PRODUCT CATEGORY

Fluorescent Dyes

The fluorescent dye family includes commonly used fluorophores such as fluorescein, rhodamines, cyanine dyes (the Cy series), and BODIPY, together with their functionalized derivatives, to meet different needs in molecular labeling, fluorescence imaging, and analytical research. Some dyes are combined with precision PEG linkers to provide hydrophilic spacers between the fluorophore and the labeling target, facilitating different fluorescent-probe designs. In life-science research, these products can label proteins, peptides, nucleic acids, antibodies, and other biomolecules for cell imaging, flow cytometry, binding assays, and molecular-interaction studies. Dyes with different emission ranges can also trace nanocarrier uptake, cellular localization, and distribution, providing visualization tools for delivery-mechanism research. In materials research, fluorescent dyes and their PEGylated derivatives are suitable for tracing polymers, liposomes, nanoparticles, and functional surfaces. Available amine, carboxyl, NHS ester, maleimide, and other reactive end groups help match different conjugation targets. Spectral properties and labeling performance should be evaluated for the specific dye structure and application system.

Fluorescent Dyes
Fluorescein-PEG-CH2CH2COONHS Ester

Fluorescein-PEG-CH2CH2COONHS Ester

Fluorescein-poly(ethylene glycol)-N-hydroxysuccinimide ester (Fluorescein-PEG-NHS) is a functional dye combining a fluorescein chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Fluorescein-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
RhodamineB-PEG-CH2CH2COONHS Ester

RhodamineB-PEG-CH2CH2COONHS Ester

Rhodamine B-poly(ethylene glycol)-N-hydroxysuccinimide ester (RhodamineB-PEG-NHS) is a functional dye combining a rhodamine B chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Rhodamine B probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
Cy3-PEG-NHS Ester

Cy3-PEG-NHS Ester

Cyanine 3-poly(ethylene glycol)-N-hydroxysuccinimide ester (Cy3-PEG-NHS) is a functional dye combining a Cy3 cyanine chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy3 cyanine-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
Cy5-PEG-NHS Ester

Cy5-PEG-NHS Ester

Cyanine 5-poly(ethylene glycol)-N-hydroxysuccinimide ester (Cy5-PEG-NHS) is a functional dye combining a Cy5 cyanine chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy5 cyanine-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
Cy7-PEG-NHS Ester

Cy7-PEG-NHS Ester

Cyanine 7-poly(ethylene glycol)-N-hydroxysuccinimide ester (Cy7-PEG-NHS) is a functional dye combining a Cy7 cyanine chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy7 cyanine-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
BODIPY-PEG-NHS Ester

BODIPY-PEG-NHS Ester

Boron-dipyrromethene-poly(ethylene glycol)-N-hydroxysuccinimide ester (BODIPY-PEG-NHS) is a functional dye combining a BODIPY chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; BODIPY-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 5–64 · 26 Catalog Nos.View Series →
Fluorescein-PEG-Mal

Fluorescein-PEG-Mal

Fluorescein-poly(ethylene glycol)-maleimide (Fluorescein-PEG-MAL) is a functional dye combining a fluorescein chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Fluorescein-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
RhodamineB-PEG-Mal

RhodamineB-PEG-Mal

Rhodamine B-poly(ethylene glycol)-maleimide (RhodamineB-PEG-MAL) is a functional dye combining a rhodamine B chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Rhodamine B probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy3-PEG-Mal

Cy3-PEG-Mal

Cyanine 3-poly(ethylene glycol)-maleimide (Cy3-PEG-MAL) is a functional dye combining a Cy3 cyanine chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy3 cyanine-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy5-PEG-Mal

Cy5-PEG-Mal

Cyanine 5-poly(ethylene glycol)-maleimide (Cy5-PEG-MAL) is a functional dye combining a Cy5 cyanine chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy5 cyanine-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy7-PEG-Mal

Cy7-PEG-Mal

Cyanine 7-poly(ethylene glycol)-maleimide (Cy7-PEG-MAL) is a functional dye combining a Cy7 cyanine chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy7 cyanine-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
BODIPY-PEG-Mal

