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

₹ 2,820.00

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
11-101-4401
Hydroxyproline Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 20,363.28
NC0853422
Sigma Aldrich Fine Chemicals Biosciences trans-4-Hydroxy-L-proline | 51-35-4 | MFCD00064320 | 10g
Sigma Aldrich Fine Chemicals Biosciences ₹ 7,178.48
11-101-4402
trans-4-Hydroxy-L-proline, ≥99% (TLC), MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 8,213.76
50-490-755
Chem-Impex International, Inc. trans-L-4-Hydroxyproline | 51-35-4 | MFCD00064320 | 100G
Chem-Impex International, Inc. ₹ 4,388.37
41875
trans-4-Hydroxy-L-proline
Supelco ₹ 6,776.45
H5534
trans-4-Hydroxy-L-proline
Sigma Aldrich ₹ 3,518.13 - ₹ 3,80,693.60
56250
trans-4-Hydroxy-L-proline
Sigma Aldrich ₹ 3,528.95 - ₹ 21,195.35
H54409
trans-4-Hydroxy-L-proline
Sigma Aldrich ₹ 2,820.00 - ₹ 14,730.00
H5534
trans-4-Hydroxy-L-proline
Sigma Aldrich ₹ 3,518.13 - ₹ 3,80,693.60
56250
trans-4-Hydroxy-L-proline
Sigma Aldrich ₹ 3,528.95 - ₹ 21,195.35

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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

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Show Difference

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Sigma Aldrich

H54409

≥99%, for peptide synthesis...


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

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SMILES string:
CCC(=O)c1ccccc1O

InChI:
1S/C9H10O2/c1-2-8(10)7-5-3-4-6-9(7)11/h3-6,11H,2H2,1H3

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SMILES string:
CN[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@@H]3OC4(O[C@H]([C@H](N)CO)[C@H](O)[C@H](O)[C@H]4O)O[C@H]23)[C@@H]1O

InChI:
1S/C20H37N3O13/c1-23-7-2-5(21)9(26)15(10(7)27)33-19-17-16(11(28)8(4-25)32-19)35-20(36-17)18(31)13(30)12(29)14(34-20)6(22)3-24/h5-19,23-31H,2-4,21-22H2,1H3/t5-,6-,7+,8-,9+,10-,11+,12-,13+,14-,15-,16+,17+,18-,19+,20+/m1/s1

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__