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

Modify Date: 2024-01-09 21:43:10

3-Carbamimidamido-L-alanine hydrochloride (1:1) structure	Common Name	3-Carbamimidamido-L-alanine hydrochloride (1:1)
	CAS Number	1482-99-1	Molecular Weight	182.609
	Density	N/A	Boiling Point	370.8ºC at 760 mmHg
	Molecular Formula	C₄H₁₁ClN₄O₂	Melting Point	-220ºC (dec.)
	MSDS	Chinese USA	Flash Point	178.1ºC
	Symbol	GHS07	Signal Word	Warning

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

(S)-2-amino-3-guanidinopropanoic acid hydrochloride is an alanine derivative[1].

Name	L-2-Amino-3-guanidinopropionic acid hydrochloride
Synonym	More Synonyms

Description	(S)-2-amino-3-guanidinopropanoic acid hydrochloride is an alanine derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
In Vitro	Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References	[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1023.

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(Chinese)

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

2-benzoylamino-...

CAS#:100057-89-4

3-Carbamimidami...

CAS#:1482-99-1

Literature: Chemical and Pharmaceutical Bulletin, , vol. 7, p. 616

Precursor 1
CAS#:100057-89-4 2-benzoylamino-...
DownStream 0

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)

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