MedKoo Cat#: 578216 | Name: C-829 dihydrochloride

Description:

WARNING: This product is for research use only, not for human or veterinary use.

C-829 dihydrochloride is an acridine derivative with sedative activity.

Chemical Structure

C-829 dihydrochloride
C-829 dihydrochloride
CAS#65094-73-7

Theoretical Analysis

MedKoo Cat#: 578216

Name: C-829 dihydrochloride

CAS#: 65094-73-7

Chemical Formula: C18H22Cl2N4O2

Exact Mass: 396.1120

Molecular Weight: 397.30

Elemental Analysis: C, 54.42; H, 5.58; Cl, 17.85; N, 14.10; O, 8.05

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
C 829 dihydrochloride; C829 dihydrochloride; C-829 dihydrochloride
IUPAC/Chemical Name
1,2-Propanediamine, N(sup 1),N(sup 1)-dimethyl-N(sup 2)-(1-nitro-9-acridinyl)-, dihydrochloride
InChi Key
VIAUTYOSTMNQLG-UHFFFAOYSA-N
InChi Code
InChI=1S/C18H20N4O2.2ClH/c1-12(11-21(2)3)19-18-13-7-4-5-8-14(13)20-15-9-6-10-16(17(15)18)22(23)24;;/h4-10,12H,11H2,1-3H3,(H,19,20);2*1H
SMILES Code
Cl.Cl.CC(CN(C)C)Nc1c2ccccc2nc3cccc(c13)[N+](=O)[O-]
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Toxicity: Mouse, LD50 - intravenous, 21.3mg/kg: No Effect Reported Mouse, LD50 - oral, 99.2mg/kg: Decreased GI Motility or Constipation. Rat, LD50, Oral, 105mg/kg: Decreased GI Motility or Constipation. Source: Archivum Immunologiae et Therapiae Experimentalis. Vol. 27, Pg. 749, 1979.

Preparing Stock Solutions

The following data is based on the product molecular weight 397.30 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Błaszczyk B, Giełdanowski J, Patkowski J, Kowalczyk-Bronisz SH. Pharmacological studies on new oncostatic acridine derivatives. I. Acute and subchronic action. Arch Immunol Ther Exp (Warsz). 1979;27(6):749-63. PMID: 549530.