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60-23-1

Basic Information
CAS No.: 60-23-1
Name: Ethanethiol, 2-amino-(8CI,9CI)
Molecular Structure:
Molecular Structure of 60-23-1 (Ethanethiol, 2-amino-(8CI,9CI))
Formula: C2H7NS
Molecular Weight: 77.16
Synonyms: 1-Amino-2-mercaptoethane;2-Amino-1-ethanethiol;2-Aminoethanethiol;2-Aminoethyl mercaptan;2-Aminoethylthiol;2-Mercaptoethanamine;2-Mercaptoethylamine;Becaptan;Cystagone;Cysteamine;Cysteinamine;Decarboxycysteine;L 1573;Lambraten;Lambratene;MEA;MEA (mercaptan);Mercamin;Mercamine;Mercaptamin;Mercaptamine;Mercaptoethylamine;Merkamin;NSC 647528;Riacon;Thioethanolamine;WR 347;b-Aminoethanethiol;b-Aminoethylthiol;b-MEA;b-Mercaptoethylamine;cysteamine HCL;
EINECS: 200-463-0
Density: 0.973 g/cm3
Melting Point: 95°C
Boiling Point: 133.6 °C at 760 mmHg
Flash Point: 34.6 °C
Solubility:
Appearance: white powder
Hazard Symbols: HarmfulXn
Risk Codes: 22-36/37/38
Safety: 26-36
Transport Information: UN 3335
PSA: 64.82000
LogP: 0.57520
Synthetic route
420-12-2

thirane

60-23-1

Cysteamine

Conditions
ConditionsYield
With ammonia at 45℃; under 11251.1 Torr; for 0.666667h; Temperature; Pressure;97%
151-56-4

ethyleneimine

60-23-1

Cysteamine

Conditions
ConditionsYield
With ethanol; hydrogen sulfide
With hydrogen sulfide unter Kuehlung;
177-07-1

2,2-pentamethylene-1,3-thiazolidine

60-23-1

Cysteamine

Conditions
ConditionsYield
With hydrogenchloride; water
51-85-4

2,2'-dithio-bis[ethylamine]

151-50-8

potassium cyanide

A

1779-81-3

4,5-Dihydro-thiazol-2-ylamin

B

60-23-1

Cysteamine

22572-33-4

S-benzylcysteamine hydrochloride

60-23-1

Cysteamine

Conditions
ConditionsYield
With ammonia; sodium
70-18-8

GLUTATHIONE

51-85-4

2,2'-dithio-bis[ethylamine]

A

13244-81-0

(S)-2-Amino-4-[(R)-2-(2-amino-ethyldisulfanyl)-1-(carboxymethyl-carbamoyl)-ethylcarbamoyl]-butyric acid

B

60-23-1

Cysteamine

Conditions
ConditionsYield
With sodium chloride In water-d2 at 25℃; Equilibrium constant;
70-18-8

GLUTATHIONE

13244-81-0

(S)-2-Amino-4-[(R)-2-(2-amino-ethyldisulfanyl)-1-(carboxymethyl-carbamoyl)-ethylcarbamoyl]-butyric acid

A

27025-41-8

Oxidized glutathione

B

60-23-1

Cysteamine

Conditions
ConditionsYield
With sodium chloride In water-d2 at 25℃; Equilibrium constant;
51-85-4

2,2'-dithio-bis[ethylamine]

60-23-1

Cysteamine

Conditions
ConditionsYield
With HO3SC6H4SH Equilibrium constant; pH 6.0;
With rac-cysteine Equilibrium constant; pH 7.4, further thiols;
With water; diothiothreitol
2937-53-3

2-aminoethylthiosulfonic acid

60-23-1

Cysteamine

Conditions
ConditionsYield
With sulfuric acid In water for 0.5h; Heating;
4490-75-9

N-(2-mercaptoethyl)-phthalimide

60-23-1

Cysteamine

Conditions
ConditionsYield
With hydrazine

Cysteamine disulfide radical anion

60-23-1

Cysteamine

Conditions
ConditionsYield
With water; dinitrogen monoxide at 22℃; Equilibrium constant; Irradiation; various pH;
2346-00-1

