ChemicalBook >> CAS DataBase List >>8-Hydroxyjulolidine

8-Hydroxyjulolidine

CAS No.
41175-50-2
Chemical Name:
8-Hydroxyjulolidine
Synonyms
2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLIN-8-OL;8-HJ;AKOS BBS-00000819;TIMTEC-BB SBB006615;8-Hydroxyjulolidine;8-HydroxyIulolidineHCl;8-Hydroxyjulolidine>8-Hydroxyjulolidine,98%;8-HYDROXYJULOLIDINE HYDROCHLORIDE;2,3,6,7-TETRAHYDRO-1H,5H-BENZO[I,J]-QUIN
CBNumber:
CB8445281
Molecular Formula:
C12H15NO
Molecular Weight:
189.25
MDL Number:
MFCD00006918
MOL File:
41175-50-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:55:43

8-Hydroxyjulolidine Properties

Melting point 132-134 °C(lit.)
Boiling point 374.4±41.0 °C(Predicted)
Density 1.22±0.1 g/cm3(Predicted)
storage temp. room temp
solubility Chloroform (Slightly), Methanol (Slightly)
pka 11.25±0.20(Predicted)
form Solid
color White to Pink
Water Solubility Soluble in water (partly), ethanol, chloroform, methanol, and acetone.
BRN 1530423
Major Application diagnostic assay manufacturing
hematology
histology
InChI InChI=1S/C12H15NO/c14-11-6-5-9-3-1-7-13-8-2-4-10(11)12(9)13/h5-6,14H,1-4,7-8H2
InChIKey FOFUWJNBAQJABO-UHFFFAOYSA-N
SMILES C12=CC=C(O)C3=C1N(CCC3)CCC2
CAS DataBase Reference 41175-50-2(CAS DataBase Reference)
FDA UNII SDF5635X33
EPA Substance Registry System 1H,5H-Benzo[ij]quinolizin-8-ol, 2,3,6,7-tetrahydro- (41175-50-2)
UNSPSC Code 12352104
NACRES NA.47

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-37/39-26-36
WGK Germany  3
10
TSCA  TSCA listed
HS Code  2933 99 80
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

8-Hydroxyjulolidine price More Price(57)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 249394 8-Hydroxyjulolidine 97% 41175-50-2 1g $112 2026-04-30 Buy
Sigma-Aldrich 249394 8-Hydroxyjulolidine 97% 41175-50-2 5g $382 2026-04-30 Buy
TCI Chemical H0928 8-Hydroxyjulolidine >97.0%(HPLC)(T) 41175-50-2 1g $55 2026-04-30 Buy
TCI Chemical H0928 8-Hydroxyjulolidine >97.0%(HPLC)(T) 41175-50-2 5g $187 2026-04-30 Buy
TRC TRC-H943675-2.5G 8-Hydroxyjulolidine 41175-50-2 2.5g $75 2026-06-03 Buy
Product number Packaging Price Buy
249394 1g $112 Buy
249394 5g $382 Buy
H0928 1g $55 Buy
H0928 5g $187 Buy
TRC-H943675-2.5G 2.5g $75 Buy

8-Hydroxyjulolidine Chemical Properties, Uses, Production

Chemical Properties

pink to beige or brown fine crystalline powder

Uses

8-Hydroxyjulolidine is used as an intermediate in the preparation of aminocoumarins via microwave-accelerated Pechmann reaction. It is also employed as a starting material for coumarin C-ribosides.

Uses

8-Hydroxyjulolidine has been used in the electrochemical switching fluorescence study.

General Description

The carboxaldehyde derivative of 8-hydroxyjulolidine is useful as a chromophore in fluorescence chemosensor and chemosensors.

