4-Bromomethyl-7-methoxycoumarin
| Code | Size | Price |
|---|
| CDX-B0022-G001 | 1 g | £121.00 |
Quantity:
| CDX-B0022-G005 | 5 g | £450.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
Short Term: +20°C. Long Term: +4°C
Documents
Further Information
Alternate Names/Synonyms:
BMC; Br-Mmc; 4-(Bromomethyl)-7-methoxy-2H-1-benzopyran-2-one
Appearance:
Off-white to beige powder.
CAS:
35231-44-8
Class:
9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302, H315, H319, H335
InChi:
InChI=1S/C11H9BrO3/c1-14-8-2-3-9-7(6-12)4-11(13)15-10(9)5-8/h2-5H,6H2,1H3
InChiKey:
CTENSLORRMFPDH-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 35231-44-8. Formula: C11H9BrO3. MW: 269.09. Synthetic. Blue fluorescent labeling reagent for fatty acids and carboxylates. Used for fluorometric analysis, derivatization, and TLC and HPLC separation of a range of naturally occurring acids. Used as a substrate for measuring histone acetyltransferase (HATs), peptidases and sirtuin activity.
MDL:
MFCD00006869
Molecular Formula:
C11H9BrO3
Molecular Weight:
269.09
Package Type:
Vial
PG:
III
Precautions:
P261, P305, P351, P338
Product Description:
Blue fluorescent labeling reagent for fatty acids and carboxylates. Used for fluorometric analysis, derivatization, and TLC and HPLC separation of a range of naturally occurring acids. Used as a substrate for measuring histone acetyltransferase (HATs), peptidases and sirtuin activity.
Purity:
>97% (HPLC)
Signal word:
Warning
SMILES:
O=C1OC2=CC(OC)=CC=C2C(CBr)=C1
Solubility Chemicals:
Soluble in chloroform (20 mg/ml), DMSO or acetone. Sparingly soluble in methanol. Slightly soluble in water.
Source / Host:
Synthetic.
Transportation:
Excepted Quantity
UN Nummer:
UN3335
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.
References
(1) W. Duenges; Anal. Chem. 49, 442 (1977) | (2) S. Lam & E. Grushka; J. Chromatogr. A 158, 207 (1978) | (3) S. Yoshida, et al.; J Chromatogr. 383, 61 (1986) | (4) J.H. Wolf & J. Korf; J. Pharm. Biomed. Anal. 10, 99 (1992) (Review) | (5) K. Wang, et al.; J. Am. Soc. Mass. Spectr. 9, 970 (1998) | (6) C. G. Knight; Lett. Pept. Sci. 5, 1 (1998) | (7) J. Peris Vicente, et al.; J. Chromatogr. A. 1076, 44 (2005) | (8) Z. Xie, et al.; J. Chromatogr. Sci. 45, 405 (2007) | (9) Z. Chen & Y.G. Zheng; Heterocycl. Commun. 13, 343 (2007) | (10) H. Abromeit, et al.; Electrophoresis 33, 1652 (2012)
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