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2-29<br />

Amino-diphenylamine (p-) H2NC6H4NHC6H5 nd./aq. al. 67 354 sl. s. s. s.<br />

-G-acid (2-)(6-,8-), Na2 salt C10H5(NH2)(SO3Na)2 v. sl. s.<br />

20<br />

-mono-potassium salt C10H5(NH2)S2O6HK 12.8<br />

18<br />

-sodium salt C10H5(NH2)S2O6HNa 2.7<br />

20<br />

-J-acid (2-)(5-,7-) C10H5(NH2)(SO3H)2 10.0<br />

18<br />

-mono-potassium salt C10H5(NH2)S2O6HK 3.4<br />

-naphthol sulfonic (1-,2-,4-)(α-) C10H5OHNH2SO3HaH2O v. s.<br />

(1-,8-,4-) NH2(OH)C10H5SO3H v. sl. s.<br />

0 -phenol (o-) 2-aminophenol H2NC6H4OH col. nd. 173 subl. 1.7 4.30 v. s.<br />

0 (m-) 3-aminophenol H2NC6H4OH pr. 122–3 2.6 s. sl. s.<br />

0 (p-) p-hydroxyaniline H2NC6H4OH lf. 184–6 d. subl. 1.1 40 i. bz.<br />

11<br />

-toluene sulfonic acid (1-,2-,3-) C6H3(CH3)(NH2)SO3H nd. 0.97<br />

20 (1-,4-,2-) C6H3(CH3)(NH2)SO3HH2O mn. d. 0.5 i.<br />

(1-,4-,3-) C6H3(CH3)(NH2)SO3HaH2O nd. 0.47<br />

11 (1-,2-,5-) C6H3(CH3)(NH2)SO3HH2O tri./aq. −H2O, 120 3 i.<br />

20/20 Amyl acetate (n-) CH3CO2CH2(CH2)3CH3 col. lq. 0.879 −70.8 148.4737 v. sl. s. ∞ ∞<br />

15/4 (i-) common amyl acetate CH3CO2CH2CH2CH(CH3)2 col. lq. 0.876 142757 0.315 ∞ ∞<br />

13 CH3CO2CH2CH(CH3)C2H5 col. lq. 0.880 141–2 v. sl. s. ∞ ∞<br />

0 (s-) α-Me-Bu-acetate CH3CO2CH(CH3)CH2C2H5 col. lq. 0.922 133.5 sl. s. ∞ ∞<br />

20/4 (s-) di Et-carbinol acetate CH3CO2CH(C2H5)2 col. lq. 0.871 133 sl. s. ∞ ∞<br />

19 (t-) CH3CO2C(CH3)2C2H5 col. lq. 0.874 124.5749 v. sl. s. ∞ ∞<br />

20/20 alcohol (n-) fusel oil, pentanol-1 CH3(CH2)3CH2OH col. lq. 0.817 −78.5 137.9 2.722 ∞ ∞<br />

20/20 (s-,n-) methyl-propyl carbinol, pentanol-2 C2H5CH2CH(OH)CH3 col. lq. 0.810 119.5 420 ∞ ∞<br />

15/4 (prim.-,i-) isobutyl carbinol, 2-methyl-butanol-4 (CH3)2CHCH2CH2OH col. lq. 0.813 −117.2 132.0 214 ∞ ∞<br />

25/4 (C2H5)2CHOH col. lq. 0.815 115.6 5.530 ∞ ∞<br />

19 (s-,i-) 2-methyl-butanol-3 (CH3)2CHCH(OH)CH3 col. lq. 0.819 113–4 2.830 ∞ ∞<br />

20/4 (t-) 2-methyl-butanol-2 (CH3)2C(OH)C2H5 col. lq. 0.809 −11.9 102 sl. s. s. s.<br />

(CH3)3CCH2OH cr. 52–3 113–4 sl. s. ∞ ∞<br />

20/4 (d-) active amyl alcohol C2H5CH(CH3)CH2OH col. lq. 0.816 128 3.630 ∞ ∞<br />

19 -amine (n-) CH3(CH2)4NH2 col. lq. 0.766 −55 103–4 s. s. s.<br />

20/4 (s-,n-) (C3H7)(CH3)CHNH2 col. lq. 0.749 91–2 ∞ ∞ ∞<br />

18/4 (i-) (CH3)2CH(CH2)2NH2 col. lq. 0.751 95 ∞ ∞ ∞<br />

25/4 (t-) (C2H5)(CH3)2CNH2 col. lq. 0.731 −105 77–8 ∞ ∞ ∞<br />

18 1-NH2-2-Me-butane C2H5CH(CH3)CH2NH2 col. lq. 0.755 95–6 ∞ ∞ ∞<br />

20/4 3-amino pentane (C2H5)2CHNH2 col. lq. 0.749 90–1 ∞ ∞ ∞<br />

18 3-NH2-2-Me-butane (CH3)2CHCH(CH3)NH2 col. lq. 0.757 83–4 ∞ ∞ ∞<br />

15/4 aniline (i-) C6H5NHC5H11 lq. 0.928 254.5 i.<br />

14/14 benzoate (i-) C6H5CO2C5H11 col. lq. 0.992 261746 i. ∞ ∞<br />

20/4 bromide (n-) 1-bromopentane CH3(CH2)3CH2Br col. lq. 1.218 −95 129.7 i. s.<br />

17/15 (i-) 4-Br-2-Me-butane (CH3)2CH(CH2)2Br col. lq. 1.220 120745 0.0216 s. s.<br />

