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D-Biotin - 98%, high purity , CAS No.58-85-5

  • Moligand™
  • ≥98%
Item Number
B105433
Grouped product items
SKUSizeAvailabilityPrice Qty
B105433-1g
1g
In stock
$90.90
B105433-5g
5g
In stock
$325.90
B105433-10g
10g
In stock
$586.90
B105433-25g
25g
In stock
$1,320.90
B105433-100g
100g
In stock
$4,753.90
B105433-500g
500g
In stock
$21,388.90

Enzyme co-factor. Protein conjugate for biochemical assays.

View related series
Vitamins and related compounds

Basic Description

Synonymsbiotin|d-biotin|58-85-5|vitamin H|Vitamin B7|Bioepiderm|coenzyme R|Bios II|Factor S|D(+)-Biotin|Biodermatin|D-(+)-Biotin|(+)-Biotin|Biotine|Biotinum|Injacom H|Biotina|Meribin|Factor S (vitamin)|Lutavit H2|Ritatin|CCRIS 3932|HSDB 346|3H-Biotin|MFCD00005541
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsEnzyme 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 TempStore at 2-8°C
Shipped InWet ice
GradeMoligand™
NoteWherever 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.
Product Description

Essential vitamin that is important for amino acid and energy metabolism


Application

Biotin may be used to elute proteins from avidin/streptavidin resins.

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.

Associated Targets

CUX1 Tbio Homeobox protein cut-like 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CNR1 Tclin Cannabinoid receptor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD1 Tclin D(1A) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD2 Tclin D(2) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ESR1 Tclin Estrogen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR3C1 Tclin Glucocorticoid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AVPR1A Tclin Vasopressin V1a receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HRH1 Tclin Histamine H1 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A2 Tclin Sodium-dependent noradrenaline transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE4D Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4D 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDE3A Tclin cGMP-inhibited 3',5'-cyclic phosphodiesterase A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CACNA1C Tclin Voltage-dependent L-type calcium channel subunit alpha-1C 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD3 Tclin D(3) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM3 Tclin Muscarinic acetylcholine receptor M3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2B Tclin Alpha-2B adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM2 Tclin Muscarinic acetylcholine receptor M2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2C Tclin Alpha-2C adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2A Tclin 5-hydroxytryptamine receptor 2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA2A Tclin Adenosine receptor A2a 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABL1 Tclin Tyrosine-protein kinase ABL1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRB1 Tclin Beta-1 adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2C Tclin 5-hydroxytryptamine receptor 2C 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA1 Tclin Adenosine receptor A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA3 Tchem Adenosine receptor A3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR3A Tclin 5-hydroxytryptamine receptor 3A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TBXA2R Tclin Thromboxane A2 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRD1 Tclin Delta-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRK1 Tclin Kappa-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRM1 Tclin Mu-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4A Tchem Lysine-specific demethylase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MLNR Tchem Motilin receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488188469
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488188469
IUPAC Name 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoic acid
INCHI 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
InChi Key YBJHBAHKTGYVGT-ZKWXMUAHSA-N
Canonical SMILES [H][C@]12CS[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2
Isomeric SMILES C1[C@H]2[C@@H]([C@@H](S1)CCCCC(=O)O)NC(=O)N2
WGK Germany 1
RTECS XJ9088200
PubChem CID 171548
Molecular Weight 244.31
Beilstein 86838

Certificates

Certificate of Analysis(COA)

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26 results found

Lot NumberCertificate TypeDateItem
H2408139Certificate of AnalysisApr 03, 2024 B105433
G2301051Certificate of AnalysisNov 12, 2022 B105433
K2330096Certificate of AnalysisNov 12, 2022 B105433
G2403045Certificate of AnalysisNov 12, 2022 B105433
G23041054Certificate of AnalysisNov 12, 2022 B105433
G2301064Certificate of AnalysisNov 12, 2022 B105433
G2301058Certificate of AnalysisNov 12, 2022 B105433
G2301053Certificate of AnalysisNov 12, 2022 B105433
G2301052Certificate of AnalysisNov 12, 2022 B105433
G2301050Certificate of AnalysisNov 12, 2022 B105433
G2301049Certificate of AnalysisNov 12, 2022 B105433
G2301048Certificate of AnalysisNov 12, 2022 B105433
G2301047Certificate of AnalysisNov 12, 2022 B105433
C2426040Certificate of AnalysisNov 12, 2022 B105433
J2217197Certificate of AnalysisSep 14, 2022 B105433
J2217198Certificate of AnalysisSep 14, 2022 B105433
J2217199Certificate of AnalysisSep 14, 2022 B105433
J2217202Certificate of AnalysisSep 14, 2022 B105433
G2230031Certificate of AnalysisJul 12, 2022 B105433
G2230030Certificate of AnalysisJul 12, 2022 B105433
G2230029Certificate of AnalysisJul 12, 2022 B105433
G2230028Certificate of AnalysisJul 12, 2022 B105433
B2225499Certificate of AnalysisDec 16, 2021 B105433
B2225626Certificate of AnalysisDec 16, 2021 B105433
B2225625Certificate of AnalysisDec 16, 2021 B105433
B2225622Certificate of AnalysisDec 16, 2021 B105433

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Chemical and Physical Properties

SolubilitySolubility 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
SensitivityLight &heat Sensitive
Specific Rotation[α]90.5 ° (C=2, 0.1mol/L NaOH)
Melt Point(°C)232-233°C

Safety and Hazards(GHS)

WGK Germany 1
RTECS XJ9088200

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Solution Calculators