Carboxylic acid hydrazides
eMolecules 2-(4-Boronobenzoyl)hydrazinecarbothioamide | 957060-76-3 | MFCD09027244 | 1g
Combi-Blocks | 2-(4-Boronobenzoyl)hydrazinecarbothioamide | 1g | 117523062 | BB-3823 | 98.000 | 957060-76-3 | MFCD09027244 | 239.060 | C8H10BN3O3S
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eMolecules Amino-PEG8-t-Boc-hydrazide | 1334169-96-8 | MFCD21363303 | 1g
Broadpharm | Amino-PEG8-t-Boc-hydrazide | 1g | 550803940 | BP-21617 | 98.000 | 1334169-96-8 | MFCD21363303 | 555.666 | C24H49N3O11
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Medchemexpress LLC BODIPY FL hydrazide 10mg | 178388-71-1 | 10 MG
BODIPY FL hydrazide is a green-fluorescent hydrazide reagent that reacts with aldehyde and ketone groups on polysaccharides and glycoproteins to form a reversible Schiff base that can be reduced to a stable linkage for detection and imaging. Its excitation maximum is about 495 nm and its emission maximum is about 516 nm.
- Reactive toward aldehyde and ketone groups
- Forms a reversible Schiff base convertible to a stable linkage by reduction
- Green fluorescence with excitation ~495 nm and emission ~516 nm
- Suitable for fluorescent labeling of carbohydrates and glycoproteins
Chem-Impex International, Inc. Isonicotinic acid hydrazide | MFCD00006426 | 100G
Isonicotinic acid hydrazide, MFCD00006426, 100G
Chem-Impex International, Inc. 4-Methoxybenzoic acid hydrazide | MFCD00017073 | 25G
4-Methoxybenzoic acid hydrazide, MFCD00017073, 25G
eMolecules Ambeed / 4-Hydroxybenzhydrazide / 5g / 552518902 / A103582 / / 5351-23-5 / MFCD00007605 / 152.153 / C7H8N2O2
Ambeed / 4-Hydroxybenzhydrazide / 5g / 552518902 / A103582 / / 5351-23-5 / MFCD00007605 / 152.153 / C7H8N2O2
eMolecules N'-Formylformic hydrazide | 628-36-4 | MFCD00003275 | 5g
Matrix Scientific | N'-Formylformic hydrazide | 5g | 389723710 | 77223 | | 628-36-4 | MFCD00003275 | 88.066 | C2H4N2O2
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eMolecules tert-butyl (3R)-3-(hydrazinecarbonyl)piperidine-1-carboxylate | 1002359-83-2 | MFCD11111950 | 1g
Pharmablock | tert-butyl (3R)-3-(hydrazinecarbonyl)piperidine-1-carboxylate | 1g | 551140595 | PBN20121447 | | 1002359-83-2 | MFCD11111950 | 243.307 | C11H21N3O3
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Medchemexpress LLC Biotin-XX hydrazide | 211237-33-1 | 95.4% | 484.66 g/mol | C22H40N6O4S | 5MG
Biotin-XX hydrazide is a carbonyl-reactive biotinylation reagent that contains two aminohexanoic acid spacers to improve avidin-binding efficiency. It couples to carbonyl groups on biomolecules to produce biotinylated targets suitable for detection, enrichment, and affinity capture using streptavidin or avidin methods.
- Contains two aminohexanoic acid spacers to enhance binding efficiency.
- Reacts selectively with carbonyl groups for targeted labeling.
- Enables affinity capture and detection with streptavidin or avidin systems.
- Supplied as a 5 mg package suitable for laboratory-scale experiments.
- High purity as determined by RP-HPLC for reliable results.
eMolecules N-(Pyridin-3-yl)hydrazinecarbothioamide | 34955-25-4 | MFCD03869992 | 100mg
Oakwood Chemicals | N-(Pyridin-3-yl)hydrazinecarbothioamide | 100mg | 532150671 | 237990 | | 34955-25-4 | MFCD03869992 | 168.220 | C6H8N4S
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eMolecules 3-Bromo-5-chloro-2-hydrazinopyridine | 1289113-27-4 | MFCD10000080 | 1g
Apollo Scientific | 3-Bromo-5-chloro-2-hydrazinopyridine | 1g | 562460166 | OR33678 | | 1289113-27-4 | MFCD10000080 | 222.470 | C5H5BrClN3
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eMolecules 2-Hydroxybenzhydrazide | 936-02-7 | MFCD00007599 | 1g
Oakwood Chemical | 2-Hydroxybenzhydrazide | 1g | 537677243 | 018713 | | 936-02-7 | MFCD00007599 | 152.153 | C7H8N2O2
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eMolecules 2-Ethoxybenzhydrazide | 21018-13-3 | 1G | Purity: 95%
Combi-Blocks | 2-Ethoxybenzhydrazide | 1G | 21018-13-3 | MFCD00017050
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4-Aminobenzhydrazide, 98%, Thermo Scientific™
CAS: 5351-17-7 Molecular Formula: C7H9N3O Molecular Weight (g/mol): 151.169 MDL Number: MFCD00007606 InChI Key: WPBZMCGPFHZRHJ-UHFFFAOYSA-N Synonym: 4-aminobenzhydrazide,amben hydrazide,p-aminobenzhydrazide,4-aminobenzoic acid hydrazide,aminostimil,4-aminobenzoylhydrazine,p-aminobenzoic acid hydrazide,p-aminobenzoyl hydrazide,benzoic acid, 4-amino-, hydrazide,p-aminobenzoic hydrazide PubChem CID: 21450 IUPAC Name: 4-aminobenzohydrazide SMILES: C1=CC(=CC=C1C(=O)NN)N