B7639
(+)-Biotin hydrazide
≥97% (TLC), powder
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About This Item
Empirical Formula (Hill Notation):
C10H18N4O2S
CAS Number:
Molecular Weight:
258.34
Beilstein:
28347
MDL number:
UNSPSC Code:
12352203
PubChem Substance ID:
NACRES:
NA.46
Assay
≥97% (TLC)
form
powder
solubility
DMSO: ≤20 mg/mL
storage temp.
2-8°C
SMILES string
[H][C@]12CS[C@@H](CCCCC(=O)NN)[C@@]1([H])NC(=O)N2
InChI
1S/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
InChI key
KOZWHQPRAOJMBN-ZKWXMUAHSA-N
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General description
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.
Application
(+)-Biotin hydrazide has been used:
- the modification of alginate
- for the labelling of mitochondrial proteins from non-muscle tissues
- as a component of glycoprotein staining solution
- in periodic acid-biotin-hydrazide (PABH) assay for mucins
- for labeling surface functional groups, biologically active molecules such as antibodies, lectins, sugars, nucleic acids or molecules with free carboxylic or keto groups.
- for coupling to glycoproteins through the carbohydrate by hydrazone formation
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Kazumi Ninomiya et al.
Nutrients, 10(10) (2018-10-18)
Inhibiting starch hydrolysis into sugar could reduce postprandial blood glucose elevation and contribute to diabetes prevention. Here, both buckwheat and wheat albumin that inhibited mammalian α-amylase in vitro suppressed blood glucose level elevation after starch loading in vivo, but it
Two-dimensional gel electrophoretic detection of protein carbonyls derivatized with biotin-hydrazide
Wu J, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 1019, 128-131 (2016)
Enhanced capture and release of circulating tumor cells using hollow glass microspheres with a nanostructured surface
Dong Z, et al.
Nanoscale, 10(35), 16795-16804 (2018)
Ajay M Shah et al.
Analytical chemistry, 84(8), 3682-3688 (2012-03-15)
Microfluidic systems for affinity-based cell isolation have emerged as a promising approach for the isolation of specific cells from complex matrices (i.e., circulating tumor cells in whole blood). However, these technologies remain limited by the lack of reliable methods for
Suppressive Effect of the o-Amylase Inhibitor Albumin from Buckwheat (Fagopyrum esculentum Moench) on Postprandial Hyperglycaemia
Impact of Bioactive Peptides on Human Health, 157-157 (2016)
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