Table 2.

Organic acids from Chamomile.

Categories	No	Name	Molecular Formula	Relative Molecular Mass	References
Primary metabolites	1	Palmitic acid	C16H32O2	256.42	[33]
	2	Linoleic acid	C18H32O2	280.45	[33]
	3	Oleic acid	C18H34O2	282.46	[33]
	4	Stearic acid	C18H36O2	284.48	[33]
Secondary metabolites	5	Isobutyric acid	C4H8O2	88.11	[36]
	6	Tiglic acid	C5H8O2	100.12	[36]
	7	Isovaleric acid	C5H10O2	102.13	[36]
	8	D,L-2-Methylbutyric acid	C5H10O2	102.13	[36]
	9	4-Hydroxybenzoic acid	C7H6O3	140.11	[35]
	10	Cinnamic acid	C9H8O2	149.02	[35]
	11	Anisic acid	C8H8O3	152.15	[33]
	12	Nonanoic acid	C9H18O2	158.24	[36]
	13	Vanillic acid	C8H8O4	168.15	[33]
	14	Decanoic acid	C10H20O2	172.26	[36]
	15	Caffeic acid	C9H8O4	179.04	[34]
	16	Quinic acid	C7H12O6	191.06	[35]
	17	Ferulic acid	C10H10O4	193.05	[35]
	18	Galacturonic acid	C6H10O7	194.14	[33]
	19	Syringic acid	C9H10O5	198.17	[33]
	20	Chlorogein acid	C16H18O9	353.09	[34]
	21	Neochlorogenic acid	C16H18O9	353.09	[34]
	22	Cryptochlorogenic acid	C16H18O9	354.31	[38]
	23	Isochlorogenic acid B	C25H24O12	516.40	[37]
	24	Isochlorogenic acid A	C25H24O12	516.45	[38]
	25	Isochlorogenic acid C	C25H24O12	516.46	[35]
	26	1,5-Dicaffeoylquinic acid	C25H24O12	517.13	[35]