A recent letter proposes a first-principle computation of the random close packing (RCP) density in spatial dimensions d = 2 and d = 3 [1]. This problem has a long history of such proposals [2-6], but none capture the full picture. Reference [1], in particular, once generalized to all d fails to describe the known behavior of jammed systems in d > 4, thus suggesting that the low-dimensional agreement is largely fortuitous.The crux of the proposed scheme is to evaluate the radial distribution function g(r, ϕ) at interparticle contact r = σ + for a (scaled) volume fraction ϕ = 2 d ϕ/d [7], and to construct an invariant g 0 = zσ/[d 2 ϕg(σ + , ϕ)] for z kissing contacts. Given the functional form g(r, ϕ), then ϕ and z can be evaluated at a known point to obtain an implicit expression, ϕ(z), that holds for other packings. The scheme uses crystal close packings (CCP), for which ϕ CCP and z CCP are known, as reference. It is then possible to solve for the marginal-stability condition, z RCP = 2d, which holds at jamming, to determine ϕ RCP . The only caveat identified in Ref. [1] is that one must choose a liquid structure expression that is defined from RCP to CCP. The two options suggestedthe Carnahan-Starling (CS) equation of state [8,9] and the Percus-Yevick (PY) closure relation-both fairly accurately describe the d = 3 liquid structure. (Another caveat is that these liquid state descriptions do not capture singular features of g(r, ϕ) at RCP [10].)Because PY fails to describe essential contact features of g(r, ϕ) in d > 3 liquids [11], the dimensional generalization here focuses on the CS form. Its one parameter, A(d), is known numerically for d = 2-13, and asymptotically scales as A(d) ∼ 3 (d+1)/2 2/(dπ) [11]. Equating the invariant in both the RCP and crystalline phases yields