
Identification
CAS Number
334-50-9
Name
Spermidine trihydrochloride
Synonyms
1,4-Butanediamine, N1-(3-aminopropyl)-, hydrochloride (1:3) [ACD/Index Name]
206-379-0 [EINECS]
334-50-9 [RN]
EJ7023000
MFCD00012918 [MDL number]
N-(3-Aminopropyl)-1,4-butandiamintrihydrochlorid [German] [ACD/IUPAC Name]
N-(3-Aminopropyl)-1,4-butanediamine trihydrochloride [ACD/IUPAC Name]
N-(3-Aminopropyl)-1,4-butanediamine, trichlorhydrate [French] [ACD/IUPAC Name]
N-(3-aminopropyl)-1,4-butanediamine, trihydrochloride
n-(3-aminopropyl)butane-1,4-diamine trihydrochloride
SPERMIDINE HYDROCHLORIDE
Spermidine trihydrochloride
(4-AMINOBUTYL)(3-AMINOPROPYL)AMINE TRIHYDROCHLORIDE
[334-50-9] [RN]
1,4-Butanediamine, N-(3-aminopropyl)-, trihydrochloride
1,4-butanediamine, N1-(3-aminopropyl)-, hydrochloride (1:3)
1,5,10-Triazadecane trihydrochloride
1,8-Diamino-4-azaoctane trihydrochloride
1173019-26-5 [RN]
35408-56-1 [RN]
4-azoniaoctamethylenediammonium trichloride
EJ 7023000
N-(3-aminopropyl)-1,4-butanediamine 3HCl
N-(3-Aminopropyl)-1,4-diamino-butane trihydrochloride
N’-(3-aminopropyl)butane-1,4-diamine
N’-(3-aminopropyl)butane-1,4-diamine and trihydrochloride
N’-(3-aminopropyl)butane-1,4-diamine trihydrochloride
N’-(3-aminopropyl)butane-1,4-diamine;trihydrochloride
N1-(3-Aminopropyl)butane-1,4-diamine trihydrochloride
S-7320
SPERMIDINE BUTANE-D8 TRIHYDROCHLORIDE
Spermidine, Trihydrochloride – CAS 334-50-9 – Calbiochem
Spermidine.3HCl
spermidine-3hcl
Spermidine-butane-d8 trihydrochloride
SPERMIDINETRIHYDROCHLORIDE
trihydrochloride
TRIHYDROGEN SPERMIDINE TRICHLORIDE
SMILES
C(CCNCCCN)CN.Cl.Cl.Cl
StdInChI
InChI=1S/C7H19N3.3ClH/c8-4-1-2-6-10-7-3-5-9;;;/h10H,1-9H2;3*1H
StdInChIKey
LCNBIHVSOPXFMR-UHFFFAOYSA-N
Molecular Formula
C7H22Cl3N3
Molecular Weight
254.629
MDL Number
MFCD00012918
Properties
Appearance
White powder
Safety Data
RIDADR
NONH for all modes of transport
Specifications and Other Information of Our Spermidine trihydrochloride CAS 334-50-9
Identification Methods
HNMR, HPLC
Purity
98% min
Shelf Life
2 years
Storage
Under room temperature away from light
Known Application
It is mainly used as an intermediate in organic synthesis and a donor in supramolecular chemistry. It can also be used as a cosmetic with anti-aging effects.
Links
This product is developed by our R&D company Caming Pharmaceutical Ltd (https://www.caming.com/).
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