
CAS Number2113-05-5
Synonyms1-(3-Chlorophenyl)biguanide hydrochloride; m-Chlorophenylbiguanide hydrochloride; MFCD00053019; N-m-Chlorophenylbiguanide hydrochloride; m-CPBG hydrochloride
Molecular FormulaC8H11Cl2N5
Molecular Weight204.10
Purity97%
Density1.49g/cm3
Boiling Point434.1ºC at 760mmHg
Melting Point190-194 °C(lit.)
Appearancesolid
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 2113-05-5 |
| Catalog No. | 2A-9000510 |
| Chinese Name | 1-(3-氯苯基)双胍盐酸盐 |
| Synonyms | 1-(3-Chlorophenyl)biguanide hydrochloride; m-Chlorophenylbiguanide hydrochloride; MFCD00053019; N-m-Chlorophenylbiguanide hydrochloride; m-CPBG hydrochloride |
| Molecular Formula | C8H11Cl2N5 |
| Molecular Weight | 204.10 |
| Purity | 97 |
| Density | 1.49g/cm3 |
| Boiling Point | 434.1ºC at 760mmHg |
| Melting Point | 190-194 °C(lit.) |
| Appearance | solid |
| Water Solubility | H2O: soluble |
| Storage Condition | The storage place must be away from oxidants and w |
| Application | m-CPBG (1-(3-chlorophenyl)biguanide) hydrochloride is a selective 5-HT3 agonist. m-CPBG hydrochloride can be used in the research of neurological diseases [1]. |
| PubChem ID | 329776186 |
| MDL Number | MFCD09028130 |
| SMILES | NC1(C2=CC=CC(Cl)=C2)CC1.[H]Cl |
| InChI | 1S/C9H10ClN.ClH/c10-8-3-1-2-7(6-8)9(11)4-5-9;/h1-3,6H,4-5,11H2;1H |
| InChI Key | AWQJBHOHCVILOR-UHFFFAOYSA-N |
| NACRES Code | NA.21 |
| UNSPSC | 12352116 |
| Hazard Symbols | Transport |
| MSDS | msds/510_1_2113_05_5.pdf |
| Bioactivity | m-CPBG (1-(3-Chlorophenyl)biguanide) hydrochloride is a selective 5-HT3 agonist. m-CPBG hydrochloride can be used for the research of neurological disease[1]. Related Catalog Research Areas >> Neurological Disease Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor In Vivo m-CPBG hydrochloride (80 and 160 nM) significantly reduces water intake induced by acute salt loading [1]. m-CPBG hydrochloride (third ventricle injection; 160 nM) significantly inhibits water intake in hypovolemic animals [1]. m-CPBG hydrochloride (third ventricle injection; 320 nM) reduces water intake in dehydrated rats [1]. m-CPBG hydrochloride (central administration) inhibits water intake induced by pharmacological activation of central cholinergic and angiotensinergic pathways [1]. Animal Model: Wistar male rats[1] Dosage: 80, 160 and 320 nM Administration: Ventricle injection Result: Decreased water intake induced by water deprivation, acute salt load and hypovolemia. References [1]. Castro L, et al. Central 5-HT(3) receptors and water intake in rats. Physiol Behav. 2002;77(2-3):349-359. Chemical & Physical Properties Density 1.49g/cm3 Boiling Point 434.1ºC at 760mmHg Melting Point 190-194 °C(lit.) Molecular Formula C8H11Cl2N5 Molecular Weight 248.11 Flash Point 216.3ºC Exact Mass 247.03900 PSA 97.78000 LogP 3.33540 Appearance of Characters solid | white Vapor Pressure 9.74E-08mmHg at 25°C InChIKey FOWAIJYHRWFTHR-UHFFFAOYSA-N SMILES Cl.NC(N)=NC(N)=Nc1cccc(Cl)c1 Storage condition Desiccate at RT Water Solubility H2O: soluble |
| Use of | m-CPBG (1-(3-Chlorophenyl)biguanide) hydrochloride is a selective 5-HT3 agonist. m-CPBG hydrochloride can be used for the research of neurological disease[1]. Properties Articles33 Name 2-(3-chlorophenyl)-1-(diaminomethylidene)guanidine,hydrochloride Synonym More Synonyms Biological Activity Description m-CPBG (1-(3-Chlorophenyl)biguanide) hydrochloride is a selective 5-HT3 agonist. m-CPBG hydrochloride can be used for the research of neurological disease[1]. Related Catalog Research Areas >> Neurological Disease Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor In Vivo m-CPBG hydrochloride (80 and 160 nM) significantly reduces water intake induced by acute salt loading [1]. m-CPBG hydrochloride (third ventricle injection; 160 nM) significantly inhibits water intake in hypovolemic animals [1]. m-CPBG hydrochloride (third ventricle injection; 320 nM) reduces water intake in dehydrated rats [1]. m-CPBG hydrochloride (central administration) inhibits water intake induced by pharmacological activation of central cholinergic and angiotensinergic pathways [1]. Animal Model: Wistar male rats[1] Dosage: 80, 160 and 320 nM Administration: Ventricle injection Result: Decreased water intake induced by water deprivation, acute salt load and hypovolemia. References [1]. Castro L, et al. Central 5-HT(3) receptors and water intake in rats. Physiol Behav. 2002;77(2-3):349-359. Chemical & Physical Properties Exact Mass 247.03900 PSA 97.78000 LogP 3.33540 Appearance of Characters solid | white InChIKey FOWAIJYHRWFTHR-UHFFFAOYSA-N Storage condition Desiccate at RT Water Solubility H2O: soluble |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 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 Names specified by the United Nations (UN) 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 Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available See reverse side of invoice or packing slip. |
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