Arthur,
I do not think light affects stannous chloride that bad.
But stannous chloride is easily degraded by oxygen or air, by being less acidic, and if there is no free tin in solution, or diluting with water stannous chloride will form an hydroxide of tin.
Excess HCl acid, excess tin metal, and the solution keeping oxygen free, will help the stannous chloride stay fresh and last longer, where it does not breakdown into another tin salt.
Because of the oxygen, when I make my stannous chloride, I make enough to fill my small bottle, this way I am not leaving my stannous chloride sitting with mostly oxygen in the bottle, as opposed to if I only had a small amount of liquid in the bottle.
Excess tin and a little extra HCl to keep the solution fresh.
I do sit my stannous in the dark cool shed, many chemicals can change in sunlight, stannous chloride may but I have not heard of it doing so. I have seen commercial tin chloride dried salts (stannous chloride) in clear plastic, chemicals that are affected by light like nitric acid, H2O2 and so on are normally stored in amber or other glass or plastic where light will not decompose the chemical, this also gives me reason to believe stannous chloride is not affected by light to any great extent.
If your stannous chloride in a test is converting a solution to brown this makes me believe a reaction is occurring, and the stannous chloride is reducing something in solution, but this something does not have to be valuable metals, stannous chloride can also reduce many base metals, most of these other base metals do not color the solution in our tests (lucky for us), although some will like copper.
If I was concerned with whether the stannous was working I would test the stannous with a known solution.
Sometimes several metals in solution together, gold and PGM can make it hard to judge from the colors, this is where a spot plate and using some of the methods Harold or Hoke's speaks of, like using copperas to test for and precipitate the gold in one well of the spot plate, and moving the remaining gold barren solution from that test to another well, and testing with another test, like SnCl2 or DMG...
Basically (testing for) and separating out one metal from the solution to be tested, so then you can test for other metals in solution.
Arthur,
I know I am probably not saying anything you that you already do not know but I thought I would try to say it anyway.