(+)-Biotin hydrazide - ≥98% , CAS No.66640-86-6

CAS: 66640-86-6 Cat. No.: B122221 Formula: C10H18N4O2S Peso molecolare: 258.34 Beilstein Registry Number: 28347 Numero EC: 613-970-0
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanehydrazide | 1H-Thieno(3,4-d)imidazole-4-pentanoic acid, hexahydro-2-oxo-, hydrazide, (3aS-(3aalpha,4beta,6aalpha))- | Biotin-NHNH2 | AS-74083 | 1H-Thieno[3,4-d]imidazole-4-pent
Storage
Store at 2-8°C
Shipped In
Wet ice
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Size
Germania (EU)
USA*
Price
Qty
25mg
B122221-25mg
—
3 Disponibile
25,08€
100mg
B122221-100mg
—
2 Disponibile
80,61€
500mg
B122221-500mg
—
3 Disponibile
357,42€
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Store at 2-8°C 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Biotin hydrazide is a biotinylation reagent used to biotinylate glycoproteins with their sugar moieties.Biotin hydrazide can be used to prepare biotin-conjugated alginate.It can also be used for covalent attachment to PAAc via carbodi-imide cross linking.
Reagent for labeling surface functional groups, biologically active molecules such as antibodies, lectins, sugars, nucleic acids or molecules with free carboxylic or keto groups. Typically used for coupling to glycoproteins through the carbohydrate by hydrazone formation.

Specifications

Sinonimi
5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanehydrazide | 1H-Thieno(3,4-d)imidazole-4-pentanoic acid, hexahydro-2-oxo-, hydrazide, (3aS-(3aalpha,4beta,6aalpha))- | Biotin-NHNH2 | AS-74083 | 1H-Thieno[3,4-d]imidazole-4-pent
Specifiche e purezza
≥98%
Condizioni di conservazione di stoccaggio
Store at 2-8°C
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Purezza
≥98%
Nomi e identificatori
Pubchem Sid504755733
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504755733
Sorrisi canoniciC1C2C(C(S1)CCCCC(=O)NN)NC(=O)N2
IUPAC Name5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanehydrazide
InChIKeyKOZWHQPRAOJMBN-ZKWXMUAHSA-N
INCHI1S/C10H18N4O2S/c11-14-8(15)4-2-1-3-7-9-6(5-17-7)12-10(16)13-9/h6-7,9H,1-5,11H2,(H,14,15)(H2,12,13,16)/t6-,7-,9-/m0/s1
Isomeri SMILES C1[C@H]2[C@@H]([C@@H](S1)CCCCC(=O)NN)NC(=O)N2
WGK Germania 3
Peso molecolare 258.34
Beilstein 28347
Reaxy-Rn 260325
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=260325&ln=

Documentazione

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseBiotin and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBiotin and derivatives
Alternative Parents Thienoimidazolidines  Imidazolidinones  Thiophenes  Thiolanes  Ureas  Carboxylic acid hydrazides  Dialkylthioethers  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Biotin_derivative - Thienoimidazolidine - Imidazolidinone - Imidazolidine - Thiolane - Thiophene - Carboxylic acid hydrazide - Carbonic acid derivative - Urea - Carboxylic acid derivative - Azacycle - Thioether - Dialkylthioether - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic heteropolycyclic compound
DescrizioneThis 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 Not available
Struttura 3D
Modello di struttura chimica interattiva





Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

6 results found

Lot NumberCertificate TypeDataOggetto
I2610154Certificate of AnalysisSep 12, 2026 B122221
H1506009Certificate of AnalysisApr 11, 2023 B122221
C2412054Certificate of AnalysisFeb 14, 2022 B122221
E2203089Certificate of AnalysisFeb 14, 2022 B122221
E2203090Certificate of AnalysisFeb 14, 2022 B122221
F2528125Certificate of AnalysisFeb 14, 2022 B122221
Proprietà chimiche e fisiche
SensibilitàHeat sensitive
Punto di fusione (°C)233 °C
Peso molecolare258.339 g/mol
XLogP3-0.700
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass258.115 Da
Monoisotopic Mass258.115 Da
Topological Polar Surface Area122.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity313.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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