19/0 (t-) 2-Br-2-Me-butane (CH3)2C(Br)C2H5 lq. 1.216 108765 i. s. s.<br />

15/4 n-butyrate (n-) C2H5CH2CO2(CH2)4CH3 col. lq. 0.871 −73.2 186.4 0.0550 ∞ ∞<br />

19/15 (i-) C2H5CH2CO2C5H11 col. lq. 0.866 178.6 i. ∞ ∞<br />

15/0 (t-) C3H7CO2C(CH3)2C2H5 col. lq. 0.865 164 sl. s. ∞ ∞<br />

0/4 i-butyrate (i-) (CH3)2CHCO2C5H11 lq. 0.876 168.8 i. s. s.<br />

20/4 chloride (n-) 1-chloropentane CH3(CH2)3CH2Cl col. lq. 0.878 −99 108.4 i. s. s.<br />

20/4 (s-) 2-chloropentane C2H5CH2CHClCH3 lq. 0.870 96.7 i. s. s.<br />

21 (s-) 3-chloropentane (C2H5)2CHCl col. lq. 0.895 97.3 i. ∞ ∞<br />

20/4 (i-) 4-Cl-2-Me-butane (CH3)2CH(CH2)2Cl col. lq. 0.893 99.7758 i. s. ∞<br />

0 (s-,i-) 3-Cl-2-Me-butane (CH3)CHCHClCH3 lq. 0.883 91753 i. s. s.<br />

20/4 (t-) 2-Cl-2-Me-butane (CH3)2CClC2H5 lq. 0.871 −72.9 85.7 i. s. s.<br />

17.5 1-Cl-2-Me-butane (CH3)(C2H5)CHCH2Cl lq. 0.881 98–9 i. s. s.<br />

i-cyanide (i-) iso-caproic iso-nitrile (CH3)2CH(CH2)2NC lq. 137–9 i. s. s.<br />

0 formate (n-) HCO2CH2(CH2)3CH3 lq. 0.902 −73.5 132 v. sl. s. ∞ ∞<br />

20/4 (i-) HCO2CH2CH2CH(CH3)2 lq. 0.882 −93.5 123.5 0.322 ∞ ∞<br />

20/4 iodide (n-) 1-iodopentane CH3(CH2)3CH2I lq. 1.510 −86 157.0 i. s. ∞<br />

18/4 (i-) 4-I-2-Me-butane (CH3)2CHCH2CH2I lq. 1.515 147765 i. ∞ ∞<br />

17/4 (s-,n-) 2-iodopentane C2H5CH2CHICH3 lq. 1.507 144–5 i. ∞ ∞<br />

19/15 (t-) 2-I-2-Me-butane (CH3)2CIC2H5 lq. 1.471 127765 i. ∞ ∞<br />

20/4 C2H5CH(CH3)CH2I lq. 1.524 148 i. ∞ ∞<br />

20 mercaptan (n-) pentanthiol-1 CH3(CH2)3CH2SH lq. 0.857 126767 i. ∞ ∞<br />

(n-) pentanthiol-3 (C2H5)2CHSH col. lq. 105 i. ∞ ∞<br />

20/4 (i-) 2-Me-butanthiol-4 (CH3)2CH(CH2)2SH lq. 0.835 120 i. ∞ ∞<br />

phenol (t-)(p-) pentaphen C5H11C6H4OH cr. 93 265–7 sl. s. s. s.<br />

15/4 propionate (n-) C2H5CO2(CH2)4CH3 lq. 0.876 −73.1 168.7 i. ∞ ∞<br />

20/4 (i-) C2H5CO2(CH2)2CH(CH3)2 col. lq. 0.870 160.2 0.125 ∞ ∞<br />

20/4 (act.) C2H5CO2C5H11 col. lq. 0.866 5816 184.24<br />

347.28<br />

341.40<br />

325.29<br />

303.31<br />

341.40<br />

248.26<br />

239.25<br />

109.13<br />

109.13<br />

109.13<br />

187.22<br />

205.23<br />

196.22<br />

205.23<br />

130.18<br />

130.18<br />

130.18<br />

130.18<br />

130.18<br />

130.18<br />

88.15<br />

88.15<br />

88.15<br />

88.15<br />

88.15<br />

88.15<br />

88.15<br />

88.15<br />

87.16<br />

87.16<br />

87.16<br />

87.16<br />

87.16<br />

87.16<br />

87.16<br />

163.26<br />

192.25<br />

151.04<br />

151.04<br />

151.04<br />

158.24<br />

158.24<br />

158.24<br />

158.24<br />

106.59<br />

106.59<br />

106.59<br />

106.59<br />

106.59<br />

106.59<br />

106.59<br />

97.16<br />

116.16<br />

116.16<br />

198.05<br />

198.05<br />

198.05<br />

198.05<br />

198.05<br />

104.21<br />

104.21<br />

104.21<br />

164.24<br />

144.21<br />

144.21<br />

144.21<br />

v. sl. s. ∞ ∞<br />

15 salicylate (n-) HOC6H4CO2C5H11 208.25 lq. 1.065 265 i. ∞ ∞<br />

20/15 Amyl i-valerate (i) C4H9CO2C5H11 172.26 col. lq. 0.858 194 v. sl. s. ∞ ∞<br />

14/0 (t-) C4H9CO2C5H11 172.26<br />

col. lq. 0.861 173–4 sl. s. s. s.<br />

*By N. A. Lange, Ph.D., H<strong>and</strong>book Publishers, Inc., S<strong>and</strong>usky, Ohio. Abridged from table of <strong>Physical</strong> Constants of Organic Compounds in Lange’s H<strong>and</strong>book of Chemistry.

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