Hierarchies

(click for more information)

4cb376f865777ae2627ed061acaaf813664e754ef281d428fca7fed02391f092

ID:

morningvoid||||0

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_10362

ID:

Comment:

A carotenol that exhibits antioxidant activity. It has been isolated from fruits such as papaya and oranges. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_12313426

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_133305

ID:

Comment:

A mixture of the four diastereoisomers arising from the two tetrahedral stereocentres of [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-λ6-sulfanylidene]cyanamide (the sulfur atom and the carbon attached to position 3 of the pyridine ring). [Both E- and Z-isomers involving the S=N double bond and the cyano group exist, but they interconvert rapidly at r.t.]. A nicotinic acetylcholine receptor agonist in insects, sulfoxaflor is used as an insecticide, particularly for the control of aphids. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_134094

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_134179

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_138089

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_140933

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15650

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15756

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15843

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15882

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15930

ID:

Comment:

A diamino-1,3,5-triazine that is 1,3,5-triazine-2,4-diamine substituted by a chloro group at position 6 while one of hydrogens of each amino group is replaced respectively by an ethyl and a propan-2-yl group. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_16101

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16113

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16130

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16196

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_164200

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_165196

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_165878

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16598

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_166459

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_166460

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_166468

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_166469

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16716

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16737

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16738

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16793

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16962

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_172368

ID:

Comment:

Any organobromine compound that is used as a flame retardant. These chemicals are widely incorporated as additives in consumer products such as electronics, vehicles, polyurethane foams etc, to make them less flammable. (Source: CHEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_17243

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17300

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17351

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17578

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17579

ID:

Comment:

A cyclic carotene obtained by dimerisation of all-trans-retinol. A strongly-coloured red-orange pigment abundant in plants and fruit and the most active and important provitamin A carotenoid. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_17642

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17650

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_17855

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_18185

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_18291

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_18723

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_189747

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_19760

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_20184

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_20469

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_22726

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_22977

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_25016

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_25107

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_25195

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_26092

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27007

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_2705

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27131

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27214

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27300

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27363

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27385

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27417

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27432

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27452

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27528

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27547

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27560

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27563

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27568

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27638

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27698

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27744

ID:

Comment:

A phosphonic acid resulting from the formal oxidative coupling of the methyl group of methylphosphonic acid with the amino group of glycine. It is one of the most commonly used herbicides worldwide, and the only one to target the enzyme 5-enolpyruvyl-3-shikimate phosphate synthase (EPSPS). Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_27789

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27929

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_27998

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28063

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28073

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28078

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28112

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28125

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28313

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28364

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28425

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28428

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28488

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28520

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28661

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28667

ID:

Comment:

A thromboxane obtained by formal oxidation of the hemiacetal hydroxy function of thromboxane B2. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_28685

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28694

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28716

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28755

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28812

ID:

Comment:

A member of the class of phosphonic acids that is phosphonic acid substituted by an aminomethyl group. It is a metabolite of the herbicide glyphosate. Source: CHEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_28838

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28842

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28866

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28875

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28941

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_28984

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_29069

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_29125

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_29287

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_29852

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_29866

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30145

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30440

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30452

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30501

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30512

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30513

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30514

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30682

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_30763

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_31575

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_31835

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_32063

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_32594

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_32888

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33115

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33204

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33216

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33284

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33301

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33324

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33341

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33344

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33364

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33375

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33387

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33388

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33666

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_33853

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34093

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34206

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34230

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34283

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34289

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34317

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34416

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34421

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34505

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34571

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34788

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34846

ID:

Comment:

A member of the class of 1,2,4-triazines that is 1,2,4-triazin-5(4H)-one substituted by an amino group at position 4, tert-butyl group at position 6 and a methylsulfanyl group at position 3. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_34852

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_34960

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_35255

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_35366

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_35546

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_35549

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_36062

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_38397

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_38855

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39068

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39069

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39096

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39163

ID:

Comment:

A carboxamidine that is acetamidine in which the amino hydrogens are substituted by a (6-chloropyridin-3-yl)methyl and a methyl group while the hydrogen attached to the imino nitrogen is replaced by a cyano group. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39171

ID:

Comment:

A C-nitro compound consisting of 2-nitroethene-1,1-diamine where one of the nitrogens bears ethyl and (6-chloro-3-pyridinyl)methyl while the other nitrogen carries a methyl group. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39175

