G6503
4-Guanidinobutyric acid
≥98%, for peptide synthesis
Synonym(s):
γ-Guanidinobutyric acid
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1 G
1 170,00 kr
5 G
3 970,00 kr
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1 G
1 170,00 kr
5 G
3 970,00 kr
About This Item
Linear Formula:
NH=C(NH2)NHCH2CH2CH2COOH
CAS Number:
Molecular Weight:
145.16
Beilstein:
1766447
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.26
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Product Name
4-Guanidinobutyric acid, ≥98%
Quality Level
Assay
≥98%
form
powder or chunks
technique(s)
drug transporter assay: suitable
color
white
mp
280-282 °C
storage temp.
2-8°C
SMILES string
NC(=N)NCCCC(O)=O
InChI
1S/C5H11N3O2/c6-5(7)8-3-1-2-4(9)10/h1-3H2,(H,9,10)(H4,6,7,8)
InChI key
TUHVEAJXIMEOSA-UHFFFAOYSA-N
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Application
Gamma-Guanidinobutyric acid (4-GBA) is used to study intestinal transport by the human proton-coupled amino acid transporter(s) (hPAT1). 4-GBA is used with other model compounds such as 1,6-diaminohexane, 1,6-diguanidinohexane, and 1,6-di(cyanoguanidino)hexane to study the biodegradability of the biocide polyhexamethylene biguanide (PHMB).
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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S Shindo et al.
Research communications in chemical pathology and pharmacology, 54(1), 73-85 (1986-10-01)
Arginine levels diminished markedly in the plasma during starvation, suggesting that plasma arginine level principally depends on food intake. Organ arginine levels were relatively stable except for an extraordinary increase in the pancreas at 96 h. Guanidinoacetic acid decreased dramatically
Guanidino compounds in hyperargininemia.
B Marescau et al.
Advances in experimental medicine and biology, 153, 427-434 (1982-01-01)
Zhipan Zhang et al.
The journal of physical chemistry. B, 109(46), 21818-21824 (2006-07-21)
Dye-sensitized solar cells based on nanocrystalline TiO(2) have been fabricated with an amphiphilic ruthenium sensitizer [Ru (4,4'-dicarboxylic acid-2,2'-bipyridine) (4,4'-bis(p-hexyloxystyryl)-2,2'-bipyridine)(NCS)(2)], coded as K-19, and 4-guanidinobutyric acid (GBA) as coadsorbent. The cells showed a approximately 50 mV increase in open-circuit voltage and
M Al Banchaabouchi et al.
Metabolism: clinical and experimental, 47(3), 355-361 (1998-03-21)
Renal failure is characterized by the retention of nitrogenous metabolites such as urea, creatinine (CTN) and other guanidino compounds (GCs), uric acid, and hippuric acid, which could be related to the clinical syndrome associated with renal insufficiency. A model of
Metabolism of arginine in invertebrates: relation to urea cycle and to other guanidine derivatives.
Y Robin
Advances in experimental medicine and biology, 153, 407-417 (1982-01-01)
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