6-guanidinohexanoic acid

Names

[ Name ]:
6-guanidinohexanoic acid

[Synonym ]:
6-Guanidino-hexansaeure
guanidinohexanoic acid
6-carbamimidamidohexanoic acid
6-Guanidinohexanoic acid
6-Guanidinocaproic acid

Chemical & Physical Properties

[ Density]:
1.25 g/cm3

[ Boiling Point ]:
385.2ºC at 760 mmHg

[ Melting Point ]:
-310ºC

[ Molecular Formula ]:
C₇H₁₅N₃O₂

[ Molecular Weight ]:
173.21300

[ Flash Point ]:
186.7ºC

[ Exact Mass ]:
173.11600

[ PSA ]:
99.20000

[ LogP ]:
1.30540

[ Index of Refraction ]:
1.541

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925290090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2925290090

[ Summary ]:
2925290090 other imines and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

New amiloride analogue as hapten to raise anti-amiloride antibodies.

Am. J. Physiol. 250(1 Pt 1) , C165-70, (1986)

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 ...

A possible approach to the suppression of side effects induced by PGE1.

Prostaglandins Leukot. Essent. Fatty Acids 52(1) , 17-20, (1995)

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 c...

(S)-2-Amino-6-guanidinohexanoic acid
6-guanidinohexanoic acid hydrochloride
2-AMINO-6-GUANIDINOHEXANOIC ACID HYDROCHLORIDE
(S)-2-Amino-6-guanidinohexanoic Acid Hydrochloride
(R)-2-Amino-6-guanidinohexanoic acid hydrochloride
2-Amino-6-guanidinohexanoic Acid-d4 Dihydrochloride
3,4,5-trimethoxy-N-(4-oxo-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)benzamide
4-fluoro-N-(4-oxo-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)benzamide
4-chloro-N-(4-oxo-1-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)benzamide
2-cyano-3-[5-(4-fluorophenyl)furan-2-yl]-N-[3-(trifluoromethyl)phenyl]prop-2-enamide
N-(4-oxo-1-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)-[1,1'-biphenyl]-4-carboxamide
2-(4-nitrophenyl)-N-(4-oxo-1-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)acetamide
2-(naphthalen-1-yl)-N-(4-oxo-1-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)acetamide
2-chloro-N-(1-(3,4-dimethylphenyl)-4-oxo-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)propanamide
N-(1-(3,4-dimethylphenyl)-4-oxo-1H-pyrazolo[3,4-d]pyrimidin-5(4H)-yl)-2-methoxybenzamide
N-[1-(3,4-dimethylphenyl)-4-oxo-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-5-yl]naphthalene-2-carboxamide

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