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B7639

Sigma-Aldrich

(+)-Biotin hydrazide

≥97% (TLC), powder

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100 MG
$86.10
1 G
$536.00

$86.10

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100 MG
$86.10
1 G
$536.00

About This Item

Empirical Formula (Hill Notation):
C10H18N4O2S
CAS Number:
Molecular Weight:
258.34
Beilstein/REAXYS Number:
28347
MDL number:
UNSPSC Code:
12352203
PubChem Substance ID:
NACRES:
NA.46

$86.10

List Price$105.00Save 18%

Availability

Available to ship onDecember 11, 2024Details


Request a Bulk Order

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[1]. Biotin hydrazide can be used to prepare biotin-conjugated alginate[2]. It can also be used for covalent attachment to PAAc via carbodi-imide cross linking[3].

Application

(+)-Biotin hydrazide has been used:
  • the modification of alginate[4]
  • for the labelling of mitochondrial proteins from non-muscle tissues[5]
  • as a component of glycoprotein staining solution[6]
  • in periodic acid-biotin-hydrazide (PABH) assay for mucins[7]
  • 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.

related product

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Studying mucin secretion from human bronchial epithelial cell primary cultures
Mucins, 259-277 (2012)
Boris Polyak et al.
Biomacromolecules, 5(2), 389-396 (2004-03-09)
Biotin was covalently coupled with alginate in an aqueous-phase reaction by means of carbodiimide-mediated activation chemistry to provide a biotin-alginate conjugate for subsequent use in biosensor applications. The synthetic procedure was optimized with respect to pH of the reaction medium
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)

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