138576
1-Adamantylamine
97%
Synonym(s):
1-Aminoadamantane
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About This Item
Empirical Formula (Hill Notation):
C10H17N
CAS Number:
Molecular Weight:
151.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-201-2
Beilstein/REAXYS Number:
2204333
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
206-208 °C (lit.)
solubility
1 M HCl: soluble 5%, clear to hazy, colorless to faint yellow or tan
SMILES string
NC12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI
1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2/t7-,8+,9-,10-
InChI key
DKNWSYNQZKUICI-CHIWXEEVSA-N
Gene Information
human ... GRIN2A(2903)
General description
1-Adamantylamine, also known as Amantadine, is an adamantane derivative where an amino group is replaced by one of the methyl groups of adamantane. It is commonly used as a starting material in various organic reaction, such as monomer synthesis and one-pot synthesis of 1-adamantylhydrazine.
Application
1-Adamantylaminecan be used as a reactant to synthesize:
- Adamantyl ureas by reacting with isocyanates in the presence of triethylamine.
- N-(1-adamantyl)-2-chloroacetamide from chloroacetyl chloride in the presence of potassium carbonate.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Zari Hooshyar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 144-150 (2016-09-18)
In this study, we describe the synthesis of a new quantum dots (QDs) by embedding glutathione capped CdTe/ZnS QDs into cationic starch biopolymer (CS-GSH-CdTe/ZnS QDs). The fluorescence intensity of prepared QDs was significantly enhanced. When QDs interacted with rifampicin, the
Adsorption isotherms and ideal selectivities of hydrogen sulfide and carbon dioxide over methane for the Si-CHA zeolite: comparison of carbon dioxide and methane adsorption with the all-silica DD3R zeolite.
Maghsoudi H, et al.
Adsorption, 19(5), 1045-1053 (2013)
Torsten Arndt et al.
Clinica chimica acta; international journal of clinical chemistry, 359(1-2), 125-131 (2005-05-26)
Amantadine (1-adamantylamine) is used for treatment of influenza, hepatitis C, parkinsonism, and multiple sclerosis. Current amantadine analysis by HPLC or gas chromatography (GC) requires a laborious sample pretreatment with extraction and/or derivatization steps. We established an LC-MS/MS method without protein
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 138576-25G | 04061838732354 |
| 138576-5G | 04061838732361 |
| 138576-100G | 04061838732347 |
| 138576-500G | 04061833498651 |