2-methyl-4,5-dihydro-thiazole

7647-01-0

hydrogenchloride

60-23-1

Cysteamine

134469-06-0

thiazolidine-2-thione

7647-01-0

hydrogenchloride

A

7783-06-4

hydrogen sulfide

B

15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

C

60-23-1

Cysteamine

Conditions
ConditionsYield
at 155℃;
7647-01-0

hydrogenchloride

154821-24-6

4,5-dihydro-3H-benzo[f][1,4]thiazocine-1,6-dione

A

88-99-3

benzene-1,2-dicarboxylic acid

B

60-23-1

Cysteamine

2-mercapto-Δ2-thiazoline

2-mercapto-Δ2-thiazoline

60-23-1

Cysteamine

Conditions
ConditionsYield
With hydrogen bromide
With 1,4-dioxane; cobalt sulfide at 175℃; Hydrogenation.unter Druck;
hydrochloride of/the/ 2-amino-ethanethiol-(1)

hydrochloride of/the/ 2-amino-ethanethiol-(1)

60-23-1

Cysteamine

Conditions
ConditionsYield
With methanol; sodium methylate
51-85-4

2,2'-dithio-bis[ethylamine]

palladium

palladium

60-23-1

Cysteamine

Conditions
ConditionsYield
Hydrogenation;
151-16-6

S-(2-aminoethyl)isothiourea

aqueous NaOH-solution

aqueous NaOH-solution

A

1190-74-5

N-(2-mercaptoethyl)guanidine

B

60-23-1

Cysteamine

67616-42-6

S-nitroso-2-aminoethanethiol

A

51-85-4

2,2'-dithio-bis[ethylamine]

B

60-23-1

Cysteamine

Conditions
ConditionsYield
With ethylenediaminetetraacetic acid; buffer reagents; ascorbic acid In water pH=3.6; Kinetics; Further Variations:; pH-values; Reagents; Decomposition;
67616-42-6

S-nitroso-2-aminoethanethiol

60-23-1

Cysteamine

Conditions
ConditionsYield
With ethylenediaminetetraacetic acid; sodium hydrogensulfite In phosphate buffer at 25℃; pH=7.4; Kinetics; Further Variations:; concentration; Substitution;
67616-42-6

S-nitroso-2-aminoethanethiol

A

60-23-1

Cysteamine

B

67776-06-1

S-nitroso-N-acetyl-DL-penicillamine

Conditions
ConditionsYield
With phosphate buffer; ethylenediaminetetraacetic acid for 0.0833333h; pH=7.4; Equilibrium constant; Further Variations:; Temperatures;
1095-85-8

2-amino tritylthio ethane

60-23-1

Cysteamine

Conditions
ConditionsYield
Stage #1: 2-amino tritylthio ethane With mercury(II) diacetate; acetic acid at 20℃;
Stage #2: With sodium tetrahydroborate In water at 20℃; pH=7 - 8; Further stages.;
151-56-4

ethyleneimine

7783-06-4

hydrogen sulfide

60-23-1

Cysteamine

Conditions
ConditionsYield
In ethanol in cold alcohol with equimolar amts.;
52-90-4

L-Cysteine

1257527-86-8

RRRQRRCcystCcystRGY

A

22801-37-2

3-(2-amino-ethyldisulfanyl)-L-alanine

B

56-89-3

L-cystine

C

60-23-1

Cysteamine

Conditions
ConditionsYield
In water at 20℃; for 24h; Inert atmosphere;
156-57-0

2-mercaptoethylamine hydrochloride

60-23-1

Cysteamine

Conditions
ConditionsYield
With sodium borohydrid; triethylamine In N,N-dimethyl-formamide
With sodium borohydrid; triethylamine In N,N-dimethyl-formamide
With sodium borohydrid; triethylamine In N,N-dimethyl-formamide

aminoethanethiol dihydrochloride

60-23-1

Cysteamine

Conditions
ConditionsYield
With sodium hydroxide In chloroform; water
With sodium hydroxide In chloroform; water
56-17-7

cystamine dihydrochioride

60-23-1

Cysteamine

Conditions
ConditionsYield
In aq. phosphate buffer for 24h; pH=7;
15579-00-7

3-<(2-aminoethyl)dithio>propionic acid

A

60-23-1

Cysteamine

B

107-96-0

3-mercaptopropionic acid

Conditions
ConditionsYield
With diothiothreitol In water at 20℃; for 2h;
60-23-1

Cysteamine

51-85-4

2,2'-dithio-bis[ethylamine]

