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2-(BOC-AMINO)ETHANETHIOL

CAS No.
67385-09-5
Chemical Name:
2-(BOC-AMINO)ETHANETHIOL
Synonyms
tert-butyl (2-Mercaptoethyl)carbaMate;BOC-CYSTEAMINE;DK861;DKSI100;DKFELEX0227;BOC-NH-ET-SH;BOC-CYSTEAMIN;SH-CH2-CH2NHBOC;N-BOC-cysteamine;BUTTPARK 147\16-59
CBNumber:
CB8215264
Molecular Formula:
C7H15NO2S
Molecular Weight:
177.26
MDL Number:
MFCD00274335
MOL File:
67385-09-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:52:49
Product description Number Pack Size Price
2-(Boc-amino)ethanethiol 97% 458910 5ml $108
2-(Boc-amino)ethanethiol 97% 458910 25ml $345
tert-Butyl (2-Mercaptoethyl)carbamate min. 95.0 % B6774 5G $49
tert-Butyl (2-Mercaptoethyl)carbamate min. 95.0 % B6774 25G $175
2-(Boc-amino)ethanethiol 98+% (GC) ≥98%(GC) 229556 5ml $200

2-(BOC-AMINO)ETHANETHIOL Properties

Boiling point 68 °C0.3 mm Hg(lit.)
Density 1.049 g/mL at 20 °C(lit.)
refractive index n20/D 1.474(lit.)
Flash point >230 °F
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly)
pka 9.95±0.10(Predicted)
form Viscous Liquid or Low Melting Solid
Specific Gravity 1.049
color Clear colorless to yellow
BRN 2243173
InChI InChI=1S/C7H15NO2S/c1-7(2,3)10-6(9)8-4-5-11/h11H,4-5H2,1-3H3,(H,8,9)
InChIKey GSJJCZSHYJNRPN-UHFFFAOYSA-N
SMILES C(OC(C)(C)C)(=O)NCCS
UNSPSC Code 12352105
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
10-13-23
HS Code  29309090
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

2-(BOC-AMINO)ETHANETHIOL price More Price(78)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 458910 2-(Boc-amino)ethanethiol 97% 67385-09-5 5ml $108 2026-04-30 Buy
Sigma-Aldrich 458910 2-(Boc-amino)ethanethiol 97% 67385-09-5 25ml $345 2026-04-30 Buy
TCI Chemical B6774 tert-Butyl (2-Mercaptoethyl)carbamate min. 95.0 % 67385-09-5 5G $49 2026-04-30 Buy
TCI Chemical B6774 tert-Butyl (2-Mercaptoethyl)carbamate min. 95.0 % 67385-09-5 25G $175 2026-04-30 Buy
Usbiological 229556 2-(Boc-amino)ethanethiol 98+% (GC) ≥98%(GC) 5ml $200 2026-06-03 Buy
Product number Packaging Price Buy
458910 5ml $108 Buy
458910 25ml $345 Buy
B6774 5G $49 Buy
B6774 25G $175 Buy
229556 5ml $200 Buy

2-(BOC-AMINO)ETHANETHIOL Chemical Properties,Uses,Production

Chemical Properties

Clear colorless viscous oil

Uses

2-(Boc-amino)ethanthiol is used in the synthesis of several organic compounds including a novel, anisamide-targeted cyclodextrin nanoformulation for the delivery of siRNA to prostate cancer cells which is a potential therapeutic option. Also used in the synthesis of bifunctional azobenzene glycoconjugates for cysteine-based photosensitive cross-linking with bioactive peptides.

reaction suitability

reagent type: cross-linking reagent

Synthesis

Synthesis of 2-(Boc-amino)ethanethiol: Cysteamine hydrochloride Ra-016 (2.0g, 44mmol) and Boc anhydride (3.5g, 16mmol) were dissolved in dichloromethane (20mL), and triethylamine (2.5mL, 18mmol) was slowly added in an ice-water bath, and the reaction was carried out for 16 hours after the addition and elevated to ambient temperature, and the organic phase was dried and spin-dried to obtain a colorless oil (2.7g, 95%), which was washed with 0.5N HCl and saturated sodium chloride. Wash with 0.5N HCl, saturated sodium chloride, the organic phase was dried and spun dry to obtain colorless oil (2.7g, yield 95%). The colorless oil obtained after NMR analysis was 2-tert-butoxycarbonylaminoethanethiol.

2-(BOC-AMINO)ETHANETHIOL Preparation Products And Raw materials

Raw materials

Preparation Products

2-(BOC-AMINO)ETHANETHIOL Suppliers

Global( 108)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Daken Advanced Materials Co.,Ltd
+86-2158073036 info@dakenam.com China 14014 58
Accela ChemBio Inc.
+1-858-6993322 info@accelachem.com United States 21193 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5906 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30224 58
Finetech Industry Limited
+86-27-8746-5837 +8619945049750 info@finetechnology-ind.com China 9539 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52704 58
Nextpeptide Inc
+86-0571-81612335 +8613336028439 sales@nextpeptide.com China 19908 58
Labnetwork lnc.
+86-27-50766799 +8618062016861 contact@labnetwork.com China 19987 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418684 +8618949823763 sales@tnjchem.com China 25356 58

View Lastest Price from 2-(BOC-AMINO)ETHANETHIOL manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-(BOC-AMINO)ETHANETHIOL pictures 2025-06-07 2-(BOC-AMINO)ETHANETHIOL
67385-09-5
100g >95.00% 100g Xian confluore Biological Technology Co., Ltd.

2-(BOC-AMINO)ETHANETHIOL Spectrum

2-(BOC-AMINO)ETHANETHIOL TERT-BUTYL N-(2-MERCAPTOETHYL)CARBAMATE N-T-BUTYLOXYCARBONYL-2-MERCAPTO-ETHYLAMIN N-TERT-BUTYLOXYCARBONYL-2-MERCAPTO-ETHYLAMINE N-TERT-BUTOXYCARBONYL-2-AMINOETHANETHIOL Carbamic acid, (2-mercaptoethyl)-, 1,1-dimethylethyl ester (9CI) Boc-Cysteamin,N-t-Butyloxycarbonyl-2-mercapto-ethylamin 2-(BOC-AMino)ethanethiol 5ML N-BOC-cysteamine 2-(Boc-aMino)ethanethiol 97% N-Boc-2-mercaptoethanamine tert-butyl N-(2-sulfanylethyl)carbamate 2-(Boc-amino)ethanethiol≥ 98% (GC) BOC-NH-ET-SH BUTTPARK 147\16-59 BOC-CYSTEAMIN SH-CH2-CH2NHBOC Carbamic acid, N-(2-mercaptoethyl)-, 1,1-dimethylethyl ester 2-(Boc-amino)ethanthiol 2-(Boc-amino)ethanthiol (>90%) DK861 DKFELEX0227 DKSI100 2-(Boc-amino)ethanethiol, 98% (2-mercaptoylethyl)aminomacetic acidtertbutyl ester BOC-CYSTEAMINE tert-butyl (2-Mercaptoethyl)carbaMate 67385-09-5 HSCH2CH2NHCO2CCH33 Building Blocks Supported Reagents Supported Synthesis Sulfur Compounds Organic Building Blocks Others Specialty Synthesis Thiols/Mercaptans N-BOC Bifunctional Crosslinkers Building Blocks Chemical Biology Chemical Synthesis Linkers Organic Building Blocks Peptide Chemistry Sulfur Compounds Thiols/Mercaptans