Benzyl Derivatives
Medchemexpress LLC 2-fluorobenzyl olaparib-d4 | 2732919-14-9 | MFCD00143661 | 438.49 | C24H19D4FN4O3 | 1mg
2-Fluorobenzyl olaparib-d4 is a deuterium labeled compound
Medchemexpress LLC n-Heptyl Alcohol-d15 25mg
n-Heptyl Alcohol-d15 is the deuterium labeled 1-Heptanol[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d4 | 1219804-10-0 | 148.60 | C7H2D4ClF | 25mg
4-Fluorobenzyl chloride-d4 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d7 | 1219804-18-8 | 98.0% | 10mg
4-Fluorobenzyl chloride-d7 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d4 | 1219804-10-0 | MFCD06658704 | 148.60 g·mol⁻¹ | C7H2D4ClF | 100mg
4-Fluorobenzyl chloride-d4 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d7 | 1219804-18-8 | 5mg
4-Fluorobenzyl chloride-d7 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d4 | 1219804-10-0 | 148.60 | C7H2D4ClF | 50mg
4-Fluorobenzyl chloride-d4 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d4 | 1219804-10-0 | >=98.0% | 148.60 g/mol | C7H2D4ClF | 5mg
4-Fluorobenzyl chloride-d4 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d7 | 1219804-18-8 | 99.7% | 146.59 | C7H4D2ClF | 25mg
4-Fluorobenzyl chloride-d7 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC 4-fluorobenzyl chloride-d4 | 1219804-10-0 | 148.60 | C7H2D4ClF | 10mg
4-Fluorobenzyl chloride-d4 is the deuterium labeled 4-Fluorobenzyl chloride[1]
Medchemexpress LLC Benzyl alcohol-13C6 | 201740-95-6 | 98.0% | 114.09 g/mol | C7H8O (ring-13C6) | 10 MG
Benzyl alcohol-13C6 is a ring-13C6 isotopically labeled benzyl alcohol used as an internal standard, tracer, or reference material in analytical chemistry and mass spectrometry. It is supplied in small, high-purity quantities suitable for MS calibration and isotopic tracing studies.
- Isotopically labeled with six 13C atoms in the phenyl ring.
- High purity: 98.0%.
- Suitable as an internal standard for mass spectrometry and tracer studies.
- Available in small quantities for analytical use (e.g., 10 mg).
- CAS number 201740-95-6 for precise identification.
Medchemexpress LLC 4-nitro-benzenemethanol, 1-methanesulfonate | 39628-94-9 | 98.8% | 231.23 g/mol | C8H9NO5S | 10 MG
p-Nitrobenzyl mesylate (PNBM) is a thiol- and phosphorothioate-specific alkylating reagent used to modify phosphorothioates to generate epitopes that are recognized by specific antibodies. It is commonly used for kinase substrate identification and thiophosphate labeling in biochemical assays, and is supplied as a small-scale solid for laboratory use.
- Alkylates phosphorothioates to form antibody-recognizable epitopes.
- Applicable to direct kinase substrate identification and thiophosphate labeling.
- High purity suitable for analytical and preparative experiments.
- Supplied as a 10 mg solid for small-scale laboratory workflows.
- Stable when stored under recommended conditions.
Medchemexpress LLC 4-(Benzyloxy)butanal | 5470-84-8 | MFCD11553544 | 97.0% | 178.23 g/mol | C11H14O2 | 100 MG
4-(Benzyloxy)butanal is a benzyl-protected primary aldehyde used as a linker and synthetic intermediate for bioconjugation and organic synthesis. The benzyl protecting group is acid-labile, while the terminal aldehyde reacts selectively with hydrazide and aminooxy nucleophiles, enabling efficient labeling and crosslinking of carbonyl-containing biomolecules such as oxidized carbohydrates.
- Benzyl-protected primary aldehyde.
- Acid-labile protecting group for controlled deprotection.
- Reactive toward hydrazide and aminooxy groups for efficient bioconjugation.
- Suitable for labeling and crosslinking oxidized carbohydrates.
- Storage recommended under nitrogen: 4°C (neat); in solvent -80°C for 6 months, -20°C for 1 month.
Medchemexpress LLC 4-(Benzyloxy)butanal | 5470-84-8 | MFCD11553544 | 178.23 g/mol | C11H14O2 | 1 G
4-(Benzyloxy)butanal is a small-molecule linker containing an acid-labile benzyl protecting group and a reactive primary aldehyde. It is used in bioconjugation and probe synthesis, where the aldehyde reacts with hydrazide and aminooxy groups to form hydrazones or oximes for labeling or crosslinking. Molecular formula C11H14O2; molecular weight 178.23 g/mol. Available in multiple small-scale package sizes for research use.
- Reactive primary aldehyde for hydrazone and oxime formation.
- Acid-labile benzyl protecting group enables controlled deprotection.
- Suitable for labeling and crosslinking oxidized carbohydrates.
- Useful as a linker in probe and conjugate synthesis.
- Available in multiple small-scale package sizes for laboratory research.
Medchemexpress LLC Benzyl butyl phthalate-d4 | 93951-88-3 | 98.38% | 316.38 | 5 MG
Benzyl butyl phthalate-d4 is the deuterium-labeled version of Benzyl butyl phthalate. Benzyl butyl phthalate, a member of phthalic acid esters (PAEs), has been shown to induce the migration and invasion of hemangioma (HA) cells by upregulating Zeb1. Additionally, it activates the aryl hydrocarbon receptor (AhR) in breast cancer cells, which stimulates SPHK1/S1P/S1PR3 signaling and promotes the formation of metastasis-initiating breast cancer stem cells (BCSCs). This compound is intended for research use only.
- Used as a tracer
- Used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Deuterium labeled compound
- Potential to affect pharmacokinetic and metabolic profiles of drugs
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