Guanidinoacetic acid

Name: Guanidinoacetic acid
Brand: Selleck Chemicals
SKU: S6340
Rating: 5 (1 reviews)

Synonyms: Guanidino acetic acid, GAA, Glycocyamine, Guanidinoacetate

Catalog No.S6340 Purity: 98.5%

Guanidinoacetic acid (Guanidino acetic acid, GAA, Glycocyamine, Guanidinoacetate), the natural precursor of creatine, is under investigation as a dietary agent. Guanidinoacetic acid exhibits potential ergogenic benefits for physically active men and women.

Guanidinoacetic acid Chemical Structure

CAS: 352-97-6

Purity & Quality Control

Batch: S634001 4-Methylpyridine] 5 mg/mL] true] DMSO] Insoluble] false] Water] Insoluble] false Purity: 98.5%

98.5

Guanidinoacetic acid Related Products

Related Products	BAPTA-AM Mitotane ATP disodium Rat IgG2b isotype control-InVivo Bendamustine Deferiprone Blebbistatin Methyl-β-cyclodextrin (MβCD) Dexrazoxane AP-III-a4 (ENOblock) 5-Aminolevulinic acid HCl Carbazochrome sodium sulfonate (AC-17) Ursolic Acid Mesna Amifostine trihydrate Guadecitabine (SGI-110) Osthole NAD+ 4-Methylumbelliferone (4-MU) Dioscin L-carnitine (Levocarnitine) Ethidium bromide Pitstop 2 Sesamin Bilobalide Formononetin Hesperidin Palmitic acid Azeliragon (TTP488) L-Mimosine Ademetionine Carbenoxolone Sodium Gadodiamide Hydrate GO-203 Vitexin N6022 Dp44mT Chlorogenic Acid Sphingosine Chrysin Coenzyme Q10 (CoQ10) Spermine Tetrahydrochloride 2-NBDG 2-NBDG D-Lin-MC3-DMA (MC3) L-Glutamine Morin Hydrate Ethylenediaminetetraacetic acid Silibinin (NSC 651520) (+)-Fangchinoline Tyloxapol Bergenin Spermine NB 598 DMNQ Trabectedin (20S)Ginsenoside Rg2 Farrerol EGCG Octaacetate D-(+)-Trehalose dihydrate Reboxetine mesylate Eprodisate disodium E7820 Gadopentetate Dimeglumine MYLS22 Hydroxytyrosol Evofosfamide (TH-302) Bromhexine HCl Gadodiamide 5-hydroxytryptophan (5-HTP) Inosine D-Mannose Anethole trithione Edetate calcium disodium DMF(N,N-Dimethylformamide) Iodoacetamide Sodium Nitroprusside Dihydrate Alendronic Acid 2,4-Pyridinedicarboxylic acid Ropivacaine GSK805 Betaine ADP Acipimox Curcumin analog C1 Clodronate Disodium Trimetazidine 2'-Deoxyadenosine monohydrate 2,2,2-Tribromoethanol Sulfopin Polaprezinc N-Acetylneuraminic acid Quinacrine Dihydrochloride Dihydrate L-methionine Brucine Glycine Tranexamic Acid Stigmasterol Oleanonic Acid Substance P TFA Achyranthes bidentata root Extract Ginsenoside Rg3 Phyllanthus Urinaria Extract Iopromide NSI-189 SR8278 Lycopene Lactulose Trometamol hydrochloride 1-Methyl-3-nitro-1-nitrosoguanidine (MNNG) Cilastatin Ureidosuccinic acid Hydrochlorothiazide Tea polyphenol Fructose (+)-JQ1 carboxylic acid Ligustilide Polybrene (Hexadimethrine Bromide) Taurocholic acid sodium salt hydrate Pinoresinol diglucoside 4-HNE (4-Hydroxynonenal) Iron Dextran Enoxaparin sodium Urea Methimazole Metolazone Sodium Picosulfate IM-54 Hydroxypropyl Cellulose Disufenton sodium Troxipide Orcinol glucoside Diludine 20R-Camptothecin (+)-Usniacin 3-Indolebutyric acid (IBA) HEPES Cremophor EL BMS-986176 DTT (Dithiothreitol) Esculin Norethindrone Methyl Eugenol Polyinosinic acid-polycytidylic acid D-Mannitol L-(-)-Glucose 1-Hydroxy-2-naphthoic acid Azomycin 3-Hydroxybenzoic acid Emlenoflast (MCC-7840) β-Alanine Alendronate sodium trihydrate β-Sitosterol Sorbitol Rat IgG1 isotype control-InVivo Magnesium lactate trihydrate Aminomalonic acid Helecin BRM/BRG1 ATP Inhibitor-1 23-Hydroxybetulinic acid PZ-2891 Meglumine L-Lactic acid Toosendanin 1,2-Propanediol Epibrassinolide Cyanidin-3-O-glucoside chloride Dihydrotanshinone I Hydrocortisone butyrate Gracillin Sodium Pyruvate Itaconic acid FH1 Cinnamic acid Guanidine HCl Diroximel Fumarate Triethylenetetramine (Trientine) 2HCl Molsidomine Calcium D-saccharate tetrahydrate Creatine monohydrate Oxybenzone D-Glucose 6-phosphate disodium salt DL-Dopa Indocyanine green FPH1 Glycochenodeoxycholic acid 5'-Adenylic acid Acetamide ML329 Pterostilbene Kinetin Acetyl Resveratrol GSK4112 LTI-291 Pramoxine HCl Plantamajoside Anhydroicaritin BZ1 Difluprednate Phloretic acid Anemoside B4 Avobenzone EGTA Sucralose 6-Chloropurine Glucosamine hydrochloride Sinoacutine 2,4-Dihydroxyacetophenone Stearic acid Stevioside Morin PMPA tetrasodium salt Monocrotaline Creatine phosphate disodium salt L-Hydroorotic acid Cholic acid Irigenin Dextrose Behenic Acid Metaxalone CTX-0294885 Fudosteine Magnesium chloride (R)-(-)-JQ1 Enantiomer β-Estradiol 17-Acetate 2'-Deoxyguanosine monohydrate L-Tryptophanamide Hydrochloride β-Cyclodextrin 3-Indolepropionic acid DL-Citrulline L-arginine Sclareol Ibandronate sodium monohydrate Talc Methyl protocatechuate Sodium nitroprusside Risedronate N-Nitrosodiethylamine Deoxyaconitine N-Acetyl-L-methionine Ethanolamine hydrochloride Sinapine thiocyanate Sodium succinate Senkyunolide A L-Tryptophan Swertiamarin Octyl gallate Brassinazole	Click to Expand
Related Compound Libraries	FDA-approved Drug Library Natural Product Library Bioactive Compound Library-I Bioactive Compound Library-Ⅱ Express-Pick Library	Click to Expand

