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Key Documents

55572

Sigma-Aldrich

6-Guanidinohexanoic acid

≥98.0%

Synonym(s):

6-Guanidinocaproic acid

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About This Item

Linear Formula:
NH2C(NH)NH(CH2)5COOH
CAS Number:
Molecular Weight:
173.21
Beilstein/REAXYS Number:
1774244
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

assay

≥98.0%

reaction suitability

reagent type: cross-linking reagent

mp

~310 °C (dec.)

SMILES string

NC(=N)NCCCCCC(O)=O

InChI

1S/C7H15N3O2/c8-7(9)10-5-3-1-2-4-6(11)12/h1-5H2,(H,11,12)(H4,8,9,10)

InChI key

NSDYIDKTTPXCRH-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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T R Kleyman et al.
The American journal of physiology, 250(1 Pt 1), C165-C170 (1986-01-11)
A new amiloride analogue, "amiloride-caproic acid," was synthesized, coupled to albumin, and used as a hapten to raise anti-amiloride antibodies in rabbits. The antibodies were affinity purified with an amiloride affinity column and characterized. Binding studies using [3H]benzamil showed a
Y Nakabou et al.
Prostaglandins, leukotrienes, and essential fatty acids, 52(1), 17-20 (1995-01-01)
Prostaglandin E1 (PGE1) is known to possess various actions in vivo. Of these actions, the contraction of the ileum and inflammation are undesirable side effects. We previously proposed a hypothesis concerning the receptors for human blood platelet aggregation and its

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