D-Sorbitol solution - AR, ≥98% , CAS No.50-70-4

Name: D-Sorbitol solution - AR, ≥98% , CAS No.50-70-4
SKU: S104833
Availability: InStock

CAS: 50-70-4 Cat. No.: S104833 Formula: C₆H₁₄O₆ Molecular Weight: 182.18 Beilstein Registry Number: 1721899 EC Number: 200-061-5

219 Citations COA

Skip to the end of the images gallery

D-Sorbitol solution - AR, ≥98% CAS No(50-70-4) S104833 by Aladdin Scientific

Skip to the beginning of the images gallery

AVAILABLE TO ORDER

GRADE & PURITY AR ? ≥98%

Synonyms

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews

🧪

Why this grade

AR, ≥98% AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal 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 219 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

May be used for washing spheroplasts and in isoelectric focusing to minimize endoosmotic flow in agarose gels.May be used to induce osmotic stress.

Specifications

Synonyms

Specifications & Purity

AR, ≥98%

Biochemical and Physiological Mechanisms

D-Sorbitol is a sugar alcohol that is commonly used as a sugar substitute. It occurs naturally and is also produced synthetically from glucose. The food industry uses D-sorbitol as an additive in the form of a sweetener, humectant, emulsifier, thickener,

Storage

Room temperature,Argon charged

Shipped In

Normal

Grade

Purity

≥98%

Names and Identifiers

Canonical Smiles	OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)CO
IUPAC Name	(2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol
InChIKey	FBPFZTCFMRRESA-JGWLITMVSA-N
INCHI	1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5-,6-/m1/s1
Isomeric SMILES	C([C@H]([C@H]([C@@H]([C@H](CO)O)O)O)O)O
WGK Germany	2
Alternate CAS	98201-93-5；68425-17-2；1259528-21-6
Molecular Weight	182.18
Beilstein	1721899
Reaxy-Rn	1721899
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721899&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

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Not available
Direct Parent	Sugar alcohols
Alternative Parents	Monosaccharides Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
External Descriptors	glucitol
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D Structure

Associated Targets(Human)

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PGR Tclin Progesterone receptor (8562 Activities)

Discover Target: PGR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

Discover Target: CHRM2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

Discover Target: HTR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

Discover Target: ADRA2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

Discover Target: GABRA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

Discover Target: DRD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

Discover Target: SLC6A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

Discover Target: ADORA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A4 Tclin Serotonin transporter (12625 Activities)

Discover Target: SLC6A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

Discover Target: ADRA1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

Discover Target: DRD3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

Discover Target: PDE3A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)

Discover Target: HTR2B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

Discover Target: TBXA2R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

Discover Target: PDE4A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH3 Tclin Histamine H3 receptor (10389 Activities)

Discover Target: HRH3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACR Tchem Acrosin (277 Activities)

Discover Target: ACR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Homo sapiens (32628 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FEN1 Tchem Flap endonuclease 1 (12055 Activities)

Discover Target: FEN1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

Discover Target: APEX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ABCB11 Tchem Bile salt export pump (2311 Activities)

