H54409
trans-4-Hydroxy-L-proline
≥99%, for peptide synthesis
Manufacturer: Sigma Aldrich
CAS Number: 51-35-4
Synonym(S): (2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid, Hyp
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 2.5 G | H54409-2.5-G | In Stock | ₹ 2,820.00 |
| 10 G | H54409-10-G | In Stock | ₹ 3,983.60 |
| 25 G | H54409-25-G | In Stock | ₹ 6,181.08 |
| 100 G | H54409-100-G | In Stock | ₹ 14,730.00 |
H54409 - 2.5 G
In Stock
Quantity
1
Base Price: ₹ 2,820.00
GST (18%): ₹ 507.60
Total Price: ₹ 3,327.60
Quality Level
200
Assay
≥99%
form
crystalline powder
optical activity
[α]25/D −75.6°, c = 1 in H2O
reaction suitability
reaction type: solution phase peptide synthesis
color
white to off-white
mp
273 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
O[C@H]1CN[C@@H](C1)C(O)=O
InChI
1S/C5H9NO3/c7-3-1-4(5(8)9)6-2-3/h3-4,6-7H,1-2H2,(H,8,9)/t3-,4+/m1/s1
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Hydroxyproline Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™ | -- | ₹ 20,363.28 | |
| | Sigma Aldrich Fine Chemicals Biosciences trans-4-Hydroxy-L-proline | 51-35-4 | MFCD00064320 | 10g | -- | ₹ 7,178.48 | |
| | trans-4-Hydroxy-L-proline, ≥99% (TLC), MilliporeSigma™ Supelco™ | -- | ₹ 8,213.76 | |
| | Chem-Impex International, Inc. trans-L-4-Hydroxyproline | 51-35-4 | MFCD00064320 | 100G | -- | ₹ 4,388.37 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 6,776.45 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 3,518.13 - ₹ 3,80,693.60 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 3,528.95 - ₹ 21,195.35 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 2,820.00 - ₹ 14,730.00 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 3,518.13 - ₹ 3,80,693.60 | |
| | trans-4-Hydroxy-L-proline | -- | ₹ 3,528.95 - ₹ 21,195.35 |
Related Products
Description
- General description: Trans-4-hydroxy-L-proline is an isomer of hydroxyproline used as a chiral building block in the production of many pharmaceuticals like neuroexcitatory kainoids.[1]
- Application: Versatile reagent for the synthesis of neuroexcitatory kainoids[2] and antifungal echinocandins.[3] Also employed in the synthesis of chiral ligands for enantioselective ethylation of aldehydes.[4]
- Other Notes: Natural constituent of animal structural proteins such as collagen and elastin.
SAFETY INFORMATION
WGK
WGK 1
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves