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N1138

Sigma-Aldrich

N-Nonanoyl-N-methylglucamine

≥98%

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Synonym(s):
N-(D-Glucityl)-N-methylnonanamide, N-Methyl-N-nonanoyl-D-glucamine, MEGA-9
Empirical Formula (Hill Notation):
C16H33NO6
CAS Number:
85261-19-4
Molecular Weight:
335.44
UNSPSC Code:
12352116
PubChem Substance ID:
24897463
NACRES:
NA.32

description

non-ionic

Quality Level

300

Assay

≥98%

form

powder

mol wt

335.44 g/mol

technique(s)

protein expression: suitable

CMC

19-25 mM (20-25°C)

suitability

suitable for molecular biology

application(s)

life science and biopharma

SMILES string

CCCCCCCCC(=O)N(C)C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

InChI

1S/C16H33NO6/c1-3-4-5-6-7-8-9-14(21)17(2)10-12(19)15(22)16(23)13(20)11-18/h12-13,15-16,18-20,22-23H,3-11H2,1-2H3/t12-,13+,15+,16+/m0/s1

InChI key

GCRLIVCNZWDCDE-SJXGUFTOSA-N

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Related Categories

Application

N-Nonanoyl-N-methylglucamine has been used to reconstitute proteins into liposomes. It has also been used to study its effects on the oligomerization of Bacillus thuringiensis Cry4Ba toxin.
Non-ionic, dialyzable detergent

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Functional assembly of 260-kDa oligomers required for mosquito-larvicidal activity of the Bacillus thuringiensis Cry4Ba toxin
Narumol Khomkhum
Peptides (2015)
Conserved Properties of Polypeptide Transport-associated (POTRA) Domains Derived from Cyanobacterial Omp85*
Patrick Koenig
The Journal of Biological Chemistry (2010)
K Häsler et al.
Biochemistry, 38(41), 13759-13765 (1999-10-16)
ATP synthase is conceived as a rotary enzyme. Proton flow drives the rotor (namely, subunits c12 epsilon gamma) relative to the stator (namely, subunits ab2 delta(alpha beta)3) and extrudes spontaneously formed ATP from three symmetrically arranged binding sites on (alpha
Dhanesh Gadre et al.
Journal of chromatography. A, 1575, 49-58 (2018-09-29)
Endotoxins are complex molecules and one of the most challenging impurities requiring separation in biopharmaceutical protein purification processes. Usually these contaminants are cleared during the downstream process, but if endotoxin interacts with the target protein it becomes difficult to remove.
Yi-Ching Hsueh et al.
Plant, cell & environment, 40(8), 1643-1657 (2017-04-23)
Glycerolipid synthesis in plants is coordinated between plastids and the endoplasmic reticulum (ER). A central step within the glycerolipid synthesis is the transport of phosphatidic acid from ER to chloroplasts. The chloroplast outer envelope protein TGD4 belongs to the LptD
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