Cas no 90-45-9 (9-Aminoacridine)

9-Aminoacridine structure

Product Name:9-Aminoacridine

CAS No:90-45-9

MF:C₁₃H₁₀N₂

MW:194.231902599335

MDL:MFCD00037839

CID:806361

PubChem ID:7019

Update Time:2024-10-26

9-Aminoacridine Chemical and Physical Properties

Names and Identifiers

- Acridin-9-amine
- 9-Acridinylamine
- 9-Aminoacridine
- 9-Acridinamine
- 9-Aminoacridine hemihydrate
- Aminacrine
- Aminoacridine
- 9-AA (purified by sublimation)
- 9-AA
- 9AA
- Aminacrin
- Izoacridina
- Monacrin
- NSC 13000
- NSC 28747
- 10-Amino-5-azaanthracene
- Aminoacridinum
- Aminoacridina
- 9-Aminoakridin
- Acridine, 9-amino-
- 9-Aminoacridin
- 9(10H)-Acridinimine
- 9-Aminoakridin [Czech]
- Aminoacridine [INN:BAN]
- Acridin-9-ylamine
- 78OY3Z0P7Z
- XJGFWWJLMVZSIG-UHFFFAOYSA-N
- acridine-9-ylamine
- Mykocert
- Aminopt
- AK10
- Acridine, 9-amino- (8CI)
- MeSH ID: D000585
- NSC-13000
- KBio1_001901
- 9-Aminoacridine, matrix substance for MALDI-MS, >=99.5% (HPLC)
- 8AD
- NCGC00094857-03
- acridin-9-yl-amine
- CS-4915
- BRD-K00535541-001-05-5
- AC2194
- AB00052180_10
- DTXSID2024456
- iminoacridan
- CS-003/03975023
- KBio2_001588
- MLS000780068
- MFCD00037839
- NSC-757794
- BCP25849
- NCGC00094857-06
- XJGFWWJLMVZSIG-UHFFFAOYSA-
- BSPBio_002154
- STK387428
- cid_2723598
- NSC13000
- CHEMBL43184
- 5-Aminoacridine
- HY-B1422
- AI3-51012
- D08AA02
- CCG-39037
- SR-01000760844
- 110166-26-2
- NCGC00094857-01
- KBio3_001654
- Spectrum5_001498
- NSC28747
- KBio2_006724
- SPECTRUM1500810
- SBI-0051612.P002
- CHEBI:74789
- EN300-17076
- AKOS000120447
- 90-45-9
- BIDD:GT0816
- Spectrum4_000580
- KBioGR_001020
- SPBio_001244
- BRD-K00535541-001-04-8
- CU-01000012501-2
- NS00005526
- SY039786
- ALBB-020726
- DB-220082
- 9-Amino-acridine
- AS-17405
- HMS1921I16
- UNII-78OY3Z0P7Z
- DTXCID104456
- Aminoacrine
- SpecPlus_000861
- NSC757794
- 9 Aminoacridine
- 4bds
- SR-01000760844-2
- DB11561
- KBioSS_001588
- BRD-K00535541-311-04-1
- AMINOACRIDINE [WHO-DD]
- 7AD
- BRD-K00535541-001-06-3
- BDBM72700
- NCGC00094857-02
- AMINOACRIDINE [INN]
- Aminoacrid
- Acramine Yellow (Salt/Mix)
- Mycosert (Salt/Mix)
- AMINACRINE [MI]
- 9-amino acridine
- KBio2_004156
- BRN 0141171
- 9-Amino-acridin
- Spectrum_001108
- Spectrum2_001112
- Pharmakon1600-01500810
- BRD-K00535541-001-02-2
- s4303
- EINECS 201-995-6
- 9-Aminoacridine (purified by sublimation)
- DB-026983
- 9-Aminoacridine free base
- SCHEMBL14999
- HMS3715H04
- A3298
- SW219793-1
- AMINACRINE [VANDF]
- NSC-28747
- NSC 7571
- WLN: T C666 BNJ IZ
- DivK1c_006957
- 65944-23-2
- CCRIS 748
- 9-Aminoacridine, 97%
- Quench (Salt/Mix)
- 9-acridinamine;hydrate;hydrochloride
- AB00052180_09
- Spectrum3_000617
- Hydrochloride, Aminoacridine
- HMS2092K22
- acridin-9-ylamine;hydrate;hydrochloride
- Q513937
- SMR000420251
- MDL： MFCD00037839
- Inchi： 1S/C13H10N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H,(H2,14,15)
- InChI Key： XJGFWWJLMVZSIG-UHFFFAOYSA-N
- SMILES： N1C2C(=CC=CC=2)C(N)=C2C=1C=CC=C2
- BRN： 0141171