ID:

Comment:

nitrile that is cyanamide in which the hydrogens are replaced by a 1,3-thiazolidin-2-ylidene group which in turn is substituted by a (6-chloropyridin-3-yl)methyl group at the ring nitrogen. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39178

ID:

Comment:

An N-nitro compound consisting of 2-nitroguanidine having a (2-chloro-1,3-thiazol-5-yl)methyl group at position 1 and a methyl group at position 3. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39183

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39185

ID:

Comment:

An oxadiazane that is tetrahydro-N-nitro-4H-1,3,5-oxadiazin-4-imine bearing (2-chloro-1,3-thiazol-5-yl)methyl and methyl substituents at positions 3 and 5 respectively. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39291

ID:

Comment:

A pyridinecarboxamide that is nicotinamide substituted by a trifluoromethyl group at position 4 and a cyanomethyl group at the carbamoyl nitrogen atom. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_39308

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39421

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_39426

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_40304

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_4045

ID:

Comment:

A member of the class of aminopyrimidine that is N-phenylpyrimidin-2-amine carrying additional cyclopropyl and methyl substituents at positions 4 and 6 respectively. A broad spectrum fungicide used to control a range of pathogens including Tapesia yallundae, Botrytis spp., Alternaria spp. and Rhynchospium secalis. Whilst it is a recognised irritant no serious human health concerns have been identified. It is moderately toxic to birds as well as most aquatic organisms and earthworms, but it is not considered toxic to honeybees. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_40909

ID:

Comment:

An aryloxypyrimidine having a 4,6-diphenoxypyrimidine skeleton in which one of the phenyl rings is cyano-substituted at C-2 and the other carries a 2-methoxy-1-(methoxycarbonyl)vinyl substituent, also at C-2. An inhibitor of mitochondrial respiration by blocking electron transfer between cytochromes b and c1, it is used widely as a fungicide in agriculture. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_44247

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_47083

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_47773

ID:

Comment:

Cholesterol esters and free cholesterol which are contained in or bound to very low density lipoproteins (VLDL).

Note:

http://purl.obolibrary.org/obo/CHEBI_47774

ID:

Comment:

Cholesterol esters and free cholesterol which are contained in or bound to low-density lipoproteins (LDL).

Note:

http://purl.obolibrary.org/obo/CHEBI_47775

ID:

Comment:

Cholesterol esters and free cholesterol which are contained in or bound to high-density lipoproteins (HDL).

Note:

http://purl.obolibrary.org/obo/CHEBI_48347

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_48765

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_49747

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_50464

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_52048

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_53156

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_53486

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_53487

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_53488

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_566274

ID:

Comment:

A dialdehyde that is propane substituted by two oxo groups at the terminal carbon atoms respectively. A biomarker of oxidative damage to lipids caused by smoking, it exists in vivo mainly in the enol form. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_5692

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_5870

ID:

Comment:

An imidazolidine that is N-nitroimidazolidin-2-imine bearing a (6-chloro-3-pyridinyl)methyl substituent at position 1. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_60151

ID:

Comment:

An oxidised form of low-density lipoprotein (LDL), regulated in vivo by a complex set of biochemical reactions and chiefly stimulated by the presence of necrotic cell debris and free radicals in the endothelium. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_67011

ID:

Comment:

An N-acyl-L-α-amino acid anion obtained by deprotonation of any folic acid. (Source: ChEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_6790

ID:

Comment:

A racemate comprising equal amounts of (R)- and (S)-metalaxyl. A systemic fungicide, it is active against phytopathogens of the order Peronosporales and is used to conrtrol Pythium in a number of vegetable crops. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_68641

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_7071

ID:

Comment:

A monocarboxylic acid amide resulting from the formal condensation of the carboxy group of m-toluic acid with the nitrogen of diethylamine. First developed by the U.S. Army in 1946 for use by military personnel in insect-infested areas, it is the most widely used insect repellent worldwide. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_70973

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_71182

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_79314

ID:

Comment:

Any compound that is added to manufactured materials to inhibit, suppress, or delay the production of flames and so prevent the spread of fire. (Source: CHEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_81518

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_81540

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_81541

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_81572

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_81781

ID:

Comment:

A racemate composed of equimolar amounts of (R)- and (S)-tebuconazole. A fungicide effective against various smut and bunt diseases in cereals and other field crops. Source:ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_81782

