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Merck

V900403

Sigma-Aldrich

双甘肽

99%, Vetec

别名:

二甘氨酸, 甘氨酰-甘氨酸

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About This Item

线性分子式:
NH2CH2CONHCH2COOH
CAS号:
分子量:
132.12
Beilstein:
1765223
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
价格与库存信息目前不能提供

产品名称

双甘肽, Vetec, reagent grade, 99%

等級

reagent grade

產品線

Vetec

化驗

99%

形狀

powder

技術

ligand binding assay: suitable

顏色

white

有用的pH值範圍

7.5-8.9

pKa (25 °C)

8.2

mp

255-260 °C

SMILES 字串

NCC(=O)NCC(O)=O

InChI

1S/C4H8N2O3/c5-1-3(7)6-2-4(8)9/h1-2,5H2,(H,6,7)(H,8,9)

InChI 密鑰

YMAWOPBAYDPSLA-UHFFFAOYSA-N

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法律資訊

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Chatterjee et al.
Langmuir : the ACS journal of surfaces and colloids, 28(34), 12502-12508 (2012-08-21)
The early adsorption stage of glycylglycine on Si(111)7×7 surface has been studied by scanning tunneling microscopy (STM). Filled-state imaging shows that glycylglycine adsorbs dissociatively in a bidentate fashion on two adjacent Si adatoms across a dimer wall or an adatom-restatom
Lasse Jenner et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(10), 3812-3816 (2013-02-23)
Here we present an X-ray crystallography structure of the clinically relevant tigecycline antibiotic bound to the 70S ribosome. Our structural and biochemical analysis indicate that the enhanced potency of tigecycline results from a stacking interaction with nucleobase C1054 within the
Eduard Schreiner et al.
Journal of the American Chemical Society, 133(21), 8216-8226 (2011-05-13)
A comprehensive study of free energy landscapes and mechanisms of COS-mediated polymerization of glycine via N-carboxy anhydrides (NCAs, "Leuchs anhydrides") and peptide hydrolysis at the water-pyrite interface at extreme thermodynamic conditions is presented. Particular emphasis is set on the catalytic
Francis Impens et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(34), 12432-12437 (2014-08-13)
SUMOylation is an essential ubiquitin-like modification involved in important biological processes in eukaryotic cells. Identification of small ubiquitin-related modifier (SUMO)-conjugated residues in proteins is critical for understanding the role of SUMOylation but remains experimentally challenging. We have set up a
Christopher M Leavitt et al.
Journal of the American Society for Mass Spectrometry, 22(11), 1941-1952 (2011-09-29)
We report vibrational predissociation spectra of the four protonated dipeptides derived from glycine and sarcosine, GlyGlyH(+)•(H(2))(1,2), GlySarH(+)•(D(2))(2), SarGlyH(+)•(H(2))(2), and SarSarH(+)•(D(2))(2), generated in a cryogenic ion trap. Sharp bands were recovered by monitoring photoevaporation of the weakly bound H(2) (D(2)) molecules

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