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L-gulo-Hexodialdose, also known as L-gulono-1,4-lactone, is a naturally occurring organic compound that plays a significant role in the biosynthesis of vitamin C (ascorbic acid) in certain organisms. It is a hexodialdose, meaning it consists of six carbon atoms and two aldehyde groups. L-gulo-Hexodialdose is an important intermediate in the metabolic pathway for the production of ascorbic acid, which is essential for various biological processes, including collagen synthesis, antioxidant activity, and immune system function. In humans, the enzyme responsible for converting L-gulo-Hexodialdose to ascorbic acid is absent, making us one of the few species that cannot synthesize vitamin C and must obtain it through diet.

3056-44-8

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3056-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3056-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3056-44:
(6*3)+(5*0)+(4*5)+(3*6)+(2*4)+(1*4)=68
68 % 10 = 8
So 3056-44-8 is a valid CAS Registry Number.

3056-44-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name glucose dialdehyde

1.2 Other means of identification

Product number -
Other names D-GLUCO-HEXODIALDOSE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3056-44-8 SDS

3056-44-8Downstream Products

3056-44-8Relevant academic research and scientific papers

Development of a transient response technique for heterogeneous catalysis in the liquid phase, Part 1: Applying an electrospray ionization mass spectrometry (ESI-MS) detector

Radivojevic,Ruitenbeek,Seshan,Lefferts

experimental part, p. 244 - 254 (2009/02/05)

We have developed a novel, transient response technique for liquid-phase heterogeneous catalytic studies, equipped with an electrospray ionization mass spectrometry (ESI-MS) detector. The technique was successfully applied as an online method for real-time detection of species dissolved in aqueous product streams at the exit of a catalytic reactor. Two test reactions, nitrite reduction with Pt/SiO2 and glucose oxidation with Pt/CNF/Ni, were used to demonstrate semi-quantitative monitoring of reactants, intermediates, and products. The capability of the novel technique is demonstrated by the fact that the ESI-MS detector is sufficiently sensitive to determine quantitatively extreme small amounts of physisorbing nitrite, down to 0.5% of a monolayer on the Pt surface. Nitrite also reacts with preadsorbed hydrogen, and the quantitative experimental results agree with the formation of both nitrogen and ammonia. The ESI-MS detector is able to distinguish between different components simultaneously, as in the case of glucose oxidation; this is its most significant advantage over existing transient techniques. A limitation of ESI-MS is its inability to detect gases dissolved in liquids, due to the relatively mild ionization process through electrospray. The second part of this article discusses an alternative detector to satisfy this deficiency.

ACTION OF ULTRASOUND ON DEOXYGENATED AQUEOUS SOLUTONS OF D-GLUCOSE

Heusinger, Helmut

, p. 67 - 76 (2007/10/02)

The action of ultrasound on deoxygenated aqueous solutions of D-glucose yielded D-gluconic acid, D-arabino-hexos-2-ulose, D-ribo-hexos-3-ulose, D-xylo-hexos-4- and -5-ulose, D-gluco-hexodialdose, 2-deoxy-D-arabino-hexonic acid, 5-deoxy-D-xylo-hexonic acid, 6-deoxy-L-threo-hexos-4,5-diulose, and 6-deoxy-D-threo-hexos-2,5-diulose.There was little cleavage of the carbon skeleton.The ratio of the deoxy compounds to the sum of the hexosuloses and the hexodialdose was smaller on sonolysis than on γ-irradiation.

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