2-Adamantylamine hydrochloride - 98%, high purity , CAS No.10523-68-9

  • ≥98%
Item Number
A113976
Grouped product items
SKUSizeAvailabilityPrice Qty
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

Basic Description

Synonyms2-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
Specifications & Purity≥98%
Shipped InNormal
Note25g、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.

Associated Targets(Human)

GRIN3A Tclin Glutamate receptor ionotropic, NMDA 3A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Influenza B virus (2113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
H2N2 subtype (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M Matrix protein 2 (436 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid488182961
Pubchem Sid Urlhttps://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

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

14 results found

Lot NumberCertificate TypeDateItem
G2404150Certificate of AnalysisApr 27, 2024 A113976
G2404151Certificate of AnalysisApr 27, 2024 A113976
G2404153Certificate of AnalysisApr 27, 2024 A113976
A2415048Certificate of AnalysisNov 23, 2023 A113976
A2415049Certificate of AnalysisNov 23, 2023 A113976
A2415050Certificate of AnalysisNov 23, 2023 A113976
H1408047Certificate of AnalysisJun 08, 2022 A113976
H1408046Certificate of AnalysisJun 08, 2022 A113976
C1414060Certificate of AnalysisFeb 23, 2022 A113976
A2225024Certificate of AnalysisDec 27, 2021 A113976
A2225025Certificate of AnalysisDec 27, 2021 A113976
A2225047Certificate of AnalysisDec 27, 2021 A113976
E2311298Certificate of AnalysisDec 27, 2021 A113976
E2311308Certificate of AnalysisDec 27, 2021 A113976

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Chemical and Physical Properties

SolubilitySoluble in water
Melt Point(°C)300°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
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

Related Documents

Citations of This Product

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]

References

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]

Solution Calculators