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1A04500

USP

L-Glucono-delta-lactone

Pharmaceutical Analytical Impurity (PAI)

Synonym(s):

L-Glucono-delta-lactone, ((3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-one)

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About This Item

Empirical Formula (Hill Notation):
C6H10O6
CAS Number:
Molecular Weight:
178.14
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
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grade

pharmaceutical analytical impurity (PAI)

agency

USP

API family

canagliflozin

manufacturer/tradename

USP

mp

142-144 °C (lit.)

application(s)

pharmaceutical
pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

-10 to -25°C

SMILES string

OC[C@@H]1OC(=O)[C@@H](O)[C@H](O)[C@H]1O

InChI key

PHOQVHQSTUBQQK-KLVWXMOXSA-N

General description

Find answers to frequently asked questions on USP products in USP FAQs.
L-Glucono-δ-lactone is a USP Pharmaceutical Analytical Impurity (PAI).


USP PAI are a product line of impurities suitable for research and analytical purposes, which help to ensure the quality and safety of medicines.


Associated Drug Substance: Canagliflozin


Therapeutic Area: Endocrine

Application

L-Glucono-δ-lactone (USP PAI) is intended for use in analytical testing to detect, identify, and measure pharmaceutical impurities.

Features and Benefits

USP PAI advance your early analytical R&D and process development. PAI can be used in the following applications:
1. Conduct analytical tests during early formulation feasibility studies.
2. Determine degradation impurities produced during stress studies.
3. Develop, validate, and transfer analytical methods.
4. Perform spiking studies during process R&D to demonstrate depletion upon recrystallization.
5. Record retention times and/or spectra
6. Determine relative response factors.
7. Identify unknown impurities that formed during ICH stability conditions.
8. Identify impurities that are present in the Reference Listed Drug
9. Test for and profile impurities not listed in drug substance and drug product monographs.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  

Other Notes

Sales restrictions may apply.
USP issued SDS can be found here

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This Item
1A0812015976171800184
description

Pharmaceutical Analytical Impurity (PAI)

description

pharmaceutical analytical impurity (PAI)

description

United States Pharmacopeia (USP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

manufacturer/tradename

USP

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical analytical impurity (PAI)

grade

pharmaceutical primary standard

grade

USP Analytical Reference Materials (ARMs)

format

neat

format

neat

format

neat

format

neat

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical small molecule

mp

142-144 °C (lit.)

mp

-

mp

-

mp

-

storage temp.

-10 to -25°C

storage temp.

2-30°C

storage temp.

2-8°C

storage temp.

2-8°C


Storage Class

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable



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