56207
1-Hydroxypiperidine
≥96.0% (GC)
Synonym(s):
1-Piperidinol
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About This Item
Empirical Formula (Hill Notation):
C5H11NO
CAS Number:
Molecular Weight:
101.15
Beilstein:
102726
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥96.0% (GC)
mp
37-39 °C
storage temp.
2-8°C
SMILES string
ON1CCCCC1
InChI
1S/C5H11NO/c7-6-4-2-1-3-5-6/h7H,1-5H2
InChI key
LKPFBGKZCCBZDK-UHFFFAOYSA-N
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Application
Base for Fmoc-based solid phase peptide synthesis
Light stabilizing agent
Light stabilizing agent
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
172.4 °F - closed cup
Flash Point(C)
78 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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D Y Wang et al.
Zhongguo yao li xue bao = Acta pharmacologica Sinica, 10(3), 252-256 (1989-05-01)
The biological N-oxidation of piperidine, a pharmacologically active biogenic amine of mammals and human beings, was studied in vitro. After incubation of piperidine-HCl in a fortified rat liver microsomal preparation (9000 x g supernatant) at 37 degrees C for 30
Akimitsu Miyaji et al.
Biochemical and biophysical research communications, 483(1), 178-182 (2017-01-04)
The dissociation of water molecules by ultrasound irradiation under aerobic conditions was demonstrated experimentally. To be able to detect the dissociation of water molecules, we performed the ultrasound irradiation of
Shipra Grover et al.
ACS infectious diseases, 7(1), 141-152 (2020-12-16)
MmpL3, an essential mycolate transporter in the inner membrane of Mycobacterium tuberculosis (Mtb), has been identified as a target of multiple, chemically diverse antitubercular drugs. However, several of these molecules seem to have secondary targets and inhibit bacterial growth by
Robert J Greenstein et al.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 13(5), e254-e263 (2009-03-24)
Without known mechanisms of action, thalidomide is used to treat a variety of non-malignant 'idiopathic' diseases. There is increasing concern that Mycobacterium avium subspecies paratuberculosis (MAP) may be zoonotic. Recently, methotrexate, azathioprine, 6-mercaptopurine (6-MP), 5-aminosalicylic acid (5-ASA), cyclosporine A, rapamycin
Areej Abuhammad et al.
PloS one, 7(12), e52790-e52790 (2013-01-04)
Latent M. tuberculosis infection presents one of the major obstacles in the global eradication of tuberculosis (TB). Cholesterol plays a critical role in the persistence of M. tuberculosis within the macrophage during latent infection. Catabolism of cholesterol contributes to the
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