T1660
Nε,Nε,Nε-Trimethyllysine hydrochloride
≥97% (TLC)
Synonym(s):
1-Pentanaminium, 5-amino-5-carboxy-N,N,N-trimethyl-, chloride (1:1), (5S)-
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About This Item
Empirical Formula (Hill Notation):
C9H20N2O2 · HCl
CAS Number:
Molecular Weight:
224.73
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
Quality Level
assay
≥97% (TLC)
form
powder
contains
salts and water as balance
composition
Amino acid content, ~75%
technique(s)
LC/MS: suitable
color
white
storage temp.
−20°C
SMILES string
[Cl-].C[N+](C)(C)CCCC[C@H](N)C(O)=O
InChI
1S/C9H20N2O2.ClH/c1-11(2,3)7-5-4-6-8(10)9(12)13;/h8H,4-7,10H2,1-3H3;1H/t8-;/m0./s1
InChI key
ZKIJKCHCMFGMCM-QRPNPIFTSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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C J Rebouche et al.
The Journal of nutrition, 116(5), 751-759 (1986-05-01)
Rates of carnitine biosynthesis in mammals depend on the availability of substrates and the activity of enzymes subserving the pathway. This study was undertaken to test the hypothesis that the availability of epsilon-N-trimethyllysine is rate-limiting for synthesis of carnitine in
Karin Strijbis et al.
IUBMB life, 62(5), 357-362 (2010-03-23)
The water-soluble zwitterion carnitine is an essential metabolite in eukaryotes required for fatty acid oxidation as it functions as a carrier during transfer of activated acyl and acetyl groups across intracellular membranes. Most eukaryotes are able to synthesize carnitine endogenously
Frank Hirche et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(22), 2158-2162 (2009-06-16)
For the investigation of the metabolism and biosynthesis of carnitine, sensitive determination of carnitine and its metabolic precursors, trimethyllysine and gamma-butyrobetaine, is required. We present here a new simplified method for the analysis of carnitine, its acetyl- and propyl esters
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T1660-25MG | 04061837338021 |