemotherapy, 57(1), 402-409 (2012-11-02)
Proline-rich antimicrobial peptides (PrAMPs) from insects and mammals have recently been evaluated for their pharmaceutical potential in treating systemic bacterial infections. Besides the native peptides, several shortened, modified, or even artificial sequences were highly effective in different murine infection models.
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Critical reviews in immunology, 32(6), 463-488 (2013-02-23)
The purpose of immunology is simple. Cure or prevent disease. M1/M2 is useful because it is simple. M1/M2 describes the two major and opposing activities of macrophages. M1 activity inhibits cell proliferation and causes tissue damage while M2 activity promotes
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Nuclear medicine and biology, 40(2), 262-272 (2012-12-15)
Radiolabeled RGD peptides that specifically target integrin α(ν)β(3) have great potential in early tumor detection through noninvasive monitoring of tumor angiogenesis. Based on previous findings of our group on radiopeptides containing positively charged aminoacids, we developed a new cyclic cRGDfK
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