D-Biotin - Moligand™, ≥98% , CAS No.58-85-5

Name: D-Biotin - Moligand™, ≥98% , CAS No.58-85-5
SKU: B105433
Availability: InStock

CAS: 58-85-5 Cat. No.: B105433 Formula: C₁₀H₁₆N₂O₃S Molecular Weight: 244.31 Beilstein Registry Number: 86838 EC Number: 200-399-3

88 Citations COA

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D-Biotin - Moligand™, ≥98% CAS No(58-85-5) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY Moligand™ ? ≥98%

Synonyms

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

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

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

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice 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 88 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Essential vitamin that is important for amino acid and energy metabolism

Application：

Biotin has been used for testing the functionality of the Avidin-displaying phages.The product has also been used for labeling the swine anti-rabbit IgG antibody and peroxidase.

It has been used for culturing of oligodendrocytes.

It has been used as a vitamin supplement for the growth of Bacillus species.

It has been used for blocking endogenous biotin during immunohistology procedures.

Specifications

Synonyms

Specifications & Purity

Moligand™, ≥98%

Biochemical and Physiological Mechanisms

Enzyme co-factor. Protein conjugate for biochemical assays. Participates in the citric acid cycle. Necessary for, and promotes cell growth, fatty acid production and the metabolism of fats and amino acids in vivo. Orally active.Biotin also acts as a cofac

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Moligand™

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥98%

Names and Identifiers

Pubchem Sid

488188469

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488188469

Canonical Smiles

[H][C@]12CS[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2

IUPAC Name

5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoic acid

InChIKey

YBJHBAHKTGYVGT-ZKWXMUAHSA-N

INCHI

1S/C10H16N2O3S/c13-8(14)4-2-1-3-7-9-6(5-16-7)11-10(15)12-9/h6-7,9H,1-5H2,(H,13,14)(H2,11,12,15)/t6-,7-,9-/m0/s1

Isomeric SMILES

C1[C@H]2[C@@H]([C@@H](S1)CCCCC(=O)O)NC(=O)N2

WGK Germany

RTECS

XJ9088200

Molecular Weight

244.31

Beilstein

86838

Reaxy-Rn

86838

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=86838&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 Organoheterocyclic compounds
  - Class Biotin and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Biotin and derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Biotin and derivatives
Alternative Parents	Imidazolyl carboxylic acids and derivatives Medium-chain fatty acids Thia fatty acids Heterocyclic fatty acids Thiolanes Imidazolines Isoureas Azacyclic compounds Carboximidamides Carboxylic acids Dialkylthioethers Monocarboxylic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides Carbonyl compounds
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Biotin - Imidazolyl carboxylic acid derivative - Medium-chain fatty acid - Heterocyclic fatty acid - Thia fatty acid - Fatty acid - Fatty acyl - Thiolane - 2-imidazoline - Isourea - Azacycle - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboxylic acid derivative - Thioether - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as biotin and derivatives. These are organic compounds containing a ureido (tetrahydroimidizalone) ring fused with a tetrahydrothiophene ring.
External Descriptors	Water-soluble vitamins
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)

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

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

Discover Target: ADRB2

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

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

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

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

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

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

Discover Target: DRD2

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

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

Discover Target: CNR1

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

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)

Discover Target: HRH2

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)

Discover Target: HTR2C

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

AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

Discover Target: AVPR2

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

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

Discover Target: AGTR1

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

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

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

Discover Target: HTR3A

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)

Discover Target: GRIN1

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

CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)

Discover Target: CACNA1C

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

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)

Discover Target: ADRA2B

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

ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)

Discover Target: ADRA2C

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)

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

ADORA2A Tclin Adenosine A2a receptor (16305 Activities)

Discover Target: ADORA2A

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

ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

Discover Target: ADORA3

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

BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)

Discover Target: BDKRB2

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

CHRNA4 Tclin Neuronal acetylcholine receptor protein alpha-4 subunit (1265 Activities)

Discover Target: CHRNA4

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

MC3R Tchem Melanocortin receptor 3 (5659 Activities)

Discover Target: MC3R

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

Associated Targets(non-human)

Mc4r Melanocortin receptor 4 (1205 Activities)

Discover Target: Mc4r

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

Pde4d Phosphodiesterase 4D (4 Activities)

Discover Target: Pde4d

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

CHO-K1 (1115 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

Streptavidin (24 Activities)

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

NS1 Nonstructural protein 1 (33327 Activities)

Discover Target: NS1

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

Slco1a4 Solute carrier organic anion transporter family member 1A4 (114 Activities)

Discover Target: Slco1a4

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

Cenchrus americanus (77 Activities)

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

Eif4a2 Eukaryotic initiation factor 4A-II (8 Activities)

Discover Target: Eif4a2

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.

