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(S)-TERT-LEUCINOL

CAS No.
112245-13-3
Chemical Name:
(S)-TERT-LEUCINOL
Synonyms
L-TERT-LEUCINOL;H-TLE-OL;L-T-LEUCINOL;H-(TBU)GLY-OL;(S)-TERT-LEACINOL;(S)-TERT-LEUCINOL;L-T-BUTYLGLYCINOL;(S)-TERT-LENCINOL;(+)-tert-Leucinol;L**L-tert-Leucinol
CBNumber:
CB4253158
Molecular Formula:
C6H15NO
Molecular Weight:
117.19
MDL Number:
MFCD00192250
MOL File:
112245-13-3.mol
Last updated:2026-01-13 11:19:20
Product description Number Pack Size Price
L-tert-Leucinol 98% 407739 1g $41.3
L-tert-Leucinol 98% 407739 5g $100.93
L-tert-Leucinol >97.0%(GC)(T) L0160 1g $62
L-tert-Leucinol >97.0%(GC)(T) L0160 5g $186
L-tert-Leucinol, 98% (99% ee) 07-7224 1g $67
More product size

(S)-TERT-LEUCINOL Properties

Melting point 30-34 °C(lit.)
Boiling point 114-116 °C (10 mmHg)
Density 0.9 g/mL at 25 °C(lit.)
refractive index 38 ° (C=1.5, EtOH)
Flash point 194 °F
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility soluble in Methanol
pka 12.88±0.10(Predicted)
form Crystalline Low Melting Mass or Liquid
color White or colorless
optical activity [α]26/D +37°, c = 1.5 in ethanol
BRN 3600321
Major Application peptide synthesis
InChI InChI=1S/C6H15NO/c1-6(2,3)5(7)4-8/h5,8H,4,7H2,1-3H3/t5-/m1/s1
InChIKey JBULSURVMXPBNA-RXMQYKEDSA-N
SMILES C(O)[C@@H](N)C(C)(C)C
CAS DataBase Reference 112245-13-3(CAS DataBase Reference)
UNSPSC Code 12352209
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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 dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
10-23
HS Code  29221990
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
2
2 0

(S)-TERT-LEUCINOL price More Price(40)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 407739 L-tert-Leucinol 98% 112245-13-3 1g $41.3 2025-07-31 Buy
Sigma-Aldrich 407739 L-tert-Leucinol 98% 112245-13-3 5g $100.93 2025-07-31 Buy
TCI Chemical L0160 L-tert-Leucinol >97.0%(GC)(T) 112245-13-3 1g $62 2025-07-31 Buy
TCI Chemical L0160 L-tert-Leucinol >97.0%(GC)(T) 112245-13-3 5g $186 2025-07-31 Buy
Strem Chemicals 07-7224 L-tert-Leucinol, 98% (99% ee) 112245-13-3 1g $67 2024-03-01 Buy
Product number Packaging Price Buy
407739 1g $41.3 Buy
407739 5g $100.93 Buy
L0160 1g $62 Buy
L0160 5g $186 Buy
07-7224 1g $67 Buy

(S)-TERT-LEUCINOL Chemical Properties,Uses,Production

Chemical Properties

white crystalline low melting mass or

Uses

Useful amino acid employed in various asymmetric reactions.

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

L-tert-Leucine

20859-02-3

(S)-TERT-LEUCINOL

112245-13-3

GENERAL STEPS: Example 8-1; To a 100 mL Schlenk tube purged with nitrogen was added 4.00 g (30.5 mmol) of (S)-tert-leucine and 40 mL of tetrahydrofuran, and the temperature of the reaction system was adjusted to 10°C. Over 5 min, 1.46 g (61.0 mmol) of lithium borohydride was added to the suspension in batches, followed by adjusting the temperature of the system to 20 °C. Over 30 minutes, 7.44 g (67.1 mmol) of trimethylmethylsilyl chloride was added slowly and dropwise, then the mixture was heated to 65 °C and stirred continuously at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to 10 °C and quenched by the slow dropwise addition of 4 mL of methanol over 20 min. After concentrating the reaction mixture using a rotary evaporator, 40 mL of 4 M aqueous sodium hydroxide solution was added and stirred for 1 hour at room temperature. Subsequently, 40 mL of tert-butyl methyl ether was added for extraction and the organic layer was separated and dried with anhydrous sodium sulfate. After filtration to remove the desiccant, the tert-butyl methyl ether was removed by atmospheric pressure distillation. Finally, the 70 to 75 °C fraction was collected by reduced pressure distillation (0.3 kPa) to give 2.96 g of (S)-tert-leucinol in 83% yield.

