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(R)-(-)-2-Amino-3-methyl-1-butanol

CAS No.
4276-09-9
Chemical Name:
(R)-(-)-2-Amino-3-methyl-1-butanol
Synonyms
D-VALINOL;2-AMINO-3-METHYLBUTAN-1-OL;D-Val-ol;D-VALINAL;R-VALINOL;H-D-VAL-OL;(-)-D-VALINOL;D-(-)-VALINOL;D-Valinol, 97%;D-Valinol,99%e.e.
CBNumber:
CB2173409
Molecular Formula:
C5H13NO
Molecular Weight:
103.16
MDL Number:
MFCD00064297
MOL File:
4276-09-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:56:57
Product description Number Pack Size Price
(R)-(?)-2-Amino-3-methyl-1-butanol 98% 284483 1g $28.5
(R)-(?)-2-Amino-3-methyl-1-butanol 98% 284483 5g $82.7
D-Valinol >98.0%(GC)(T) V0077 1g $24
D-Valinol >98.0%(GC)(T) V0077 5g $75
D-Valinol 237271 1g $156
More product size

(R)-(-)-2-Amino-3-methyl-1-butanol Properties

Melting point 35-36 °C(lit.)
Boiling point 189-190 °C(lit.)
alpha -16.5 º (c=10, EtOH)
Density 0.931 g/mL at 20 °C(lit.)
refractive index n20/D 1.455
Flash point 194 °F
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Low Melting Crystals or Crystalline Mass
pka 12.82±0.10(Predicted)
color White to light yellow
optical activity [α]20/D 16°, c = 10 in ethanol
Sensitive Air Sensitive
BRN 1719138
InChI 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m0/s1
InChIKey NWYYWIJOWOLJNR-YFKPBYRVSA-N
SMILES CC(C)[C@@H](N)CO
CAS DataBase Reference 4276-09-9(CAS DataBase Reference)
FDA UNII 829QNS6ERZ
UNSPSC Code 12352116
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P305+P351+P338-P321-P332+P313-P337+P313
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37-36-36/37/38
WGK Germany  3
10-34
HS Code  29051990
Storage Class 11 - Combustible Solids
NFPA 704
2
2 1

(R)-(-)-2-Amino-3-methyl-1-butanol price More Price(108)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 284483 (R)-(?)-2-Amino-3-methyl-1-butanol 98% 4276-09-9 1g $28.5 2026-04-30 Buy
Sigma-Aldrich 284483 (R)-(?)-2-Amino-3-methyl-1-butanol 98% 4276-09-9 5g $82.7 2026-04-30 Buy
TCI Chemical V0077 D-Valinol >98.0%(GC)(T) 4276-09-9 1g $24 2026-04-30 Buy
TCI Chemical V0077 D-Valinol >98.0%(GC)(T) 4276-09-9 5g $75 2026-04-30 Buy
Usbiological 237271 D-Valinol 1g $156 2026-06-03 Buy
Product number Packaging Price Buy
284483 1g $28.5 Buy
284483 5g $82.7 Buy
V0077 1g $24 Buy
V0077 5g $75 Buy
237271 1g $156 Buy

(R)-(-)-2-Amino-3-methyl-1-butanol Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powde

Uses

D-Valinol is used as a reagent in the synthesis of the HIV type 1 integrase inhibitor Elvitegravir (E509000). D-Valinol is also used in the preparation of novel 2-(alkylmorpholin-4-yl)-6-(3-fluoropyridin-4-yl)-pyrimidin-4(3H)-ones as orally active GSK-3β inhibitors for Alzheimer''s disease.

