41336
DL-α-氨基-ε-己内酰胺 盐酸盐
≥99.0%
别名:
(±)-3-氨基六氢-2H-氮杂卓-2-酮 盐酸盐, 3-氨基-2-氧代六亚基亚胺 盐酸盐, DL-赖氨酸内酰胺 盐酸盐
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关于此项目
经验公式（希尔记法）:
C6H12N2O · HCl
化学文摘社编号:
分子量:
164.63
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
DL-α-氨基-ε-己内酰胺 盐酸盐, ≥99.0%
InChI
1S/C6H12N2O.ClH/c7-5-3-1-2-4-8-6(5)9;/h5H,1-4,7H2,(H,8,9);1H
SMILES string
Cl[H].NC1CCCCNC1=O
InChI key
LWXJCGXAYXXXRU-UHFFFAOYSA-N
assay
≥99.0%
storage temp.
2-8°C
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Application
DL-α-Amino-ε-caprolactam hydrochloride may be used to prepare the optically active forms of DL-α-amino-ε-caprolactam. It may be used for the enzymatic synthesis of L-lysine by new microbial strains.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Conversion of d-and dl-a-amino-e-caprolactam into l-lysine using both yeast cells and bacterial cells.
Fukumura T.
Agricultural and Biological Chemistry, 41(8), 1327-1330 (1977)
K Plhácková et al.
Folia microbiologica, 27(6), 382-389 (1982-01-01)
The production of L-lysine from DL-alpha-amino-epsilon-caprolactam (DL-ACL) by new strains producing L-alpha-amino-epsilon-caprolactamase and aminocaprolactam racemase is described. Optimal conditions for hydrolysis of L-ACL by Cryptococcus sp. and for racemization of ACL by cells of a strain isolated in nature and
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