text.skipToContent text.skipToNavigation

Maximum quantity allowed is 999

Please select the quantity

CAS RN: 10199-89-0 | Product Number: A5592

NBD-Cl (=4-Chloro-7-nitro-2,1,3-benzoxadiazole) [for HPLC Labeling]


Purity: >98.0%(T)
Synonyms:
  • 4-Chloro-7-nitrobenzofurazan
  • 4-Chloro-7-nitro-2,1,3-benzoxadiazole
Product Documents:
1G
25,00 €
1   ≥100 
5G
98,00 €
5   ≥100 

*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Product Number A5592
Purity / Analysis Method >98.0%(T)
Molecular Formula / Molecular Weight C__6H__2ClN__3O__3 = 199.55 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 10199-89-0
Reaxys Registry Number 614212
PubChem Substance ID 87563199
SDBS (AIST Spectral DB) 5444
MDL Number

MFCD00005808

Specifications
Appearance Light yellow to Yellow powder to crystal
Purity(Volumetric Analysis) min. 98.0 %
Melting point 97.0 to 100.0 °C
Solubility in Methanol almost transparency
Properties (reference)
Melting Point 98 °C
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
EC Number 233-496-4
RTECS# DF8002400
Transport Information:
HS Number 2934999090
Application
HPLC Labeling Reagent for Amines and Thiols

The compound 1 which is an HPLC fluorescence labeling reagent having a 2,1,3-benzoxadiazole skeleton, can easily react with a secondary amine and thiol. The resultant derivative is stable enough to reach the detector without any decomposition under general reversed phase HPLC. An excellent chromatogram can be obtained by fluorescence detection analysis at the excitation and emission wavelengths of 460 nm and 535 nm, respectively.

Application example:
[Alkylamines] 1)
To 25~500 µL of a methanol solution containing an amine (1~20 µg), 4~8 eq. excess amount of 0.05% labeling reagent 1 / methanol solution is added. After adding 50~100 µL of 0.1 M NaHCO3, incubate at 55 °C for 1~5 h. After cooling the reaction mixture to room temperature, use it as an HPLC sample.
[Others]
TLC and HPLC of N-methylcarbamates, N,N-dimethylcarbamates in agrichemicals2,3) Hydrolyze the carbamates to label the amine derivatives.
TLC of amphetamines in urine4,5), HPLC of prolines (precolumn derivatization method)6)

References


PubMed Literature


TCIMAIL
Product Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.

The requested SDS is not available.

Please Contact Us for more information.

Specifications
C of A & Other Certificates
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The product with the lot number searched for has been discontinued and no related documentation is available.

Sample C of A
This is a sample C of A and may not represent a recently manufactured lot of the product.

A sample C of A for this product is not available at this time.

Analytical Charts
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The requested analytical chart is not available. Sorry for the inconvenience.

The product with the lot number searched for has been discontinued and no related documentation is available.

Other Documents

Session Status
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.

Your session has timed out. You will be redirected to the HOME page.