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Merck
CN

12110

Benzhydrylamine hydrochloride polymer-bound

100-200 mesh, extent of labeling: ~1.5 mmol/g amine loading

Synonym(s):

α-Aminodiphenylmethane hydrochloride polymer-bound, BHA-polystyrene, Polystyrene crosslinked with divinylbenzene, α-aminobenzylated hydrochloride

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About This Item

UNSPSC Code:
12352200
MDL number:
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extent of labeling

~1.5 mmol/g amine loading

matrix

crosslinked with 2% DVB

particle size

100-200 mesh

Other Notes

Support for the solid-phase synthesis of peptides; Preparation of the NBB-resin

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Automated solid phase synthesis of thymosin alpha 1.
S S Wang et al.
International journal of peptide and protein research, 15(1), 1-4 (1980-01-01)
D H Coy et al.
International journal of peptide and protein research, 15(1), 73-78 (1980-01-01)
The 28-residue sequence of porcine vasoactive peptide (VIP) was assembled on a benzhydrylamine resin support, cleaved by HF treatment, and purified by ion-exchange and partition chromatography. In addition to the normal criteria, the homogeneity of the final material, obtained in
E. Giralt et al.
Tetrahedron, 38, 1193-1193 (1982)
S A Gaehde et al.
International journal of peptide and protein research, 18(5), 451-458 (1981-11-01)
N-tert.-butoxycarbonyl-aminomethyl( alpha-phenyl)phenoxyacetic acid was synthesized and found to be suitable for use as a handle in the solid-phase synthesis of peptide alpha-carboxamides. This handle was prepared with an 82% yield when N-tert.-butoxycarbonyl-( rho-hydroxy)benzhydrylamine was treated with excess sodium iodoacetate under

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