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R-tetrahydropapaverine HCl

Product Name
R-tetrahydropapaverine HCl
CAS No.
54417-53-7
Chemical Name
R-tetrahydropapaverine HCl
Synonyms
R-BINAP;R-Tetrahydropapaverine;R-(+)-Tetrahydropapaverin;R-tetrahydropapaverine HC;R-tetrahydropapaverine HCl;R-TATRAHYDROPAPAVERINE HCL;Atracurium Besylate Impurity 7;D-(-)-Norlaudanosine hydrochloride;Cisatracurium Besilate Impurity 19;(R)-(-)-Norlaudanosine hydrochloride
CBNumber
CB5718052
Molecular Formula
C20H26ClNO4
Formula Weight
379.88
MOL File
54417-53-7.mol
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R-tetrahydropapaverine HCl Property

Boiling point:
475.8℃
Density 
1.32 at 22℃
vapor pressure 
0Pa at 25℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
InChI
InChI=1/C20H25NO4.ClH/c1-22-17-6-5-13(10-18(17)23-2)9-16-15-12-20(25-4)19(24-3)11-14(15)7-8-21-16;/h5-6,10-12,16,21H,7-9H2,1-4H3;1H/t16-;/s3
InChIKey
VMPLLPIDRGXFTQ-LSQUZMQTNA-N
SMILES
C(C1C=CC(OC)=C(OC)C=1)[C@H]1NCCC2=CC(OC)=C(OC)C=C12.Cl |&1:11,r|
LogP
-0.63 at 25℃
CAS DataBase Reference
54417-53-7(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
22-52/53
Safety Statements 
22-61
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

AK Scientific
Product number
B660
Product name
R-TetrahydropapaverineHCl
Packaging
5g
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD132887
Product name
1-(3,4-Dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydroiodide
Packaging
10g
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD132887
Product name
1-(3,4-Dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydroiodide
Packaging
25g
Price
$145
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
47940
Product name
(R)-(-)-NorlaudanosineHCl
Packaging
100mg
Price
$635
Updated
2021/12/16
Crysdot
Product number
CD11107248
Product name
(R)-1-(3,4-Dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolinehydrochloride
Purity
97%
Packaging
1g
Price
$45
Updated
2021/12/16
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R-tetrahydropapaverine HCl Chemical Properties,Usage,Production

Application

R-tetrahydropapaverine HCl is a useful research chemical.

Synthesis

6429-04-5

54417-53-7

The general procedure for the synthesis of the target compound using 1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride as raw material was as follows: 20 g of 1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride was dissolved in 400 mL of distilled water, and stirred until completely dissolved. Subsequently, ammonia was added to the solution to adjust the pH, and after observing that no white oily material precipitated, 400 mL of toluene was added and mixed with thorough stirring. The organic phase (toluene layer) and the aqueous phase were separated to ensure that there was no residual raw material in the aqueous phase. The organic phase was dried with anhydrous sodium sulfate to obtain 17.3 g of racemate. The racemate was dissolved in 173 mL of acetonitrile and heated to 70 °C. 3.93 g of the splitting agent N-acetyl-D-leucine was slowly added and the reaction was stirred for 20 minutes. Next, 0.522 g of the splitting agent N-acetyl-D-phenylalanine was added and the reaction was continued with stirring for 35 minutes. Upon completion of the reaction, it was slowly cooled to room temperature and subsequently stored in a refrigerator at 4°C for 24 hours to promote crystallization. Upon completion of crystallization, the solid product was collected by filtration. The product was converted to hydrochloride form, treated by adding appropriate amount of hydrochloric acid and dried to give 8.325 g of 1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride in R-configuration. The total yield was 83.25% and the purity was 97.6%.

References

[1] Patent: CN107056700, 2017, A. Location in patent: Paragraph 0040-0043; 0046; 0058

R-tetrahydropapaverine HCl Preparation Products And Raw materials

Raw materials

Preparation Products

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R-tetrahydropapaverine HCl Suppliers

Carbosynth
Tel
--
Fax
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Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
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58
CARBONE SCIENTIFIC CO.,LTD
Tel
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Fax
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Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
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Eurolabs Limited
Tel
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Fax
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Country
United Kingdom
ProdList
6309
Advantage
46
Fluorochem Ltd
Tel
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Fax
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Email
vernam@fluorochem.co.uk
Country
United Kingdom
ProdList
6375
Advantage
65
Fluorochem Ltd.
Tel
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Fax
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Email
enquiries@fluorochem.co.uk
Country
United Kingdom
ProdList
6401
Advantage
74
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View Lastest Price from R-tetrahydropapaverine HCl manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
R-tetrahydropapaverine HCl 54417-53-7
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1KG 10KG 100KG
Release date
2025-05-22
Shaanxi Dideu New Materials Co. Ltd
Product
R-tetrahydropapaverine HCl 54417-53-7
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10000KGS
Release date
2025-03-06
R&D Scientific Inc.
Product
R-tetrahydropapaverine HCl 54417-53-7
Price
US $890.00/Kg
Min. Order
1Kg
Purity
98
Supply Ability
500 Kg
Release date
2024-05-07

54417-53-7, R-tetrahydropapaverine HClRelated Search:


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  • R-TATRAHYDROPAPAVERINE HCL
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  • Atracurium Impurity 7(R-Tetrahydropapaverine HCl)
  • Atracurium Besylate Impurity 7
  • (1R,2R)-1-(3,4-dimethoxybenzyl)-2-(3-ethoxy-3-oxopropyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium benzenesulfonate
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  • 54417-53-7
  • Analgesic series