NMR Compound Spectrum Catalog

Experimental ¹H / ¹³C pages for common laboratory compounds. Filter by letter or carbon count, then open a compound for peak tables and stick spectra. Also try ¹H prediction and ¹³C prediction.

Browse All 2593

A–ZA 93 B 92 C 104 D 199 E 103 F 17 G 32 H 53 I 83 J 1 K 3 L 15 M 143 N 101 O 39 P 149 Q 4 R 5 S 37 T 133 U 41 V 30WX 2YZ 1 # 1113

CarbonsC1–C4 539 C5–C8 1285 C9–C12 768 C13–C18 1C19+

Showing 1–80 of 133 · letter T · page 1/2

Name	CAS	Formula	Slug
Tdbpp	126-72-7	C9H15Br6O4P	`tdbpp`
Tdcpp	13674-87-8	C9H15Cl6O4P	`tdcpp`
Tellurophene	288-08-4	C4H4Te	`tellurophene`
Temed	110-18-9	C6H16N2	`temed`
Terephthalonitrile	623-26-7	C8H4N2	`terephthalonitrile`
Terpinolene	586-62-9	C10H16	`terpinolene`
tert-Amylamine	594-39-8	C5H13N	`tert-amylamine`
tert-Butanol	75-65-0	C4H10O	`tert-butanol`
tert-Butyl 2-bromopropanoate	39149-80-9	C7H13BrO2	`tert-butyl-2-bromopropanoate`
tert-Butyl 3-butenoate	14036-55-6	C8H14O2	`tert-butyl-3-butenoate`
tert-Butyl acrylate	1663-39-4	C7H12O2	`tert-butyl-acrylate`
tert-Butyl carbamate	4248-19-5	C5H11NO2	`tert-butyl-carbamate`
tert-Butyl cyanoacetate	1116-98-9	C7H11NO2	`tert-butyl-cyanoacetate`
tert-Butyl ethyl ether	637-92-3	C6H14O	`tert-butyl-ethyl-ether`
Tert-Butyl Isocyanate	1609-86-5	C5H9NO	`tert-butyl-isocyanate`
tert-Butyl methyl ether	1634-04-4	C5H12O	`tert-butyl-methyl-ether`
tert-Butyl N-(2-hydroxyethyl)carbamate	26690-80-2	C7H15NO3	`tert-butyl-n-2-hydroxyethylcarbamate`
tert-Butyl N-(3-hydroxypropyl)carbamate	58885-58-8	C8H17NO3	`tert-butyl-n-3-hydroxypropylcarbamate`
tert-Butyl nitrite	540-80-7	C4H9NO2	`tert-butyl-nitrite`
tert-Butyl sulfide	107-47-1	C8H18S	`tert-butyl-sulfide`
tert-Butylamine	75-64-9	C4H11N	`tert-butylamine`
tert-Butyldiethanolamine	2160-93-2	C8H19NO2	`tert-butyldiethanolamine`
tert-Butylquinone	3602-55-9	C10H12O2	`tert-butylquinone`
tert-Octylamine	107-45-9	C8H19N	`tert-octylamine`
Tetraacetylethylenediamine	10543-57-4	C10H16N2O4	`tetraacetylethylenediamine`
Tetrabromo-o-Cresol	576-55-6	C7H4Br4O	`tetrabromo-o-cresol`
Tetrachloroacetone	632-21-3	C3H2Cl4O	`tetrachloroacetone`
Tetraethyl orthocarbonate	78-09-1	C9H20O4	`tetraethyl-orthocarbonate`
Tetraethyl orthosilicate	78-10-4	C8H20O4Si	`tetraethyl-orthosilicate`
Tetraethylgermane	597-63-7	C8H20Ge	`tetraethylgermane`
Tetraethylsilane	631-36-7	C8H20Si	`tetraethylsilane`
Tetraethylurea	1187-03-7	C9H20N2O	`tetraethylurea`
Tetrafluorobenzoic acid	1201-31-6	C7H2F4O2	`tetrafluorobenzoic-acid`
Tetrahydro-2-furancarboxylic acid	16874-33-2	C5H8O3	`tetrahydro-2-furancarboxylic-acid`
tetrahydrobiopterin	17528-72-2	C9H15N5O3	`tetrahydrobiopterin`
Tetrahydrofuran	109-99-9	C4H8O	`tetrahydrofuran`
Tetrahydrofurfuryl acrylate	2399-48-6	C8H12O3	`tetrahydrofurfuryl-acrylate`
Tetrahydrofurfuryl bromide	1192-30-9	C5H9BrO	`tetrahydrofurfuryl-bromide`
Tetrahydrofurfuryl chloride	3003-84-7	C5H9ClO	`tetrahydrofurfuryl-chloride`
