β-Cyclodextrin - ≥98% , CAS No.7585-39-9

Name: β-Cyclodextrin - ≥98% , CAS No.7585-39-9
SKU: C104384
Availability: InStock

CAS: 7585-39-9 Cat. No.: C104384 Formule: C₄₂H₇₀O₃₅ Poids moléculaire: 1134.98 Beilstein Registry Number: 78623 Numéro CE: 231-493-2 PubChem CID: 444041

667 Citations COA

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β-Cyclodextrin - ≥98% CAS No(7585-39-9) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥98%

Synonyms

Cyclomaltoheptaose | Cycloheptaamylose | Betadex | Cycloheptaglucan | Schardinger β-Dextrin

Storage

Room temperature,Desiccated

Shipped In

Normal

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

🧪

Why this grade

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

🌡

Storage & shipping

Room temperature,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 667 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Useful for forming water-soluble complexes for fluorescent labeling of proteins.

Product Application:

Use to solubilize non-polar compounds such as fatty acids, lipids and cholesterol. Reported useful for the selective precipitation of enantiomeric, positional or structural isomersβ-Cyclodextrin is used with dansyl chloride to form water-soluble complexes for fluorescent labeling of proteins. It is an active ingredient of household odor eliminator. It is also used in personal care products like toothpastes, skin creams and dusting powders. It finds applications in the cosmetic industry for products like detergents and perfumes for the controlled release of fragrances. Further, it is used to produce HPLC columns allowing chiral enantiomers separation. In addition to this, it is used to decrease the level of cholesterol in milk fat.

Specifications

Synonymes

Cyclomaltoheptaose | Cycloheptaamylose | Betadex | Cycloheptaglucan | Schardinger β-Dextrin

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

β-Cyclodextrin is made of homogeneous cyclic α1,4-linked D-glucopyranose units in a seven member ring. Forms clathrates and suitable for use with dansyl chloride to form water-soluble complexes for fluorescent labeling of proteins.

Conditions de stockage de stockage

Room temperature,Desiccated

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

Pubchem Sid	488189822
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488189822
Sourires canoniques	OC[C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@@H]3CO)O[C@H]4[C@H](O)[C@@H](O)[C@H](O[C@@H]4CO)O[C@H]5[C@H](O)[C@@H](O)[C@H](O[C@@H]5CO)O[C@H]6[C@H](O)[C@@H](O)[C@H](O[C@@H]6CO)O[C@H]7[C@H](O)[C@@H](O)[C@H](O[C@@H]7CO)O[C@H]8[C@H](O)[C@@H](O)[C@H](O[C@@H]8CO)O[C@H]1[C@H](O)[C@H]2O
IUPAC Name	(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36R,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6.28,11.213,16.218,21.223,26.228,31]nonatetracontane-36,37,38,39,40,41,42,43,44,45,46,47,48,49-tetradecol
InChIKey	WHGYBXFWUBPSRW-FOUAGVGXSA-N
INCHI	1S/C42H70O35/c43-1-8-29-15(50)22(57)36(64-8)72-30-9(2-44)66-38(24(59)17(30)52)74-32-11(4-46)68-40(26(61)19(32)54)76-34-13(6-48)70-42(28(63)21(34)56)77-35-14(7-49)69-41(27(62)20(35)55)75-33-12(5-47)67-39(25(60)18(33)53)73-31-10(3-45)65-37(71-29)23(58)16(31)51/h8-63H,1-7H2/t8-,9-,10-,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-/m1/s1
Isomères SMILES	C([C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H]([C@@H]([C@H]6O)O)O[C@@H]7[C@H](O[C@@H]([C@@H]([C@H]7O)O)O[C@@H]8[C@H](O[C@H](O2)[C@@H]([C@H]8O)O)CO)CO)CO)CO)CO)CO)O)O)O
WGK Allemagne	2
RTECS	GU2293000
PubChem CID	444041
Poids moléculaire	1134.98
Beilstein	78623

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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 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
  - Classe Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Classe	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Not available
Direct Parent	Oligosaccharides
Alternative Parents	Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Oligosaccharide - Oxane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
External Descriptors	cyclodextrin
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

Structure 3D

Cibles associées (humaines)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

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

F2 Tclin Thrombin (11687 Activities)

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

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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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

HMGCR Tclin HMG-CoA reductase (2475 Activities)

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

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

INSR Tclin Insulin receptor (5558 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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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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

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

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

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

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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

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

TSHR Tclin Thyroid stimulating hormone receptor (29986 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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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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

DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

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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

HRH2 Tclin Histamine H2 receptor (5428 Activities)

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

ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

Discover Target: ADRA1D

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

HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

Discover Target: HTR1B

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

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

Discover Target: HTR2A

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

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

CALCR Tclin Calcitonin receptor (2215 Activities)

Discover Target: CALCR

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

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

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

HRH1 Tclin Histamine H1 receptor (7573 Activities)

Discover Target: HRH1

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

ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

Discover Target: ADRA1B

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

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

Discover Target: AVPR1A

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

OPRD1 Tclin Delta opioid receptor (15096 Activities)