Computed Properties

Exact Mass: 194.08400
Monoisotopic Mass: 194.084398327g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Heavy Atom Count: 15
Rotatable Bond Count: 0
Complexity: 207
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Topological Polar Surface Area: 38.9
Surface Charge: 0
Tautomer Count: 2
XLogP3: 2.8

Experimental Properties

Color/Form: Yellow needle like crystals. Medium strength alkaline
Density: 1.268
Melting Point: 236.0 to 240.0 deg-C
Boiling Point: 320.68°C (rough estimate)
Refractive Index: 1.5014 (estimate)
Solubility: ethanol: hazy
Stability/Shelf Life: Stable. Incompatible with strong oxidizing agents.
PSA: 38.91000
LogP: 3.55140
Merck: 407
pka: 9.99(at 20℃)
λmax: 406nm(DMF)(lit.)
Solubility: Soluble in ethanol, acetone and chloroform

9-Aminoacridine Security Information

Symbol:
Prompt：warning
Signal Word：Warning
Hazard Statement： H302-H315-H319
Warning Statement： P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501
Hazardous Material transportation number：2811
WGK Germany：3
Hazard Category Code： 36/37/38
Safety Instruction： S26; S36
RTECS：AR7300000
Hazardous Material Identification：
HazardClass：6.1(b)
PackingGroup：III
Storage Condition：Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
Safety Term：6.1(b)
Packing Group：III
Risk Phrases：R36/37/38

9-Aminoacridine Pricemore >>

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TRC	A190880-1g	9-Aminoacridine	90-45-9		1g	$ 110.00	2023-09-09
TRC	A190880-2g	9-Aminoacridine	90-45-9		2g	$ 145.00	2022-06-08
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S e l l e c k ZHONG GUO	S4303-25mg	9-Aminoacridine	90-45-9	99.87%	25mg	￥794.48	2023-09-16
S e l l e c k ZHONG GUO	S4303-50mg	9-Aminoacridine	90-45-9	99.87%	50mg	￥1392.3	2022-04-26
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ChemScence	CS-4915-5g	9-Aminoacridine	90-45-9	99.50%	5g	$70.0	2022-04-26

9-Aminoacridine Production Method

Production Method 1

90-45-9

Reaction Conditions

1.1 Reagents: Urea , Sodium hydride Solvents: Dimethyl sulfoxide ; rt
1.2 24 h, rt
1.3 Solvents: Water ; rt

Reference

: Direct and facile synthesis of 9-aminoacridine and acridin-9-yl-ureas

Borovlev, Ivan V.; et al, Tetrahedron Letters, 2016, 57(32), 3608-3611

Production Method 2

90-45-9

Reaction Conditions

1.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP1A1 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 3

21330-56-3

90-45-9

Reaction Conditions

1.1 Reagents: Hydrogen sulfide

Reference

: Real-time quantification of nuclear RNA export using an intracellular relocation probe

Shen, Jie; et al, Chinese Chemical Letters, 2022, 33(8), 3865-3868

Production Method 4

74054-24-3

90-45-9

Reaction Conditions

1.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP1A1 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 5

77472-50-5

90-45-9

Reaction Conditions

1.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP1A1 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 6

94129-62-1

90-45-9

Reaction Conditions

1.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP2D6 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 7

10399-73-2

90-45-9

Reaction Conditions

1.1 Reagents: Phosphorus pentachloride
2.1 Reagents: Phenol , Ammonium carbonate

Reference

: Preparation of 9-amino-1,2,3,4-tetrahydroacridines as agents for treatment of Alzheimer's disease

, Japan, , ,

Production Method 8

1207-69-8

90-45-9

Reaction Conditions

1.1 Solvents: Chloroform , Phenol ; rt → -10 °C; -10 °C; 1 h, -10 °C; -10 °C → rt; 2 h, rt; rt → 55 °C; overnight, 50 - 55 °C
1.2 Reagents: Hydrochloric acid
2.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP1A1 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 9

1207-69-8

90-45-9

Reaction Conditions

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

Production Method 10

134-50-9

90-45-9

Reaction Conditions

1.1 Reagents: Potassium hydroxide

Reference

: Fluorogenic, specific detection of sarin gas mimic, diethylchlorophosphate

Rahman, Ziaur ; et al, Journal of Photochemistry and Photobiology, 2023, 444,

Production Method 11

90-45-9

Reaction Conditions

1.1 Solvents: Xylene ; 1 h, reflux

Reference

: Direct and facile synthesis of 9-aminoacridine and acridin-9-yl-ureas

Borovlev, Ivan V.; et al, Tetrahedron Letters, 2016, 57(32), 3608-3611

Production Method 12

90-45-9

Reaction Conditions

1.1 Reagents: Sodium, (2,2-dimethylhydrazino)- Solvents: Benzene

Reference

: Terpenes as constituents of fats. II. Constitution of kahweol. 1

Kaufmann, H. P.; et al, Chemische Berichte, 1963, 96(9), 2489-98

Production Method 13

90-45-9

Reaction Conditions

1.1 Reagents: Sodium hydrazide (Na(N2H3))

Reference

: Sodium hydrazide

Kauffmann, Thomas, e-EROS Encyclopedia of Reagents for Organic Synthesis, 2001, 1, 1-2