60 results found

Lot Number	Certificate Type	Date	Item
J2217202	Certificate of Analysis	Jul 30, 2026	B105433
J2217198	Certificate of Analysis	Jul 30, 2026	B105433
J2522304	Certificate of Analysis	Oct 27, 2025	B105433
J2522416	Certificate of Analysis	Oct 27, 2025	B105433
J2522417	Certificate of Analysis	Oct 27, 2025	B105433
J2522418	Certificate of Analysis	Oct 27, 2025	B105433
C2609276	Certificate of Analysis	Oct 14, 2025	B105433
J2610031	Certificate of Analysis	Oct 14, 2025	B105433
C2616072	Certificate of Analysis	Oct 14, 2025	B105433
C2609278	Certificate of Analysis	Oct 14, 2025	B105433
C2609277	Certificate of Analysis	Oct 14, 2025	B105433
C2609269	Certificate of Analysis	Oct 14, 2025	B105433
C2609268	Certificate of Analysis	Oct 14, 2025	B105433
C2609267	Certificate of Analysis	Oct 14, 2025	B105433
G2616072	Certificate of Analysis	Oct 14, 2025	B105433
H2508242	Certificate of Analysis	Jun 20, 2025	B105433
H2508243	Certificate of Analysis	Jun 20, 2025	B105433
H2508239	Certificate of Analysis	Jun 20, 2025	B105433
H2508244	Certificate of Analysis	Jun 20, 2025	B105433
H2508240	Certificate of Analysis	Jun 20, 2025	B105433
H2508241	Certificate of Analysis	Jun 20, 2025	B105433
C2521633	Certificate of Analysis	Mar 10, 2025	B105433
C2521603	Certificate of Analysis	Mar 10, 2025	B105433
C2521089	Certificate of Analysis	Mar 10, 2025	B105433
C2521088	Certificate of Analysis	Mar 10, 2025	B105433
C2521087	Certificate of Analysis	Mar 10, 2025	B105433
C2521086	Certificate of Analysis	Mar 10, 2025	B105433
L2417035	Certificate of Analysis	Nov 16, 2024	B105433
F2516064	Certificate of Analysis	Nov 16, 2024	B105433
L2404484	Certificate of Analysis	Nov 16, 2024	B105433
L2404489	Certificate of Analysis	Nov 16, 2024	B105433
L2404490	Certificate of Analysis	Nov 16, 2024	B105433
J2431063	Certificate of Analysis	Oct 14, 2024	B105433
J2431129	Certificate of Analysis	Oct 14, 2024	B105433
J2431151	Certificate of Analysis	Oct 14, 2024	B105433
J2431197	Certificate of Analysis	Oct 14, 2024	B105433
H2408139	Certificate of Analysis	Apr 03, 2024	B105433
K2330096	Certificate of Analysis	Nov 12, 2022	B105433
G2301058	Certificate of Analysis	Nov 12, 2022	B105433
G23041054	Certificate of Analysis	Nov 12, 2022	B105433
C2426040	Certificate of Analysis	Nov 12, 2022	B105433
G2301047	Certificate of Analysis	Nov 12, 2022	B105433
G2301048	Certificate of Analysis	Nov 12, 2022	B105433
G2301049	Certificate of Analysis	Nov 12, 2022	B105433
G2301050	Certificate of Analysis	Nov 12, 2022	B105433
G2301051	Certificate of Analysis	Nov 12, 2022	B105433
G2301052	Certificate of Analysis	Nov 12, 2022	B105433
G2301053	Certificate of Analysis	Nov 12, 2022	B105433
G2301064	Certificate of Analysis	Nov 12, 2022	B105433
G2403045	Certificate of Analysis	Nov 12, 2022	B105433
J2217199	Certificate of Analysis	Sep 14, 2022	B105433
J2217197	Certificate of Analysis	Sep 14, 2022	B105433
G2230031	Certificate of Analysis	Jul 12, 2022	B105433
G2230030	Certificate of Analysis	Jul 12, 2022	B105433
G2230029	Certificate of Analysis	Jul 12, 2022	B105433
G2230028	Certificate of Analysis	Jul 12, 2022	B105433
B2225499	Certificate of Analysis	Dec 16, 2021	B105433
B2225626	Certificate of Analysis	Dec 16, 2021	B105433
B2225625	Certificate of Analysis	Dec 16, 2021	B105433
B2225622	Certificate of Analysis	Dec 16, 2021	B105433