Biological Activity

Description	Guanidinoacetic acid (Guanidino acetic acid, GAA, Glycocyamine, Guanidinoacetate), the natural precursor of creatine, is under investigation as a dietary agent. Guanidinoacetic acid exhibits potential ergogenic benefits for physically active men and women.

NCT Number	Recruitment	Conditions	Sponsor/Collaborators	Start Date	Phases
Clinical Trial Information (data from https://clinicaltrials.gov, updated on 2024-01-11)
NCT06150820	Recruiting	Pompe Disease (Late-onset)	Astellas Gene Therapies\|Astellas Pharma Inc	November 30 2023	Not Applicable
NCT05312736	Recruiting	Gyrate Atrophy\|Gyrata of Choroid and Retina; Atrophy\|Ornithine-δ-aminotransferase\|OAT\|Chorioretinal Degeneration	Jaeb Center for Health Research\|Conquering Gyrate Atrophy Foundation\|Food and Drug Administration (FDA)\|Department of Health and Human Services	November 21 2023	--
NCT05874388	Not yet recruiting	Friedreich Ataxia	Institut National de la Santé Et de la Recherche Médicale France	September 1 2023	Not Applicable
NCT05448131	Recruiting	Pompe-Disease	Centre for Analytical Biochemistry and Biomedical Mass Spectrometry\|University of Giessen	February 1 2023	--
NCT04981210	Recruiting	Pompe Disease	National Taiwan University Hospital	August 1 2021	--

References

[1] Sergej M Ostojic. Amino Acids. 2016 Aug;48(8):1867-75.

Chemical Information & Solubility

Molecular Weight	117.11	Formula	C₃H₇N₃O₂
CAS No.	352-97-6	SDF	--
Storage (From the date of receipt)	3 years -20°C powder	Storage of Stock Solutions Aliquot the stock solutions to avoid repeated freeze-thaw cycles	1 year-80°Cin solvent
Storage (From the date of receipt)	3 years -20°C powder		1 month-20°Cin solvent

In vitro
Batch:

4-Methylpyridine : 5 mg/mL

DMSO : Insoluble ( Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Molecular Weight Calculator

In vivo
Batch:

Add solvents to the product individually and in order.

In vivo Formulation Calculator

Preparing Stock Solutions

Molarity Calculator

Dilution Calculator Molecular Weight Calculator

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

Dosage: mg/kg Average weight of animals: g Dosing volume per animal:μL Number of animals:

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO + % + % Tween 80 + % ddH₂O

%DMSO+ %

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH₂O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

Tel: +1-832-582-8158 Ext:3
If you have any other enquiries, please leave a message.

* Indicates a Required Field

C1=C0/X	C1:	LOG(C1):
C2=C1/X	C2:	LOG(C2):
C3=C2/X	C3:	LOG(C3):
C4=C3/X	C4:	LOG(C4):
C5=C4/X	C5:	LOG(C5):
C6=C5/X	C6:	LOG(C6):
C7=C6/X	C7:	LOG(C7):
C8=C7/X	C8:	LOG(C8):