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Merck
CN

G11608

Sigma-Aldrich

乙酸胍

99%

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别名:
N-脒基甘氨酸, 甘氨酸氰胺, 胍基乙酸
线性分子式:
H2NC(=NH)NHCH2CO2H
CAS号:
分子量:
117.11
Beilstein:
1759179
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

mp

300 °C (lit.)

SMILES字符串

NC(=N)NCC(O)=O

InChI

1S/C3H7N3O2/c4-3(5)6-1-2(7)8/h1H2,(H,7,8)(H4,4,5,6)

InChI key

BPMFZUMJYQTVII-UHFFFAOYSA-N

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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J Michiels et al.
Poultry science, 91(2), 402-412 (2012-01-19)
Creatine, (CREA) a central constituent in energy metabolism, is obtained from dietary animal protein or de novo synthesis from guanidinoacetic acid (GAA). Especially in all-vegetable diets, supplemental CREA or GAA may restore the CREA availability in tissues, and hence, improve
Rafael Deminice et al.
The Journal of nutrition, 141(10), 1799-1804 (2011-09-02)
The aim of the present study was to examine the effects of creatine supplementation on liver fat accumulation induced by a high-fat diet in rats. Rats were fed 1 of 3 different diets for 3 wk: a control liquid diet
Carla Valongo et al.
Clinica chimica acta; international journal of clinical chemistry, 348(1-2), 155-161 (2004-09-17)
A new gas chromatography-mass spectrometry method for routine quantification of urine creatine and guanidinoacetic acid (GAA) has been developed to provide a fast, reliable and inexpensive metabolic screening. Our method uses a two-step derivatization procedure which involves a reaction with
S Stöckler et al.
Pediatric research, 36(3), 409-413 (1994-09-01)
In a patient with extrapyramidal movement disorder and extremely low creatinine concentrations in serum and urine, in vivo proton magnetic resonance spectroscopy disclosed a generalized depletion of creatinine in the brain. Oral substitution of arginine, a substrate for creatine synthesis
Joseph D T Ndika et al.
Molecular genetics and metabolism, 106(1), 48-54 (2012-03-06)
Arginine:glycineamidinotransferase (AGAT/GATM) deficiency has been described in 9 patients across 4 families. Here we describe the clinical outcome and response to creatine supplementation in a patient of the second family affected with AGAT deficiency-a 9-year-old girl. Delayed motor milestones were

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