D-(+)-Gluconic acid δ-lactone - 10mM in DMSO , CAS No.90-80-2

CAS: 90-80-2 Cat. No.: D426861 分子式: C6H10O6 分子量: 178.14 Beilstein Registry Number: 83286 EC番号: 202-016-5
注文可能
GRADE & PURITY 10mM in DMSO
Synonyms
1,5-D-Gluconolactone | D-(+)-Gluconic acid d-lactone | D-(+)-Gluconic acid-delta lactone | EINECS 202-016-5 | D-Gluconic acid lactone | delta-Gluconic acid lactone | UNII-WQ29KQ9POT | delta-Gluconic acid-delta-lactone | NSC34393 | NSC-34393 | Glucolactone
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
USA
ドイツ (EU)*
Price
Qty
1ml
D426861-1ml
2 在庫あり
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$26.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 155 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

Product Application:

Glucono delta-lactone (GDL) is a kind of excellent multifunctional food additive. It is mainly used as protein coagulant, acidifier, pickling, or leavening agent. expander, preservative, seasonings, sequestrant, chelating agent, color-preserver, etc. it is widely applied to food, daily chemical industry, pharmaceuticals, cosmetics. Plastic and resinous modification, electrode position and polish, metal-surface cleaning and organic synthesis.

Specifications

同義語
1,5-D-Gluconolactone | D-(+)-Gluconic acid d-lactone | D-(+)-Gluconic acid-delta lactone | EINECS 202-016-5 | D-Gluconic acid lactone | delta-Gluconic acid lactone | UNII-WQ29KQ9POT | delta-Gluconic acid-delta-lactone | NSC34393 | NSC-34393 | Glucolactone
仕様と純度
10mM in DMSO
生化学的・生理学的メカニズム
Gluconolactone is a product of the oxidation of glucose by glucose oxidase. It has been found to be a mixed type, noncompetitive inhibitor for the hydrolysis of p-nitrophenyl alpha-D-glucoside by glucoamylase, an enzyme that breaks down starch into glucos
保管条件
Store at -80°C
入荷
Dry ice packs + Cold packs
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
名前と識別子
パブケム・シド
カノニカル・スマイル
C(C1C(C(C(C(=O)O1)O)O)O)O
IUPAC Name
(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-one
InChIKey
PHOQVHQSTUBQQK-SQOUGZDYSA-N
INCHI
1S/C6H10O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-5,7-10H,1H2/t2-,3-,4+,5-/m1/s1
異性体SMILES
C([C@@H]1[C@H]([C@@H]([C@H](C(=O)O1)O)O)O)O
WGKドイツ
3
RTECS
LZ5184000
分子量
178.14
Beilstein
83286
Reaxy-Rn
13905182
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13905182&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
分類Organooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides - Hexoses
Direct ParentGluconolactones
Alternative Parents Delta valerolactones  Oxanes  Secondary alcohols  Carboxylic acid esters  Polyols  Oxacyclic compounds  Monocarboxylic acids and derivatives  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Gluconolactone - Delta valerolactone - Delta_valerolactone - Oxane - Carboxylic acid ester - Lactone - Secondary alcohol - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Polyol - Hydrocarbon derivative - Organic oxide - Alcohol - Primary alcohol - Carbonyl group - Aliphatic heteromonocyclic compound
説明This compound belongs to the class of organic compounds known as gluconolactones. These are polyhydroxy acids containing a gluconolactone molecule, which is characterized by a tetrahydropyran substituted by three hydroxyl groups, one ketone group, and one hydroxymethyl group.
External Descriptors aldono-1,5-lactone - gluconolactone
3 D構造
インタラクティブ化学構造モデル





関連ターゲット(人間)
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
作用メカニズム
証明書(CoA、COO、BSE/TSEと分析図)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
化学的性質と物理的性質
感度Moisture sensitive; light sensitive
比旋光度[α]63.5 ° (C=10, H2O)
融点(°C)160°C
分子量178.140 g/mol
XLogP3-2.000
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count1
Exact Mass178.048 Da
Monoisotopic Mass178.048 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity181.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
よくある質問と記事
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)
Alginate : An Overview of Extraction and Purification Processes, Quality Identification, and Multidomain Applications
Galactose-Related Precursor Conversion and Redox Regulation in Plant Ascorbate Biosynthesis
The Dual-Targeted Skin-Brightening Mechanism of 4-MSK: Inhibiting Melanin Production and Reducing Epidermal Pigment Retention
Potential Mechanisms of Succinic Acid in Acne Care: From Dicarboxylic Acid–Base Equilibria to Metabolic Antagonism Among Skin Microorganisms
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
Citations of This Product
ソリューション計算機
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