Your a damn nice bee THC.
Yup I'm quite certain on the eph soly in tone. But if it's at the start of a procedure the tone wash, less will dissolve (but still some).
To demonstrate this pour a boiling wash thru a filter, you'll see fragments of crystal when you look at the filter paper from various angles.
when convinced bring the wash back up to boiling and throw it all back in the main pot as this is unacceptable and was only an experiment.
actually now im fucken confused, the merck only has an entry for paracetamol for the freebase, ill just paste all of it so you can look through it too:
Monograph number: Title: Acetaminophen. CAS Registry number: [103-90- CAS name(s): N- (4-Hydroxyphenyl)acetamide; 4prime-hydroxyacetanilide Additional name(s): p- hydroxyacetanilide; p- acetamido phenol; p- acetaminophenol; p- acetylaminophenol; N- acetyl- p- aminophenol; paracetamol Trade name(s): Acamol (Teva) ; Acetalgine (Streuli) ; Alpiny (SS Pharm.) ; Anaflon (SKB) ; Anhiba (Hokuriku) ; Apamide (Bayer) ; Ben-u-ron (Bene-Arzneimittel) ; Calpol (Warner-Lambert) ; Captin (Krewel) ; Dafalgan (UPSA) ; Datril (Bristol-Myers Squibb) ; Dirox (Sanofi Winthrop) ; Disprol (Reckitt and Colman) ; Doliprane (RPR) ; Dolprone (Bottu) ; Enelfa (Dolorgiet) ; Feb rilex (Raven) ; Gelocatil (Gelos) ; Hedex (SKB) ; Momentum (Much) ; Ortensan (Cimex) ; Pacemol (Gemballa) ; Panadol (SKB) ; Pana leve (Pinewood) ; Panasorb (SKB) ; Panodil (SKB) ; Paraspen (Fisons) ; Pasolind N (Stada) ; Salzone (Wallace) ; Tabalgin (Berk) ; Tapar (Parke, Davis) ; Tempra (Mead Johnson) ; Tylenol (McNeil) ; Valadol (Bristol-Myers Squibb) Molecular formula: C 8 H 9 NO 2 Molecular weight: Percent Composition: C 63.56%, H 6.00%, N 9.27%, O Literature references: Prepn from p- nitrophenol: Morse, Ber. 11, 232 (1878); Tingle, Williams, Am. Chem. J. 37, 63 (1907); from p- aminophenol: Lumiegravere et al., Bull. Soc. Chim. France [3] 33, 785 (1905); Fierz-David, Kuster, Helv. Chim. Acta 22, 94 (1939); Wilbert, De Angelis, U.S. pat. 2,998,450 (1961 to Warner-Lambert); Bergmann, Ger. pat. 453,577; Chem. Zentr. 1928, I, 2663; Frdl. 16, 238; from p- hydroxyaceto phenone hydrazone: Pearson et al., J. Am. Chem. Soc. 75, 5907 (1953). Toxicity data: G. A. Starmer et al., Toxicol. Appl. Pharmacol. 19, 20 (1971); D. C. Dahlin, S. D. Nelson, J. Med. Chem. 25, 885 (1982). Evalu ation of renal effects: D. P. Sandler et al., N. Engl. J. Med. 320, 1238 (1989). Comprehensive description: J. E. Fairbrother, Anal . Profiles Drug Subs . 3, 1-109 (1974). Review of pharmacology: B. Ameer, D. J. Greenblatt, Ann. Int. Med. 87, 202-209 (1977). Review of acetaminophen-indu ced hepato toxicity: J. A. Hinson, Rev. Biochem. Toxicol. 2, 103-129 (1980); idem, Life Sci. 29, 107-116 (1981); and proposed protective agents: M. Davis, Sem. Liver Dis. 6, 138-147 (1986). For proposed toxic metabolite see Acet imidoquinone. Properties: Large monoclinic prisms from water, mp 169-170.5degrees . d 4 21 1.293 . uv max (ethanol): 250 nm (epsi 13800) . Very slightly sol in cold water, considerably more sol in hot water. Sol in methanol, ethanol, dimethylformamide, ethylene dichloride, acetone, ethyl acetate. Slightly sol in ether. Practically insol in petr ether, pentane, benzene. LD 50 in mice ( mg/kg ): 338 orally (Starmer), 500 i.p. (Dahlin, Nelson) . Density: d 4 21 Melting Point: 169-170.5 UV Maxima: USE: Manuf azo dyes, photographic chemicals. THERAP CAT: Analgesic; antipyretic.