Conditions
ConditionsYield
With polystyrene-bound diaryl selenoxide In dichloromethane for 1.5h;100%
borohydride exchange resin (Amberlit IRA-400); copper(II) sulfate In methanol for 3h; Ambient temperature;98%
With dihydrogen peroxide In water for 2h; Inert atmosphere;97.5%
60-23-1

Cysteamine

10191-60-3

dimethyl N-cyanodithioiminocarbonate

26364-65-8

2-(N-cyanoimino)thiazolidine

Conditions
ConditionsYield
In ethanol at 90℃; for 2h;100%
In ethanol for 3h; Heating / reflux;67.1%
In ethanol Heating;
59565-09-2

2-(vinyloxy)ethyl isothiocyanate

60-23-1

Cysteamine

121612-54-2

N-(2-vinyloxyethyl)-N'-(2-mercaptoethyl)thiourea

Conditions
ConditionsYield
100%
119197-24-9, 119197-25-0, 146936-34-7

3-chloro-4,4,4-trifluoro-2-phenyl-but-2-enal

60-23-1

Cysteamine

2-<(3-chloro-4,4,4-trifluoro-2-phenylbut-2-enylidene)amino>ethanethiol

Conditions
ConditionsYield
In tetrahydrofuran for 0.25h; Ambient temperature;100%
81937-15-7, 81937-22-6

2,3-O-isopropylidene-α,β-D-mannose

60-23-1

Cysteamine

2-(1,2-O-isopropylidene-D-manno-pentahydroxypentyl)thiazolidine

Conditions
ConditionsYield
With triethylamine In methanol at 65℃;100%
105-45-3

acetoacetic acid methyl ester

60-23-1

Cysteamine

503616-48-6

(Z)-3-(2-Mercapto-ethylamino)-but-2-enoic acid methyl ester

Conditions
ConditionsYield
for 24h; Ambient temperature;100%
42330-12-1

5-bromo-6-undecanone

60-23-1

Cysteamine

undecan-5-oxo-spiro-6-(1',3'-thiazolidine)

Conditions
ConditionsYield
In benzene at 20℃; for 55h;100%
2114-00-3

2-bromo-1-phenyl-1-propanone

60-23-1

Cysteamine

1-phenyl-spiro-1-(1',3'-thiazolidine)propan-2-one

Conditions
ConditionsYield
In benzene at 20℃; for 24h;100%
2680-03-7

N,N-Dimethylacrylamide

60-23-1

Cysteamine

3-(2-aminoethylsulfanyl)-N,N-dimethylpropanamide

Conditions
ConditionsYield
In methanol at 20℃; for 2h;100%
3194-70-5

2-vinyl-4,6-diamino-S-triazine

60-23-1

Cysteamine

2,4-diamino-6-[2-(2-aminoethylthio)ethyl]-1,3,5-triazine

Conditions
ConditionsYield
In methanol at 65℃; for 1h;100%
60-23-1

Cysteamine

cystamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; Cumene hydroperoxide; tert-butyl (S)-(tetrahydrotellurophen-3-yl)carbamate In dichloromethane; water at 25℃; Flow reactor;100%
108-24-7

acetic anhydride

60-23-1

Cysteamine

1420-88-8

S-[2-(acetylamino)ethyl] ethanethioate

Conditions
ConditionsYield
With silica gel for 0.0666667h; Microwave irradiation; neat (no solvent);99%
With hydrogenchloride; potassium hydroxide In water for 1h;98%
With pyridine
100-48-1

pyridine-4-carbonitrile

60-23-1

Cysteamine

106735-89-1

2-(pyridin-4-yl)-4,5-dihydrothiazole

Conditions
ConditionsYield
With tribromomelamine at 100℃; for 0.05h; Neat (no solvent);99%
With 1-butyl-3-methylimidazolium tribromide at 100℃; for 0.133333h;98%
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione at 110℃; for 0.05h; chemoselective reaction;96%
In ethanol Heating;
873-32-5

2-Chlorobenzonitrile

60-23-1

Cysteamine

49672-22-2

2-(2-chlorophenyl)-4,5-dihydro-1,3-thiazole

Conditions
ConditionsYield
With tribromomelamine at 100℃; for 0.0666667h; Neat (no solvent);99%
In ethanol for 5h; Heating;40%
542-85-8

