Cinolazepam
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MedKoo CAT#: 317533

CAS#: 75696-02-5

Description: Cinolazepam is a benzodiazepine derivative drug. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Due to its strong sedative properties, it is primarily used as an hypnotic.


Chemical Structure

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Cinolazepam
CAS# 75696-02-5

Theoretical Analysis

MedKoo Cat#: 317533
Name: Cinolazepam
CAS#: 75696-02-5
Chemical Formula: C18H13ClFN3O2
Exact Mass: 357.07
Molecular Weight: 357.770
Elemental Analysis: C, 60.43; H, 3.66; Cl, 9.91; F, 5.31; N, 11.75; O, 8.94

Price and Availability

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5mg USD 800 2 Weeks
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Synonym: Cinolazepam; Gerodorm; OX-373;

IUPAC/Chemical Name: 3-[7-chloro-5-(2-fluorophenyl)-3-hydroxy-2-oxo-3H-1,4-benzodiazepin-1-yl]propanenitrile

InChi Key: XAXMYHMKTCNRRZ-UHFFFAOYSA-N

InChi Code: InChI=1S/C18H13ClFN3O2/c19-11-6-7-15-13(10-11)16(12-4-1-2-5-14(12)20)22-17(24)18(25)23(15)9-3-8-21/h1-2,4-7,10,17,24H,3,9H2

SMILES Code: C1=CC=C(C(=C1)C2=NC(C(=O)N(C3=C2C=C(C=C3)Cl)CCC#N)O)F

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, not in water

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 357.77 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: Saletu B, Kindshofer G, Anderer P, Grünberger J. Short-term sleep laboratory
studies with cinolazepam in situational insomnia induced by traffic noise. Int J
Clin Pharmacol Res. 1987;7(5):407-18. PubMed PMID: 2889679.


2: Oelschläger H, Volke J, Belal F. Analysis of drugs by polarography, XXXV: The
polarographic behaviour of
cinolazepam[1-(2-cyanoethyl)-7-chloro-3-hydroxy-5-(2-fluorophe n
yl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one] and assay of its tablets. Arch Pharm
(Weinheim). 1992 Feb;325(2):65-8. PubMed PMID: 1605717.


3: Richards BL, Whittle SL, Buchbinder R. Muscle relaxants for pain management in
rheumatoid arthritis. Cochrane Database Syst Rev. 2012 Jan 18;1:CD008922. doi:
10.1002/14651858.CD008922.pub2. Review. PubMed PMID: 22258993.


4: Walash MI, Belal F, Metwally ME, Hefnawy MM. A selective fluorimetric method
for the determination of some 1,4-benzodiazepine drugs containing a hydroxyl
group at C-3. J Pharm Biomed Anal. 1994 Nov;12(11):1417-23. PubMed PMID: 7849137.


5: Mascher H, Nitsche V, Schütz H. Separation, isolation and identification of
optical isomers of 1,4-benzodiazepine glucuronides from biological fluids by
reversed-phase high-performance liquid chromatography. J Chromatogr. 1984 Mar
9;306:231-9. PubMed PMID: 6715462.