Production Method 14

2042-37-7

90-45-9

Reaction Conditions

1.1 Reagents: Cesium carbonate Catalysts: Palladium diacetate , BINAP Solvents: Toluene ; 15 h, 100 °C; 100 °C → 0 °C
1.2 Reagents: Boron trifluoride etherate ; 0 °C; 24 h, 100 °C

Reference

: Pd-catalyzed one-pot approach for installation of 9-aminoacridines via Buchwald-Hartwig amination and cycloaromatization

Gopalaiah, Kovuru; et al, ARKIVOC (Gainesville, 2022, (6), 24-37

Production Method 15

90-45-9

Reaction Conditions

1.1 Reagents: Hydrochloric acid Solvents: Water

Reference

: Studies on thiazolidinones. Part XV. Synthesis of thiazolidinones from mono- and disubstituted thioureas possessing alicyclic and heterocyclic substituents

Sahu, J.; et al, Journal of the Indian Chemical Society, 1985, 62(1), 71-3

Production Method 16

20141-87-1

90-45-9

Reaction Conditions

1.1 Catalysts: Aniline

Reference

: Synthesis of pyridinium heterocyclic ylides. Degradation of the pyridinium group

Esteve, Marta E.; et al, Journal of Heterocyclic Chemistry, 1981, 18(5), 1061-3

Production Method 17

22739-29-3

90-45-9

Reaction Conditions

1.1 Reagents: NADPH Catalysts: Cytochrome P450 CYP2D6 Solvents: Dimethyl sulfoxide , Water ; pH 7.2, 30 °C

Reference

: A real-time fluorescence assay for measuring N-dealkylation

Mayer, Richard T.; et al, Drug Metabolism and Disposition, 2007, 35(1), 103-109

9-Aminoacridine Raw materials

9-Aminoacridine Preparation Products

9-Aminoacridine (90-45-9)

9-Aminoacridine Suppliers

Suzhou Senfeida Chemical Co., Ltd

Gold Member

Audited Supplier

(CAS:90-45-9)9-Aminoacridine

Order Number:1682724;sfd17142

Stock Status:in Stock

Quantity:Company Customization/200kg

Purity:98%/99.9%

Pricing Information Last Updated:Monday, 14 April 2025 18:21

Price ($):discuss personally

Email:[email protected]

Tiancheng Chemical (Jiangsu) Co., Ltd

Gold Member

Audited Supplier

(CAS:90-45-9)9-氨基吖啶

Order Number:LE1682724

Stock Status:in Stock

Quantity:25KG,200KG,1000KG

Purity:99%

Pricing Information Last Updated:Friday, 20 June 2025 12:32

Price ($):discuss personally

Email:[email protected]

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2. An approach to C–N activation: coupling of arenesulfonyl hydrazides and arenesulfonyl chlorides with tert-amines via a metal-, oxidant- and halogen-free anodic oxidation??

M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
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Related Categories

90-45-9 (9-Aminoacridine) Related Products

Recommended suppliers

Suzhou Senfeida Chemical Co., Ltd

(CAS:90-45-9)9-Aminoacridine

Purity:98%/99.9%

Quantity:Company Customization/200kg

Price ($):Inquiry/Inquiry

Tiancheng Chemical (Jiangsu) Co., Ltd

(CAS:90-45-9)9-氨基吖啶

Purity:99%

Quantity:25KG,200KG,1000KG

Price ($):Inquiry

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Cas no 90-45-9 (9-Aminoacridine)

9-Aminoacridine Chemical and Physical Properties

Names and Identifiers

Computed Properties

Experimental Properties

9-Aminoacridine Security Information

9-Aminoacridine Pricemore >>

9-Aminoacridine Production Method

Production Method 1

Production Method 2

Production Method 3

Production Method 4

Production Method 5

Production Method 6

Production Method 7

Production Method 8

Production Method 9

Production Method 10

Production Method 11

Production Method 12

Production Method 13

Production Method 14

Production Method 15

Production Method 16

Production Method 17

9-Aminoacridine Raw materials

9-Aminoacridine Preparation Products

9-Aminoacridine Suppliers

9-Aminoacridine Related Literature

Related Categories

90-45-9 (9-Aminoacridine) Related Products