BODIPY-PEG-Mal

Boron-dipyrromethene-poly(ethylene glycol)-maleimide (BODIPY-PEG-MAL) is a functional dye combining a BODIPY chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; BODIPY-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
TAMRA-PEG-NHS Ester

TAMRA-PEG-NHS Ester

Tetramethylrhodamine-poly(ethylene glycol)-N-hydroxysuccinimide ester (TAMRA-PEG-NHS) is a functional dye combining a tetramethylrhodamine chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Tetramethylrhodamine-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
TAMRA-PEG-Mal

TAMRA-PEG-Mal

Tetramethylrhodamine-poly(ethylene glycol)-maleimide (TAMRA-PEG-MAL) is a functional dye combining a tetramethylrhodamine chromophore, a defined-length PEG spacer, and a maleimide conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The maleimide can add to cysteine thiols or other thiolated modules, providing a handle for conjugation at thiol sites. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Tetramethylrhodamine-probe construction; Cysteine-site modification; Thiol-selective bioconjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Dansyl-PEG-NHS Ester

Dansyl-PEG-NHS Ester

5-Dimethylaminonaphthalene-1-sulfonyl-poly(ethylene glycol)-N-hydroxysuccinimide ester (Dansyl-PEG-NHS) is a functional dye combining a dansyl chromophore, a defined-length PEG spacer, and an N-hydroxysuccinimide ester conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The NHS ester can form amide bonds with primary amines, enabling conjugation to amine-containing small molecules, peptides, proteins, or material surfaces. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Dansyl-probe construction; Amine modification in proteins and peptides; Amine-functionalized surface conjugation. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Palladium(II) Tetraphenyltetrabenzoporphyrin

Palladium(II) Tetraphenyltetrabenzoporphyrin

Palladium(II) Tetraphenyltetrabenzoporphyrin (PdTPTBP) is a structurally defined functional small molecule. The principal structural feature is a palladium(II)-coordinated tetraphenyltetrabenzoporphyrin. Absorption, dispersion, and relevant reaction behavior can be studied under matched media and optical measurement conditions to select attachment strategies based on structural changes. The metal–porphyrin conjugated scaffold provides a starting structure for photosensitizer–carrier combinations, energy transfer, and oxygen-related response studies. Applications: Photosensitizing and photocatalytic materials; Energy-transfer systems; Phosphorescence and oxygen-related response studies. Customization available.

1 Catalog No.View Series →
Hydroxymethylbiphenyl-functionalized palladium(II) tetraphenyltetrabenzoporphyrin (PdTPTBP-OH)

Hydroxymethylbiphenyl-functionalized palladium(II) tetraphenyltetrabenzoporphyrin (PdTPTBP-OH)

Hydroxymethylbiphenyl-functionalized palladium(II) tetraphenyltetrabenzoporphyrin (PdTPTBP-OH) is a structurally defined functional small molecule. The principal structural feature is a palladium porphyrin with hydroxymethylbiphenyl substituents. The hydroxymethyl groups provide handles for further esterification or conjugation to attach the photosensitive scaffold to carriers or polymers with compatible sites. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: Conjugatable photosensitive materials; Photosensitive-component immobilization; Carrier and polymer modification. Customization available.

1 Catalog No.View Series →
Methacrylate-functionalized palladium(II) tetraphenyltetrabenzoporphyrin monomer (PdTPTBP monomer)

Methacrylate-functionalized palladium(II) tetraphenyltetrabenzoporphyrin monomer (PdTPTBP monomer)

Methacrylate-functionalized palladium(II) tetraphenyltetrabenzoporphyrin monomer (PdTPTBP monomer) is a structurally defined functional small molecule. The principal structural feature is a palladium porphyrin bearing polymerizable methacrylate groups. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The methacrylate sites can undergo suitable radical polymerization or copolymerization, covalently incorporating the photosensitive units into a polymer structure. Applications: Photosensitive comonomers; Photosensitive-material immobilization; Functional-polymer construction. Customization available.