Synthesis

Methyl D-valinate hydrochloride

7146-15-8

(R)-(-)-2-Amino-3-methyl-1-butanol

4276-09-9

trans-3,6-Diisopropyl-2,5-Piperazinedione

19943-14-7

General procedure for the synthesis of D-valinol and compounds (CAS:19943-14-7) from D-valine methyl ester hydrochloride: Hydrogenation of R-phenylglycine methyl ester was carried out in a 0.5 L stainless steel electrolyzer with stirring at 500 rpm to test the catalyst activity. First, 1 g of catalyst (20-40 mesh) was loaded into the reactor and subsequently purged five times with H2 to remove air. The catalyst was reduced at 1 MPa H2 pressure and 250 °C for 4 hours. After the autoclave was cooled to room temperature in H2 atmosphere, 1.5 g of R-phenylglycine methyl ester (R-p-m) diluted by 150 mL of ethanol (R-p-m/Cat = 1.5, w/w) was added. The reaction conditions were set at 5 MPa H2 pressure and 80 °C temperature for 10 hours. Upon completion of the reaction, the autoclave was cooled to room temperature in H2 atmosphere, followed by separation of the solid catalyst by centrifugation. The product was purified by silica gel column chromatography using ethyl acetate/methanol (3/2, v/v) as eluent. Finally, the light yellow powdery product was obtained by rotary evaporation. The analysis of the reactants and products was carried out using a high performance liquid chromatograph (HPLC, Agilent 1260 Infinity) equipped with a UV detector and an Eclipse XDB-C18 column (150 × 4.6 mm, 5 μm particles), which in turn was used to calculate the conversion of R-phenylglycine methyl ester (X), yield (Y), and chemoselectivity for R-phenylglycine (S), where yield is the liquid chromatographic yield. The enantiomeric excess values (ee values) of the products were determined by HPLC equipped with a UV detector (wavelength 258 nm) and a chiral column (CHIRALPAK AY-H, 250 × 4.6 mm, 5 μm particle size).

References

[1] Catalysis Letters, 2017, vol. 147, # 8, p. 2160 - 2166

640-68-6
4276-09-9
Synthesis of (R)-(-)-2-Amino-3-methyl-1-butanol from D-Valine
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View Lastest Price from (R)-(-)-2-Amino-3-methyl-1-butanol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(R)-(-)-2-Amino-3-methyl-1-butanol pictures 2026-07-24 (R)-(-)-2-Amino-3-methyl-1-butanol
4276-09-9
1KG 98.0% 50kg/month WUHAN FORTUNA CHEMICAL CO., LTD
(R)-(-)-2-Amino-3-methyl-1-butanol pictures 2026-03-20 (R)-(-)-2-Amino-3-methyl-1-butanol
4276-09-9
1KG 99% 20 mt Hebei Chuanghai Biotechnology Co., Ltd
(R)-(-)-2-Amino-3-methyl-1-butanol pictures 2021-07-13 (R)-(-)-2-Amino-3-methyl-1-butanol
4276-09-9
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
(R)-(-)-2-Amino-3-methyl-1-butanol 98% D-Valinol≥ 99% (GC) D-Valinol,99%e.e. (R)-(-)-2-AMINO-3-METHYLBUTANOL FOR SYNT (R)-2-Amino-3-mehylbutanol (R)-()-2-Amino-3-methyl-1-butanol,D-Valinol (R)-(-)-2-Amino-3-me (R)-(-)-2-AMino-3-Methyl-1-butanol, 98% 5GR (R)-(-)-2-AMino-3-Methyl-1-butanol, 95+% (R)-(-)-2-Amino-3-methyl-1-butanol, 98.5% (D)-VALINOL/(R)-(-)-2-AMINO-3-METHYL-1-BUTANOL (-)-D-VALINOL D-(-)-VALINOL D-VALINAL D-2-AMINO-3-METHYL-1-BUTANOL H-D-VAL-OL R-VALINOL (R)-(-)-2-AMINO-3-METHYLBUTAN-1-OL (R)-(-)-2-AMINO-3-METHYLBUTANOL D-(-)-VALINOL 98% (R)-(-)-Z-Amino-3-Methyl-1-Butanol D-(-)-Valinol,98% 1-Butanol, 2-amino-3-methyl-, (2R)- (R)-(-)-2-Amino-3-methyl-1-butanol (2R)-2-Amino-3-methyl-1-butanol (R)-3-Methyl-2-aminobutane-1-ol (R)-(-)-2-Amino-3-methyl-1-butanol,98% (R)-(-)-2-Amino-3-methylbutan-1-ol 98% (R)-(-)-2-Amino-3-methyL (R)-(-)-2-Amino-3-methyl-1-butanol USP/EP/BP Elvitegravir Impurity 5 (R)-(?)-2-Amino-3-methyl-1-butanol D-Valinol, 97% 2-AMINO-3-METHYLBUTAN-1-OL D-VALINOL D-Val-ol 4276-09-9 4276-O9-9 4276-9-9 868070 44276-09-9 427-69-9 4726-09-9 868-07-0 4270-09-9 C5H13NO AMINE Organic Building Blocks Peptide Synthesis Specialty Synthesis Amino Alcohols (Chiral) Chiral Building Blocks Asymmetric Synthesis Amino Alcohols Amino Acid Derivatives Amino Alcohols (Chiral) Asymmetric Synthesis Chiral Building Blocks