Tetrahydroindene	3048-65-5	C9H12	`tetrahydroindene`
Tetrahydrolinalool	78-69-3	C10H22O	`tetrahydrolinalool`
Tetrahydrophthalic Acid	88-98-2	C8H10O4	`tetrahydrophthalic-acid`
Tetrahydrophthalic acid imide	85-40-5	C8H9NO2	`tetrahydrophthalic-acid-imide`
Tetrahydropyran-2-Methanol	100-72-1	C6H12O2	`tetrahydropyran-2-methanol`
Tetrahydroquinone	637-88-7	C6H8O2	`tetrahydroquinone`
tetrahydrothiophene	110-01-0	C4H8S	`tetrahydrothiophene`
Tetralin	119-64-2	C10H12	`tetralin`
Tetramethylene diacetate	628-67-1	C8H14O4	`tetramethylene-diacetate`
Tetramethylene dibromide	110-52-1	C4H8Br2	`tetramethylene-dibromide`
Tetramethylene dichloride	110-56-5	C4H8Cl2	`tetramethylene-dichloride`
Tetramethylene glutaric acid	16713-66-9	C9H14O4	`tetramethylene-glutaric-acid`
Tetramethylenedithiol	1191-08-8	C4H10S2	`tetramethylenedithiol`
Tetramethylgermanium	865-52-1	C4H12Ge	`tetramethylgermanium`
Tetramethylputrescine	111-51-3	C8H20N2	`tetramethylputrescine`
Tetramethylsuccinonitrile	3333-52-6	C8H12N2	`tetramethylsuccinonitrile`
Tetramethylthiourea	2782-91-4	C5H12N2S	`tetramethylthiourea`
Tetramethyltrimethylenediamine	110-95-2	C7H18N2	`tetramethyltrimethylenediamine`
Tetramethylurea	632-22-4	C5H12N2O	`tetramethylurea`
Thiazolidine-2-carboxylic acid	16310-13-7	C4H7NO2S	`thiazolidine-2-carboxylic-acid`
Thiirane	420-12-2	C2H4S	`thiirane`
Thioacetamide	62-55-5	C2H5NS	`thioacetamide`
thioctic acid	1077-28-7	C8H14O2S2	`thioctic-acid`
thiodiglycol	111-48-8	C4H10O2S	`thiodiglycol`
Thiodiglycolic acid	123-93-3	C4H6O4S	`thiodiglycolic-acid`
Thiodisuccinic acid	4917-76-4	C8H10O8S	`thiodisuccinic-acid`
thiophen-3-amine	17721-06-1	C4H5NS	`thiophen-3-amine`
Thiophene	110-02-1	C4H4S	`thiophene`
Thiophene-2-carbohydrazide	2361-27-5	C5H6N2OS	`thiophene-2-carbohydrazide`
Thiophene-3-carboxylic acid	88-13-1	C5H4O2S	`thiophene-3-carboxylic-acid`
thiram	137-26-8	C6H12N2S4	`thiram`
Thymoquinone	490-91-5	C10H12O2	`thymoquinone`
Tmee	563-79-1	C6H12	`tmee`
TMPD (alcohol)	144-19-4	C8H18O2	`tmpd-alcohol`
Tobias acid	81-16-3	C10H9NO3S	`tobias-acid`
Toluene	108-88-3	C7H8	`toluene`
Tosyl isocyanate	4083-64-1	C8H7NO3S	`tosyl-isocyanate`
Tosylacetonitrile	5697-44-9	C9H9NO2S	`tosylacetonitrile`
tri(propan-2-yl)silane	19186-97-1	C9H22Si	`tripropan-2-ylsilane`
Triacetonamine	826-36-8	C9H17NO	`triacetonamine`
Triacetonamine oxime	4168-79-0	C9H18N2O	`triacetonamine-oxime`

References & data sources

NMRShiftDB2 — open experimental NMR chemical shift database.
Steinbeck, C.; Kuhn, S. NMRShiftDB — nmrshiftdb.nmr.uni-koeln.de
Gottlieb, H. E.; Kotlyar, V.; Nudelman, A. NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities. J. Org. Chem. 1997, 62, 7512–7515.
Fulmer, G. R. et al. NMR Chemical Shifts of Trace Impurities. Organometallics 2010, 29, 2176–2179.
PubChem — compound identifiers and structure depictions (NIH/NCBI).
Related tools: nmrdb.org (community NMR prediction reference).