Sucrose - AR , CAS No.57-50-1

Name: Sucrose - AR , CAS No.57-50-1
SKU: S112228
Availability: InStock

CAS: 57-50-1 Cat. No.: S112228 Fórmula: C₁₂H₂₂O₁₁ Peso molecular: 342.30 Beilstein Registry Number: 90825 Número EC: 200-334-9

940 Citations COA

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Sucrose - AR CAS No(57-50-1) S112228 by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY AR ?

Synonyms

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Descripción general Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Preguntas frecuentes y artículos Citations of This Product Calculadoras de soluciones Reseñas

🧪

Why this grade

AR AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged,Desiccated 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 940 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Sucrose is a disaccharide (glucose and fructose), which is commonly known as table sugar. It is a non-reducing sugar abundantly found in nature. It is present as the main constituent of soft drinks, beverages, and many food products.

Sucrose can be used:

· As a component of culture media for microorganisms.

· As an impermeant solute in the study of forward osmosis membrane parameters.

Specifications

Sinónimos

Especificaciones y pureza

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged,Desiccated

Enviado en

Normal

Grado

Nombres e identificadores

Pubchem Sid

508816530

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508816530

Sonrisas canónicas

C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O

IUPAC Name

(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

InChIKey

CZMRCDWAGMRECN-UGDNZRGBSA-N

INCHI

1S/C12H22O11/c13-1-4-6(16)8(18)9(19)11(21-4)23-12(3-15)10(20)7(17)5(2-14)22-12/h4-11,13-20H,1-3H2/t4-,5-,6-,7-,8+,9-,10+,11-,12+/m1/s1

Isómeros SMILES

C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@]2([C@H]([C@@H]([C@H](O2)CO)O)O)CO)O)O)O)O

WGK Alemania

RTECS

WN6500000

Peso molecular

342.30

Beilstein

90825

Reaxy-Rn

11343410

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11343410&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
  - Clase Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates
      - Level5 Glycosyl compounds
        Level6 O-glycosyl compounds

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Clase	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Glycosyl compounds
Direct Parent	O-glycosyl compounds
Alternative Parents	Disaccharides C-glycosyl compounds Ketals Oxanes Tetrahydrofurans Secondary alcohols Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	O-glycosyl compound - Disaccharide - C-glycosyl compound - Ketal - Oxane - Tetrahydrofuran - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
External Descriptors	Disaccharides
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

Estructura 3D

Objetivos asociados (humanos)

F2 Tclin Thrombin (11687 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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

PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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

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

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

AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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

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

MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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

HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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

AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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

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

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

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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

HRH1 Tclin Histamine H1 receptor (7573 Activities)

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

OPRM1 Tclin Mu opioid receptor (19785 Activities)

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

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

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

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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

OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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

HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)

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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

GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)

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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)

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

SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)

Discover Target: SLC29A1

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

ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)

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

CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)

Discover Target: CHRM3

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

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

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

TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

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

EDNRA Tclin Endothelin receptor ET-A (5008 Activities)

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

ADORA2A Tclin Adenosine A2a receptor (16305 Activities)

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

PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

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

ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

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

Objetivos asociados (no humanos)

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

Discover Target: Npy1r

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

Cckar Cholecystokinin A receptor (90 Activities)

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

Pde4d Phosphodiesterase 4D (4 Activities)

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

Hdac6 Histone deacetylase 6 (222 Activities)

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

Pseudomonas aeruginosa (123386 Activities)

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Staphylococcus aureus (210822 Activities)

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Escherichia coli (133304 Activities)

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Bacillus subtilis (32866 Activities)

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Candida albicans (78123 Activities)

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Cavia porcellus (23802 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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BV-2 (3710 Activities)

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

rep Replicase polyprotein 1ab (378 Activities)

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

Sciatic nerve (18 Activities)

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Hypothalamus (44 Activities)

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Thalamus (188 Activities)

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Cerebellum (165 Activities)

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SARS-CoV-2 (38078 Activities)

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Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

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.

