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Merck
CN

30434

Dansylhydrazine

BioReagent, suitable for fluorescence, ≥90% (HPLC)

Synonym(s):

5-(Dimethylamino)-1-naphthalenesulfonic hydrazide, 5-(Dimethylamino)naphthalene-1-sulfono­hydra­zide, Dns-Hz

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About This Item

Linear Formula:
(CH3)2NC10H6SO2NHNH2
CAS Number:
33008-06-9
Molecular Weight:
265.33
Beilstein:
2868662
EC Number:
251-337-7
MDL number:
MFCD00003986
UNSPSC Code:
12352103
PubChem Substance ID:
329753512
NACRES:
NA.32

Key Documents

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product line

BioReagent

Assay

≥90% (HPLC)

mp

126-130 °C (lit.)

solubility

ethanol: soluble

fluorescence

λex 340 nm; λem 525 nm in ethanol

suitability

suitable for fluorescence

storage temp.

2-8°C

SMILES string

CN(C)c1cccc2c(cccc12)S(=O)(=O)NN

InChI

1S/C12H15N3O2S/c1-15(2)11-7-3-6-10-9(11)5-4-8-12(10)18(16,17)14-13/h3-8,14H,13H2,1-2H3

InChI key

KPQYDVAFRDWIBW-UHFFFAOYSA-N

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Application

Dansylhydrazine (DH) is widely used as a fluorometric reagent for carbonyl compounds. Dansylated carbonyl molecules can be separated and identified by analytical techniques.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Fluorescent marker for carbonyl compounds

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCM7166
BCCL3174
BCCK6905
BCCK1108
BCCK6309

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1-Dimethylaminonaphthalene-5-sulfonyl hydrazine (dansyl hydrazine): a fluorometric reagent for carbonyl compounds.
R Chayes et al.
Analytical biochemistry, 42(1), 283-286 (1971-07-01)
Cheuk Fai Chiu et al.
The journal of physical chemistry. A, 115(34), 9579-9584 (2011-07-20)
The development of chromophore-carbon nanotube hybrids requires efficient and accurate methods to investigate their photophysical properties. Using the ability of the fluorescence labeling of surface species (FLOSS) technique to determine the density of covalently attached dyes to the surface of
Osama Y Al-Dirbashi et al.
Biomedical chromatography : BMC, 22(11), 1181-1185 (2008-07-25)
We describe an improved diagnostic method for tyrosinemia type 1 based on quantifying succinylacetone in dried blood spots by ultra-performance liquid chromatography tandem mass spectrometry. Succinylacetone extracted from a single 3/16 inch disk of specimen collection paper containing a dried
Heather L Lord et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(13), 1292-1298 (2009-01-07)
Analytical derivatization (AD) increases the sensitivity of analysis by one to three orders of magnitude, stabilizes labile analytes and converts them into readily extractable products. Using a variant of this technique, we applied solid phase analytical derivatization (SPAD) to fully
J M Anderson
Analytical biochemistry, 152(1), 146-153 (1986-01-01)
Methods for the determination of carbonyl compounds of biological origin by high-performance liquid chromatography were improved by the use of new fluorescent derivatizing agents. Eight fluorescent hydrazides were either synthesized or obtained commercially and compared to dansyl hydrazine (1-dimethylaminonaphthalene-5-sulfonylohydrazide). Four
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