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

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

1 Citations

≥98%

CAS#: 2212-75-1
Molecular Weight: 280.32
Beilstein Registry Number: 2153826
EC Number: 218-662-6
MDL number: MFCD00038204
PubChem CID: 75172
PubChem SID: 504754920

In stock

Item Number

Z105920

Grouped product items
SKU	Size	Availability	Price
Z105920-1g	1g	9	$9.90
Z105920-5g	5g	9	$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	9	$123.90
Z105920-100g	100g	9	$443.90

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Chemical Biology (0) N-protected amino acids (0)

Basic Description

Synonyms	cbz-lysine \| SCHEMBL287474 \| (S)-6-amino-2-(benzyloxycarbonylamino)hexanoic acid \| Z-Lys-OH \| cobalt(2+);dinitrate;hexahydrate \| N-alpha-Carbobenzoxy-L-lysine \| Nalpha-Carbobenzoxy-L-lysine \| L-Lysine, N2-((phenylmethoxy)carbonyl)- \| ((benzyloxy)carbonyl)
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice
Product Description	An educt for the convenient preparation of L-α-aminoadipic acid.

AI Insight

Names and Identifiers

Pubchem Sid	504754920
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504754920
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（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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7 results found

Lot Number	Certificate Type	Date	Item
H1510267	Certificate of Analysis	Apr 12, 2023	Z105920
J2229626	Certificate of Analysis	Jul 12, 2022	Z105920
J2229625	Certificate of Analysis	Jul 12, 2022	Z105920
J2229624	Certificate of Analysis	Jul 12, 2022	Z105920
J2229623	Certificate of Analysis	Jul 12, 2022	Z105920
H1802043	Certificate of Analysis	Jun 13, 2022	Z105920
K2316171	Certificate of Analysis	Oct 11, 2021	Z105920

Chemical and Physical Properties

Sensitivity	Heat sensitive
Specific Rotation[α]	-13° (C=2,0.2mol/L HCl)
Melt Point(°C)	226-231 °C
Molecular Weight	280.320 g/mol
XLogP3	-1.100
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	9
Exact Mass	280.142 Da
Monoisotopic Mass	280.142 Da
Topological Polar Surface Area	102.000 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	304.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Safety and Hazards(GHS)

WGK Germany	3
Reaxy-Rn	2153826

Specifications

Specification Sheet

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Shan Li, Haifeng Wu, Yuanxi Liu, Baoli Zhang, Shichao Xu, Zhen-Gang Wang. (2023) Oxidase-Mimetic Nanocatalyst Based on Geometry-Dependent Biomolecular Self-Assembly. CHEMISTRY OF MATERIALS, [PMID:] [10.1021/acs.chemmater.3c02028]

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]
7. Shan Li, Haifeng Wu, Yuanxi Liu, Baoli Zhang, Shichao Xu, Zhen-Gang Wang. (2023) Oxidase-Mimetic Nanocatalyst Based on Geometry-Dependent Biomolecular Self-Assembly. CHEMISTRY OF MATERIALS, [PMID:] [10.1021/acs.chemmater.3c02028]

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