Hydroxybenzotriazole

Hydroxybenzotriazole

Names
Preferred IUPAC name 1H-1,2,3-Benzotriazol-1-ol
Other names N-Hydroxybenzotriazole HOBt
Identifiers
CAS Number	2592-95-2  Y (monohydrate): 80029-43-2  Y
3D model (JSmol)	Interactive image
ChemSpider	68282  Y
ECHA InfoCard	100.018.173
EC Number	219-989-7 (monohydrate):602-929-2
PubChem CID	75771 (monohydrate): 2796029
UNII	A2T929DMG4  Y (monohydrate): S72K7GY45F  Y
CompTox Dashboard (EPA)	DTXSID3044627
InChI InChI=1S/C6H5N3O/c10-9-6-4-2-1-3-5(6)7-8-9/h1-4,10H Y Key: ASOKPJOREAFHNY-UHFFFAOYSA-N N InChI=1/C6H5N3O/c10-9-6-4-2-1-3-5(6)7-8-9/h1-4,10H Key: ASOKPJOREAFHNY-UHFFFAOYAP
SMILES n1nn(O)c2ccccc12
Properties
Chemical formula	C6H5N3O
Molar mass	135.1234 g mol−1 (anhydrous)
Melting point	156 to 159 °C (313 to 318 °F; 429 to 432 K) (decomposes)
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H203
Precautionary statements	P210, P230, P240, P250, P280, P370+P380, P372, P373, P401, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N  verify  (what is  YN ?) Infobox references

Hydroxybenzotriazole (abbreviated HOBt) is an organic compound that is a derivative of benzotriazole. It is a white crystalline powder, which as a commercial product contains some water (~11.7% wt as the HOBt monohydrate crystal). Anhydrous HOBt is explosive.

It is mainly used to suppress the racemization of single-enantiomer chiral molecules and to improve the efficiency of peptide synthesis.

Use in peptide synthesis

Automated peptide synthesis involves the condensation of the amino group of protected amino acids with the activated ester. HOBt is used to produce such activated esters which react with amines at ambient temperature to give amides. ^[1]

HOBt is also used for the synthesis of amides from carboxylic acids aside from amino acids. These substrates may not be convertible to the acyl chlorides. ^[2]

Safety

Due to reclassification as UN0508, a class 1.3C explosive, hydroxybenzotriazole and its monohydrate crystal are no longer allowed to be transported by sea or air as per 49CFR (USDOT hazardous materials regulations). However, UNECE draft proposal ECE/TRANS/WP.15/AC.1/HAR/2009/1 has been circulated to UN delegates and, if implemented, would amend current regulations thus allowing for the monohydrate crystal to be shipped under the less-stringent code of UN3474 as a class 4.1 desensitized explosive. HOBt was demonstrated to not exhibit dermal corrosion or irritation but did exhibit eye irritation. ^[3] The sensitization potential of HOBt was shown to be low (non-sensitizing at 1% in LLNA testing according to OECD 429 ^[4] ).

References

1. W. König, R. Geiger (1970). "Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1-Hydroxy-benzotriazolen". Chem. Ber. 103 (3): 788–798. doi:10.1002/cber.19701030319. PMID   5436656.
2. Myers, Andrew G.; Yang, Bryant H.; Chen, Hou (2000). "Transformation of Pseudoephedrine Amides Into Highly Enantiomerically Enriched Aldehydes, Alcohols, and Ketones". Organic Syntheses. Vol. 77. p. 29. doi:10.1002/0471264180.os077.04. ISBN   0471264229.
3. Graham, Jessica C.; Trejo-Martin, Alejandra; Chilton, Martyn L.; Kostal, Jakub; Bercu, Joel; Beutner, Gregory L.; Bruen, Uma S.; Dolan, David G.; Gomez, Stephen; Hillegass, Jedd; Nicolette, John; Schmitz, Matthew (2022-06-20). "An Evaluation of the Occupational Health Hazards of Peptide Couplers". Chemical Research in Toxicology. 35 (6): 1011–1022. doi:10.1021/acs.chemrestox.2c00031. ISSN   0893-228X. PMC   9214767 . PMID   35532537.
4. OECD (2010). Test No. 429: Skin Sensitisation: Local Lymph Node Assay. Paris: Organisation for Economic Co-operation and Development.