3-Carbamimidamido-L-alanine hydrochloride (1:1)

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Names

[ Name ]:
3-Carbamimidamido-L-alanine hydrochloride (1:1)

[Synonym ]:
Ethanaminium, 1-carboxy-2-[(diaminomethylene)amino]-, chloride (1:1)
1-Carboxy-2-[(diaminomethylene)amino]ethanaminium chloride
L-Alanine, 3-[(aminoiminomethyl)amino]-, hydrochloride (1:1)
(S)-2-Amino-3-guanidinopropanoic acid hydrochloride
L-2-Amino-3-guanidinopropionic acid hydrochloride
3-Guanidino-L-alanine hydrochloride
3-Carbamimidamido-L-alanine hydrochloride (1:1)
(2S)-2-amino-3-(diaminomethylideneamino)propanoic acid,hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
370.8ºC at 760 mmHg

[ Melting Point ]:
-220ºC (dec.)

[ Molecular Formula ]:
C₄H₁₁ClN₄O₂

[ Molecular Weight ]:
182.609

[ Flash Point ]:
178.1ºC

[ Exact Mass ]:
182.057053

[ PSA ]:
125.22000

[ LogP ]:
0.57460

[ Vapour Pressure ]:
1.62E-06mmHg at 25°C

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Noncoded amino acid replacement probes of the aspartate aminotransferase mechanism.

Biochemistry 36 , 10517-10525, (1997)

The primary role of Tyr225 in the aspartate aminotransferase mechanism is to provide a hydrogen bond to stabilize the 3'O- functionality of bound pyridoxal phosphate. The strength of this hydrogen bon...

Binding of the unreactive substrate analog L-2-amino-3-guanidinopropionic acid (dinor-L-arginine) to human arginase I.

Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun. 68(Pt 8) , 889-93, (2012)

Human arginase I (HAI) is a binuclear manganese metalloenzyme that catalyzes the hydrolysis of L-arginine to form L-ornithine and urea through a metal-activated hydroxide mechanism. Since HAI regulate...

Analysis of 1- and 3-methylhistidines, aromatic and basic amino acids in rat and human urine. Feldhoff RC, Ledden DJ, et al.

J. Chromatogr. A. 311 , 267-276, (1984)

3-(Methylselanyl)-L-alanine hydrochloride (1:1)
(S)-2-Amino-3-guanidinopropanoic acid dihydrochloride
(S)-2-AMINO-3-PIPERAZIN-1-YL-PROPIONIC ACID HCL
(S)-2-AMINO-3-(PYRIDIN-3-YL)PROPANOIC ACID HYDROCHLORIDE
(S)-(-)-5-Fluorowillardiine hydrochloride
2-Amino-3-(2-oxo-1,2-dihydroquinolin-4-yl)propanoic acid hydrochloride
3-(aminomethyl)-5-chloro-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one
1-Bromo-5-chloro-3-methylisoquinoline
1,4-Dibromo-6-fluoro-3-methylisoquinoline
1-Bromo-5-fluoroisoquinoline-3-carboxylic acid
3-(1H-1,2,4-triazol-3-yl)butan-1-aminedihydrochloride
rac-ethyl (1R,2S)-2-(aminomethyl)cyclohexane-1-carboxylate hydrochloride, cis
1-[(4-Methylbenzenesulfonyl)oxy]cyclopropane-1-carboxylic acid
(1H-1,2,4-triazol-3-yl)methyl 4-methylbenzene-1-sulfonate
2-(Aminomethyl)-6-methylanilinedihydrochloride
3-Methyloxolan-3-yl 4-methylbenzene-1-sulfonate

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