54802
1-Hydroxybenzotriazole hydrate
≥97.0% dry basis (T), for peptide synthesis
동의어(들):
HOBt Hydrate
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C6H5N3O · xH2O
CAS Number:
Molecular Weight:
135.12 (anhydrous basis)
Beilstein:
4515
EC Number:
MDL number:
UNSPSC 코드:
12352000
PubChem Substance ID:
NACRES:
NA.22
추천 제품
제품명
1-Hydroxybenzotriazole hydrate, ≥97.0% dry basis (T)
Quality Level
분석
≥97.0% dry basis (T)
양식
solid
구성
water, ~12%
반응 적합성
reaction type: Addition Reactions
mp
155-158 °C (lit.)
solubility
DMF: 0.1 g/mL, clear
응용 분야
peptide synthesis
SMILES string
[H]O[H].On1nnc2ccccc12
InChI
1S/C6H5N3O.H2O/c10-9-6-4-2-1-3-5(6)7-8-9;/h1-4,10H;1H2
InChI key
PJUPKRYGDFTMTM-UHFFFAOYSA-N
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일반 설명
1-Hydroxybenzotriazole is a coupling reagent used to synthesize amides by the condensation reaction between the activated ester/acid and the amino group of protected amino acids. It is also used as a racemization suppressor during peptide synthesis.
애플리케이션
1-Hydroxybenzotriazole hydrate can be used as a condensation reagent to prepare:
- Poly-γ-glutamic acid methyl ester from a dimer of γ-glutamic acid.
- Oxadiazoles via cyclo condensation of amidoximes with trifluoroacetic anhydride or benzoic acid derivatives.
기타 정보
Widely used additive to decrease racemization in the carbodiimide peptide coupling; Racemization-free condensation of peptide fragments
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Chronic 3 - Desen. Expl. 2 - Eye Irrit. 2
Storage Class Code
4.1A - Other explosive hazardous materials
WGK
WGK 1
Flash Point (°F)
314.6 °F
Flash Point (°C)
157 °C
이미 열람한 고객
S. Ishizuka et al.
Pept. Sci., 37, 39-39 (2001)
Chemical synthesis of poly-?-glutamic acid by polycondensation of ?-glutamic acid dimer: Synthesis and reaction of poly-?-glutamic acid methyl ester
Sanda F, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 39(5), 732-741 (2001)
T. Miyazawa et al.
Tetrahedron Letters, 25, 771-771 (1984)
[A new method for synthesis of peptides: activation of the carboxyl group with dicyclohexylcarbodiimide using 1-hydroxybenzotriazoles as additives].
W König et al.
Chemische Berichte, 103(3), 788-798 (1970-01-01)
Adel Badria et al.
Journal of materials science. Materials in medicine, 29(11), 175-175 (2018-11-11)
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