Synthesis

8-Methoxyjulolidine

63468-83-7

8-HYDROXYJULOLIDINE

41175-50-2

The general procedure for the synthesis of 1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol from 8-methoxyjulolidine was as follows: 8-methoxyjulolidine (10 g, 50 mmol) was dissolved in a mixed solution consisting of 50 mL of 47% hydriodic acid, 80 mL of concentrated hydrochloric acid and 200 mL of water. The reaction mixture was heated to reflux and the progress of the reaction was monitored by thin layer chromatography (TLC). After 15 hours of reaction, 50 mL of concentrated hydrochloric acid was added to the mixture. The total reaction time was 60 hours. Upon completion of the reaction, the solution was cooled in an ice bath and first neutralized to pH 6 with 50% sodium hydroxide solution, followed by the addition of phosphate buffer (prepared by dissolving 6.9 g NaH2PO4-H2O and 1.4 g Na2HPO4 in 100 mL of water). The product was extracted with dichloromethane and the organic phase was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The resulting crude product was redissolved in dichloromethane and extracted repeatedly with 10% sodium hydroxide solution until the aqueous phase was colorless. Subsequently, the organic phase was acidified, dried and extracted again, and the solvent was removed as described above, resulting in the product 1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol (6.24 g) in 67% yield and with a melting point of 126-130°C. The product was extracted with sodium sulfate under reduced pressure.

References

[1] Journal of Organic Chemistry, 1987, vol. 52, # 8, p. 1465 - 1468
[2] Journal of Fluorescence, 2015, vol. 25, # 6, p. 1615 - 1628
[3] Chemical Communications, 2011, vol. 47, # 47, p. 12691 - 12693
[4] Chemistry - A European Journal, 2014, vol. 20, # 12, p. 3510 - 3519
[5] Patent: US2018/280543, 2018, A1. Location in patent: Paragraph 0041; 0098

8-Hydroxyjulolidine Preparation Products And Raw materials

Global Suppliers ( 250)
Supplier Tel Email Country ProdList Advantage
Shanghai ChuangYan Chemical Technology Co., Ltd. 021-11111111 11111111111 546919421@qq.com China 3770 55
Shanghai joygo pharmacetical tech., Co., Ltd. 13621615409 sale1@joygooo.com China 108 50
Zhongxin Chenshi (Wuhan) Technology Co., Ltd 18942922096 2662561040@qq.com China 980 58
Hunan HuaTeng Pharmaceutical Co., Ltd., 400-8592883 15367835770 sales@huatengsci.com China 5869 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Syntechem Co.,Ltd info@syntechem.com China 12973 57

View Latest Price from 8-Hydroxyjulolidine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
8-Hydroxyjulolidine pictures 2026-09-02 8-Hydroxyjulolidine
41175-50-2
$1.00-200.00 1KG 99%, 99.5% Sublimated Henan Fengda Chemical Co., Ltd
8-HYDROXYJULOLIDINE pictures 2026-06-30 8-HYDROXYJULOLIDINE
41175-50-2
1kg 98% Shaanxi Dideu New Materials Co. Ltd
8-HYDROXYJULOLIDINE pictures 2025-12-24 8-HYDROXYJULOLIDINE
41175-50-2
1KG 98.0% 10 Shaanxi Dideu Medichem Co. Ltd
2,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-ol 97% AKOS BBS-00000819 8-HYDROXY-2,3,6,7-TETRAHYDRO-1H,5H-BENZO[IJ]QUINOLIZINE 8-HYDROXYJULOLIDINE HYDROCHLORIDE 2,3,6,7-TETRAHYDRO-1H,5H-BENZO[IJ]QUINOLIZIN-8-OL 8-HydroxyIulolidineHCl 1H,5H-Benzoijquinolizin-8-ol, 2,3,6,7-tetrahydro- 8-Hydroxyjulolidine,98% 2,3,6,7-TETRAHYDRO-1H,5H-BENZO[I,J]-QUIN 1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quinolin-8-ol 2,3,6,7-Tetrahydro-1H,5H-benzo[i,j]-quinolizin-8-ol for synthesis 2,3,6,7-Tetrahydro-1H,5H-benzop[ij]quinolizine-8-ol TIMTEC-BB SBB006615 ,3,6,7-Tetrahydro-1H,5H-benzo(ij)quinolizin-8-ol ,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-ol 5h-benzo[ij]quinolizin-8-ol,2,3,6,7-tetrahydro-1 8-Hydroxyjulolidine> 1,2,3,5,6,7-Hexahydropyrido[3,2,1-ij]quin 1-azatricyclo[7.3.1.0?13]trideca-5(13),6,8-trien-6-ol 1-azatricyclo7.3.1.0^{5,13}trideca-5,7,9(13)-trien-6-ol 8-HJ 2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLIN-8-OL 8-Hydroxyjulolidine 41175-50-2 ALCOHOL Building Blocks Organic Building Blocks Oxygen Compounds Phenols