Chemical and Physical Properties

Solubility	Solubility in water: 0.22 g/L (25°C) Solubility in other solvents: more soluble in hot water and dil. alkali 0.8 g/L alcohol insoluble in most other common organic solvents
Sensitivity	Light &heat Sensitive
Specific Rotation[α]	90.5 ° (C=2, 0.1mol/L NaOH)
Melt Point(°C)	232-233°C
Molecular Weight	244.310 g/mol
XLogP3	0.300
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	5
Exact Mass	244.088 Da
Monoisotopic Mass	244.088 Da
Topological Polar Surface Area	104.000 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	298.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
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

Professional Guide to Streptavidin-Modified Proteins

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

Tags:

Avidin Streptavidin

Why Can Biotinylated Peptides Test Negative in Biotin Assays?

Categories: Frequently Asked Questions: Products, Experiments and Troubleshooting

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Peptides

Strategies for Eluting Biotinylated Proteins and Nucleic Acids from Streptavidin Supports

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

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Streptavidin Biotin

How to Dissolve Biotin for Streptavidin Elution Buffers

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Tags:

Buffer Streptavidin Biotin

How Biotinylated Molecules are Purified with Streptavidin Beads

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

Tags:

protein Streptavidin

How to Elute Biotinylated Proteins and Nucleic Acids from Streptavidin Beads？

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

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Streptavidin

Biotin-Labeled Protein Purification

Categories: Laboratory Protocols & SOPs Library

Tags:

Biotin-Labeled Protein Purification Biotinylation

A Practical Guide to Small-Molecule Chemical Probes: Concept Clarification, Causal Validation, and Experimental Selection (with Product Navigation and Tables A–D)

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

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Chemical probe Small-Molecule Chemical Probes

Vitamins, Coenzymes, and Enzymes: A Metabolic Synergy Network and Its Disease Associations

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REDOX Vitamins Coenzymes Enzymes holoenzymes cofactors group transfer one-carbon metabolism metabolic flux disease associations

Protein Tags Demystified: Classification, Properties, and Suitable Experimental Applications

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

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protein tags affinity tags epitope tags fluorescent tags affinity purification

Glycoprotein Hormone Family: Molecular Features, Signaling Bias, and In Vivo Pharmacokinetics

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

Tags:

Glycosylation Pharmacokinetics FSH LH hCG TSH Glycoprotein hormones Common α-subunit Specific β-subunit Signaling bias

Experimental Selection of NHS-LC-Biotin and Sulfo-NHS-LC-Biotin: Water Solubility, Membrane Permeability, and Differences in Application Scenarios

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

Tags:

NHS-LC-Biotin Sulfo-NHS-LC-Biotin N-hydroxysuccinimide

Signal Transduction Mechanism of Graphene Biosensors: From Molecular Recognition to Electrical/Optical Signal Readout and Materials Selection

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

Tags:

Graphene Biosensor

What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications

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

Tags:

Synthetic Biology SB

Reactions and Applications of 3,3-Difluoroallyl Sulfonium Salts (DFASs): Small-Molecule gem-Difluoroallylation, Selective Peptide Modification, and Subsequent Functionalization

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

Tags:

Polypeptide Fluorinated groups

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📚 Citations by Application

Other applications35

Organic synthesis — reaction medium23

Extraction & workup solvent14

Controlled-release & nanoparticle carrier32

Drug / compound screening39

Cytotoxicity screening15

Cell viability4

Nanoparticle / material biocompatibility3

Chromatography (HPLC / GC / TLC)2

Spectroscopy sample preparation6

IC50 determination1

Cancer cell line characterization4

Cross-coupling reactions1

Cell proliferation1

Industrial & non-pharma application2

Electrochemistry & battery electrolyte3

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