Guanidineacetic acid

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;352-97-6
Mol File:352-97-6.mol
Guanidineacetic acid Structure
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
pka2.82(at 25℃)
form Solid
color White to Off-White
Water Solubility 3.6g/L(15 ºC)
Merck 14,4495
BRN 1759179
InChIKeyBPMFZUMJYQTVII-UHFFFAOYSA-N
CAS DataBase Reference352-97-6(CAS DataBase Reference)
EPA Substance Registry SystemGlycocyamine (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
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Guanidineacetic acid English
SigmaAldrich English
ACROS English
ALFA English
Guanidineacetic acid Usage And Synthesis
Chemical PropertiesWHITE TO SLIGHTLY BEIGE FINE CRYSTALLINE POWDER
UsesGuanidinoacetic Acid is an important marker for renal failure, in kidney transplantation, and for the renal metabolic activity.
DefinitionChEBI: The N-amidino derivative of glycine.
Purification MethodsRecrystallise 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 materialsThiourea-->Bromoethane-->ETHYLTHIOUREA
Preparation Products2-amino-1,5-dihydro-4H-imidazol-4-one
CREATINE-(METHYL-13C) MONOHYDRATE CYCLOCREATINE (2-AMINO-4-METHYL-6-OXOPYRIMIDIN-1(6H)-YL)ACETIC ACID (4,5-DIHYDRO-1 H-IMIDAZOL-2-YLAMINO)-ACETIC ACID GUANIDINOSUCCINIC ACID 2-GUANIDINOPROPIONIC ACID Creatine phosphate 2-([[(4-METHYLBENZYL)AMINO](PHENYLIMINO)METHYL]AMINO)ACETIC ACID CREATINE PHOSPHATE, DIPOTASSIUM SALT GUANIDINEACETIC ACID, [1-14C]- CREATINE, [4-14C] PHOSPHOCREATINE DI-TRIS SALT (3-ALLYL-2-IMINO-2,3-DIHYDRO-BENZOIMIDAZOL-1-YL)-ACETIC ACID ALPHA-GUANIDINOGLUTARIC ACID (2-IMINO-3-METHYL-2,3-DIHYDRO-BENZOIMIDAZOL-1-YL)-ACETIC ACID ARGININOSUCCINIC ACID DISODIUM SALT 6-HYDROXYTRYPTAMINE, CREATINE SULFATE (2-IMINO-3-METHYL-2,3-DIHYDRO-BENZOIMIDAZOL-1-YL)-ACETIC ACID HYDROBROMIDE

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