1 Catalog No.View Series →
3-Hydroxypropyl-functionalized Sulfur-Substituted Nile Blue (NBS-OH)

3-Hydroxypropyl-functionalized Sulfur-Substituted Nile Blue (NBS-OH)

3-Hydroxypropyl-functionalized Sulfur-Substituted Nile Blue (NBS-OH) is a structurally defined functional small molecule. The principal structural feature is a thio-Nile Blue scaffold bearing a 3-hydroxypropyl group. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Combining a sulfur-substituted chromophore with a hydroxypropyl modification site enables studies of photosensitizer attachment, dispersion, and photoreaction behavior. The dye scaffold shown carries a single positive charge. The listed molecular formula excludes any unspecified counterion. Applications: Type I photosensitization studies; Modifiable photosensitive materials; Photoreaction-system construction. Customization available.

1 Catalog No.View Series →
3-Hydroxypropyl-functionalized Selenium-Substituted Nile Blue (NBSe-OH)

3-Hydroxypropyl-functionalized Selenium-Substituted Nile Blue (NBSe-OH)

3-Hydroxypropyl-functionalized Selenium-Substituted Nile Blue (NBSe-OH) is a structurally defined functional small molecule. The principal structural feature is a seleno-Nile Blue scaffold bearing a 3-hydroxypropyl group. Selenium substitution provides an elemental-composition comparison within related chromophore systems, while the hydroxyl site enables attachment to carriers or polymers. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The dye scaffold shown carries a single positive charge. The listed molecular formula excludes any unspecified counterion. Applications: Selenium-substituted photosensitive materials; Sulfur/selenium structural comparisons; Carrier–dye conjugation. Customization available.

1 Catalog No.View Series →
2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-thione (SHF-NH2)

2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-thione (SHF-NH2)

2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-thione (SHF-NH2) is a structurally defined functional small molecule. The principal structural feature is a 3-hydroxythioflavone bearing an aminoethoxy substituent. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The primary amine facilitates attachment to activated carboxyl derivatives, incorporating the sulfur-containing donor scaffold into polymers, ligands, or carriers. Applications: CO/H2S donor studies; Sulfur-containing photoreactive materials; Amino-functional donor conjugation. Customization available.

1 Catalog No.View Series →
2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-selenone (SeHF-NH2)

2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-selenone (SeHF-NH2)

2-(4-(2-aminoethoxy)phenyl)-3-hydroxy-4H-chromene-4-selenone (SeHF-NH2) is a structurally defined functional small molecule. The principal structural feature is a 3-hydroxyselenoflavone bearing an aminoethoxy substituent. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The primary amine supports further amidation, while the selenium-containing scaffold can be compared with its sulfur analogue for elemental substitution and photoreaction behavior. Applications: CO donor studies; Sulfur/selenium substitution effects; Amino-functional photoreactive materials. Customization available.

1 Catalog No.View Series →
N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-nitrobenzyl)nitrous amide (CouNO-NO2)

N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-nitrobenzyl)nitrous amide (CouNO-NO2)

N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-nitrobenzyl)nitrous amide (CouNO-NO2) is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing o-nitrobenzyl and hydroxymethylcoumarin groups. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The o-nitrobenzyl and coumarin chromophores provide different aryl environments, while the hydroxymethyl site provides a material-conjugation handle. Applications: o-Nitrobenzyl NO donor studies; Coumarin-donor immobilization; Aryl substituent effects. Customization available.

1 Catalog No.View Series →
N-benzyl-N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)nitrous amide (CouNO-H)

N-benzyl-N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)nitrous amide (CouNO-H)

N-benzyl-N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)nitrous amide (CouNO-H) is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing benzyl and hydroxymethylcoumarin groups. The benzyl moiety without an ortho nitro group can be compared with the corresponding nitro-substituted structure, while the hydroxymethyl group enables attachment to carriers or other synthetic modules. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: Benzylcoumarin NO donor studies; Donor–carrier conjugation; Nitro-substituted structure comparisons. Customization available.

1 Catalog No.View Series →
N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-methoxybenzyl)nitrous amide (CouNO-OCH3)

N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-methoxybenzyl)nitrous amide (CouNO-OCH3)

N-(4-(hydroxymethyl)-2-oxo-2H-chromen-7-yl)-N-(2-methoxybenzyl)nitrous amide (CouNO-OCH3) is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing o-methoxybenzyl and coumarin groups. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The o-methoxybenzyl group provides an independent variable for aryl substituent effects, while the coumarin hydroxymethyl group supports further functionalization. Applications: Methoxybenzyl NO donor studies; Aryl electronic-environment comparisons; Hydroxymethyl-functional donor conjugation. Customization available.