ID:

Comment:

A racemate comprising equal amounts of (R)- and (S)-tetraconazole. A fungicide used to control a range of fungal infections including powdery mildew, rusts, bunt, loose smut and scab. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_82392

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_83445

ID:

Comment:

A pyrimidone that is pyrimidin-4(1H)-one substituted by a methyl group at position 6 and an isopropyl group at position 2. It is a metabolite of diazinon. (Source: CHEBI)

Note:

http://purl.obolibrary.org/obo/CHEBI_83491

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_83492

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_83493

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_83506

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_8489

ID:

Comment:

The cyclic ketal obtained by formal condensation of 1-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone with pentane-1,2-diol. A triazole fungicide, it is used commercially as a diastereoisomeric mixture on soft fruit (including apricots, peaches, nectarines, plums and prunes), nuts (including peanuts, pecans and almonds), mushrooms, and grasses grown for seeds. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_85122

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_8674

ID:

Comment:

A member of the class of aminopyrimidines that is N-phenylpyrimidin-2-amine carrying two additional methyl substituents at positions 4 and 6. A fungicide used to control grey mould on fruit, vegetables and ornamentals as well as leaf scab on pome fruit. Also commonly employed to control Botrytis cinerea throughout the winemaking process in grapes, must, fermenting must and wine. Source: ChEBI

Note:

http://purl.obolibrary.org/obo/CHEBI_88522

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_88542

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_89645

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_89749

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/NCIT_C25744

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/chebi/35019

ID:

Comment:

A trialkyl phosphate that is the tributyl ester of phosphoric acid. (Source: ChEBI)

Note:

http://purl.org/twc/HHEAR_00001

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00005

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00006

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00016

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00017

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00018

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00250

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00260

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00262

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00273

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00286

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00293

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00308

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00316

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00317

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00318

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00319

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00320

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00321

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00322

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00323

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00324

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00325

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00326

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00327

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00328

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00329

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00330

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00331

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00332

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00333

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00335

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00336

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00337

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00338

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00339

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00340

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00344

ID:

Comment:

Note:

Duplicate of OXB?

http://purl.org/twc/HHEAR_00348

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00358

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00359

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00361

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00363

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00365

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00366

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00367

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00368

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00369

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00370

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00371

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00372

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00373

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00374

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00375

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00376

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00377

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00378

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00379

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00380

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00381

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00382

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00383

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00384

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00385

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00387

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00388

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00389

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00390

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00391

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00392

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00393

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00394

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00395

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00396

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00397

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00398

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00399

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00400

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00401

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00402

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00403

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00404

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00405

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00406

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00410

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00411

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00412

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00426

ID:

Comment:

Note:

Duplicate of NIC?

http://purl.org/twc/HHEAR_00431

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00432

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00433

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00434

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00435

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00436

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00437

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00438

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00439

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00441

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00443

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00444

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00445

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00448

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00449

ID:

Comment:

Note:

To Do: align with CHEBI.

http://purl.org/twc/HHEAR_00450

ID:

Comment:

Note:

Only found in one journal article, no where else. Maybe mis-spelled?

http://purl.org/twc/HHEAR_00451

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00452

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00453

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00454

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00457

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00467

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00468

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00469

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00470

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00471

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00731

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_00798

ID:

morningvoid||||1

Comment:

Note:

http://purl.org/twc/HHEAR_01333

ID:

Comment:

The mereological sum of all three cholesterols, VLDL, LDL, and HDL

Note:

http://purl.org/twc/HHEAR_01372

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01373

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01374

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01375

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01381

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01382

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01383

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01384

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01385

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01386

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01387

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01388

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01389

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01390

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01391

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01392

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01393

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01394

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01399

ID:

Comment:

A substance that contains both Dibutyl phosphate and Di-isobutyl phosphate as its constituent parts

Note:

http://purl.org/twc/HHEAR_01400

ID:

Comment:

Note:

http://purl.org/twc/HHEAR_01685

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/100503

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/101640759

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/10229

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/104820

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/10546

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/10587157

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/110394

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/110678

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/11344811

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/114481

ID:

Comment:

