Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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A113976-1g | 1g | In stock | $21.90 | |
A113976-5g | 5g | In stock | $84.90 | |
A113976-25g | 25g | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $291.90 |
Synonyms | 2-Aminoadamantane hydrochloride; Tricyclo[3.3.1.1(3.7)]dec-2-ylamine hydrochloride;Adamantan-2-amine hydrochloride | AKOS017343998 | MFCD00074743 | A0718 | Adamantan-2-amine HCl | AKOS000104803 | SY011241 | W-204551 | 2-adamantan amine HCl | 2-Adamantylam |
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Specifications & Purity | ≥98% |
Shipped In | Normal |
Note | 25g、1g卖完停产,不再备货 |
Product Description | Product Description The HPLC assay of 2-adamantylamine hydrochloride after pre-column derivatization with 4-fluoro-7-nitro-2,1,3-benzoxadiazole has been studied. Product Application 2-Adamantylamine hydrochloride was used to prepare 2-adamantylamide of 2'-(carboxymethoxime)-olivomycin I. The HPLC assay of 2-adamantylamine hydrochloride after pre-column derivatization with 4-fluoro-7-nitro-2,1,3-benzoxadiazole has been studied. It is also used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Pubchem Sid | 488182961 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488182961 |
IUPAC Name | adamantan-2-amine;hydrochloride |
INCHI | InChI=1S/C10H17N.ClH/c11-10-8-2-6-1-7(4-8)5-9(10)3-6;/h6-10H,1-5,11H2;1H |
InChi Key | WLDWDRZITJEWRJ-UHFFFAOYSA-N |
Canonical SMILES | C1C2CC3CC1CC(C2)C3N.Cl |
Isomeric SMILES | C1C2CC3CC1CC(C2)C3N.Cl |
WGK Germany | 3 |
RTECS | AU4375100 |
PubChem CID | 25331 |
Molecular Weight | 187.71 |
Beilstein | 4297901 |
Reaxy-Rn | 4297901 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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G2404150 | Certificate of Analysis | Apr 27, 2024 | A113976 |
G2404151 | Certificate of Analysis | Apr 27, 2024 | A113976 |
G2404153 | Certificate of Analysis | Apr 27, 2024 | A113976 |
A2415048 | Certificate of Analysis | Nov 23, 2023 | A113976 |
A2415049 | Certificate of Analysis | Nov 23, 2023 | A113976 |
A2415050 | Certificate of Analysis | Nov 23, 2023 | A113976 |
H1408047 | Certificate of Analysis | Jun 08, 2022 | A113976 |
H1408046 | Certificate of Analysis | Jun 08, 2022 | A113976 |
C1414060 | Certificate of Analysis | Feb 23, 2022 | A113976 |
A2225024 | Certificate of Analysis | Dec 27, 2021 | A113976 |
A2225025 | Certificate of Analysis | Dec 27, 2021 | A113976 |
A2225047 | Certificate of Analysis | Dec 27, 2021 | A113976 |
E2311298 | Certificate of Analysis | Dec 27, 2021 | A113976 |
E2311308 | Certificate of Analysis | Dec 27, 2021 | A113976 |
Solubility | Soluble in water |
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Melt Point(°C) | 300°C |
Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation |
Precautionary Statements | P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P271:Use only outdoors or in a well-ventilated area. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P362+P364:Take off contaminated clothing and wash it before reuse. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help. P319:Get medical help if you feel unwell. |
WGK Germany | 3 |
RTECS | AU4375100 |
Reaxy-Rn | 4297901 |
1. Yahui Zhang, Haifeng Yao, Yongping Dong. (2024) Electrochemiluminescence of an iridium complex doped with SiO2 nanoparticles to detect 2-adamantanamine based on the host–guest interaction of cucurbit[7]uril. ANALYST, 149 (4): (1160-1168). [PMID:38167663] [10.1039/D3AN02021E] |
1. Yasuhiko Higashi,Shota Nakamura,Hiroki Matsumura,Youichi Fujii. (2005-09-15) Simultaneous liquid chromatographic assay of amantadine and its four related compounds in phosphate-buffered saline using 4-fluoro-7-nitro-2,1,3-benzoxadiazole as a fluorescent derivatization reagent.. Biomedical chromatography : BMC, 20 ((5)): (423-428). [PMID:16161183] |
2. Alina A Okhina,Artem D Rogachev,Olga I Yarovaya,Mikhail V Khvostov,Tatyana G Tolstikova,Andrey G Pokrovsky,Veniamin A Khazanov,Nariman F Salakhutdinov. (2019-12-23) Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent.. Journal of pharmaceutical and biomedical analysis, 180 (113039-113039). [PMID:31865208] |
3. C Clark,M M Woodson,H T Nagasawa. (1991-01-01) Inhibition of lymphocyte proliferation by amantadine and its isomer, 2-aminoadamantane; impact on Lyt-2+ T cells while sparing L3T4+ T cells.. Immunopharmacology, 21 ((1)): (41-50). [PMID:1860784] |
4. Iu V Vakhitova,R S Iamidanov,V A Vakhitov,S B Seredenin. (2005-04-29) [DNA macroarray analysis of gene expression changes in rat brain after single administration of 2-aminoadamantane compound].. Molekuliarnaia biologiia, 39 ((2)): (276-285). [PMID:15856951] |
5. Anna N Tevyashova,Eugenia N Olsufyeva,Eugenia N Zbarsky,Jan Balzarini,Alexander A Shtil,Lyubov G Dezhenkova,Vladimir M Bukhman,Victor B Zbarsky,Maria N Preobrazhenskaya. (2009-01-10) Modification of the antibiotic olivomycin I at the 2'-keto group of the side chain. Novel derivatives, antitumor and topoisomerase I-poisoning activity.. The Journal of antibiotics, 62 ((1)): (37-41). [PMID:19132061] |
6. Yahui Zhang, Haifeng Yao, Yongping Dong. (2024) Electrochemiluminescence of an iridium complex doped with SiO2 nanoparticles to detect 2-adamantanamine based on the host–guest interaction of cucurbit[7]uril. ANALYST, 149 (4): (1160-1168). [PMID:38167663] [10.1039/D3AN02021E] |