Identification | More | [Name]
Guanidineacetic acid | [CAS]
352-97-6 | [Synonyms]
2-([AMINO(IMINO)METHYL]AMINO)ACETIC ACID 2-GUANIDINOACETIC ACID GLYCOCYAMINE GUANIDINEACETIC ACID GUANIDINOACETIC ACID GUANIDOACETIC ACID N-AMIDINOGLYCINE N-GUANYLGLYCINE N-(Aminoiminomethyl)glycine N-Amidinoglycine~Glycocyamine GUANIDINOACETIC ACID 99+% BIOTECH GRADE GLYCOYAMINE Gaa(Glycocyamine) Glycocyamine(Gaa) Guanidineaceticacid,99% Glyucocyamine Guanidinoacetic acid, 99+% Guanidinooacetic Acid N-Amidinoglycine, N-Guanylglycine, Glycocyamine Guanidinoacetic acid, N-Amidinoglycine, N-Guanylglycine | [EINECS(EC#)]
206-529-5 | [Molecular Formula]
C3H7N3O2 | [MDL Number]
MFCD00004278 | [Molecular Weight]
117.11 | [MOL File]
352-97-6.mol |
Chemical Properties | Back Directory | [Appearance]
WHITE TO SLIGHTLY BEIGE FINE CRYSTALLINE POWDER | [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
| [form ]
Solid | [pka]
2.82(at 25℃) | [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]
352-97-6(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
MB7700000 | [HS Code ]
29252000 |
Hazard Information | Back Directory | [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. | [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.] |
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