Discover Target: ABCB11

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

74 results found

Lot Number	Certificate Type	Date	Item
H2617594	Certificate of Analysis	Aug 28, 2026	S104833
H2617595	Certificate of Analysis	Aug 28, 2026	S104833
H2617589	Certificate of Analysis	Aug 26, 2026	S104833
H2617590	Certificate of Analysis	Aug 26, 2026	S104833
E2626501	Certificate of Analysis	Jun 10, 2026	S104833
E2626502	Certificate of Analysis	Jun 10, 2026	S104833
E2626505	Certificate of Analysis	Jun 10, 2026	S104833
A2604521	Certificate of Analysis	Jan 21, 2026	S104833
A2604540	Certificate of Analysis	Jan 21, 2026	S104833
A2604500	Certificate of Analysis	Jan 15, 2026	S104833
A2604541	Certificate of Analysis	Jan 15, 2026	S104833
K2510575	Certificate of Analysis	Nov 12, 2025	S104833
K2510576	Certificate of Analysis	Nov 12, 2025	S104833
I2503493	Certificate of Analysis	Sep 12, 2025	S104833
I2503807	Certificate of Analysis	Sep 12, 2025	S104833
I2503782	Certificate of Analysis	Sep 11, 2025	S104833
I2503806	Certificate of Analysis	Sep 11, 2025	S104833
G2528393	Certificate of Analysis	Aug 04, 2025	S104833
G2528394	Certificate of Analysis	Aug 04, 2025	S104833
F2506678	Certificate of Analysis	Jun 16, 2025	S104833
F2506675	Certificate of Analysis	Jun 16, 2025	S104833
F2506676	Certificate of Analysis	Jun 16, 2025	S104833
F2506677	Certificate of Analysis	Jun 16, 2025	S104833
E2516062	Certificate of Analysis	May 20, 2025	S104833
C2528576	Certificate of Analysis	Apr 14, 2025	S104833
C2528575	Certificate of Analysis	Apr 14, 2025	S104833
C2528398	Certificate of Analysis	Apr 10, 2025	S104833
C2528574	Certificate of Analysis	Apr 10, 2025	S104833
K2414314	Certificate of Analysis	Nov 20, 2024	S104833
K2414345	Certificate of Analysis	Nov 20, 2024	S104833
K2414365	Certificate of Analysis	Nov 20, 2024	S104833
I2409230	Certificate of Analysis	Sep 14, 2024	S104833
I2409231	Certificate of Analysis	Sep 14, 2024	S104833
I2409229	Certificate of Analysis	Sep 14, 2024	S104833
H2401232	Certificate of Analysis	Aug 06, 2024	S104833
H2401233	Certificate of Analysis	Aug 06, 2024	S104833
H2401234	Certificate of Analysis	Aug 06, 2024	S104833
H2401235	Certificate of Analysis	Aug 06, 2024	S104833
D2428509	Certificate of Analysis	May 08, 2024	S104833
D2428507	Certificate of Analysis	May 08, 2024	S104833
D2428508	Certificate of Analysis	May 08, 2024	S104833
D2428510	Certificate of Analysis	May 08, 2024	S104833
B2421316	Certificate of Analysis	Feb 23, 2024	S104833
B2421319	Certificate of Analysis	Feb 23, 2024	S104833
B2421318	Certificate of Analysis	Feb 23, 2024	S104833
B2421317	Certificate of Analysis	Feb 23, 2024	S104833
L2318260	Certificate of Analysis	Dec 19, 2023	S104833
L2318263	Certificate of Analysis	Dec 19, 2023	S104833
L2318264	Certificate of Analysis	Dec 19, 2023	S104833
L2318298	Certificate of Analysis	Dec 19, 2023	S104833
K2314072	Certificate of Analysis	Nov 22, 2023	S104833
K2308164	Certificate of Analysis	Nov 16, 2023	S104833
J2311094	Certificate of Analysis	Oct 17, 2023	S104833
G2324109	Certificate of Analysis	Jul 29, 2023	S104833
G2324110	Certificate of Analysis	Jul 29, 2023	S104833
G2324117	Certificate of Analysis	Jul 27, 2023	S104833
G2324122	Certificate of Analysis	Jul 27, 2023	S104833
E2323420	Certificate of Analysis	May 31, 2023	S104833
E2323422	Certificate of Analysis	May 30, 2023	S104833
C2306528	Certificate of Analysis	Mar 15, 2023	S104833
L2220315	Certificate of Analysis	Dec 24, 2022	S104833
L2220317	Certificate of Analysis	Dec 24, 2022	S104833
L2220318	Certificate of Analysis	Dec 24, 2022	S104833
L2220319	Certificate of Analysis	Dec 24, 2022	S104833
H2205356	Certificate of Analysis	Aug 09, 2022	S104833
H2205357	Certificate of Analysis	Aug 09, 2022	S104833
B2226100	Certificate of Analysis	Feb 28, 2022	S104833
B2226101	Certificate of Analysis	Feb 28, 2022	S104833
H2205354	Certificate of Analysis	Feb 28, 2022	S104833
B2226124	Certificate of Analysis	Feb 28, 2022	S104833
H2205355	Certificate of Analysis	Feb 28, 2022	S104833
B2226053	Certificate of Analysis	Feb 28, 2022	S104833
B2216101	Certificate of Analysis	Dec 11, 2021	S104833
L2103709	Certificate of Analysis	Dec 11, 2021	S104833

