Naphthol AS acetate
| Code | Size | Price |
|---|
| CDX-N0354-G010 | 10 g | £97.00 |
Quantity:
| CDX-N0354-G025 | 25 g | £184.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
Short term: +4°C, Long term: -20°C
Documents
Further Information
Alternate Names/Synonyms:
3-Acetoxy-2-naphthoic acid anilide
Appearance:
White to off-white powder.
CAS:
1163-67-3
EClass:
32160000
Form (Short):
solid
Handling Advice:
Keep under inert gas.Very hygroscopic.
InChi:
InChI=1S/C19H15NO3/c1-13(21)23-18-12-15-8-6-5-7-14(15)11-17(18)19(22)20-16-9-3-2-4-10-16/h2-12H,1H3,(H,20,22)
InChiKey:
CVJGNNYDVQYHEO-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 1163-67-3. Formula: C19H15NO3. MW: BD9837. Naphthol AS acetate is a fluorogenic substrate for unspecified esterases. After cleavage of the fluorigenic substrate by esterases the free Naphthol AS can couple with diazonium salts to form different types of fluorescent azo dyes. Human and bovine serum albumin are active against Naphthol AS acetate, resulting in a fluorescence excited at 320nm and monitored at 500nm. Can also be used as a bulding block or intermediate for organic synthesis.
MDL:
MFCD00004095
Molecular Formula:
C19H15NO3
Molecular Weight:
305.33
Package Type:
Vial
Product Description:
Naphthol AS acetate is a fluorogenic substrate for unspecified esterases. After cleavage of the fluorigenic substrate by esterases the free Naphthol AS can couple with diazonium salts to form different types of fluorescent azo dyes. Human and bovine serum albumin are active against Naphthol AS acetate, resulting in a fluorescence excited at 320nm and monitored at 500nm. Can also be used as a bulding block or intermediate for organic synthesis.
Purity:
>99% (HPLC)
SMILES:
O=C(NC1=CC=CC=C1)C2=CC3=CC=CC=C3C=C2OC(C)=O
Solubility Chemicals:
Soluble in methanol.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) A.H. Baillie; J. Micr. Sci. 105, 247 (1964) | (2) V.K. Hopsu, et al.; J. Histochem. Cytochem. 13, 117 (1965) | (3) M.T. Rakhawy; Acta Anatomica 95, 572 (1976) | (4) M. Tavassoli; Scand. J. Haematol. 20, 330 (1978) | (5) Y. Eishi, et al.; Bull. Tokyo Med. Dent. Univ. 29, 47 (1982) | (6) R.F. Chen & C.H. Scott; Anal. Lett. 17, 857 (1984) | (7) U. Waspi, et al.; Eur. J. Biochem. 254, 32 (1998)