Ethyl isothiocyanate

103076-71-7

2-{2-[4-(3-Fluoro-phenyl)-piperazin-1-yl]-ethoxy}-benzaldehyde

60-23-1

Cysteamine

103074-89-1

2-(2-{2-[4-(3-Fluoro-phenyl)-piperazin-1-yl]-ethoxy}-phenyl)-thiazolidine-3-carbothioic acid ethylamide

Conditions
ConditionsYield
99%
60-23-1

Cysteamine

55991-67-8

5-phenylfuran-2,3-dione

81385-08-2

N-(2-Mercapto-ethyl)-2,4-dioxo-4-phenyl-butyramide

Conditions
ConditionsYield
In 1,4-dioxane for 1h; Heating;99%
591-50-4

iodobenzene

201230-82-2

carbon monoxide

60-23-1

Cysteamine

A

55065-04-8

S-2-(N-benzoylamino)ethyl benzothioathe

B

C20H23NO3

Conditions
ConditionsYield
With dichlorido[2,2'-(4-methylbenzene-1,2-diyl)bis(4,4-dimethyl-4,5-dihydro-1,3-oxazole)-N,N']palladium(II); potassium carbonate In acetonitrile at 120℃; under 5171.62 Torr; for 3 - 12h; Catalytic behavior; Time; Autoclave;A 99%
B 12%
75-36-5

acetyl chloride

60-23-1

Cysteamine

17612-91-8

1-[(2-aminoethyl)sulfanyl]ethan-1-one hydrochloride

Conditions
ConditionsYield
With trifluoroacetic acid at 0 - 20℃; for 2h;99%
60-23-1

Cysteamine

Conditions
ConditionsYield
With 2,2,6,6-tetramethyl-piperidine In water at 140℃; under 3000.3 Torr; for 0.166667h; Reagent/catalyst; Temperature; Pressure;98.4%
With dihydrogen peroxide; acetic acid
100-47-0

benzonitrile

60-23-1

Cysteamine

2722-34-1

2-phenylthiazoline

Conditions
ConditionsYield
With tribromomelamine at 100℃; for 0.05h; Neat (no solvent);98%
With 1-butyl-3-methylimidazolium tribromide at 100℃; for 0.0833333h;96%
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione at 110℃; for 0.116667h; chemoselective reaction;95%
102-01-2

N-phenylacetoacetamide

60-23-1

Cysteamine

122717-93-5

2-(2-Methyl-thiazolidin-2-yl)-N-phenyl-acetamide

Conditions
ConditionsYield
With toluene-4-sulfonic acid In benzene for 16h; Heating;98%
With toluene-4-sulfonic acid In benzene for 6h; Heating;98%
443-48-1

metronidazole

60-23-1

Cysteamine

78949-89-0

4-<(2-aminoethyl)thio>-2-methylimidazole-1-ethanol

Conditions
ConditionsYield
With pH 5.0 In water at 37℃; for 120h;98%
With pH 5.0 at 37℃; for 120h; Product distribution; Mechanism; other reaction conditions;
32869-75-3

4-(2-formylbenzyl)-2-phenylnaphtho<1,8-bc>furan-5-one

60-23-1

Cysteamine

78752-79-1

4-<2-(1,3-thiazolidin-2-yl)benzyl>-2-phenylnaphtho<1,8-bc>furan-5-one

Conditions
ConditionsYield
In benzene for 12h; Heating; N2, dark;98%
201230-82-2

carbon monoxide

60-23-1

Cysteamine

2682-49-7

thiazolidine-2-one

Conditions
ConditionsYield
With selenium; oxygen; acetonitrile98%
Stage #1: carbon monoxide; Cysteamine With potassium carbonate; sulfur In N,N-dimethyl-formamide at 20℃; under 760 Torr; for 4h;
Stage #2: With oxygen In N,N-dimethyl-formamide at 20℃; under 760 Torr; for 2h;
87%
72155-45-4

Boc-L-phenylalaninal

60-23-1

Cysteamine

120205-64-3, 120205-65-4, 133164-09-7, 133164-10-0, 144775-23-5

(2RS,1'S)-2-<1'-((tert-butoxycarbonyl)amino)-2'-phenylethyl>-1,3-thiazolidine

Conditions
ConditionsYield
In benzene for 4h; Ambient temperature;98%
In benzene Yield given;
60-23-1

