MedKoo Cat#: 413353 | Name: Homochlorcyclizine

Description:

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

Homochlorcyclizine is an antihistamine of the diphenylmethylpiperazine group which has been marketed in Japan since 1965. It is used in the treatment of allergies and other conditions. It also has some anticholinergic, antidopaminergic, and antiserotonergic properties.

Chemical Structure

Homochlorcyclizine
Homochlorcyclizine
CAS#848-53-3

Theoretical Analysis

MedKoo Cat#: 413353

Name: Homochlorcyclizine

CAS#: 848-53-3

Chemical Formula: C19H23ClN2

Exact Mass: 314.1550

Molecular Weight: 314.86

Elemental Analysis: C, 72.48; H, 7.36; Cl, 11.26; N, 8.90

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
Homochlorcyclizine; NSC25132; NSC-25132; NSC 25132
IUPAC/Chemical Name
1-(p-Chloro-alpha-phenylbenzyl)hexahydro-4-methyl-1H-1,4-diazepine
InChi Key
WEUCDJCFJHYFRL-UHFFFAOYSA-N
InChi Code
InChI=1S/C19H23ClN2/c1-21-12-5-13-22(15-14-21)19(16-6-3-2-4-7-16)17-8-10-18(20)11-9-17/h2-4,6-11,19H,5,12-15H2,1H3
SMILES Code
CN1CCN(C(C2=CC=CC=C2)C3=CC=C(Cl)C=C3)CCC1
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
Solvent mg/mL mM
Solubility
Soluble in DMSO 0.0 100.00
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 314.86 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: FISHERMAN EW, FEINBERG SM, FEINBERG AR, PRUZANSKY JJ. Homochlorcyclizine: an antiallergic drug with multiple clinical properties. J Allergy. 1960 May- Jun;31:232-6. doi: 10.1016/0021-8707(60)90051-4. PMID: 13823261. 2: Chang TS, Chen CT. Inhibitory effect of homochlorcyclizine on melanogenesis in α-melanocyte stimulating hormone-stimulated mouse B16 melanoma cells. Arch Pharm Res. 2012 Jan;35(1):119-27. doi: 10.1007/s12272-012-0113-z. Epub 2012 Feb 2. PMID: 22297750. 3: Suzuki A, Yasui-Furukori N, Mihara K, Kondo T, Furukori H, Inoue Y, Kaneko S, Otani K. Histamine H1-receptor antagonists, promethazine and homochlorcyclizine, increase the steady-state plasma concentrations of haloperidol and reduced haloperidol. Ther Drug Monit. 2003 Apr;25(2):192-6. doi: 10.1097/00007691-200304000-00008. PMID: 12657913. 4: Nishikata M, Nakai A, Fushida H, Miyake K, Arita T, Iseki K, Miyazaki K. Enantioselective pharmacokinetics of homochlorcyclizine: disposition of (+)- and (-)-homochlorcyclizine after intravenous and oral administration of racemic homochlorcyclizine to rats. J Pharm Pharmacol. 1994 Jul;46(7):591-5. doi: 10.1111/j.2042-7158.1994.tb03863.x. PMID: 7996389. 5: Miyazawa T. [Experimental allergic contact dermatitis and homochlorcyclizine]. Clin Pediatr (Phila). 1968 Sep;7(9):302-3. Japanese. PMID: 4386436. 6: Nishikata M, Nakai A, Fushida H, Miyake K, Arita T, Iseki K, Miyazaki K, Nomura A. Enantioselective pharmacokinetics of homochlorcyclizine. III. Simultaneous determination of (+)- and (-)- homochlorcyclizine in human urine by high-performance liquid chromatography. J Chromatogr. 1993 Feb 26;612(2):239-44. PMID: 8096848. 7: Taniguchi K, Masuda Y, Takanaka K. Inhibitory effects of histamine H1 receptor blocking drugs on metabolic activations of neutrophils. J Pharmacobiodyn. 1991 Feb;14(2):87-93. doi: 10.1248/bpb1978.14.87. PMID: 1678430. 8: Oishi R, Shishido S, Yamori M, Saeki K. Comparison of the effects of eleven histamine H1-receptor antagonists on monoamine turnover in the mouse brain. Naunyn Schmiedebergs Arch Pharmacol. 1994 Feb;349(2):140-4. doi: 10.1007/BF00169830. PMID: 7513381. 9: Nishikata M, Nomura A, Iseki K, Miyazaki K, Nakai A, Fushida H, Miyake K, Arita T. Enantioselective pharmacokinetics of homochlorcyclizine. II: Disposition and metabolism of (+)-, (-)- and racemic homochlorcyclizine after oral administration to man. Eur J Clin Pharmacol. 1992;43(5):533-8. doi: 10.1007/BF02285097. PMID: 1362384. 10: GIRARD JP. [Clinical trials with a new anti-allergic agent, homochlorcyclizine. Effects on urinary elimination of the metabolite of serotonin]. Ther Umsch. 1962 Feb;19:50-3. French. PMID: 13898853.