57 results found

Lot Number	Certificate Type	Fecha	Articulo
H2605342	Certificate of Analysis	Jul 27, 2026	S112228
H2605470	Certificate of Analysis	Jul 27, 2026	S112228
H2605471	Certificate of Analysis	Jul 27, 2026	S112228
C2613366	Certificate of Analysis	Mar 02, 2026	S112228
C2613312	Certificate of Analysis	Mar 02, 2026	S112228
C2613311	Certificate of Analysis	Mar 02, 2026	S112228
B2604168	Certificate of Analysis	Jan 08, 2026	S112228
B2604192	Certificate of Analysis	Jan 08, 2026	S112228
H2427470	Certificate of Analysis	Dec 27, 2022	S112228
H2528357	Certificate of Analysis	Dec 27, 2022	S112228
H2528356	Certificate of Analysis	Dec 27, 2022	S112228
H2528355	Certificate of Analysis	Dec 27, 2022	S112228
G2510377	Certificate of Analysis	Dec 27, 2022	S112228
H2427367	Certificate of Analysis	Dec 27, 2022	S112228
H2427241	Certificate of Analysis	Dec 27, 2022	S112228
G2510614	Certificate of Analysis	Dec 27, 2022	S112228
G2510379	Certificate of Analysis	Dec 27, 2022	S112228
G2510378	Certificate of Analysis	Dec 27, 2022	S112228
F2518517	Certificate of Analysis	Dec 27, 2022	S112228
H2528567	Certificate of Analysis	Dec 27, 2022	S112228
I2311680	Certificate of Analysis	Dec 27, 2022	S112228
J2516576	Certificate of Analysis	Dec 27, 2022	S112228
J2516707	Certificate of Analysis	Dec 27, 2022	S112228
K2301408	Certificate of Analysis	Dec 27, 2022	S112228
K2301409	Certificate of Analysis	Dec 27, 2022	S112228
L2405301	Certificate of Analysis	Dec 27, 2022	S112228
L2405302	Certificate of Analysis	Dec 27, 2022	S112228
L2405441	Certificate of Analysis	Dec 27, 2022	S112228
L2405611	Certificate of Analysis	Dec 27, 2022	S112228
F2518440	Certificate of Analysis	Dec 27, 2022	S112228
F2518439	Certificate of Analysis	Dec 27, 2022	S112228
F2404395	Certificate of Analysis	Dec 27, 2022	S112228
F2404234	Certificate of Analysis	Dec 27, 2022	S112228
F2315298	Certificate of Analysis	Dec 27, 2022	S112228
F2314497	Certificate of Analysis	Dec 27, 2022	S112228
A2424420	Certificate of Analysis	Dec 27, 2022	S112228
A2426142	Certificate of Analysis	Dec 27, 2022	S112228
E2304067	Certificate of Analysis	Dec 27, 2022	S112228
E2304029	Certificate of Analysis	Dec 27, 2022	S112228
D2328239	Certificate of Analysis	Dec 27, 2022	S112228
C2426407	Certificate of Analysis	Dec 27, 2022	S112228
K2303068	Certificate of Analysis	Dec 27, 2022	S112228
C2301318	Certificate of Analysis	Dec 27, 2022	S112228
C2301430	Certificate of Analysis	Dec 27, 2022	S112228
B2301502	Certificate of Analysis	Dec 27, 2022	S112228
B2301501	Certificate of Analysis	Dec 27, 2022	S112228
A2305770	Certificate of Analysis	Dec 27, 2022	S112228
K2229950	Certificate of Analysis	Oct 18, 2022	S112228
K2229951	Certificate of Analysis	Oct 18, 2022	S112228
I2219004	Certificate of Analysis	Sep 22, 2022	S112228
I2219005	Certificate of Analysis	Sep 22, 2022	S112228
F2201150	Certificate of Analysis	Mar 15, 2022	S112228
F2201154	Certificate of Analysis	Mar 15, 2022	S112228
F2215270	Certificate of Analysis	Mar 15, 2022	S112228
F2215271	Certificate of Analysis	Mar 15, 2022	S112228
A2220518	Certificate of Analysis	Dec 20, 2021	S112228
A2220522	Certificate of Analysis	Dec 20, 2021	S112228

Propiedades químicas y físicas

Solubilidad	Soluble in water (342 g/l at 20 °C), alcohol (slightly), ethanol (1 9/170ml), methanol (1 g/100ml), glycerol (moderately ), pyridine (moderately ), water (1 g/0.5ml at 25 °C), and boiling water (1 g/0.2ml). Insoluble in chloroform, and ether.
Sensibilidad	Moisture sensitive.
Rotación específica [α]	66.5 ° (C=26, H2O)
Punto de fusión (°C)	185-187℃
Peso molecular	342.300 g/mol
XLogP3	-3.700
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	11
Rotatable Bond Count	5
Exact Mass	342.116 Da
Monoisotopic Mass	342.116 Da
Topological Polar Surface Area	190.000 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	395.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	9
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

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

Pyran and the “Pyran Family” Research Selection Guide: Key Structural Points, a Classification Roadmap, and Experimental Selection Navigation

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Pyran Oxygen-containing heterocycle

What a Disagreement in Specific Rotation Results Reveals About Method Control: Why Specific Rotation Values for Chiral Samples Cannot Be Discussed Apart from Measurement Conditions

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Specific rotation measurement Specific rotation

From Sucrose to Monosaccharides: Key Enzymatic Nodes and Regulatory Logic in Sugar Conversion

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sucrose Glucose monosaccharides invertase sucrose synthase sucrose phosphorylase

Structural Characteristics, Operational Methods, and Separation Applications of Dextran Gels

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dextran gel gel filtration crosslinked dextran molecular sieving desalting buffer exchange chromatographic packing material

Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface

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High-performance liquid chromatography Porous Graphitic Carbon

Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles

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Establishment and Evaluation Methods of Diabetic Animal Models

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diabetic animal modeling STZ-induced model alloxan model high-fat diet model HFD+STZ model NOD mice db/db mice ZDF rats

GC-IRMS: Detecting purity and adulteration of tequila with isotope fingerprints

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Isotopes Mass spectrometry GC-IRMS Gas Chromatography Isotope Fingerprint

Comparison of Reducing Sugar Detection Methods: Selection of Fehling’s Reagent, Benedict’s Method, DNS Method, and HPLC

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Evaluation of Blood-Brain Barrier Permeability: Tracer Extravasation, TEER Measurement, and Interpretation of In Vitro Model Results

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blood-brain barrier TEER Papp BBB permeability Tracer Extravasation Tight Junction Proteins Brain Microvascular Endothelial Cells

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

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Mechanisms by Which Fructan-Rich Ophiopogon japonicus Tuberous Root Extract Supports Skin Moisturization and Barrier Function

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

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

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Sucrose - AR , CAS No.57-50-1

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Sucrose - AR , CAS No.57-50-1

Storage & shipping

Quality documents

Literature proof

Descripción general

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Reseñas de cliente

📚 Citations by Application

Need help choosing the grade?

View related series

Artículos relacionados