Cysteamine

619-24-9

3-nitrobenzonitrile

96159-88-5

2-(3-nitrophenyl)-4,5-dihydro-1,3-thiazole

Conditions
ConditionsYield
With trichloroisocyanuric acid In neat (no solvent) at 110℃; for 0.0333333h; chemoselective reaction;98%
With 1-butyl-3-methylimidazolium tribromide at 100℃; for 0.1h;88%
With tribromomelamine at 100℃; for 0.0833333h; Neat (no solvent);87%
In ethanol for 5h; Heating;63%
60-23-1

Cysteamine

2-(1,2:4,5-di-O-isopropylidene-D-manno-pentahydroxypentyl)thiazolidine

Conditions
ConditionsYield
In methanol for 48h; Heating;98%
24424-99-5

di-tert-butyl dicarbonate

60-23-1

Cysteamine

67385-09-5

2-[(tert-butoxycarbonyl)amino]-1-ethanethiol

Conditions
ConditionsYield
In tetrahydrofuran; water at 20℃; for 4h; Inert atmosphere;98%
With triethylamine In dichloromethane at 12℃; for 16h;79.9%
With triethylamine In dichloromethane at 12℃; for 16h;79.9%
60-23-1

Cysteamine

158849-69-5

(1'R,2'S)-bicyclomycin C(2'),C(3') acetonide

(1S,6R)-5-(2-Amino-ethylsulfanylmethyl)-6-hydroxy-1-[(R)-hydroxy-((S)-2,2,4-trimethyl-[1,3]dioxolan-4-yl)-methyl]-2-oxa-7,9-diaza-bicyclo[4.2.2]decane-8,10-dione

Conditions
ConditionsYield
With sodium hydroxide In methanol; water Ambient temperature;98%
34075-91-7, 14871-98-8

benzoylacetonatoboron difluoride

60-23-1

Cysteamine

(2Z)-1-Phenyl-3-[(2-sufanylethyl)amino]-2-buten-1-one

Conditions
ConditionsYield
In acetonitrile at 20℃; for 0.5h;98%
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    Cysteamine

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  • Ethanethiol, 2-amino-(8CI,9CI) 60-23-1

  • Casno:

    60-23-1

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  • Casno:

    60-23-1

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  • Casno:

    60-23-1

    MSDS/COA Download

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    60-23-1

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    60-23-1

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    60-23-1

    Cysteamine manufacturer

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  • 2-AMINOETHANETHIOL CAS 60-23-1

  • Casno:

    60-23-1

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  • Ethanethiol, 2-amino-(8CI,9CI)

  • Casno:

    60-23-1

    Ethanethiol, 2-amino-(8CI,9CI)

    Min.Order: 0

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  • 2-AMINOETHANETHIOL (High quality and competitive product)

  • Casno:

    60-23-1

    2-AMINOETHANETHIOL (High quality and competitive product)

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    60-23-1

    2-AMINOETHANETHIOL

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  • Casno:

    60-23-1

    CYSTEAMINE

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    Address:No. 206 Zhen Hua Road, Hangzhou 310030, Zhejiang, China

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  • Casno:

    60-23-1

    Cysteamine

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  • Casno:

    60-23-1

    High quality 2-Aminpoethanethiol

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    60-23-1

    High purity 2-Aminpoethanethiol

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  • Ethanethiol, 2-amino-(8CI,9CI)

  • Casno:

    60-23-1

    Ethanethiol, 2-amino-(8CI,9CI)

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  • 60-23-1 2-AMINOETHANETHIOL

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    60-23-1

    60-23-1 2-AMINOETHANETHIOL

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    60-23-1

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    60-23-1

    CYSTEAMINE

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  • Casno:

    60-23-1

    2-Aminoethanethiol

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    60-23-1

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    60-23-1

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    60-23-1

    Ethanethiol, 2-amino-(8CI,9CI)

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  • Casno:

    60-23-1

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  • cysteamine

  • Casno:

    60-23-1

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    60-23-1

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    Business Type:Manufacturers

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  • Casno:

    60-23-1

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    Business Type:Manufacturers

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  • Casno:

    60-23-1

    2-AMINOETHANETHIOL

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  • Casno:

    60-23-1

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    60-23-1

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  • Casno:

    60-23-1

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Chemistry

Molecular Structure of Cysteamine (60-23-1):

