1,4-Diaminobutane dihydrochloride

1,4-Diaminobutane dihydrochloride Basic information
Product Name:1,4-Diaminobutane dihydrochloride
Synonyms:1,4-BUTANEDIAMINE DIHYDROCHLORIDE;1,4-BUTANEDIAMMONIUM DICHLORIDE;1,4-DIAMINOBUTANE 2HCL;1,4-Diaminobutane dihydrochloride,1,4-Butanediamine dihydrochloride, 1,4-Diaminobutane dihydrochloride, Putrescine dihydrochloride, Tetramethylenediamine dihydrochloride;Putrescine dihydrochloride,1,4-Butanediamine dihydrochloride, 1,4-Diaminobutane dihydrochloride, Tetramethylenediamine dihydrochloride;1,4-DiaMinobutane dihydrochloride, 99+% 25GR;1,4-DIAMINOBUTANE DIHYDROCHLORIDE:PUTRESCINE 2HCL;1,4-DIAMINOBUTANE DIHYDROCHLORIDE 98+%
CAS:333-93-7
MF:C4H14Cl2N2
MW:161.07
EINECS:206-375-9
Product Categories:Heterocyclic Compounds;antibiotic
Mol File:333-93-7.mol
1,4-Diaminobutane dihydrochloride Structure
1,4-Diaminobutane dihydrochloride Chemical Properties
Melting point 280 °C (dec.)(lit.)
Boiling point 265.47°C (rough estimate)
density 1.2524 (rough estimate)
refractive index 1.6300 (estimate)
storage temp. Store below +30°C.
solubility H2O: 100 mg/mL
form powder
color White
Water Solubility almost transparency
Sensitive Hygroscopic
Merck 14,7947
BRN 3906680
Stability:Stable, but hygroscopic. Substances to be avoided: strong oxidizing agents. Combustible.
InChIKeyXXWCODXIQWIHQN-UHFFFAOYSA-N
CAS DataBase Reference333-93-7(CAS DataBase Reference)
EPA Substance Registry System1,4-Diaminobutane dihydrochloride (333-93-7)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36-37/39
WGK Germany 3
RTECS EJ7280000
TSCA Yes
HS Code 29212900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
1,4-Diaminobutane dihydrochloride Usage And Synthesis
Chemical Propertieswhite powder
UsesPutrescine dihydrochloride has been used as medium component in F-12 + GlutaMax medium for mice ganglia culture, retinal ganglion cell culture and in HCT116 colon carcinoma cells for ornithine decarboxylase (ODC) assay.
General DescriptionPutrescine is an end product of fatty acid metabolism in dead tissues. It is a volatile diamine with pungent odour. It is synthesized by the decarboxylation of ornithine in the presence of enzyme, ornithine decarboxylase. Molecular docking studies reveal the binding of putrescine to human receptors called the trace amine-associated receptors (TAAR6 and TAAR8), present in olfactory epithelium.
Biochem/physiol ActionsBinds to the polyamine modulatory site of the NMDA receptor and potentiates NMDA-induced currents; precursor of spermidine.
Purification MethodsCrystallise the salt from EtOH/H2O. [Beilstein 4 IV 1284.]
1,4-Diaminobutane dihydrochloride Preparation Products And Raw materials
N-(4-AMINOBUTYL)-5-CHLORO-2-NAPHTHALENESULFONAMIDE HYDROCHLORIDE H-ARG-ARG-4M-BETA-NA 3 HCL DIPHENYLAMINE HYDROCHLORIDE QUINACRINE MUSTARD DIHYDROCHLORIDE D-ORNITHINE DIHYDROCHLORIDE N,N'-bis-(N-dodecyl-N,N-dimethylglycine)-1,4-diaminobutane dihydrochloride 2-Aminoethylammonium chloride Methoxyammonium chloride PHE-ARG BETA-NAPHTHYLAMIDE DIHYDROCHLORIDE Mepacrine hydrochloride N-METHYL-BUTANE-1,4-DIAMINE 2HCL ARG-ARG BETA-NAPHTHYLAMIDE TRIHYDROCHLORIDE (R,R)-2,3-DIAMINOBUTANE DIHYDROCHLORIDE 1,4-DIAMINOBUTANE DIHYDROCHLORIDE, [15N2] Dihydrochloride PPACK, DIHYDROCHLORIDE Cyclohexylamine hydrochloride (S,S)-2,3-DIAMINOBUTANE DIHYDROCHLORIDE

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