Protocols with Chlorophorm-Methanol 2:1 mixtures are also quite common, yet not as efficient as acetone or hexane. From what organism do you want to extract? This has also an influence on extraction efficiency!
For photometric quantification you can use a normal spectrophotometer and cuvettes suitable for UV measurements. But of course you have to purify or separate carotenoids from your extract by TLC or HPLC to get decent peaks for quantification.