References

[1] Journal of the American Chemical Society, 2003, vol. 125, # 21, p. 6362 - 6363
[2] Chemical Communications, 2010, vol. 46, # 3, p. 445 - 447
[3] Beilstein Journal of Organic Chemistry, 2013, vol. 9, p. 1637 - 1642
[4] Journal of Organic Chemistry, 1992, vol. 57, # 17, p. 4732 - 4740
[5] Organic Letters, 2018, vol. 20, # 16, p. 4806 - 4810

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View Lastest Price from (S)-TERT-LEUCINOL manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(S)-TERT-LEUCINOL pictures 2025-12-01 (S)-TERT-LEUCINOL
112245-13-3
US $0.00 / kg 1kg 98% 1000kg Shaanxi Dideu New Materials Co. Ltd
(S)-tert-Leucinol pictures 2019-07-06 (S)-tert-Leucinol
112245-13-3
US $1.00 / kg 1kg 95%-99% as request Career Henan Chemical Co
2-AMINO-3,3-DIMETHYL-1-BUTANOL L-T-LEUCINOL L-(+)-TERT-LEUCINOL L-T-BUTYLGLYCINOL (S)-2-AMINO-3,3-DIMETHYLBUTANOL (S)-2-AMINO-3,3-DIMETHYL-1-BUTANOL (S)-TERT-LEUCINOL (S)-TERT-LEACINOL (2S)-1-HYDROXY-3,3-DIMETHYL-BUTAN-2-YL]AZANIUM H-TLE-OL H-(TBU)GLY-OL (S)-TERT-LENCINOL (S)-2-Amino-3,3-dimethyl-1-butanol, L-tert-Leucinol (2R)-2-Amino-3,3-dimethyl-1-butanol (R)-3,3-Dimethyl-2-aminobutane-1-ol (+)-tert-Leucinol (2S)-2-Amino-3,3-dimethyl-1-butanol (S)-2-tert-Butyl-2-aminoethanol (S)-3,3-Dimethyl-2-amino-1-butanol (S)-tert-Leucinol,95% (S)-tert-Leucinol,98% L-tert-Leucinol,(S)-2-Amino-3,3-dimethyl-1-butanol (S)-tert-Leucinol,(S)-2-Amino-3,3-dimethyl-1-butanol, L-tert-Leucinol (2S)-2-Amino-3,3-dimethylbutan-1-ol (2S)-2-Amino-3,3-dimethylbutan-1-ol 99% L-tert-Leucinol, (2S)-2-Amino-3,3-dimethyl-1-hydroxybutane L-tert-Leucinol 98% L-tert-Leucinol L-Tert-Leucinol≥ 98% (GC) L-tert-Leucinol,99%e.e. L-tert-Leucinol, 98% (99% ee) L**L-tert-Leucinol (S)-2-Amino-3,3-dimethyl-1-hydroxybutane L-tert-Leucinol, 98%, for synthesis L-tert-Leucinol> 1-Butanol, 2-amino-3,3-dimethyl-, (2S)- (S)-TERT-LEUCINOL USP/EP/BP L-TERT-LEUCINOL L-tert leucine alcohol L-2-amino-3,3-dimethylbutan-1-ol L-tert-Leucinol,97% L-tert-Leucinol 112245-13-3 CH33CCHNH2CH2OH C6H16NO AMINE Peptide Synthesis Specialty Synthesis Chiral Building Blocks Amino Alcohols (Chiral) Amino Alcohols Amino Acid Derivatives Pharmaceutical Intermediates Amino Alcohols Amino Alcohols (Chiral) Chiral Building Blocks Synthetic Organic Chemistry Amino alcohols