Mebhydrolin napadisylate structure, CAS 6153-33-9

Mebhydrolin napadisylate

CAS Number6153-33-9

SynonymsMebhydroline 1,5-naphthalenedisulfonate salt; diazoline; Naphthalene-1,5-disulfonic acid - 5-benzyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1:2); 1,5-Naphthalenedisulfonic acid - 5-benzyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1:2); Mebhydrolin napadisylate; Mebhydroline Napadisylate

Molecular FormulaC48H48N4O6S2

Molecular Weight841.06

Purity98.00%

Density0.9799 (rough estimate)

Boiling Point457.3ºC at 760 mmHg

Melting Point280°C (rough estimate)

Flash Point

AppearanceWhite or almost white crystal

EINECS

MSDSChineseEnglish

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Cat. No.: 2A-9032532 Purity: 98.00%
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Quality Control of [ 6153-33-9 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number6153-33-9
Catalog No.2A-9032532
Chinese Name美海屈林萘二磺酸盐
SynonymsMebhydroline 1,5-naphthalenedisulfonate salt; diazoline; Naphthalene-1,5-disulfonic acid - 5-benzyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1:2); 1,5-Naphthalenedisulfonic acid - 5-benzyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1:2); Mebhydrolin napadisylate; Mebhydroline Napadisylate
Molecular FormulaC48H48N4O6S2
Molecular Weight841.06
Purity98.00
Density0.9799 (rough estimate)
Boiling Point457.3ºC at 760 mmHg
Melting Point280°C (rough estimate)
AppearanceWhite or almost white crystal
Storage Conditionroom temperature, inert gas
ApplicationMebhydrolin napadisylate is a specific histamine H1 receptor antagonist.
HTC2933990090
MDL NumberC19H20N2·1/2C10H8O6S2
SMILESCN1CCc2c(c3ccccc3n2Cc2ccccc2)C1.CN1CCc2c(c3ccccc3n2Cc2ccccc2)C1.O=S(=O)(O)c1cccc2c(S(=O)(=O)O)cccc12
InChIInChI=1S/2C19H20N2.C10H8O6S2/c2*1-20-12-11-19-17(14-20)16-9-5-6-10-18(16)21(19)13-15-7-3-2-4-8-15;11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16/h2*2-10H,11-14H2,1H3;1-6H,(H,11,12,13)(H,14,15,16)
InChI KeyCJUOSBUQOWKEKJ-UHFFFAOYSA-N
Hazard Symbolstransportation
MSDSmsds/32532_1_6153_33_9.pdf
BioactivityMebhydrolin napadisylate is a specific histamine H1 receptor antagonist. Related Catalog Signaling Pathways >> GPCR/G Protein >> Histamine Receptor Signaling Pathways >> Immunology/Inflammation >> Histamine Receptor Research Areas >> Inflammation/Immunology Target Histamine H1-receptor[1] In Vitro Mebhydrolin is a specific histamine H1-receptor antagonist with minimal sedative properties and comparing it with the effects of chlorpromazine, the archetypical phenothiazine[1]. Mebhydrolin exerts an antihistaminic effect over the period of the ethanol interaction study[2]. References [1]. O'Neill PA, et al. Chlorpromazine-a specific effect on breathlessness? Br J Clin Pharmacol. 1985 Jun;19(6):793-7. [2]. Franks HM, et al. Interaction between ethanol and antihistamines: 3. Mebhydrolin. Med J Aust. 1981 Oct 31;2(9):477-9. Chemical & Physical Properties Density 0.9799 (rough estimate) Boiling Point 457.3ºC at 760 mmHg Melting Point 280°C (rough estimate) Molecular Formula C48H48N4O6S2 Molecular Weight 841.048 Flash Point 230.4ºC Exact Mass 840.301514 PSA 141.84000 LogP 10.72560 Index of Refraction 1.8676 (estimate) InChIKey CJUOSBUQOWKEKJ-UHFFFAOYSA-N SMILES CN1CCc2c(c3ccccc3n2Cc2ccccc2)C1.CN1CCc2c(c3ccccc3n2Cc2ccccc2)C1.O=S(=O)(O)c1cccc2c(S(=O)(=O)O)cccc12
Use ofMebhydrolin napadisylate is a specific histamine H1 receptor antagonist. Properties Articles13 Name Mebhydrolin Napadisylate Synonym More Synonyms Mebhydrolin napadisylate Biological Activity Description Mebhydrolin napadisylate is a specific histamine H1 receptor antagonist. Related Catalog Signaling Pathways >> GPCR/G Protein >> Histamine Receptor Signaling Pathways >> Immunology/Inflammation >> Histamine Receptor Research Areas >> Inflammation/Immunology Histamine H1-receptor[1] In Vitro Mebhydrolin is a specific histamine H1-receptor antagonist with minimal sedative properties and comparing it with the effects of chlorpromazine, the archetypical phenothiazine[1]. Mebhydrolin exerts an antihistaminic effect over the period of the ethanol interaction study[2]. References [1]. O'Neill PA, et al. Chlorpromazine-a specific effect on breathlessness? Br J Clin Pharmacol. 1985 Jun;19(6):793-7. [2]. Franks HM, et al. Interaction between ethanol and antihistamines: 3. Mebhydrolin. Med J Aust. 1981 Oct 31;2(9):477-9. Chemical & Physical Properties Molecular Formula C48H48N4O6S2 Exact Mass 840.301514 PSA 141.84000 LogP 10.72560 Index of Refraction 1.8676 (estimate) InChIKey CJUOSBUQOWKEKJ-UHFFFAOYSA-N
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Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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