Quinacrine methanesulfonate

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MedKoo CAT#: 591036

CAS#: 316-05-2 (mesylate)

Description: Quinacrine methanesulfonate is a bioactive chemical.


Chemical Structure

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Quinacrine methanesulfonate
CAS# 316-05-2 (mesylate)

Theoretical Analysis

MedKoo Cat#: 591036
Name: Quinacrine methanesulfonate
CAS#: 316-05-2 (mesylate)
Chemical Formula: C25H38ClN8O7S2
Exact Mass: 591.18
Molecular Weight: 591.160
Elemental Analysis: C, 50.71; H, 6.47; Cl, 5.99; N, 7.10; O, 18.91; S, 10.83

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

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Related CAS #: 83-89-6 (free base)   69-05-6 (HCl)   316-05-2 (mesylate)   6151-30-0 (HCl hydrate)   6598-46-5 (mesylate hydrate)   78901-94-7 (acetate)  

Synonym: Mepacrine dimethanesulfonate salt

IUPAC/Chemical Name: Acridine, 6-chloro-9-((4-(diethylamino)-1-methylbutyl)amino)-2-methoxy-, dimethanesulfonate

InChi Key: BSSDNUXUOKRRHO-UHFFFAOYSA-N

InChi Code: InChI=1S/C23H30ClN3O.2CH4O3S/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23;2*1-5(2,3)4/h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26);2*1H3,(H,2,3,4)

SMILES Code: COC1=CC2=C(NC(C)CCCN(CC)CC)C3=CC=C(Cl)C=C3N=C2C=C1.CS(=O)(O)=O.CS(=O)(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: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 591.16 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Soto C, Aguilar G, Jiménez L. Interdependence between sodium transport, external chloride, and sodium/calcium exchanger in the isolated skin of the Rana pipiens. J Exp Zool. 2001 Jan 1;289(1):23-32. PubMed PMID: 11169490.

2: Nishi Y, Hasegawa MM, Taketomi M, Ohkawa Y, Inui N. Comparison of 6-thioguanine-resistant mutation and sister chromatid exchanges in Chinese hamster V79 cells with forty chemical and physical agents. Cancer Res. 1984 Aug;44(8):3270-9. PubMed PMID: 6744262.

3: Marfin SV, Zakharov IA. [Genetic control of mitotic crossing over in yeasts. IV. The induction of mitotic crossing over by chemical mutagens with different mechanisms of action]. Genetika. 1983 Aug;19(8):1227-32. Russian. PubMed PMID: 6354843.

4: Rogers AM, Back KC. Comparative mutagenicity of 4 DNA-intercalating agents in L5178Y mouse lymphoma cells. Mutat Res. 1982 Dec;102(4):447-55. PubMed PMID: 7177152.

5: Muscarella DE, Bloom SE. The longevity of chemically induced sister chromatid exchanges in Chinese hamster ovary cells. Environ Mutagen. 1982;4(6):647-55. PubMed PMID: 6891633.

6: Heard JT Jr, Matney TS. Requirement of a partially diploid donor for the chemical induction of mutations in transforming DNA. Mutat Res. 1980 Feb;69(2):217-24. PubMed PMID: 6767181.

7: Haglund U, Zech L. Simultaneous staining of sister chromatid exchanges and Q-bands in human chromosomes after treatment with methyl methane sulphonate, quinacrine mustard, and quinacrine. Hum Genet. 1979 Jul 18;49(3):307-17. PubMed PMID: 478538.

8: Morrow J, Prickett MS, Fritz S, Vernick D, Deen D. Mutagenesis studies on cultured mammalian cells. The sensitivity of the asparagine-requiring phenotype to several chemical agents. Mutat Res. 1976 Mar;34(3):481-8. PubMed PMID: 177865.

9: Cook TM, Goldman CK. Hycanthone and its congeners as bacterial mutagens. J Bacteriol. 1975 May;122(2):549-56. PubMed PMID: 1092656; PubMed Central PMCID: PMC246090.