Hi there, i have a question about formaldehyde. Using formaldehyde to react with Grignard reagent or orgaolithium reagent results in alcohol. But i checked formaldehyde in Aldrich and found they are all stored in 37%wt-40%wt in H2O. When people do the above reaction, don't Grignard reagent or organolithium be deprotonated before attacking the carbonyl? Is there any dry formaldehyde commerically available? Please help me to find out this. Thank you.