Guanidineacetic acid 352-97-6 CAS NO.352-97-6

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Guanidineacetic acid Basic information

Product Name:	Guanidineacetic acid
Synonyms:	N-Amidinoglycin;(Aminoiminomethyl)aminoacetic acid;GLYCOCYAMINE(GUANIDINOACETIC ACID)(P);Guanidineacetic acid,N-Amidinoglycine, N-Guanylglycine, Glycocyamine;Guanidineacetic acid 99%;Guanidineacetic acid,glucocyamine,Glycocyamine;BetacyaMine;NSC 1901
CAS:	352-97-6
MF:	C3H7N3O2
MW:	117.11
EINECS:	206-529-5
Product Categories:	Pharmaceutical Intermediates;Amino acids;Building Blocks;Chemical Synthesis;Guanidines;Nitrogen Compounds;Intermediates & Fine Chemicals;Pharmaceuticals;Organic Building Blocks
Mol File:	352-97-6.mol

Guanidineacetic acid Chemical Properties

Melting point	300 °C(lit.)
Boiling point	218.88°C (rough estimate)
density	1.4020 (rough estimate)
refractive index	1.4900 (estimate)
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
solubility	6 M NaOH : 50 mg/mL, clear, colorless
pka	2.82(at 25℃)
form	Solid
color	White to Off-White
Water Solubility	3.6g/L(15 ºC)
Merck	14,4495
BRN	1759179
InChIKey	BPMFZUMJYQTVII-UHFFFAOYSA-N
CAS DataBase Reference	352-97-6(CAS DataBase Reference)
EPA Substance Registry System	Glycocyamine (352-97-6)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
WGK Germany	3
RTECS	MB7700000
HS Code	29252000

MSDS Information

Provider	Language
Guanidineacetic acid	English
SigmaAldrich	English
ACROS	English
ALFA	English

Guanidineacetic acid Usage And Synthesis

Chemical Properties	WHITE TO SLIGHTLY BEIGE FINE CRYSTALLINE POWDER
Uses	An important marker for renal failure, in kidney transplantation, and for the renal metabolic activity.
Uses	Guanidinoacetic Acid is an important marker for renal failure, in kidney transplantation, and for the renal metabolic activity.
Definition	ChEBI: The N-amidino derivative of glycine.
Purification Methods	Recrystallise it from 15 parts of hot H2O, or by dissolving it in slightly more than the calculated amount of 2N HCl and precipitating it by adding an equivalent of 2N NaOH, filtering, washing with cold H2O and drying first in vacuo, then at 60o in vacuo. The hydrochloride has m 200o(dec) after recrystallisation from aqueous HCl as plates. The picrate forms needles from hot H2O with m 210o(dec). [Brand & Brand Org Synth Coll Vol III 440 1955, Failey & Brand J Biol Chem 102 768 1933, King J Chem Soc 2375 1930, Beilstein 4 H 359, 4 I 477, 4 II 793, 4 III 1165.]

Guanidineacetic acid Preparation Products And Raw materials

Raw materials	Thiourea-->Bromoethane-->ETHYLTHIOUREA
Preparation Products	2-amino-1,5-dihydro-4H-imidazol-4-one

 

 

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