Chemical and Physical Properties

Solubility	Soluble in water; Insoluble in Ether
Sensitivity	moisture sensitive
Refractive Index	1.3477
Specific Rotation[α]	106° (C=0.4,Acidified (NH4)6Mo7O24)
Boil Point(°C)	200 °C/0.002 mmHg
Melt Point(°C)	110 °C
Molecular Weight	182.170 g/mol
XLogP3	-3.100
Hydrogen Bond Donor Count	6
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	5
Exact Mass	182.079 Da
Monoisotopic Mass	182.079 Da
Topological Polar Surface Area	121.000 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	105.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Documents & Articles

Buffer Additives to Prevent Protein Precipitation

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Protein purification

Bio-based Chemicals: From Platform Molecules to Application Scenarios — Trend Insights and Aladdin’s Product Portfolio

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Bio-based Chemicals Biobased materials

Functional Sweetener Maltitol: Physicochemical Properties, Application Practices, and Aladdin Product Selection Guide

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Sweetener Maltitol

An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Carbohydrates

Functional Properties, Application Scenarios, and Manufacturing Processes of Maltotetraose (G4): A Review

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

G4 Maltotetraose Maltooligosaccharide α-1,4-glycosidic bond Low sweetness High viscosity Anti-crystallization Acid and heat stability

Functional Framework of Starch Metabolism-Related Enzymes in Food Science Research and Mechanistic Analysis of Quality Regulation

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

α-amylase Rheology Starch Metabolism-Related Enzymes Food Science Research Quality-Regulation Mechanisms Glucoamylase Debranching Enzymes Transglycosylases Staling Digestive Properties

Why Do Alcohols Differ in Function: Why Is Glycerol Mainly Moisturizing, Propylene Glycol Mainly Solubilizing, and Isopropyl Alcohol Fast-Drying? — Understanding Personal Care Formulation Functions from Structural Differences

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Propylene Glycol

Analysis of Structural Differences in Diols: Moisturization, Co-solvency, Skin Feel, and Formulation Selection for Propylene Glycol, Butylene Glycol, and Medium- to Long-Chain 1,2-Alkanediols

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Daily chemical formula Humectant

Mechanisms and Troubleshooting of Foam Reduction in Personal and Household Care Formulations: Film Rupture, Weak Interfacial Films, Insufficient Surfactant Supply, and Phase-State Disturbance

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Foam performance

Experimental Applications of Carboxymethyl Cellulose (CMC) Solution in Enzyme Assays, Suspension Systems, and Functional Materials

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Carboxymethyl Cellulose CMC solution sodium carboxymethyl cellulose cellulase substrate CMCase activity suspension system film-forming material rheological regulation

The Moisturizing and Low-Moisture Protective Mechanisms of Trehalose: From Its α,α-1,1 Structure and Hydration Dynamics to In Vitro Skin Barrier Research

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Trehalose

Moisturizing Mechanisms of Tremella fuciformis Polysaccharides: From Polysaccharide Structure and Hydration Rheology to Dynamic Film Formation on the Skin Surface

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Tremella fuciformis Polysaccharides

1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

1,8-naphthyridine aldose reductase ALR2 AKR1B1 aldose reductase inhibitor pharmacophore benzylic bromination

What Is Direct Compression? Process Characteristics, Suitability Criteria, and Excipient Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Direct Compression Wet granulation and tablet compression Dry granulation and tablet compression

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Reconstitution Calculator

Reviews

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View AR grade guide →

Bulk & Custom Packaging Need larger quantities or custom specifications? Contact our team for a tailored quote.

D-Sorbitol solution - AR, ≥98% , CAS No.50-70-4

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Customer Reviews

📚 Citations by Application

Need help choosing the grade?

D-Sorbitol solution - AR, ≥98% , CAS No.50-70-4

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Customer Reviews

📚 Citations by Application

Need help choosing the grade?

View related series