1 Catalog No.View Series →
N-(4-(hydroxymethyl)benzyl)-N-(4-methyl-2-oxo-2H-chromen-7-yl)nitrous amide

N-(4-(hydroxymethyl)benzyl)-N-(4-methyl-2-oxo-2H-chromen-7-yl)nitrous amide

N-(4-(hydroxymethyl)benzyl)-N-(4-methyl-2-oxo-2H-chromen-7-yl)nitrous amide (CouNO-OH) is a structurally defined functional small molecule. The principal structural feature is a coumarin N-nitrosamine with the hydroxymethyl group on the benzyl moiety. This modifiable hydroxymethyl position can be compared with analogues bearing hydroxymethyl on the coumarin moiety to study attachment-position effects. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: Coumarin NO donor attachment-site comparisons; Benzyl-side hydroxymethyl modification; Donor-material immobilization. Customization available.

1 Catalog No.View Series →
N-(2-hydroxyethyl)-N-(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)nitrous amide (NBDNO-OH)

N-(2-hydroxyethyl)-N-(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)nitrous amide (NBDNO-OH)

N-(2-hydroxyethyl)-N-(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)nitrous amide (NBDNO-OH) is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing nitrobenzoxadiazole and hydroxyethyl groups. Nitrobenzoxadiazole provides an aromatic scaffold distinct from coumarin, and the hydroxyethyl terminus can be further derivatized for carrier attachment. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: NBD-chromophore NO donor studies; Hydroxyethyl-functional donor conjugation; Chromophore scaffold and photoreaction comparisons. Customization available.

1 Catalog No.View Series →
N-(2-hydroxyethyl)-N-(4-nitrophenyl)nitrous amide (NBNO-OH)

N-(2-hydroxyethyl)-N-(4-nitrophenyl)nitrous amide (NBNO-OH)

N-(2-hydroxyethyl)-N-(4-nitrophenyl)nitrous amide (NBNO-OH) is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing p-nitrophenyl and hydroxyethyl groups. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The p-nitrophenyl group provides an aromatic substitution pattern, while the hydroxyethyl group retains an independent attachment site for comparing donor immobilization and release behavior. Applications: Nitrophenyl NO donor studies; Hydroxyethyl-site conjugation; Aryl nitrosamine immobilization. Customization available.

1 Catalog No.View Series →
N-(2-hydroxyethyl)-N-(4-nitro-3-(trifluoromethyl)phenyl)nitrous amide

N-(2-hydroxyethyl)-N-(4-nitro-3-(trifluoromethyl)phenyl)nitrous amide

N-(2-hydroxyethyl)-N-(4-nitro-3-(trifluoromethyl)phenyl)nitrous amide is a structurally defined functional small molecule. The principal structural feature is an aryl N-nitrosamine containing nitro, trifluoromethyl, and hydroxyethyl groups. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The trifluoromethyl and nitro groups jointly modify the aromatic substitution environment, while the hydroxyethyl group provides a handle for subsequent material attachment. Applications: Fluorinated NO donor studies; Trifluoromethyl substituent effects; Donor molecule–material conjugation. Customization available.

1 Catalog No.View Series →
N-benzyl-N-(2-(2-hydroxyethyl)-1,3-dioxo-2,3-dihydro-1H-phenalen-6-yl)nitrous amide

N-benzyl-N-(2-(2-hydroxyethyl)-1,3-dioxo-2,3-dihydro-1H-phenalen-6-yl)nitrous amide

N-benzyl-N-(2-(2-hydroxyethyl)-1,3-dioxo-2,3-dihydro-1H-phenalen-6-yl)nitrous amide is a structurally defined functional small molecule. The principal structural feature is a fused-ring dicarbonyl N-nitrosamine scaffold bearing a hydroxyethyl group. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. The fused-ring dicarbonyl scaffold provides an optical-structure comparison with phenyl or coumarin donors, while the hydroxyethyl site remains available for further derivatization. Applications: Fused-ring dicarbonyl NO donor studies; Chromophoric-donor immobilization; Aromatic scaffold optical comparisons. Customization available.

