2-Amino-9H-pyrido[2-3-b]indole - ≥98% , CAS No.26148-68-5

CAS: 26148-68-5 Cat. No.: A169118 Molecular Weight: 183.21 EC Number: 811-637-6
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
HSDB 7086 | 2-Amino-a-carboline | BRN 0744369 | CCRIS 38 | AMINO-9H-PYRIDO(2,3-B)INDOLE, 2- | J-016280 | 9H-PYRIDO(2,3-B)INDOL-2-AMINE | FJTNLJLPLJDTRM-UHFFFAOYSA-N | 2-AMINO-9H-PYRIDO(2,3-B)INDOLE [HSDB] | A818215 | Q27155854 | 2-Amino-alpha-carboline;Aa
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
A169118-5mg
3
$38.90
25mg
A169118-25mg
3
$108.90
100mg
A169118-100mg
2
$339.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
HSDB 7086 | 2-Amino-a-carboline | BRN 0744369 | CCRIS 38 | AMINO-9H-PYRIDO(2, 3-B)INDOLE, 2- | J-016280 | 9H-PYRIDO(2, 3-B)INDOL-2-AMINE | FJTNLJLPLJDTRM-UHFFFAOYSA-N | 2-AMINO-9H-PYRIDO(2, 3-B)INDOLE [HSDB] | A818215 | Q27155854 | 2-Amino-alpha-carboline;Aa
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
AαC (2-Amino-9H-pyrido[2-3-b]indole) is a potential human carcinogen, which is generated by the combustion of tobacco, or by pyrolysis of protein. AαC potentially contributes to liver or digestive tract cancers. Inside body AαC is metabolized to intermedi
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Canonical SmilesC1=CC=C2C(=C1)C3=C(N2)N=C(C=C3)N
IUPAC Name9H-pyrido[2,3-b]indol-2-amine
InChIKeyFJTNLJLPLJDTRM-UHFFFAOYSA-N
INCHI1S/C11H9N3/c12-10-6-5-8-7-3-1-2-4-9(7)13-11(8)14-10/h1-6H,(H3,12,13,14)
Isomeric SMILES C1=CC=C2C(=C1)C3=C(N2)N=C(C=C3)N
Molecular Weight 183.21
Reaxy-Rn 744369
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=744369&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassIndoles and derivatives
SubclassPyridoindoles
Intermediate Tree Nodes Not available
Direct ParentAlpha carbolines
Alternative Parents Pyrrolopyridines  Indoles  Pyridines and derivatives  Imidolactams  Benzenoids  Pyrroles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Alpha-carboline - Pyrrolopyridine - Indole - Imidolactam - Benzenoid - Pyridine - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha carbolines. These are organic compounds containing a pyrido[2,3-b]indole core (which is a pyridine fused to an indole).
External Descriptors pyridoindole
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA5A Tclin Carbonic anhydrase 5A, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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

3 results found

Lot NumberCertificate TypeDateItem
J2310021Certificate of AnalysisSep 20, 2023 A169118
J2310022Certificate of AnalysisSep 20, 2023 A169118
J2310023Certificate of AnalysisSep 20, 2023 A169118
Chemical and Physical Properties
SensitivityAir Sensitive,Heat Sensitive
Boil Point(°C)441 °C
Melt Point(°C)201 °C
Molecular Weight183.210 g/mol
XLogP32.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass183.08 Da
Monoisotopic Mass183.08 Da
Topological Polar Surface Area54.700 Ų
Heavy Atom Count14
Formal Charge0
Complexity219.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Peijian Sun, Yipeng Wang, Song Yang, Xuehui Sun, Bin Peng, Lining Pan, Yunzhen Jia, Xiaobing Zhang, Cong Nie.  (2023)  Molecularly Imprinted Polymer Nanospheres with Hydrophilic Shells for Efficient Molecular Recognition of Heterocyclic Aromatic Amines in Aqueous Solution.  MOLECULES,  28  (5): (2052).  [PMID:36903298] [10.3390/molecules28052052]
2. Xiaohan Zang, Yongcheng Wang, Cong Han, Lishuang Cui, Haojie Liu, Shuimiao Tian, Kechun Liu, Peihai Li, Chen Sun, Qing Xia, Yun Zhang.  (2024)  2-Acetamidophenol (2-AAP) Suppresses the Progression of Atherosclerosis by Alleviating Hyperlipidemia and Attenuating the Ferroptosis Pathway.  Marine Drugs,  22  (11): (513).  [PMID:39590793] [10.3390/md22110513]
3. Junhao Cui, Zhiyang Zhao, Yongqi Ren, Bailong Chen, Chase Rheinlander, Antonio Xavier Moore, Longzhi Li.  (2024)  Excellent cycle stability of Fe loaded on N-doped activated carbon for microwave hydrogenolysis of lignin.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.158001]
4. Hina Ramzan, Faiqa Nadeem, Muhammad Usman, Muhammad Shahzaib, Muneeb Ur Rahman, Fuhua Shen, Zhiping Zhang, Reeta Rani Singhania, Farzana Jabeen, Waheed Afzal, Nadeem Tahir.  (2024)  Investigating the quantum size effects of multi-walled carbon nanotubes (MWCNTs) in photocatalytic fermentative biohydrogen production.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2024.141738]
5. Xiaobo Li, Kaifeng Yang, Fangming Han, Yafeng Jin, Haonan Zhang, Heng Gao.  (2024)  Simultaneous and sensitive detection of dopamine and acetaminophen at a glassy carbon electrode modified with a carbonized-ZIF-67/Super P nanocomposite.  NEW JOURNAL OF CHEMISTRY,  48  (7): (3294-3303).  [PMID:] [10.1039/D3NJ05135H]
6. Jie Kang, Jiangyi Di, Hao Zhang, Yuting Hao, Yongqin Guo, Zixin Tian, Shuang Zhao.  (2024)  Simultaneous voltammetric detection of acetaminophen and levofloxacin based on barley leaves derived carbon decorated with gold nanoparticles.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111335]
7. Yu-Ting Cao, Shuai-Wei Lu, Yu-hang Zhou, Jun Wei.  (2024)  The synthesis and research of a novel organosilicon-modified waterborne blocked polyisocyanate crosslinker with a semi-interpenetrating network structure.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2024.108413]
Solution Calculators
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