Discover Target: OPRD1

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

OPRK1 Tclin Kappa opioid receptor (16155 Activities)

Discover Target: OPRK1

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

HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

Discover Target: HTR4

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

ESR2 Tclin Estrogen receptor beta (9272 Activities)

Discover Target: ESR2

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

CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

Discover Target: CYSLTR1

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

Cibles associées (non humaines)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

Discover Target: Agtr2

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

Mc4r Melanocortin receptor 4 (1205 Activities)

Discover Target: Mc4r

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

Ltc4s Leukotriene C4 synthase (1 Activities)

Discover Target: Ltc4s

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

Sigmar1 Sigma opioid receptor (160 Activities)

Discover Target: Sigmar1

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

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)

Discover Target: Cckar

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

Nos2 Nitric oxide synthase, inducible (3573 Activities)

Discover Target: Nos2

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

Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

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

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

Mmp9 Matrix metalloproteinase 9 (38 Activities)

Discover Target: Mmp9

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

Staphylococcus aureus (210822 Activities)

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

Cavia porcellus (23802 Activities)

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

Mus musculus (284745 Activities)

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

Rattus norvegicus (775804 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)

Discover Target: rep

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

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

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

Glra2 Glycine receptor (1745 Activities)

Discover Target: Glra2

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

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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

Analytical Chart:

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71 results found

Lot Number	Certificate Type	Date	Article
E2628347	Certificate of Analysis	May 14, 2026	C104384
E2628325	Certificate of Analysis	May 14, 2026	C104384
E2628324	Certificate of Analysis	May 14, 2026	C104384
E2628323	Certificate of Analysis	May 14, 2026	C104384
L2529270	Certificate of Analysis	Dec 05, 2025	C104384
C2609554	Certificate of Analysis	Dec 05, 2025	C104384
C2609394	Certificate of Analysis	Dec 05, 2025	C104384
C2609393	Certificate of Analysis	Dec 05, 2025	C104384
C2609390	Certificate of Analysis	Dec 05, 2025	C104384
L2529269	Certificate of Analysis	Dec 05, 2025	C104384
L2529268	Certificate of Analysis	Dec 05, 2025	C104384
L2529131	Certificate of Analysis	Dec 05, 2025	C104384
J2530016	Certificate of Analysis	Aug 11, 2025	C104384
I2501228	Certificate of Analysis	Aug 11, 2025	C104384
I2501227	Certificate of Analysis	Aug 11, 2025	C104384
I2501226	Certificate of Analysis	Aug 11, 2025	C104384
I2501224	Certificate of Analysis	Aug 11, 2025	C104384
H2504149	Certificate of Analysis	Jun 30, 2025	C104384
F2511349	Certificate of Analysis	May 29, 2025	C104384
F2511350	Certificate of Analysis	May 29, 2025	C104384
F2511351	Certificate of Analysis	May 29, 2025	C104384
F2511363	Certificate of Analysis	May 29, 2025	C104384
D2502209	Certificate of Analysis	Jan 17, 2025	C104384
D2502210	Certificate of Analysis	Jan 17, 2025	C104384
D2502296	Certificate of Analysis	Jan 17, 2025	C104384
D2502382	Certificate of Analysis	Jan 17, 2025	C104384
B2528282	Certificate of Analysis	Jan 17, 2025	C104384
B2528283	Certificate of Analysis	Jan 17, 2025	C104384
B2528341	Certificate of Analysis	Jan 17, 2025	C104384
B2528301	Certificate of Analysis	Jan 17, 2025	C104384
L2413637	Certificate of Analysis	Aug 17, 2024	C104384
L2413633	Certificate of Analysis	Aug 17, 2024	C104384
H2428343	Certificate of Analysis	Aug 17, 2024	C104384
H2428352	Certificate of Analysis	Aug 17, 2024	C104384
H2428353	Certificate of Analysis	Aug 17, 2024	C104384
H2428354	Certificate of Analysis	Aug 17, 2024	C104384
L2413634	Certificate of Analysis	Aug 17, 2024	C104384
L2413635	Certificate of Analysis	Aug 17, 2024	C104384
L2413636	Certificate of Analysis	Aug 17, 2024	C104384
A2510236	Certificate of Analysis	Jul 09, 2024	C104384
A2510235	Certificate of Analysis	Jul 09, 2024	C104384
F2411168	Certificate of Analysis	May 24, 2024	C104384
F2411137	Certificate of Analysis	May 24, 2024	C104384
F2411169	Certificate of Analysis	May 24, 2024	C104384
F2411167	Certificate of Analysis	May 24, 2024	C104384
B2422172	Certificate of Analysis	Jan 22, 2024	C104384
B2422170	Certificate of Analysis	Jan 22, 2024	C104384
B2422168	Certificate of Analysis	Jan 22, 2024	C104384
B2422167	Certificate of Analysis	Jan 22, 2024	C104384
K2321074	Certificate of Analysis	Nov 01, 2023	C104384
K2321073	Certificate of Analysis	Nov 01, 2023	C104384
K2321072	Certificate of Analysis	Nov 01, 2023	C104384
K2321017	Certificate of Analysis	Nov 01, 2023	C104384
B2322518	Certificate of Analysis	Dec 10, 2022	C104384
B2322698	Certificate of Analysis	Dec 10, 2022	C104384
B2322697	Certificate of Analysis	Dec 03, 2022	C104384
B2322525	Certificate of Analysis	Dec 03, 2022	C104384
B2322528	Certificate of Analysis	Dec 03, 2022	C104384
B2322693	Certificate of Analysis	Dec 03, 2022	C104384
J2226303	Certificate of Analysis	Aug 03, 2022	C104384
J2226302	Certificate of Analysis	Aug 03, 2022	C104384
J2226301	Certificate of Analysis	Aug 03, 2022	C104384
F2206071	Certificate of Analysis	Mar 15, 2022	C104384
F2206072	Certificate of Analysis	Mar 15, 2022	C104384
F2206080	Certificate of Analysis	Mar 15, 2022	C104384
F2206082	Certificate of Analysis	Mar 15, 2022	C104384
B2212196	Certificate of Analysis	Dec 13, 2021	C104384
B2212195	Certificate of Analysis	Dec 13, 2021	C104384
B2212194	Certificate of Analysis	Dec 13, 2021	C104384
B2212193	Certificate of Analysis	Dec 13, 2021	C104384
H2204226	Certificate of Analysis	Sep 03, 2021	C104384