EINECS: 200-463-0
IUPAC Name: 2-Aminoethanethiol 
Molecular Formula: C2H7NS
Molecular Weight: 77.148680 g/mol
XLogP3-AA: -0.4
H-Bond Donor: 1
H-Bond Acceptor: 1
Canonical SMILES: C(CS)N
InChI: InChI=1S/C2H7NS/c3-1-2-4/h4H,1-3H2
InChIKey: UFULAYFCSOUIOV-UHFFFAOYSA-N
Index of Refraction: 1.485
Molar Refractivity: 22.74 cm3
Molar Volume: 79.2 cm3
Surface Tension: 34.8 dyne/cm
Density: 0.973 g/cm3
Flash Point: 34.6 °C
Enthalpy of Vaporization: 37.11 kJ/mol
Boiling Point: 133.6 °C at 760 mmHg
Vapour Pressure: 8.39 mmHg at 25 °C
Melting Point: 95 °C
Water Solubility: 1e+006 mg/L at 25 °C
Storage Temp.: 2-8 °C

Toxicity Data With Reference

1.    

pic-esc 50 mg/L

    APMBAY    Applied Microbiology. 12 (1964),234.
2.    

cyt-ham:ovr 1 mmol/L

    CALEDQ    Cancer Letters (Shannon, Ireland). 5 (1978),199.
3.    

dns-ham:fbr 1 mmol/L

    CALEDQ    Cancer Letters (Shannon, Ireland). 5 (1978),199.
4.    

sce-ham:ovr 100 µmol/L

    MUREAV    Mutation Research. 68 (1979),351.
5.    

ipr-rat LD50:232 mg/kg

    ARZNAD    Arzneimittel-Forschung. Drug Research. 5 (1955),421.
6.    

scu-rat LD50:84 mg/kg

    OSDIAF    Osaka Shiritsu Daigaku Igaku Zasshi. Journal of the Osaka City Medical Center. 5 (1956),128.
7.    

orl-mus LD50:625 mg/kg

    JMCMAR    Journal of Medicinal Chemistry. 18 (1975),798.
8.    

ipr-mus LD50:250 mg/kg

    JMCMAR    Journal of Medicinal Chemistry. 12 (1969),510.
9.    

scu-mus LD50:84 mg/kg

    OSDIAF    Osaka Shiritsu Daigaku Igaku Zasshi. Journal of the Osaka City Medical Center. 5 (1956),128.
10.    

ivn-mus LD50:190 mg/kg

    CHDDAT    Comptes Rendus Hebdomadaires des Seances de l’Academie des Sciences, Serie D. 262 (1966),206.

Consensus Reports

EPA Genetic Toxicology Program.

Safety Profile

Safety Information of Cysteamine (60-23-1):
Hazard Codes: Xn
Risk Statements: 22-36/37/38
22: Harmful if swallowed
36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-36
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36: Wear suitable protective clothing
RIDADR: 3259
WGK Germany: 3
RTECS: KJ0175000
F: 1-3-10-13-34
Poison by intravenous, subcutaneous, and intraperitoneal routes. Moderately toxic by ingestion. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits very toxic fumes of SOx and NOx.

Specification

  Cysteamine (60-23-1) is white powder, known as Cysteamine [USAN:BAN] ; Mercaptamine [INN] ; (2-Mercaptoethyl)amine ; 1-Amino-2-mercaptoethylamine ; 2-Amino-1-ethanethiol ; 2-Aminoethanethiol ; 2-Aminoethyl mercaptan ; 2-Mercaptoethanamine ; Becaptan ; CCRIS 3083 ; Cisteamina ; Cisteamina [Italian] ; Cystagon ; Cysteamin ; Cysteinamine ; Decarboxycysteine ; HSDB 7353 ; L 1573 ; L-1573 ; Lambraten ; Lambratene ; MEA ; MEA (mercaptan) ; Mercamine ; Mercaptamina ; Mercaptamina [INN-Spanish] ; Mercaptamine ; Mercaptaminum ; Mercaptaminum [INN-Latin] ; Mercaptoethylamine ; NSC 647528 ; Riacon ; Thioethanolamine ; UNII-5UX2SD1KE2 ; WR 347 ; beta-Aminoethanethiol ; beta-Aminoethylthiol ; beta-Mercaptoethylamine ; Ethanethiol, 2-amino- . Cysteamine (60-23-1) is used to form Coenzyme A by combining with pantothenate and adenosine triphosphate in the body. It is also used for treatment of radiation sickness and disorders of cystine excretion.