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Z-Lys-OH - 98%, high purity , CAS No.2212-75-1

  • ≥98%
Item Number
Z105920
Grouped product items
SKUSizeAvailabilityPrice Qty
Z105920-1g
1g
In stock
$9.90
Z105920-5g
5g
In stock
$30.90
Z105920-10g
10g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$54.90
Z105920-25g
25g
In stock
$123.90
Z105920-100g
100g
In stock
$443.90
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Discover Z-Lys-OH by Aladdin Scientific in 98% for only $9.90. Available - in Ligands at Aladdin Scientific. Tags: Chemical Biology, N-protected amino acids.

View related series
Chemical Biology N-protected amino acids

Basic Description

SynonymsZ-Lys-OH|2212-75-1|Nalpha-Cbz-L-lysine|Cbz-Lys-OH|(S)-6-Amino-2-(((benzyloxy)carbonyl)amino)hexanoic acid|N-alpha-Carbobenzoxy-L-lysine|L-Lysine, N2-[(phenylmethoxy)carbonyl]-|MFCD00038204|L-Lysine, N2-((phenylmethoxy)carbonyl)-|Lysine, N2-[(phenylmethoxy
Specifications & Purity98%
Storage TempStore at 2-8°C
Shipped InWet ice
Product Description

An educt for the convenient preparation of L-α-aminoadipic acid.

Names and Identifiers

IUPAC Name (2S)-6-amino-2-(phenylmethoxycarbonylamino)hexanoic acid
INCHI InChI=1S/C14H20N2O4/c15-9-5-4-8-12(13(17)18)16-14(19)20-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,15H2,(H,16,19)(H,17,18)/t12-/m0/s1
InChi Key OJTJKAUNOLVMDX-LBPRGKRZSA-N
Canonical SMILES C1=CC=C(C=C1)COC(=O)NC(CCCCN)C(=O)O
Isomeric SMILES C1=CC=C(C=C1)COC(=O)N[C@@H](CCCCN)C(=O)O
WGK Germany 3
PubChem CID 75172
Molecular Weight 280.32
Beilstein 2153826
Reaxy-Rn 2153826

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

5 results found

Lot NumberCertificate TypeDateItem
J2229623Certificate of AnalysisJul 12, 2022 Z105920
J2229624Certificate of AnalysisJul 12, 2022 Z105920
J2229625Certificate of AnalysisJul 12, 2022 Z105920
J2229626Certificate of AnalysisJul 12, 2022 Z105920
K2316171Certificate of AnalysisOct 11, 2021 Z105920

Chemical and Physical Properties

SensitivityHeat sensitive
Specific Rotation[α]-13° (C=2,0.2mol/L HCl)
Melt Point(°C)226-231 °C

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 2153826

Related Documents

 SDS

 Specification Sheet

References

1. A S Bajkowski,A Frankfater.  (1983-02-10)  The pH dependency of bovine spleen cathepsin B-catalyzed transfer of N alpha-benzyloxycarbonyl-L-lysine from p-nitrophenol to water and dipeptide nucleophiles. Comparisons with papain..  The Journal of biological chemistry,  258  ((3)): (1650-1655).  [PMID:6401725]
2. Kimiyasu Isobe,Shouko Nagasawa.  (2007-10-30)  Characterization of Nalpha-benzyloxycarbonyl-L-lysine oxidizing enzyme from Rhodococcus sp. AIU Z-35-1..  Journal of bioscience and bioengineering,  104  ((3)): (218-223).  [PMID:17964487]
3. Rong Kuang,Zhanpeng Zhang,Xiaobing Jin,Jiang Hu,Melanie J Gupte,Longxing Ni,Peter X Ma.  (2015-07-04)  Nanofibrous spongy microspheres enhance odontogenic differentiation of human dental pulp stem cells..  Advanced healthcare materials,  4  ((13)): (1993-2000).  [PMID:26138254]
4. Kimiyasu Isobe,Nahoko Fukuda,Shouko Nagasawa,Kaoru Saitou.  (2010-06-22)  Enzymes responsible for the conversion of N alpha-[(Benzyloxy)carbonyl]-D-lysine to N alpha-[(Benzyloxy)carbonyl]-D-aminoadipic acid by Rhodococcus sp. AIU Z-35-1..  Chemistry & biodiversity,  7  ((6)): (1549-1554).  [PMID:20564569]
5. Jong-Woo Lim,Woonsung Na,Hyun-Ouk Kim,Minjoo Yeom,Geunseon Park,Aram Kang,Haejin Chun,Chaewon Park,Seungseok Oh,Van Phan Le,Hyoung Hwa Jeong,Daesub Song,Seungjoo Haam.  (2018-12-15)  Cationic Poly(Amino Acid) Vaccine Adjuvant for Promoting Both Cell-Mediated and Humoral Immunity Against Influenza Virus..  Advanced healthcare materials,  8  ((2)): (e1800953-e1800953).  [PMID:30549426]
6. Akifumi Kato,Kazumasa Ohtake,Yoshitaka Tanaka,Shigeyuki Yokoyama,Kensaku Sakamoto,Yasuhisa Shiraishi.  (2021-02-10)  An expanded genetic code facilitates antibody chemical conjugation involving the lambda light chain..  Biochemical and biophysical research communications,  546  (35-39).  [PMID:33561746]

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