Propriétés chimiques et physiques

Solubilité	Soluble in water (10 mg/ml), and 1 M NH4OH (50 mg/ml).
Indice de réfraction	1.59
Rotation spécifique [α]	+162o, c = 1.5 in water
Point d'ébullition (°C)	1541.18°C/760mmHg
Point de fusion (°C)	290-300°C
Poids moléculaire	1135.000 g/mol
XLogP3	-15.000
Hydrogen Bond Donor Count	21
Hydrogen Bond Acceptor Count	35
Rotatable Bond Count	7
Exact Mass	1134.37 Da
Monoisotopic Mass	1134.37 Da
Topological Polar Surface Area	554.000 Å²
Heavy Atom Count	77
Formal Charge	0
Complexity	1480.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	35
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

FAQ et articles

N-Bromosuccinimide (NBS)

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OxidizingAgents Organic Reaction Toolbox C-H Functionalization NBS N-Bromosuccinimide

Cyclodextrins, Explained: Structure, Inclusion Mechanism, Derivatization Types, and a Quick Selection Guide (with a 5-Category Checklist)

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

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Cyclodextrins

A Practical Guide to Fragrance Compositions: Turning a Black-Box Formula into an Engineerable System—Compatibility, Stability, Controlled Release, Traceability, and Selection

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

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Fragrance Fragrance composition Fragrance base

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

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Carbohydrates

Review of the Structural Characteristics, Biological Functions, and Application Advances of Lycopene

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

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Carotenoids Antioxidant Natural Pigment lycopene functional food

Extraction Methods and Process Selection for Flavonoid Compounds

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

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flavonoid compounds extraction methods solvent extraction ultrasound-assisted extraction microwave-assisted extraction enzyme-assisted extraction supercritical fluid extraction process optimization

Structure, Properties, and Mechanisms of Powdered Fragrances and Fragrance Delivery Materials: Stability, Release Mechanisms, and Selection Logic

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

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Fragrance Powdered Fragrances

How to Extend Fragrance Longevity in Personal and Home Care Products: Fragrance Structure, Surface Deposition, and Release Modulation

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

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Cationic surfactants Daily chemical products Fragrance molecules

2-Iodylbenzoic Acid (IBX)

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

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Organic Reaction Toolbox Oxidation Reagents Oxidation Reaction IBX Hypervalent Iodine

Antioxidant Mechanisms, Stability, and Delivery Strategies of Resveratrol in Skincare Research

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

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Resveratrol

UVA Absorption Mechanism of Avobenzone: Keto–Enol Tautomerism, Photochemical Instability, and Formulation Photostabilization Strategies

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

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cosmetics

Potential Mechanisms of p-Cymene in Problem-Prone Skin: Membrane Perturbation, Inflammatory Signaling Modulation, and Localized Delivery

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

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p-cymene 1-isopropyl-4-methylbenzene

Why Are Adamantane Compounds Special? From Rigid Cage Structures and Selective Functionalization to Medicinal Chemistry and Functional Materials Applications

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

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Medicinal Chemistry adamantane adamantane compounds diamondoids three-dimensional cage structure bridgehead position bridge position selective functionalization conformational restriction hydrophobic volume photoresist materials low-dielectric polymers host–guest recognition porous organic materials

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β-Cyclodextrin - ≥96% , CAS No.7585-39-9

β-Cyclodextrin - for cell culture, ≥98% , CAS No.7585-39-9

β-Cyclodextrin - 10mM in DMSO , CAS No.7585-39-9

β-Cyclodextrin - ≥98% , CAS No.7585-39-9

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Produits apparentés

β-Cyclodextrin - ≥98% , CAS No.7585-39-9

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations by Application

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Produits apparentés