Skip to Content
Merck
All Photos(1)

Documents

H0377

Sigma-Aldrich

DL-5-Hydroxylysine hydrochloride

Synonym(s):

2,6-Diamino-5-hydroxycaproic acid hydrochloride, 2,6-Diamino-5-hydroxyhexanoic acid hydrochloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
NH2CH2CH(OH)CH2CH2CH(NH2)COOH · HCl
CAS Number:
13204-98-3
Molecular Weight:
198.65
Beilstein:
3914368
EC Number:
236-168-9
MDL number:
MFCD00012878
UNSPSC Code:
12352209
PubChem Substance ID:
24895397
NACRES:
NA.26

Assay

≥98% (TLC)

Quality Level

200

form

powder

color

white

mp

225 °C (dec.) (lit.)

application(s)

detection
peptide synthesis

SMILES string

Cl.NCC(O)CCC(N)C(O)=O

InChI

1S/C6H14N2O3.ClH/c7-3-4(9)1-2-5(8)6(10)11;/h4-5,9H,1-3,7-8H2,(H,10,11);1H

InChI key

MJXVOTKVFFAZQJ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application


  • Characterization of acetyl-CoA: L-lysine N6-acetyltransferase, which catalyses the first step of carbon catabolism from lysine in Saccharomyces cerevisiae.: This research investigates the enzyme acetyl-CoA: L-lysine N6-acetyltransferase, which initiates the catabolism of lysine in Saccharomyces cerevisiae. Utilizing DL-5-Hydroxylysine hydrochloride, the study provides insights into the metabolic pathways and regulatory mechanisms of lysine degradation, contributing to the broader understanding of amino acid metabolism in yeast (Bode et al., 1993).

Biochem/physiol Actions

DL-5-Hydroxylysine is a racemic mixture of D- and L- enantiomers of 5-hydroxylysine which may be used as potential target markers for radical-induced protein oxidation.

Other Notes

Mixed DL and DL-allo

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 5

1 of 5

3-Methyl-L-histidine

Sigma-Aldrich

M9005

3-Methyl-L-histidine

H-L-Photo-lysine HCl ≥98%

Sigma-Aldrich

907251

H-L-Photo-lysine HCl

1-Methyl-L-histidine ≥98.0% (TLC)

Sigma-Aldrich

67520

1-Methyl-L-histidine

5-Hydroxy-L-tryptophan 98% (calc. on dried substance)

Sigma-Aldrich

107751

5-Hydroxy-L-tryptophan

L-Cystathionine ≥98% (TLC)

Sigma-Aldrich

C7505

L-Cystathionine

R Bode et al.
Archives of microbiology, 160(5), 397-400 (1993-01-01)
The carbon catabolism of L-lysine starts in Saccharomyces cerevisiae with acetylation by an acetyl-CoA:L-lysine N6-acetyltransferase. The enzyme is strongly induced in cells grown on L-lysine as sole carbon source and has been purified about 530-fold. Its activity was specific for
B Morin et al.
Chemical research in toxicology, 11(11), 1265-1273 (1998-11-17)
gamma-Irradiation of several amino acids (Val, Leu, Ile, Lys, Pro, and Glu) in the presence of O2 generates hydroperoxides. We have previously isolated and characterized valine and leucine hydroperoxides, and hydroxides, and have detected these products in both isolated systems
M Droux et al.
Archives of biochemistry and biophysics, 316(1), 585-595 (1995-01-10)
Cystathionine beta-lyase, the second enzyme of the transsulfuration pathway leading to homocysteine synthesis was purified over 16,000-fold from spinach (Spinacia oleracea L.) leaf chloroplasts (soluble fraction). Enzyme activity was followed along the purification scheme by either a colorimetric method for
N Zhang et al.
International journal of plant sciences, 160(3), 511-519 (2001-09-07)
Lactuca sativa cv. Baijianye seedlings do not normally produce lateral roots, but removal of the root tip or application of auxin, especially indole-butyric acid, triggered the formation of lateral roots. Primordia initiated within 9 h and were fully developed after
Lasanthi P Jayathilaka et al.
Organic letters, 6(21), 3659-3662 (2004-10-08)
[reaction: see text] L-alpha-(1-Cyclobutenyl)glycine (1-Cbg) was targeted as a potentially translatable analogue of isoleucine and valine and as a useful building block for peptides. An enantioselective synthesis was executed in which the key step was diastereoselective addition of 1-cyclobutenylmagnesium bromide
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service