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Fmoc-D-Trp(Boc)-OH(CAS# 163619-04-3)

Chemical Property:

Molecular Formula C31H30N2O6
Molar Mass 526.58
Density 1.28±0.1 g/cm3(Predicted)
Melting Point 86 – 92℃ (D℃omposes)
Appearance White to off-white crystalline powder
BRN 7062970
pKa 3.71±0.10(Predicted)
Storage Condition 2-8°C
Refractive Index 1.632
MDL MFCD00153367
In vitro study ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker.

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Risk and Safety

Safety Description S22 – Do not breathe dust.
S24/25 – Avoid contact with skin and eyes.
WGK Germany 3
FLUKA BRAND F CODES 10
HS Code 29339900

Fmoc-D-Trp(Boc)-OH(CAS# 163619-04-3) introduction

N-alpha-fluorene methoxycarbonyl-N-in-tert-butoxycarbonyl-D-tryptophan is an amino acid derivative, also known as Fmoc-Trp(Boc)-OH. Here is some information about its properties, uses, manufacturing methods, and safety:

Quality:
- Appearance: White crystalline solid
- Solubility: Soluble in organic solvents such as methylene chloride and dimethyl sulfoxide, insoluble in water

Use:
- Fmoc-Trp(Boc)-OH is widely used in the field of peptide synthesis and is used as a protective group in organic synthesis.

Method:
- The preparation of Fmoc-Trp(Boc)-OH typically consists of two steps. The amino groups of tryptophan side chains are protected with a protecting group, usually with dihydrazine spinachlate (Fmoc). Second, tert-butylhydroxymethylic acid acetal (Boc) is used to protect the hydroxyl group of tryptophan.

Safety Information:
- Fmoc-TRP (Boc)-OH may be irritating to the skin, eyes, and respiratory system, and should be used with appropriate protective equipment to ensure adequate ventilation.
- Care should be taken to avoid inhalation, swallowing, or contact when using or handling Fmoc-Trp(Boc)-OH.


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