N-(Propionyloxy)succinimide

Name: <I>N</I>-(Propionyloxy)succinimide
Brand: SIAL
Price: 331 USD
Availability: InStock

for LC-MS derivatization, LiChropur^™, ≥95% (HPLC)

Synonym(s):

1-(1-Oxopropoxy)-2,5-pyrrolidinedione, 2,5-Dioxopyrrolidin-1-yl-propanoate, Propanoic acid-NHS ester, Propionyl-Osu, Succinimidyl propionate

Slide 1 of 1

Select a Size

1 G

$331.00

Available to ship TODAYDetails

One Time Order

Request a Bulk Order

Subscriptions are currently unavailable.

About This Item

Empirical Formula (Hill Notation):

C₇H₉NO₄

CAS Number:

30364-55-7

Molecular Weight:

171.15

MDL number:

MFCD03427483

UNSPSC Code:

41116105

NACRES:

NA.22

Key Documents

View All Documentation

Quality Level

100

assay

≥95% (HPLC)

form

solid

quality

LiChropur^™
for LC-MS derivatization

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations

technique(s)

LC/MS: suitable

SMILES string

O=C(CCC1=O)N1OC(CC)=O

InChI

1S/C7H9NO4/c1-2-7(11)12-8-5(9)3-4-6(8)10/h2-4H2,1H3

InChI key

AASBXERNXVFUEJ-UHFFFAOYSA-N

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item	774324	633259	764221
Supelco 93535 N-(Propionyloxy)succinimide	Sigma-Aldrich 774324 N-(Benzoyloxy)succinimide	Sigma-Aldrich 633259 N-Acetoxy-d₃-succinimide	Sigma-Aldrich 764221 Propargyl-N-hydroxysuccinimidyl ester
assay ≥95% (HPLC)	assay 96%	assay -	assay -
form solid	form solid	form solid	form solid
quality LiChropur^™	quality -	quality -	quality -
reaction suitability reagent type: derivatization reagent reaction type: Acylations	reaction suitability -	reaction suitability -	reaction suitability -
technique(s) LC/MS: suitable	technique(s) -	technique(s) protein expression: suitable	technique(s) -
Quality Level 100	Quality Level 100	Quality Level -	Quality Level 100

General description

N-(Propionyloxy)succinimide is commonly used as a mobile phase additive in liquid chromatography-mass spectrometry (LC-MS) and its typical application involves the derivatization of histones. It involves the following properties:

Extensive QC testing ensures the highest specifications.
Optimized to improve ionization and resolution.
Extremely low levels of inorganic and organic impurities.
Manufactured specifically for accurate and fast LC-MS.

Other Notes

Discover LiChropur^™ reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.

Description

Pricing

73345

Dibutylammonium acetate solution, 0.5 M in H₂O, LiChropur^™, suitable for ion pair chromatography

70221

Ammonium formate, eluent additive for LC-MS, LiChropur^™, ≥99.0%

73594

Ammonium acetate, LiChropur^™, eluent additive for LC-MS

89789

Dipropylammonium acetate solution, 0.5 M in H₂O, suitable for ion pair chromatography

80457

Trifluoroacetic acid, eluent additive for LC-MS, LiChropur^™, ≥99.0% (GC)

18370

2,2,2-Trifluoroethanol, suitable for mass spectrometry (MS), LiChropur^™, ≥99.8% (GC)

93645

Dihexylammonium acetate solution, 0.5 M in H₂O, suitable for ion pair chromatography, LiChropur^™

51197

Sodium formate solution, suitable for LC-MS, LiChropur^™

00922

Difluoroacetic acid, for LC-MS LiChropur^™, ≥97.5% (GC)

00940

Formic acid, for LC-MS LiChropur^™, 97.5-98.5% (T)

5.33004

Ammonium acetate, for LC-MS LiChropur^™

5.33001

Acetic acid 100%, for LC-MS LiChropur^™

5.33002

Formic acid 98% - 100%, for LC-MS LiChropur^™

5.33005

Ammonium hydrogen carbonate, for LC-MS LiChropur^™

18127

1,1,1,3,3,3-Hexafluoro-2-propanol, for LC-MS LiChropur^™

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mitragynine, an euphoric compound inhibits hERG1a/1b channel current and upregulates the complexation of hERG1a-Hsp90 in HEK293-hERG1a/1b cells.

Yea Lu Tay et al.

Scientific reports, 9(1), 19757-19757 (2019-12-26)

Mitragyna speciosa Korth (M. speciosa) has been widely used as a recreational product, however, there are growing concerns on the abuse potentials and toxicity of the plant. Several poisoning and fatal cases involving kratom and mitragynine have been reported but

Longin R-SNARE is retrieved from the plasma membrane by ANTH domain-containing proteins in Arabidopsis.

Masaru Fujimoto et al.

Proceedings of the National Academy of Sciences of the United States of America, 117(40), 25150-25158 (2020-09-25)

The plasma membrane (PM) acts as the interface between intra- and extracellular environments and exhibits a tightly regulated molecular composition. The composition and amount of PM proteins are regulated by balancing endocytic and exocytic trafficking in a cargo-specific manner, according

Archaeal Chromatin Proteins Cren7 and Sul7d Compact DNA by Bending and Bridging.

Zhenfeng Zhang et al.

mBio, 11(3) (2020-06-11)

Archaeal chromatin proteins Cren7 and Sul7d from Sulfolobus are DNA benders. To better understand their architectural roles in chromosomal DNA organization, we analyzed DNA compaction by Cren7 and Sis7d, a Sul7d family member, from Sulfolobus islandicus at the single-molecule (SM)

Role of C-mannosylation in the secretion of mindin.

Yoko Inai et al.

Biochimica et biophysica acta. General subjects, 1864(8), 129632-129632 (2020-05-18)

Mindin (spondin2), a secretory protein related to neural development and immunity, is a member of thrombospondin type I repeat (TSR) superfamily proteins, and has a unique glycosylation of C-mannosylation in its structure. However, it remains unclear whether C-mannosylation plays a

A Kelch13-defined endocytosis pathway mediates artemisinin resistance in malaria parasites.

Jakob Birnbaum et al.

Science (New York, N.Y.), 367(6473), 51-59 (2020-01-04)

Artemisinin and its derivatives (ARTs) are the frontline drugs against malaria, but resistance is jeopardizing their effectiveness. ART resistance is mediated by mutations in the parasite's Kelch13 protein, but Kelch13 function and its role in resistance remain unclear. In this

View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service