2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoic acid is a perfluorinated compound that is 2-propoxypentanoic acid in which all 11 of the hydrogens attached to carbon atoms have been replaced by fluorine atoms. Used as an alternative to perfluorooctanoic acid in the fluoropolymer industry for years, its widespread environmental distribution, high bioaccumulation capability, and human exposure have caused great concern, particularly as its potential toxicity and health risk is still largely unknown. It is a monocarboxylic acid, a perfluorinated compound and an ether. (Source: Pubchem)

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/118770

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/119096

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/13089

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/131668297

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/131668311

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/139036037

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/1480

ID:

Comment:

2,4,5-trichlorophenoxyacetic acid is a light tan solid (melting point 153 °C). Insoluble in water. Contact may irritate the skin. (2,4,5-trichlorophenoxy)acetic acid is a chlorophenoxyacetic acid that is phenoxyacetic acid in which the ring hydrogens at postions 2, 4 and 5 are substituted by chlorines. It has a role as a defoliant, a synthetic auxin and a phenoxy herbicide. It is a chlorophenoxyacetic acid and a trichlorobenzene. It is a conjugate acid of a (2,4,5-trichlorophenoxy)acetate. An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed) Source: Pubchem

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/148386

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/1486

ID:

Comment:

2,4-dichlorophenoxyacetic acid is an odorless white to tan solid. Sinks in water. (USCG, 1999) 2,4-Dichlorophenoxyacetic acid (2,4-D) does not occur naturally in the environment. 2,4-D is the active ingredient in many products used in the United States and throughout the world as an herbicide to kill weeds on land and in the water. There are nine forms of 2,4-D that can be used as an herbicide and it is typically sold as a powder or in a liquid form. 2,4-D is a chlorophenoxyacetic acid that is phenoxyacetic acid in which the ring hydrogens at postions 2 and 4 are substituted by chlorines. It has a role as a synthetic auxin, a defoliant, an agrochemical, an EC 1.1.1.25 (shikimate dehydrogenase) inhibitor, an environmental contaminant and a phenoxy herbicide. It is a chlorophenoxyacetic acid and a dichlorobenzene. It is a conjugate acid of a (2,4-dichlorophenoxy)acetate. Source: Pubchem

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/14985

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/150694

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/154683

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/155712

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/155713

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/15709948

ID:

Comment:

2,3,4,5-Tetrabromobenzoic acid is a member of benzoic acids and an organohalogen compound. (Source: Pubchem)

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/16212161

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/164720

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/165618

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/170295

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/18134

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/182767

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/18427030

ID:

Comment:

Synonyms: Mono-3-hydroxybutyl phthalate SCHEMBL4078490 DTXSID601027746 Phthalic acid 1-(3-hydroxybutyl) ester

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/184601

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/187353

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/20269373

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/20569227

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/21013

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/211457

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/2286

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/232446

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/23448

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/23671439

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/2760954

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/2829396

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/287064

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/31355

ID:

Comment:

Tri-isobutylphosphate is a trialkyl phosphate. (Source: PubChem)

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/31736

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/36218

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/3736298

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/37766

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/44284

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/44286

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/44357137

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/443848

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/445354

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/47782

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/53435014

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6028

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/623849

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/630355

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6535

ID:

Comment:

Triethyl phosphate appears as a colorless, corrosive liquid. Combustible. Slowly dissolves in water and sinks in water. Severely irritates skin, eyes and mucous membranes. (Source: Pubchem)

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6540

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/66166

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6618

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6619

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/6626

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/67734

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/67815

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/67818

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/67820

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/68123

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/7005

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/71371900

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/73864

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/74189

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/74318

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/74544

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/75575

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/76438

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/77547

ID:

Comment:

Note:

http://rdf.ncbi.nlm.nih.gov/pubchem/compound/7881

ID:

Comment:

Dibutyl phosphate is a pale-amber odorless liquid. Mp: -13 °C, bp: 135-138 °C. Density: 1.06 g cm-3. Moderately soluble in water (18 g / L at 20 °C). (Source: Pubchem)

Targeted Analyte

4cb376f865777ae2627ed061acaaf813664e754ef281d428fca7fed02391f092

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_10362

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_12313426

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_133305

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_134094

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_134179

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_138089

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_140933

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15650

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15756

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15843

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15882

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_15930

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16101

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16113

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16130

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_16196

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_164200

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_165196

ID:

Comment:

Note:

http://purl.obolibrary.org/obo/CHEBI_165878

ID:

Comment: