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
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
≥99.0%
储存温度
2-8°C
SMILES字符串
Cl[H].NC1CCCCNC1=O
InChI
1S/C6H12N2O.ClH/c7-5-3-1-2-4-8-6(5)9;/h5H,1-4,7H2,(H,8,9);1H
InChI key
LWXJCGXAYXXXRU-UHFFFAOYSA-N
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应用
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.
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
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)
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