1 Catalog No.View Series →
N-benzyl-N-(4-(hydroxymethyl)phenyl)nitrous amide

N-benzyl-N-(4-(hydroxymethyl)phenyl)nitrous amide

N-benzyl-N-(4-(hydroxymethyl)phenyl)nitrous amide is a structurally defined functional small molecule. The principal structural feature is an N-nitrosamine containing hydroxymethylphenyl and benzyl groups. The hydroxymethyl group lies on the phenyl ring attached to the nitrosamine, providing a carrier-attachment site while retaining the benzyl structure. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: Hydroxymethylaryl NO donors; Benzyl structure and attachment-site studies; Donor immobilization. Customization available.

1 Catalog No.View Series →
N-benzyl-N-(4-(hydroxymethyl)-2-nitrophenyl)nitrous amide

N-benzyl-N-(4-(hydroxymethyl)-2-nitrophenyl)nitrous amide

N-benzyl-N-(4-(hydroxymethyl)-2-nitrophenyl)nitrous amide is a structurally defined functional small molecule. The principal structural feature is a benzyl N-nitrosamine containing ortho-nitro and hydroxymethylphenyl groups. The ortho nitro and hydroxymethyl groups provide aromatic substitution variables for comparison with the non-nitrated counterpart in release and optical-response studies. Absorption, dispersion, and relevant reaction behavior can be compared under matched media and optical measurement conditions to guide attachment strategies. Applications: o-Nitro hydroxymethyl NO donors; Aromatic substitution and release-behavior studies; Conjugatable donor synthesis. Customization available.

1 Catalog No.View Series →
BODIPY-PEG-CH2CH2COOH

BODIPY-PEG-CH2CH2COOH

Boron-dipyrromethene-poly(ethylene glycol)-carboxylic acid (BODIPY-PEG-COOH) is a functional dye combining a BODIPY chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; BODIPY-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy3-PEG-CH2CH2COOH

Cy3-PEG-CH2CH2COOH

Cyanine 3-poly(ethylene glycol)-carboxylic acid (Cy3-PEG-COOH) is a functional dye combining a Cy3 cyanine chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy3 cyanine-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy5-PEG-CH2CH2COOH

Cy5-PEG-CH2CH2COOH

Cyanine 5-poly(ethylene glycol)-carboxylic acid (Cy5-PEG-COOH) is a functional dye combining a Cy5 cyanine chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy5 cyanine-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Cy7-PEG-CH2CH2COOH

Cy7-PEG-CH2CH2COOH

Cyanine 7-poly(ethylene glycol)-carboxylic acid (Cy7-PEG-COOH) is a functional dye combining a Cy7 cyanine chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Cy7 cyanine-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
TAMRA-PEG-CH2CH2COOH

TAMRA-PEG-CH2CH2COOH

Tetramethylrhodamine-poly(ethylene glycol)-carboxylic acid (TAMRA-PEG-COOH) is a functional dye combining a tetramethylrhodamine chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Tetramethylrhodamine-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
RhodamineB-PEG-CH2CH2COOH

RhodamineB-PEG-CH2CH2COOH

Rhodamine B-poly(ethylene glycol)-carboxylic acid (RhodamineB-PEG-COOH) is a functional dye combining a rhodamine B chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Rhodamine B probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →
Fluorescein-PEG-CH2CH2COOH

Fluorescein-PEG-CH2CH2COOH

Fluorescein-poly(ethylene glycol)-carboxylic acid (Fluorescein-PEG-COOH) is a functional dye combining a fluorescein chromophore, a defined-length PEG spacer, and a carboxyl conjugation terminus. The PEG spacer is available in discrete chain lengths with different degrees of polymerization. The carboxyl group can be activated for amide coupling with primary-amine-containing molecules, retaining a handle for subsequent ligand or carrier attachment. The PEG spacer separates the chromophore from the target attachment site. Chain length can be selected in relation to labeling position, local environment, and conjugate dispersion. Applications: Fluorescent labeling and tracing; Fluorescein-probe construction; Amine-containing molecule conjugation; Drug and ligand modification. Customization available.

n = 4–96 · 26 Catalog Nos.View Series →

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