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50199

Gly-Gly

≥99.5% (NT), BioUltra

Synonym(s):

Diglycine, Glycyl-glycine

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About This Item

Linear Formula:
NH2CH2CONHCH2COOH
CAS Number:
Molecular Weight:
132.12
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12161700
EC Number:
209-127-8
MDL number:
Beilstein/REAXYS Number:
1765223
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Product Name

Gly-Gly, BioUltra, ≥99.5% (NT)

product line

BioUltra

Quality Level

assay

≥99.5% (NT)

form

powder

impurities

insoluble matter, passes filter test

ign. residue

≤0.05% (as SO4)

loss

≤0.05% loss on drying, 110 °C

color

white

pH

4.5-6.0 (20 °C, 1 M in H2O)

useful pH range

7.5-8.9

pKa (25 °C)

8.2

mp

220-240 °C

solubility

H2O: 1 M at 20 °C, clear, colorless

anion traces

chloride (Cl-): ≤50 mg/kg, sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤5 mg/kg, As: ≤0.1 mg/kg, Ba: ≤5 mg/kg, Bi: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤50 mg/kg, Li: ≤5 mg/kg, Mg: ≤5 mg/kg, Mn: ≤5 mg/kg, Mo: ≤5 mg/kg, NH4+: ≤200 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Sr: ≤5 mg/kg, Zn: ≤5 mg/kg

λ

1 M in H2O

UV absorption

λ: 260 nm Amax: 0.075, λ: 280 nm Amax: 0.072

SMILES string

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 key

YMAWOPBAYDPSLA-UHFFFAOYSA-N

Gene Information

human ... SLC15A1(6564)

Application

  • Structural and molecular insights into a bifunctional glycoside hydrolase 30 xylanase specific to glucuronoxylan: This study provides a detailed analysis of the enzyme′s structure and function, demonstrating D-(+)-Xylose′s role in enhancing our understanding of xylose metabolism in industrial applications such as biofuel production and biotechnological innovations (Pentari et al., 2024).

  • Efficient production of 1,2,4-butanetriol from corn cob hydrolysate by metabolically engineered Escherichia coli: Highlights the utilization of D-(+)-Xylose from agricultural waste, optimizing processes for sustainable biofuel production, emphasizing the sugar′s pivotal role in renewable energy research (Li et al., 2024).

  • Biochemical characterization of a xylose-tolerant GH43 β-xylosidase from Geobacillus thermodenitrificans: Provides insights into the enzyme′s biophysical properties and its utility in biotechnological applications, furthering the understanding of D-(+)-Xylose′s role in enhancing enzyme performance under various industrial conditions (Melo et al., 2023).

  • Genome-scale metabolic modeling reveals metabolic trade-offs associated with lipid production in Rhodotorula toruloides: Explores how D-(+)-Xylose can be used to optimize metabolic pathways for improved lipid production, highlighting its potential in synthetic biology and metabolic engineering to enhance bioproduct synthesis efficiency (Reķēna et al., 2023).

Other Notes

Superior buffer for the growth of Aphanosthece halophytica (Chroococcales) in hypersaline media

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This Item
G3915G1002G0674
form

powder

form

powder

form

powder

form

powder

assay

≥99.5% (NT)

assay

≥99%

assay

≥99% (titration)

assay

-

product line

BioUltra

product line

-

product line

-

product line

-

cation traces

Al: ≤5 mg/kg, Ba: ≤5 mg/kg, Ca: ≤10 mg/kg, Co: ≤5 mg/kg, Cu: ≤5 mg/kg, K: ≤50 mg/kg, Mg: ≤5 mg/kg, Mo: ≤5 mg/kg, Na: ≤50 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg, As: ≤0.1 mg/kg, Cd: ≤5 mg/kg, Fe: ≤5 mg/kg, Mn: ≤5 mg/kg, Ni: ≤5 mg/kg, Bi: ≤5 mg/kg, Li: ≤5 mg/kg, Sr: ≤5 mg/kg, Cr: ≤5 mg/kg, NH4+: ≤200 mg/kg

cation traces

heavy metals (as Pb): ≤5 ppm

cation traces

-

cation traces

-

color

white

color

white

color

white

color

-

mp

220-240 °C

mp

255-260 °C

mp

262-264 °C

mp

-


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Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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D.R. Tindall et al.
Phycologia, 17, 179-179 (1978)
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
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



Global Trade Item Number

SKUGTIN
50199-50G04061832422640
50199-10G04061832422633

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