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About This Item
Empirical Formula (Hill Notation):
C4H7NO4 · C6H14N4O2
CAS Number:
Molecular Weight:
307.30
UNSPSC Code:
12352200
EC Number:
231-656-8
InChI key
SUUWYOYAXFUOLX-PGMHMLKASA-N
InChI
1S/C6H14N4O2.C4H7NO4/c7-4(5(11)12)2-1-3-10-6(8)9;5-2(4(8)9)1-3(6)7/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);2H,1,5H2,(H,6,7)(H,8,9)/t4-;/m1./s1
storage temp.
−20°C
Biochem/physiol Actions
Substrate of nitric oxide synthase, which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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A Besset et al.
Acta endocrinologica, 99(1), 18-23 (1982-01-01)
Arginine aspartate was administered orally (250 mg/dg/day) for one week to 5 healthy male human volunteers aged 20-35. After this period, the 24 h patterns of growth hormone (GH) and prolactin (Prl) secretion were determined by radioimmunoassay on blood samples
Sylvie Blazejewski et al.
Fundamental & clinical pharmacology, 23(3), 339-344 (2009-06-17)
To investigate the effect of chronic oral arginine aspartate on the growth hormone (GH), GH-releasing hormone (GHRH), insulin-like growth factor-1 (IGF-1) and IGF-binding protein-3 (IGFBP-3) secretions in healthy volunteers. Twenty-three healthy non-athlete volunteer males were administered arginine aspartate (30 g)
R Stanislavov et al.
Phytotherapy research : PTR, 23(3), 297-302 (2009-01-15)
In a randomly allocated, double-blind, placebo-controlled, cross-over design, 50 infertile patients were treated for 1 month with placebo or a combination of l-arginine aspartate and Pycnogenol (Prelox). Semen samples were examined at 4 week intervals according to WHO criteria. Treatment
[Arginine aspartate and muscular activity].
G Gremion et al.
Schweizerische Zeitschrift fur Sportmedizin, 35(1), 21-24 (1987-03-01)
Y Neuzillet et al.
Andrology, 1(2), 223-228 (2013-02-16)
Efficacy and safety of l-arginine aspartate 8 g combined with 200 mg of adenosine monophosphate (AA) with placebo (PL) alone for intermittent treatment of mild-to-moderate erectile dysfunction (ED) were compared. The study design was a double-blind, PL-controlled, two-way crossover randomized
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